Klaus Willecke - Publications

Affiliations: 
Bonn University, Bonn, Nordrhein-Westfalen, Germany 

308 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Bickert A, Kern P, van Uelft M, Herresthal S, Ulas T, Gutbrod K, Breiden B, Degen J, Sandhoff K, Schultze JL, Dörmann P, Hartmann D, Bauer R, Willecke K. Inactivation of ceramide synthase 2 catalytic activity in mice affects transcription of genes involved in lipid metabolism and cell division. Biochimica Et Biophysica Acta. 1863: 734-749. PMID 29653252 DOI: 10.1016/J.Bbalip.2018.04.006  0.374
2018 Ströh S, Puller C, Swirski S, Hölzel MB, van der Linde LIS, Segelken J, Schultz K, Block C, Monyer H, Willecke K, Weiler R, Greschner M, Janssen-Bienhold U, Dedek K. Eliminating Glutamatergic Input onto Horizontal Cells Changes the Dynamic Range and Receptive Field Organization of Mouse Retinal Ganglion Cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29352045 DOI: 10.1523/Jneurosci.0141-17.2018  0.356
2017 Zhang J, Griemsmann S, Wu Z, Dobrowolski R, Willecke K, Theis M, Steinhäuser C, Bedner P. Connexin43, but not connexin30, contributes to adult neurogenesis in the dentate gyrus. Brain Research Bulletin. PMID 28689039 DOI: 10.1016/j.brainresbull.2017.07.001  0.481
2017 Press E, Alaga KC, Barr K, Shao Q, Bosen F, Willecke K, Laird DW. Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice. Cell Death & Disease. 8: e2845. PMID 28569788 DOI: 10.1038/Cddis.2017.234  0.37
2017 Lall VK, Bruce G, Voytenko L, Drinkhill M, Wellershaus K, Willecke K, Deuchars J, Deuchars SA. Physiologic regulation of heart rate and blood pressure involves connexin 36-containing gap junctions. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 28533325 DOI: 10.1096/Fj.201600919Rr  0.425
2016 Wörsdörfer P, Bosen F, Gebhardt M, Russ N, Zimmermann K, Komla Kessie D, Sekaran T, Egert A, Ergün S, Schorle H, Pfeifer A, Edenhofer F, Willecke K. Abrogation Of Gap Junctional Communication In Es Cells Results In A Disruption Of Primitive Endoderm Formation In Embryoid Bodies. Stem Cells (Dayton, Ohio). PMID 27870307 DOI: 10.1002/stem.2545  0.44
2016 Brüggen B, Kremser C, Bickert A, Ebel P, Vom Dorp K, Schultz K, Dörmann P, Willecke K, Dedek K. Defective ceramide synthases in mice cause reduced amplitudes in electroretinograms and altered sphingolipid composition in retina and cornea. The European Journal of Neuroscience. PMID 27086873 DOI: 10.1111/ejn.13260  0.41
2016 Cea LA, Puebla C, Cisterna BA, Escamilla R, Vargas AA, Frank M, Martínez-Montero P, Prior C, Molano J, Esteban-Rodríguez I, Pascual I, Gallano P, Lorenzo G, Pian H, Barrio LC, ... Willecke K, et al. Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis. Cellular and Molecular Life Sciences : Cmls. PMID 26803842 DOI: 10.1007/s00018-016-2132-2  0.377
2016 García IE, Bosen F, Mujica P, Pupo A, Flores-Muñoz C, Jara O, González C, Willecke K, Martínez AD. From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome. The Journal of Investigative Dermatology. PMID 26777423 DOI: 10.1016/J.Jid.2015.11.017  0.32
2015 Bosen F, Celli A, Crumrine D, vom Dorp K, Ebel P, Jastrow H, Dörmann P, Winterhager E, Mauro T, Willecke K. Altered epidermal lipid processing and calcium distribution in the KID syndrome mouse model Cx26S17F. Febs Letters. 589: 1904-10. PMID 26070424 DOI: 10.1016/J.Febslet.2015.05.047  0.371
2015 Eberle M, Ebel P, Mayer CA, Barthelmes J, Tafferner N, Ferreiros N, Ulshöfer T, Henke M, Foerch C, de Bazo AM, Grösch S, Geisslinger G, Willecke K, Schiffmann S. Exacerbation of experimental autoimmune encephalomyelitis in ceramide synthase 6 knockout mice is associated with enhanced activation/migration of neutrophils. Immunology and Cell Biology. PMID 25833068 DOI: 10.1038/icb.2015.47  0.313
2015 Bickert A, Ginkel C, Kol M, vom Dorp K, Jastrow H, Degen J, Jacobs RL, Vance DE, Winterhager E, Jiang XC, Dörmann P, Somerharju P, Holthuis JC, Willecke K. Functional characterization of enzymes catalyzing ceramide phosphoethanolamine biosynthesis in mice. Journal of Lipid Research. 56: 821-35. PMID 25667419 DOI: 10.1194/Jlr.M055269  0.359
2015 Lübkemeier I, Bosen F, Kim JS, Sasse P, Malan D, Fleischmann BK, Willecke K. Human Connexin43E42K mutation from a sudden infant death victim leads to impaired ventricular activation and neonatal death in mice. Circulation. Cardiovascular Genetics. 8: 21-9. PMID 25504652 DOI: 10.1161/CIRCGENETICS.114.000793  0.332
2014 Eberle M, Ebel P, Wegner MS, Männich J, Tafferner N, Ferreiros N, Birod K, Schreiber Y, Krishnamoorthy G, Willecke K, Geisslinger G, Grösch S, Schiffmann S. Regulation of ceramide synthase 6 in a spontaneous experimental autoimmune encephalomyelitis model is sex dependent. Biochemical Pharmacology. 92: 326-35. PMID 25173988 DOI: 10.1016/j.bcp.2014.08.016  0.332
2014 Agullo-Pascual E, Lin X, Leo-Macias A, Zhang M, Liang FX, Li Z, Pfenniger A, Lübkemeier I, Keegan S, Fenyö D, Willecke K, Rothenberg E, Delmar M. Super-resolution imaging reveals that loss of the C-terminus of connexin43 limits microtubule plus-end capture and NaV1.5 localization at the intercalated disc. Cardiovascular Research. 104: 371-81. PMID 25139742 DOI: 10.1093/cvr/cvu195  0.373
2014 Griemsmann S, Höft SP, Bedner P, Zhang J, von Staden E, Beinhauer A, Degen J, Dublin P, Cope DW, Richter N, Crunelli V, Jabs R, Willecke K, Theis M, Seifert G, et al. Characterization of Panglial Gap Junction Networks in the Thalamus, Neocortex, and Hippocampus Reveals a Unique Population of Glial Cells. Cerebral Cortex (New York, N.Y. : 1991). PMID 25037920 DOI: 10.1093/Cercor/Bhu157  0.448
2014 Ebel P, Imgrund S, Vom Dorp K, Hofmann K, Maier H, Drake H, Degen J, Dörmann P, Eckhardt M, Franz T, Willecke K. Ceramide synthase 4 deficiency in mice causes lipid alterations in sebum and results in alopecia. The Biochemical Journal. 461: 147-58. PMID 24738593 DOI: 10.1042/BJ20131242  0.403
2014 Bosen F, Schütz M, Beinhauer A, Strenzke N, Franz T, Willecke K. The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in mice. Febs Letters. 588: 1795-801. PMID 24685692 DOI: 10.1016/J.Febslet.2014.03.040  0.382
2013 Ströh S, Sonntag S, Janssen-Bienhold U, Schultz K, Cimiotti K, Weiler R, Willecke K, Dedek K. Cell-specific cre recombinase expression allows selective ablation of glutamate receptors from mouse horizontal cells. Plos One. 8: e83076. PMID 24349437 DOI: 10.1371/Journal.Pone.0083076  0.46
2013 Lübkemeier I, Andrié R, Lickfett L, Bosen F, Stöckigt F, Dobrowolski R, Draffehn AM, Fregeac J, Schultze JL, Bukauskas FF, Schrickel JW, Willecke K. The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice. Journal of Molecular and Cellular Cardiology. 65: 19-32. PMID 24060583 DOI: 10.1016/J.Yjmcc.2013.09.008  0.426
2013 Cea LA, Cisterna BA, Puebla C, Frank M, Figueroa XF, Cardozo C, Willecke K, Latorre R, Sáez JC. De novo expression of connexin hemichannels in denervated fast skeletal muscles leads to atrophy. Proceedings of the National Academy of Sciences of the United States of America. 110: 16229-34. PMID 24043768 DOI: 10.1073/Pnas.1312331110  0.355
2013 Ebel P, Vom Dorp K, Petrasch-Parwez E, Zlomuzica A, Kinugawa K, Mariani J, Minich D, Ginkel C, Welcker J, Degen J, Eckhardt M, Dere E, Dörmann P, Willecke K. Inactivation of ceramide synthase 6 in mice results in an altered sphingolipid metabolism and behavioral abnormalities. The Journal of Biological Chemistry. 288: 21433-47. PMID 23760501 DOI: 10.1074/Jbc.M113.479907  0.429
2013 May D, Tress O, Seifert G, Willecke K. Connexin47 protein phosphorylation and stability in oligodendrocytes depend on expression of Connexin43 protein in astrocytes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 7985-96. PMID 23637189 DOI: 10.1523/JNEUROSCI.5874-12.2013  0.487
2013 Kremser C, Klemm AL, van Uelft M, Imgrund S, Ginkel C, Hartmann D, Willecke K. Cell-type-specific expression pattern of ceramide synthase 2 protein in mouse tissues. Histochemistry and Cell Biology. 140: 533-47. PMID 23591958 DOI: 10.1007/s00418-013-1091-z  0.495
2013 Lübkemeier I, Requardt RP, Lin X, Sasse P, Andrié R, Schrickel JW, Chkourko H, Bukauskas FF, Kim JS, Frank M, Malan D, Zhang J, Wirth A, Dobrowolski R, Mohler PJ, ... ... Willecke K, et al. Deletion of the last five C-terminal amino acid residues of connexin43 leads to lethal ventricular arrhythmias in mice without affecting coupling via gap junction channels. Basic Research in Cardiology. 108: 348. PMID 23558439 DOI: 10.1007/S00395-013-0348-Y  0.463
2013 Chapman RJ, Lall VK, Maxeiner S, Willecke K, Deuchars J, King AE. Localization of neurones expressing the gap junction protein Connexin45 within the adult spinal dorsal horn: a study using Cx45-eGFP reporter mice. Brain Structure & Function. 218: 751-65. PMID 22638825 DOI: 10.1007/S00429-012-0426-1  0.685
2013 Agullo-Pascual E, Lin X, Pfenniger A, Lübkemeier I, Willecke K, Rothenberg E, Delmar M. A Novel Noncanonical Role of Cx43 in the Heart: Ensuring the Arrival of Nav1.5 to the Intercalated Disk Heart Rhythm. 10: 1742. DOI: 10.1016/J.HRTHM.2013.09.016  0.402
2012 Khodosevich K, Zuccotti A, Kreuzberg MM, Le Magueresse C, Frank M, Willecke K, Monyer H. Connexin45 modulates the proliferation of transit-amplifying precursor cells in the mouse subventricular zone. Proceedings of the National Academy of Sciences of the United States of America. 109: 20107-12. PMID 23169657 DOI: 10.1073/Pnas.1217103109  0.775
2012 Jobs A, Schmidt K, Schmidt VJ, Lübkemeier I, van Veen TA, Kurtz A, Willecke K, de Wit C. Defective Cx40 maintains Cx37 expression but intact Cx40 is crucial for conducted dilations irrespective of hypertension. Hypertension. 60: 1422-9. PMID 23090768 DOI: 10.1161/HYPERTENSIONAHA.112.201194  0.471
2012 Ginkel C, Hartmann D, vom Dorp K, Zlomuzica A, Farwanah H, Eckhardt M, Sandhoff R, Degen J, Rabionet M, Dere E, Dörmann P, Sandhoff K, Willecke K. Ablation of neuronal ceramide synthase 1 in mice decreases ganglioside levels and expression of myelin-associated glycoprotein in oligodendrocytes. The Journal of Biological Chemistry. 287: 41888-902. PMID 23074226 DOI: 10.1074/Jbc.M112.413500  0.449
2012 Frank M, Wirth A, Andrié RP, Kreuzberg MM, Dobrowolski R, Seifert G, Offermanns S, Nickenig G, Willecke K, Schrickel JW. Connexin45 provides optimal atrioventricular nodal conduction in the adult mouse heart. Circulation Research. 111: 1528-38. PMID 22982984 DOI: 10.1161/CIRCRESAHA.112.270561  0.796
2012 Degen J, Dublin P, Zhang J, Dobrowolski R, Jokwitz M, Karram K, Trotter J, Jabs R, Willecke K, Steinhäuser C, Theis M. Dual reporter approaches for identification of Cre efficacy and astrocyte heterogeneity. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 26: 4576-83. PMID 22859373 DOI: 10.1096/fj.12-207183  0.432
2012 Sonntag S, Dedek K, Dorgau B, Schultz K, Schmidt KF, Cimiotti K, Weiler R, Löwel S, Willecke K, Janssen-Bienhold U. Ablation of retinal horizontal cells from adult mice leads to rod degeneration and remodeling in the outer retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 10713-24. PMID 22855819 DOI: 10.1523/Jneurosci.0442-12.2012  0.359
2012 Schmidt VJ, Jobs A, von Maltzahn J, Wörsdörfer P, Willecke K, de Wit C. Connexin45 is expressed in vascular smooth muscle but its function remains elusive. Plos One. 7: e42287. PMID 22848755 DOI: 10.1371/journal.pone.0042287  0.482
2012 Zlomuzica A, Tress O, Binder S, Rovira C, Willecke K, Dere E. Changes in object recognition and anxiety-like behaviour in mice expressing a Cx47 mutation that causes Pelizaeus-Merzbacher-like disease. Developmental Neuroscience. 34: 277-87. PMID 22832166 DOI: 10.1159/000339305  0.407
2012 Tress O, Maglione M, May D, Pivneva T, Richter N, Seyfarth J, Binder S, Zlomuzica A, Seifert G, Theis M, Dere E, Kettenmann H, Willecke K. Panglial gap junctional communication is essential for maintenance of myelin in the CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 7499-518. PMID 22649229 DOI: 10.1523/Jneurosci.0392-12.2012  0.435
2012 Jennemann R, Rabionet M, Gorgas K, Epstein S, Dalpke A, Rothermel U, Bayerle A, van der Hoeven F, Imgrund S, Kirsch J, Nickel W, Willecke K, Riezman H, Gröne HJ, Sandhoff R. Loss of ceramide synthase 3 causes lethal skin barrier disruption. Human Molecular Genetics. 21: 586-608. PMID 22038835 DOI: 10.1093/Hmg/Ddr494  0.342
2012 Zlomuzica A, Viggiano D, Degen J, Binder S, Ruocco LA, Sadile AG, Willecke K, Huston JP, Dere E. Behavioral alterations and changes in Ca/calmodulin kinase II levels in the striatum of connexin36 deficient mice. Behavioural Brain Research. 226: 293-300. PMID 21889545 DOI: 10.1016/j.bbr.2011.08.028  0.404
2011 Bao M, Kanter EM, Huang RY, Maxeiner S, Frank M, Zhang Y, Schuessler RB, Smith TW, Townsend RR, Rohrs HW, Berthoud VM, Willecke K, Laing JG, Yamada KA. Residual Cx45 and its relationship to Cx43 in murine ventricular myocardium. Channels (Austin, Tex.). 5: 489-99. PMID 22127232 DOI: 10.4161/chan.5.6.18523  0.689
2011 Lynn BD, Tress O, May D, Willecke K, Nagy JI. Ablation of connexin30 in transgenic mice alters expression patterns of connexin26 and connexin32 in glial cells and leptomeninges. The European Journal of Neuroscience. 34: 1783-93. PMID 22098503 DOI: 10.1111/j.1460-9568.2011.07900.x  0.486
2011 Degen J, Schütz M, Dicke N, Strenzke N, Jokwitz M, Moser T, Willecke K. Connexin32 can restore hearing in connexin26 deficient mice. European Journal of Cell Biology. 90: 817-24. PMID 21813206 DOI: 10.1016/J.Ejcb.2011.05.001  0.464
2011 Dicke N, Pielensticker N, Degen J, Hecker J, Tress O, Bald T, Gellhaus A, Winterhager E, Willecke K. Peripheral lymphangiogenesis in mice depends on ectodermal connexin-26 (Gjb2). Journal of Cell Science. 124: 2806-15. PMID 21807945 DOI: 10.1242/jcs.084186  0.483
2011 Tress O, Maglione M, Zlomuzica A, May D, Dicke N, Degen J, Dere E, Kettenmann H, Hartmann D, Willecke K. Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans. Plos Genetics. 7: e1002146. PMID 21750683 DOI: 10.1371/Journal.Pgen.1002146  0.49
2011 Blankenship AG, Hamby AM, Firl A, Vyas S, Maxeiner S, Willecke K, Feller MB. The role of neuronal connexins 36 and 45 in shaping spontaneous firing patterns in the developing retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 9998-10008. PMID 21734291 DOI: 10.1523/Jneurosci.5640-10.2011  0.667
2011 Nagy JI, Lynn BD, Tress O, Willecke K, Rash JE. Connexin26 expression in brain parenchymal cells demonstrated by targeted connexin ablation in transgenic mice. The European Journal of Neuroscience. 34: 263-71. PMID 21714813 DOI: 10.1111/j.1460-9568.2011.07741.x  0.492
2011 Lübkemeier I, Machura K, Kurtz L, Neubauer B, Dobrowolski R, Schweda F, Wagner C, Willecke K, Kurtz A. The connexin 40 A96S mutation causes renin-dependent hypertension. Journal of the American Society of Nephrology : Jasn. 22: 1031-40. PMID 21597036 DOI: 10.1681/ASN.2010101047  0.349
2011 Campbell RE, Ducret E, Porteous R, Liu X, Herde MK, Wellerhaus K, Sonntag S, Willecke K, Herbison AE. Gap junctions between neuronal inputs but not gonadotropin-releasing hormone neurons control estrous cycles in the mouse. Endocrinology. 152: 2290-301. PMID 21447638 DOI: 10.1210/En.2010-1311  0.384
2011 von Maltzahn J, Wulf V, Matern G, Willecke K. Connexin39 deficient mice display accelerated myogenesis and regeneration of skeletal muscle. Experimental Cell Research. 317: 1169-78. PMID 21272575 DOI: 10.1016/j.yexcr.2011.01.017  0.417
2011 Gosejacob D, Dublin P, Bedner P, Hüttmann K, Zhang J, Tress O, Willecke K, Pfrieger F, Steinhäuser C, Theis M. Role of astroglial connexin30 in hippocampal gap junction coupling. Glia. 59: 511-9. PMID 21264956 DOI: 10.1002/glia.21120  0.463
2011 Kurt B, Kurtz L, Sequeira-Lopez ML, Gomez RA, Willecke K, Wagner C, Kurtz A. Reciprocal expression of connexin 40 and 45 during phenotypical changes in renin-secreting cells. American Journal of Physiology. Renal Physiology. 300: F743-8. PMID 21209011 DOI: 10.1152/ajprenal.00647.2010  0.501
2011 Hilgen G, von Maltzahn J, Willecke K, Weiler R, Dedek K. Subcellular distribution of connexin45 in OFF bipolar cells of the mouse retina. The Journal of Comparative Neurology. 519: 433-50. PMID 21192077 DOI: 10.1002/Cne.22526  0.46
2011 Schütz M, Auth T, Gehrt A, Bosen F, Körber I, Strenzke N, Moser T, Willecke K. The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome. Human Molecular Genetics. 20: 28-39. PMID 20926451 DOI: 10.1093/Hmg/Ddq429  0.426
2010 Söhl G, Joussen A, Kociok N, Willecke K. Expression of connexin genes in the human retina. Bmc Ophthalmology. 10: 27. PMID 20979653 DOI: 10.1186/1471-2415-10-27  0.453
2010 Tykocinski LO, Sinemus A, Rezavandy E, Weiland Y, Baddeley D, Cremer C, Sonntag S, Willecke K, Derbinski J, Kyewski B. Epigenetic regulation of promiscuous gene expression in thymic medullary epithelial cells. Proceedings of the National Academy of Sciences of the United States of America. 107: 19426-31. PMID 20966351 DOI: 10.1073/pnas.1009265107  0.388
2010 Frank M, Eiberger B, Janssen-Bienhold U, de Sevilla Müller LP, Tjarks A, Kim JS, Maschke S, Dobrowolski R, Sasse P, Weiler R, Fleischmann BK, Willecke K. Neuronal connexin-36 can functionally replace connexin-45 in mouse retina but not in the developing heart. Journal of Cell Science. 123: 3605-15. PMID 20930146 DOI: 10.1242/Jcs.068668  0.824
2010 Schütz M, Scimemi P, Majumder P, De Siati RD, Crispino G, Rodriguez L, Bortolozzi M, Santarelli R, Seydel A, Sonntag S, Ingham N, Steel KP, Willecke K, Mammano F. The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice. Human Molecular Genetics. 19: 4759-73. PMID 20858605 DOI: 10.1093/Hmg/Ddq402  0.478
2010 Parenti R, Cicirata F, Zappalà A, Catania A, La Delia F, Cicirata V, Tress O, Willecke K. Dynamic expression of Cx47 in mouse brain development and in the cuprizone model of myelin plasticity. Glia. 58: 1594-609. PMID 20578039 DOI: 10.1002/glia.21032  0.407
2010 Müller LP, Dedek K, Janssen-Bienhold U, Meyer A, Kreuzberg MM, Lorenz S, Willecke K, Weiler R. Expression and modulation of connexin 30.2, a novel gap junction protein in the mouse retina. Visual Neuroscience. 27: 91-101. PMID 20537217 DOI: 10.1017/S0952523810000131  0.799
2010 Zlomuzica A, Reichinnek S, Maxeiner S, Both M, May E, Wörsdörfer P, Draguhn A, Willecke K, Dere E. Deletion of connexin45 in mouse neurons disrupts one-trial object recognition and alters kainate-induced gamma-oscillations in the hippocampus. Physiology & Behavior. 101: 245-53. PMID 20471991 DOI: 10.1016/J.Physbeh.2010.05.007  0.673
2010 Maglione M, Tress O, Haas B, Karram K, Trotter J, Willecke K, Kettenmann H. Oligodendrocytes in mouse corpus callosum are coupled via gap junction channels formed by connexin47 and connexin32. Glia. 58: 1104-17. PMID 20468052 DOI: 10.1002/Glia.20991  0.465
2010 Kozoriz MG, Bechberger JF, Bechberger GR, Suen MW, Moreno AP, Maass K, Willecke K, Naus CC. The connexin43 C-terminal region mediates neuroprotection during stroke. Journal of Neuropathology and Experimental Neurology. 69: 196-206. PMID 20084014 DOI: 10.1097/NEN.0b013e3181cd44df  0.417
2010 Gros D, Théveniau-Ruissy M, Bernard M, Calmels T, Kober F, Söhl G, Willecke K, Nargeot J, Jongsma HJ, Mangoni ME. Connexin 30 is expressed in the mouse sino-atrial node and modulates heart rate. Cardiovascular Research. 85: 45-55. PMID 19679680 DOI: 10.1093/Cvr/Cvp280  0.456
2009 Imgrund S, Hartmann D, Farwanah H, Eckhardt M, Sandhoff R, Degen J, Gieselmann V, Sandhoff K, Willecke K. Adult ceramide synthase 2 (CERS2)-deficient mice exhibit myelin sheath defects, cerebellar degeneration, and hepatocarcinomas. The Journal of Biological Chemistry. 284: 33549-60. PMID 19801672 DOI: 10.1074/Jbc.M109.031971  0.396
2009 Dedek K, Breuninger T, de Sevilla Müller LP, Maxeiner S, Schultz K, Janssen-Bienhold U, Willecke K, Euler T, Weiler R. A novel type of interplexiform amacrine cell in the mouse retina. The European Journal of Neuroscience. 30: 217-28. PMID 19614986 DOI: 10.1111/J.1460-9568.2009.06808.X  0.656
2009 Kunze A, Congreso MR, Hartmann C, Wallraff-Beck A, Hüttmann K, Bedner P, Requardt R, Seifert G, Redecker C, Willecke K, Hofmann A, Pfeifer A, Theis M, Steinhäuser C. Connexin expression by radial glia-like cells is required for neurogenesis in the adult dentate gyrus. Proceedings of the National Academy of Sciences of the United States of America. 106: 11336-41. PMID 19549869 DOI: 10.1073/pnas.0813160106  0.485
2009 Sipos A, Vargas SL, Toma I, Hanner F, Willecke K, Peti-Peterdi J. Connexin 30 deficiency impairs renal tubular ATP release and pressure natriuresis. Journal of the American Society of Nephrology : Jasn. 20: 1724-32. PMID 19478095 DOI: 10.1681/Asn.2008101099  0.398
2009 von Maltzahn J, Kreuzberg MM, Matern G, Euwens C, Höher T, Wörsdörfer P, Willecke K. C-terminal tagging with eGFP yields new insights into expression of connexin45 but prevents rescue of embryonic lethal connexin45-deficient mice. European Journal of Cell Biology. 88: 481-94. PMID 19473725 DOI: 10.1016/j.ejcb.2009.04.004  0.826
2009 Dobrowolski R, Hertig G, Lechner H, Wörsdörfer P, Wulf V, Dicke N, Eckert D, Bauer R, Schorle H, Willecke K. Loss of connexin43-mediated gap junctional coupling in the mesenchyme of limb buds leads to altered expression of morphogens in mice. Human Molecular Genetics. 18: 2899-911. PMID 19439426 DOI: 10.1093/hmg/ddp227  0.467
2009 Palacios-Prado N, Sonntag S, Skeberdis VA, Willecke K, Bukauskas FF. Gating, permselectivity and pH-dependent modulation of channels formed by connexin57, a major connexin of horizontal cells in the mouse retina. The Journal of Physiology. 587: 3251-69. PMID 19433576 DOI: 10.1113/Jphysiol.2009.171496  0.422
2009 Schrickel JW, Kreuzberg MM, Ghanem A, Kim JS, Linhart M, Andrié R, Tiemann K, Nickenig G, Lewalter T, Willecke K. Normal impulse propagation in the atrioventricular conduction system of Cx30.2/Cx40 double deficient mice. Journal of Molecular and Cellular Cardiology. 46: 644-52. PMID 19248787 DOI: 10.1016/j.yjmcc.2009.02.012  0.789
2009 Cina C, Maass K, Theis M, Willecke K, Bechberger JF, Naus CC. Involvement of the cytoplasmic C-terminal domain of connexin43 in neuronal migration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 2009-21. PMID 19228955 DOI: 10.1523/JNEUROSCI.5025-08.2009  0.42
2009 Auth T, Schlüter S, Urschel S, Kussmann P, Sonntag S, Höher T, Kreuzberg MM, Dobrowolski R, Willecke K. The TSG101 protein binds to connexins and is involved in connexin degradation. Experimental Cell Research. 315: 1053-62. PMID 19210987 DOI: 10.1016/j.yexcr.2008.12.025  0.772
2009 Janssen-Bienhold U, Trümpler J, Hilgen G, Schultz K, Müller LP, Sonntag S, Dedek K, Dirks P, Willecke K, Weiler R. Connexin57 is expressed in dendro-dendritic and axo-axonal gap junctions of mouse horizontal cells and its distribution is modulated by light. The Journal of Comparative Neurology. 513: 363-74. PMID 19177557 DOI: 10.1002/Cne.21965  0.427
2009 Kreuzberg MM, Liebermann M, Segschneider S, Dobrowolski R, Dobrzynski H, Kaba R, Rowlinson G, Dupont E, Severs NJ, Willecke K. Human connexin31.9, unlike its orthologous protein connexin30.2 in the mouse, is not detectable in the human cardiac conduction system. Journal of Molecular and Cellular Cardiology. 46: 553-9. PMID 19168070 DOI: 10.1016/j.yjmcc.2008.12.007  0.781
2009 Trovato-Salinaro A, Belluardo N, Frinchi M, von Maltzahn J, Willecke K, Condorelli DF, Mudò G. Regulation of connexin gene expression during skeletal muscle regeneration in the adult rat. American Journal of Physiology. Cell Physiology. 296: C593-606. PMID 19129462 DOI: 10.1152/ajpcell.00458.2008  0.369
2009 Requardt RP, Kaczmarczyk L, Dublin P, Wallraff-Beck A, Mikeska T, Degen J, Waha A, Steinhäuser C, Willecke K, Theis M. Quality control of astrocyte-directed Cre transgenic mice: the benefits of a direct link between loss of gene expression and reporter activation. Glia. 57: 680-92. PMID 18942753 DOI: 10.1002/glia.20796  0.42
2009 Sonntag S, Söhl G, Dobrowolski R, Zhang J, Theis M, Winterhager E, Bukauskas FF, Willecke K. Mouse lens connexin23 (Gje1) does not form functional gap junction channels but causes enhanced ATP release from HeLa cells. European Journal of Cell Biology. 88: 65-77. PMID 18849090 DOI: 10.1016/J.Ejcb.2008.08.004  0.466
2009 Dobrowolski R, Willecke K. Connexin-caused genetic diseases and corresponding mouse models. Antioxidants & Redox Signaling. 11: 283-95. PMID 18831677 DOI: 10.1089/ars.2008.2128  0.348
2008 Tanaka M, Yamaguchi K, Tatsukawa T, Theis M, Willecke K, Itohara S. Connexin43 and bergmann glial gap junctions in cerebellar function. Frontiers in Neuroscience. 2: 225-33. PMID 19225596 DOI: 10.3389/neuro.01.038.2008  0.479
2008 Alev C, Urschel S, Sonntag S, Zoidl G, Fort AG, Höher T, Matsubara M, Willecke K, Spray DC, Dermietzel R. The neuronal connexin36 interacts with and is phosphorylated by CaMKII in a way similar to CaMKII interaction with glutamate receptors. Proceedings of the National Academy of Sciences of the United States of America. 105: 20964-9. PMID 19095792 DOI: 10.1073/pnas.0805408105  0.329
2008 Rouach N, Koulakoff A, Abudara V, Willecke K, Giaume C. Astroglial metabolic networks sustain hippocampal synaptic transmission. Science (New York, N.Y.). 322: 1551-5. PMID 19056987 DOI: 10.1126/science.1164022  0.304
2008 Li X, Penes M, Odermatt B, Willecke K, Nagy JI. Ablation of Cx47 in transgenic mice leads to the loss of MUPP1, ZONAB and multiple connexins at oligodendrocyte-astrocyte gap junctions. The European Journal of Neuroscience. 28: 1503-17. PMID 18973575 DOI: 10.1111/J.1460-9568.2008.06431.X  0.637
2008 Tanaka M, Yamaguchi K, Tatsukawa T, Nishioka C, Nishiyama H, Theis M, Willecke K, Itohara S. Lack of Connexin43-mediated bergmann glial gap junctional coupling does not affect cerebellar long-term depression, motor coordination, or eyeblink conditioning. Frontiers in Behavioral Neuroscience. 2: 1. PMID 18958191 DOI: 10.3389/neuro.08.001.2008  0.48
2008 Hanner F, Schnichels M, Zheng-Fischhöfer Q, Yang LE, Toma I, Willecke K, McDonough AA, Peti-Peterdi J. Connexin 30.3 is expressed in the kidney but not regulated by dietary salt or high blood pressure. Cell Communication & Adhesion. 15: 219-30. PMID 18649192 DOI: 10.1080/15419060802013836  0.411
2008 Elzarrad MK, Haroon A, Willecke K, Dobrowolski R, Gillespie MN, Al-Mehdi AB. Connexin-43 upregulation in micrometastases and tumor vasculature and its role in tumor cell attachment to pulmonary endothelium. Bmc Medicine. 6: 20. PMID 18647409 DOI: 10.1186/1741-7015-6-20  0.334
2008 Hanner F, von Maltzahn J, Maxeiner S, Toma I, Sipos A, Krüger O, Willecke K, Peti-Peterdi J. Connexin45 is expressed in the juxtaglomerular apparatus and is involved in the regulation of renin secretion and blood pressure. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 295: R371-80. PMID 18579650 DOI: 10.1152/Ajpregu.00468.2007  0.717
2008 Van Der Giessen RS, Koekkoek SK, van Dorp S, De Gruijl JR, Cupido A, Khosrovani S, Dortland B, Wellershaus K, Degen J, Deuchars J, Fuchs EC, Monyer H, Willecke K, De Jeu MT, De Zeeuw CI. Role of olivary electrical coupling in cerebellar motor learning. Neuron. 58: 599-612. PMID 18498740 DOI: 10.1016/J.Neuron.2008.03.016  0.358
2008 Dere E, Zheng-Fischhöfer Q, Viggiano D, Gironi Carnevale UA, Ruocco LA, Zlomuzica A, Schnichels M, Willecke K, Huston JP, Sadile AG. Connexin31.1 deficiency in the mouse impairs object memory and modulates open-field exploration, acetylcholine esterase levels in the striatum, and cAMP response element-binding protein levels in the striatum and piriform cortex. Neuroscience. 153: 396-405. PMID 18384970 DOI: 10.1016/j.neuroscience.2008.01.077  0.381
2008 Dedek K, Pandarinath C, Alam NM, Wellershaus K, Schubert T, Willecke K, Prusky GT, Weiler R, Nirenberg S. Ganglion cell adaptability: does the coupling of horizontal cells play a role? Plos One. 3: e1714. PMID 18320035 DOI: 10.1371/Journal.Pone.0001714  0.388
2008 Wellershaus K, Degen J, Deuchars J, Theis M, Charollais A, Caille D, Gauthier B, Janssen-Bienhold U, Sonntag S, Herrera P, Meda P, Willecke K. A new conditional mouse mutant reveals specific expression and functions of connexin36 in neurons and pancreatic beta-cells. Experimental Cell Research. 314: 997-1012. PMID 18258229 DOI: 10.1016/J.Yexcr.2007.12.024  0.485
2008 Lin JH, Lou N, Kang N, Takano T, Hu F, Han X, Xu Q, Lovatt D, Torres A, Willecke K, Yang J, Kang J, Nedergaard M. A central role of connexin 43 in hypoxic preconditioning. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 681-95. PMID 18199768 DOI: 10.1523/JNEUROSCI.3827-07.2008  0.39
2008 Wörsdörfer P, Maxeiner S, Markopoulos C, Kirfel G, Wulf V, Auth T, Urschel S, von Maltzahn J, Willecke K. Connexin expression and functional analysis of gap junctional communication in mouse embryonic stem cells. Stem Cells (Dayton, Ohio). 26: 431-9. PMID 18055446 DOI: 10.1634/stemcells.2007-0482  0.713
2008 Dobrowolski R, Sasse P, Schrickel JW, Watkins M, Kim JS, Rackauskas M, Troatz C, Ghanem A, Tiemann K, Degen J, Bukauskas FF, Civitelli R, Lewalter T, Fleischmann BK, Willecke K. The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans. Human Molecular Genetics. 17: 539-54. PMID 18003637 DOI: 10.1093/Hmg/Ddm329  0.422
2008 Kreuzberg MM, Deuchars J, Weiss E, Schober A, Sonntag S, Wellershaus K, Draguhn A, Willecke K. Expression of connexin30.2 in interneurons of the central nervous system in the mouse. Molecular and Cellular Neurosciences. 37: 119-34. PMID 17942321 DOI: 10.1016/J.Mcn.2007.09.003  0.802
2007 Roell W, Lewalter T, Sasse P, Tallini YN, Choi BR, Breitbach M, Doran R, Becher UM, Hwang SM, Bostani T, von Maltzahn J, Hofmann A, Reining S, Eiberger B, Gabris B, ... ... Willecke K, et al. Engraftment of connexin 43-expressing cells prevents post-infarct arrhythmia. Nature. 450: 819-24. PMID 18064002 DOI: 10.1038/Nature06321  0.796
2007 Zheng-Fischhöfer Q, Kibschull M, Schnichels M, Kretz M, Petrasch-Parwez E, Strotmann J, Reucher H, Lynn BD, Nagy JI, Lye SJ, Winterhager E, Willecke K. Characterization of connexin31.1-deficient mice reveals impaired placental development. Developmental Biology. 312: 258-71. PMID 17961533 DOI: 10.1016/j.ydbio.2007.09.025  0.449
2007 Maass K, Shibayama J, Chase SE, Willecke K, Delmar M. C-terminal truncation of connexin43 changes number, size, and localization of cardiac gap junction plaques. Circulation Research. 101: 1283-91. PMID 17932323 DOI: 10.1161/CIRCRESAHA.107.162818  0.47
2007 Zheng-Fischhöfer Q, Schnichels M, Dere E, Strotmann J, Loscher N, McCulloch F, Kretz M, Degen J, Reucher H, Nagy JI, Peti-Peterdi J, Huston JP, Breer H, Willecke K. Characterization of connexin30.3-deficient mice suggests a possible role of connexin30.3 in olfaction. European Journal of Cell Biology. 86: 683-700. PMID 17728008 DOI: 10.1016/J.Ejcb.2007.01.005  0.428
2007 Qu Y, Tang W, Dahlke I, Ding D, Salvi R, Söhl G, Willecke K, Chen P, Lin X. Analysis of connexin subunits required for the survival of vestibular hair cells. The Journal of Comparative Neurology. 504: 499-507. PMID 17702002 DOI: 10.1002/Cne.21459  0.488
2007 Dobrowolski R, Sommershof A, Willecke K. Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels. The Journal of Membrane Biology. 219: 9-17. PMID 17687502 DOI: 10.1007/s00232-007-9055-7  0.368
2007 Ciolofan C, Lynn BD, Wellershaus K, Willecke K, Nagy JI. Spatial relationships of connexin36, connexin57 and zonula occludens-1 in the outer plexiform layer of mouse retina. Neuroscience. 148: 473-88. PMID 17681699 DOI: 10.1016/j.neuroscience.2007.06.003  0.387
2007 Brehm R, Zeiler M, Rüttinger C, Herde K, Kibschull M, Winterhager E, Willecke K, Guillou F, Lécureuil C, Steger K, Konrad L, Biermann K, Failing K, Bergmann M. A sertoli cell-specific knockout of connexin43 prevents initiation of spermatogenesis. The American Journal of Pathology. 171: 19-31. PMID 17591950 DOI: 10.2353/ajpath.2007.061171  0.491
2007 Schnichels M, Wörsdörfer P, Dobrowolski R, Markopoulos C, Kretz M, Schwarz G, Winterhager E, Willecke K. The connexin31 F137L mutant mouse as a model for the human skin disease erythrokeratodermia variabilis (EKV). Human Molecular Genetics. 16: 1216-24. PMID 17446259 DOI: 10.1093/hmg/ddm068  0.482
2007 Winterhager E, Pielensticker N, Freyer J, Ghanem A, Schrickel JW, Kim JS, Behr R, Grümmer R, Maass K, Urschel S, Lewalter T, Tiemann K, Simoni M, Willecke K. Replacement of connexin43 by connexin26 in transgenic mice leads to dysfunctional reproductive organs and slowed ventricular conduction in the heart. Bmc Developmental Biology. 7: 26. PMID 17408477 DOI: 10.1186/1471-213X-7-26  0.405
2007 Ahmad S, Tang W, Chang Q, Qu Y, Hibshman J, Li Y, Söhl G, Willecke K, Chen P, Lin X. Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness. Proceedings of the National Academy of Sciences of the United States of America. 104: 1337-41. PMID 17227867 DOI: 10.1073/Pnas.0606855104  0.476
2007 Corvalán LA, Araya R, Brañes MC, Sáez PJ, Kalergis AM, Tobar JA, Theis M, Willecke K, Sáez JC. Injury of skeletal muscle and specific cytokines induce the expression of gap junction channels in mouse dendritic cells. Journal of Cellular Physiology. 211: 649-60. PMID 17226782 DOI: 10.1002/Jcp.20971  0.604
2007 Rackauskas M, Kreuzberg MM, Pranevicius M, Willecke K, Verselis VK, Bukauskas FF. Gating properties of heterotypic gap junction channels formed of connexins 40, 43, and 45. Biophysical Journal. 92: 1952-65. PMID 17189315 DOI: 10.1529/Biophysj.106.099358  0.8
2007 Döring B, Pfitzer G, Adam B, Liebregts T, Eckardt D, Holtmann G, Hofmann F, Feil S, Feil R, Willecke K. Ablation of connexin43 in smooth muscle cells of the mouse intestine: functional insights into physiology and morphology. Cell and Tissue Research. 327: 333-42. PMID 17058052 DOI: 10.1007/s00441-006-0281-6  0.408
2007 Li J, Habbes HW, Eiberger J, Willecke K, Dermietzel R, Meier C. Analysis of connexin expression during mouse Schwann cell development identifies connexin29 as a novel marker for the transition of neural crest to precursor cells. Glia. 55: 93-103. PMID 17024657 DOI: 10.1002/glia.20427  0.475
2006 Kreuzberg MM, Willecke K, Bukauskas FF. Connexin-mediated cardiac impulse propagation: connexin 30.2 slows atrioventricular conduction in mouse heart. Trends in Cardiovascular Medicine. 16: 266-72. PMID 17055382 DOI: 10.1016/J.Tcm.2006.05.002  0.79
2006 Dedek K, Schultz K, Pieper M, Dirks P, Maxeiner S, Willecke K, Weiler R, Janssen-Bienhold U. Localization of heterotypic gap junctions composed of connexin45 and connexin36 in the rod pathway of the mouse retina. The European Journal of Neuroscience. 24: 1675-86. PMID 17004931 DOI: 10.1111/J.1460-9568.2006.05052.X  0.688
2006 Chung DJ, Castro CH, Watkins M, Stains JP, Chung MY, Szejnfeld VL, Willecke K, Theis M, Civitelli R. Low peak bone mass and attenuated anabolic response to parathyroid hormone in mice with an osteoblast-specific deletion of connexin43. Journal of Cell Science. 119: 4187-98. PMID 16984976 DOI: 10.1242/Jcs.03162  0.305
2006 Eckardt D, Kirchhoff S, Kim JS, Degen J, Theis M, Ott T, Wiesmann F, Doevendans PA, Lamers WH, de Bakker JM, van Rijen HV, Schneider MD, Willecke K. Cardiomyocyte-restricted deletion of connexin43 during mouse development. Journal of Molecular and Cellular Cardiology. 41: 963-71. PMID 16963078 DOI: 10.1016/j.yjmcc.2006.07.017  0.391
2006 Urschel S, Höher T, Schubert T, Alev C, Söhl G, Wörsdörfer P, Asahara T, Dermietzel R, Weiler R, Willecke K. Protein kinase A-mediated phosphorylation of connexin36 in mouse retina results in decreased gap junctional communication between AII amacrine cells. The Journal of Biological Chemistry. 281: 33163-71. PMID 16956882 DOI: 10.1074/Jbc.M606396200  0.798
2006 Krüger O, Maxeiner S, Kim JS, van Rijen HV, de Bakker JM, Eckardt D, Tiemann K, Lewalter T, Ghanem A, Lüderitz B, Willecke K. Cardiac morphogenetic defects and conduction abnormalities in mice homozygously deficient for connexin40 and heterozygously deficient for connexin45. Journal of Molecular and Cellular Cardiology. 41: 787-97. PMID 16919680 DOI: 10.1016/j.yjmcc.2006.07.005  0.687
2006 Shelley J, Dedek K, Schubert T, Feigenspan A, Schultz K, Hombach S, Willecke K, Weiler R. Horizontal cell receptive fields are reduced in connexin57-deficient mice. The European Journal of Neuroscience. 23: 3176-86. PMID 16820008 DOI: 10.1111/J.1460-9568.2006.04848.X  0.414
2006 Bukauskas FF, Kreuzberg MM, Rackauskas M, Bukauskiene A, Bennett MV, Verselis VK, Willecke K. Properties of mouse connexin 30.2 and human connexin 31.9 hemichannels: implications for atrioventricular conduction in the heart. Proceedings of the National Academy of Sciences of the United States of America. 103: 9726-31. PMID 16772377 DOI: 10.1073/Pnas.0603372103  0.794
2006 Ott T, Jokwitz M, Lenhard D, Romualdi A, Dombrowski F, Ittrich C, Schwarz M, Willecke K. Ablation of gap junctional communication in hepatocytes of transgenic mice does not lead to disrupted cellular homeostasis or increased spontaneous tumourigenesis. European Journal of Cell Biology. 85: 717-28. PMID 16740338 DOI: 10.1016/J.Ejcb.2006.03.004  0.453
2006 Wallraff A, Köhling R, Heinemann U, Theis M, Willecke K, Steinhäuser C. The impact of astrocytic gap junctional coupling on potassium buffering in the hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 5438-47. PMID 16707796 DOI: 10.1523/Jneurosci.0037-06.2006  0.462
2006 Kretz M, Eckardt D, Krüger O, Kim JS, Maurer J, Theis M, van Rijen HV, Schorle H, Willecke K. Normal embryonic development and cardiac morphogenesis in mice with Wnt1-Cre-mediated deletion of connexin43. Genesis (New York, N.Y. : 2000). 44: 269-76. PMID 16703618 DOI: 10.1002/dvg.20204  0.464
2006 von Maltzahn J, Wulf V, Willecke K. Spatiotemporal expression of connexin 39 and -43 during myoblast differentiation in cultured cells and in the mouse embryo. Cell Communication & Adhesion. 13: 55-60. PMID 16613780 DOI: 10.1080/15419060600631508  0.441
2006 Döring B, Shynlova O, Tsui P, Eckardt D, Janssen-Bienhold U, Hofmann F, Feil S, Feil R, Lye SJ, Willecke K. Ablation of connexin43 in uterine smooth muscle cells of the mouse causes delayed parturition. Journal of Cell Science. 119: 1715-22. PMID 16595547 DOI: 10.1242/jcs.02892  0.444
2006 Kreuzberg MM, Schrickel JW, Ghanem A, Kim JS, Degen J, Janssen-Bienhold U, Lewalter T, Tiemann K, Willecke K. Connexin30.2 containing gap junction channels decelerate impulse propagation through the atrioventricular node. Proceedings of the National Academy of Sciences of the United States of America. 103: 5959-64. PMID 16571663 DOI: 10.1073/pnas.0508512103  0.788
2006 Zheng-Fischhöfer Q, Ghanem A, Kim JS, Kibschull M, Schwarz G, Schwab JO, Nagy J, Winterhager E, Tiemann K, Willecke K. Connexin31 cannot functionally replace connexin43 during cardiac morphogenesis in mice. Journal of Cell Science. 119: 693-701. PMID 16449318 DOI: 10.1242/jcs.02800  0.531
2006 Haefliger JA, Krattinger N, Martin D, Pedrazzini T, Capponi A, Döring B, Plum A, Charollais A, Willecke K, Meda P. Connexin43-dependent mechanism modulates renin secretion and hypertension. The Journal of Clinical Investigation. 116: 405-13. PMID 16440062 DOI: 10.1172/JCI23327  0.389
2006 Eiberger J, Kibschull M, Strenzke N, Schober A, Büssow H, Wessig C, Djahed S, Reucher H, Koch DA, Lautermann J, Moser T, Winterhager E, Willecke K. Expression pattern and functional characterization of connexin29 in transgenic mice. Glia. 53: 601-11. PMID 16435366 DOI: 10.1002/Glia.20315  0.471
2006 Van Der Giessen RS, Maxeiner S, French PJ, Willecke K, De Zeeuw CI. Spatiotemporal distribution of Connexin45 in the olivocerebellar system. The Journal of Comparative Neurology. 495: 173-84. PMID 16435305 DOI: 10.1002/cne.20873  0.668
2006 Bedner P, Niessen H, Odermatt B, Kretz M, Willecke K, Harz H. Selective permeability of different connexin channels to the second messenger cyclic AMP. The Journal of Biological Chemistry. 281: 6673-81. PMID 16373337 DOI: 10.1074/Jbc.M511235200  0.627
2006 Haas B, Schipke CG, Peters O, Söhl G, Willecke K, Kettenmann H. Activity-dependent ATP-waves in the mouse neocortex are independent from astrocytic calcium waves. Cerebral Cortex (New York, N.Y. : 1991). 16: 237-46. PMID 15930372 DOI: 10.1093/Cercor/Bhi101  0.31
2005 Schubert T, Maxeiner S, Krüger O, Willecke K, Weiler R. Connexin45 mediates gap junctional coupling of bistratified ganglion cells in the mouse retina. The Journal of Comparative Neurology. 490: 29-39. PMID 16041717 DOI: 10.1002/Cne.20621  0.681
2005 Ravier MA, Güldenagel M, Charollais A, Gjinovci A, Caille D, Söhl G, Wollheim CB, Willecke K, Henquin JC, Meda P. Loss of connexin36 channels alters beta-cell coupling, islet synchronization of glucose-induced Ca2+ and insulin oscillations, and basal insulin release. Diabetes. 54: 1798-807. PMID 15919802 DOI: 10.2337/Diabetes.54.6.1798  0.361
2005 Kreuzberg MM, Söhl G, Kim JS, Verselis VK, Willecke K, Bukauskas FF. Functional properties of mouse connexin30.2 expressed in the conduction system of the heart. Circulation Research. 96: 1169-77. PMID 15879306 DOI: 10.1161/01.Res.0000169271.33675.05  0.793
2005 Theis M, Söhl G, Eiberger J, Willecke K. Emerging complexities in identity and function of glial connexins. Trends in Neurosciences. 28: 188-95. PMID 15808353 DOI: 10.1016/J.Tins.2005.02.006  0.415
2005 Schubert T, Degen J, Willecke K, Hormuzdi SG, Monyer H, Weiler R. Connexin36 mediates gap junctional coupling of alpha-ganglion cells in mouse retina. The Journal of Comparative Neurology. 485: 191-201. PMID 15791644 DOI: 10.1002/Cne.20510  0.428
2005 Söhl G, Maxeiner S, Willecke K. Expression and functions of neuronal gap junctions. Nature Reviews. Neuroscience. 6: 191-200. PMID 15738956 DOI: 10.1038/Nrn1627  0.7
2005 Scherer SS, Xu YT, Messing A, Willecke K, Fischbeck KH, Jeng LJ. Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 1550-9. PMID 15703409 DOI: 10.1523/Jneurosci.3082-04.2005  0.482
2005 Maxeiner S, Dedek K, Janssen-Bienhold U, Ammermüller J, Brune H, Kirsch T, Pieper M, Degen J, Krüger O, Willecke K, Weiler R. Deletion of connexin45 in mouse retinal neurons disrupts the rod/cone signaling pathway between AII amacrine and ON cone bipolar cells and leads to impaired visual transmission. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 566-76. PMID 15659592 DOI: 10.1523/Jneurosci.3232-04.2005  0.717
2005 Frisch C, De Souza-Silva MA, Söhl G, Güldenagel M, Willecke K, Huston JP, Dere E. Stimulus complexity dependent memory impairment and changes in motor performance after deletion of the neuronal gap junction protein connexin36 in mice. Behavioural Brain Research. 157: 177-85. PMID 15617784 DOI: 10.1016/J.Bbr.2004.06.023  0.806
2005 Araya R, Eckardt D, Maxeiner S, Krüger O, Theis M, Willecke K, Sáez JC. Expression of connexins during differentiation and regeneration of skeletal muscle: functional relevance of connexin43. Journal of Cell Science. 118: 27-37. PMID 15601660 DOI: 10.1242/Jcs.01553  0.734
2004 Kretz M, Maass K, Willecke K. Expression and function of connexins in the epidermis, analyzed with transgenic mouse mutants. European Journal of Cell Biology. 83: 647-54. PMID 15679109 DOI: 10.1078/0171-9335-00422  0.514
2004 Söhl G, Odermatt B, Maxeiner S, Degen J, Willecke K. New insights into the expression and function of neural connexins with transgenic mouse mutants. Brain Research. Brain Research Reviews. 47: 245-59. PMID 15572175 DOI: 10.1016/J.Brainresrev.2004.05.006  0.792
2004 von Maltzahn J, Euwens C, Willecke K, Söhl G. The novel mouse connexin39 gene is expressed in developing striated muscle fibers. Journal of Cell Science. 117: 5381-92. PMID 15466892 DOI: 10.1242/Jcs.01413  0.395
2004 Wallraff A, Odermatt B, Willecke K, Steinhäuser C. Distinct types of astroglial cells in the hippocampus differ in gap junction coupling. Glia. 48: 36-43. PMID 15326613 DOI: 10.1002/Glia.20040  0.662
2004 Maass K, Ghanem A, Kim JS, Saathoff M, Urschel S, Kirfel G, Grümmer R, Kretz M, Lewalter T, Tiemann K, Winterhager E, Herzog V, Willecke K. Defective epidermal barrier in neonatal mice lacking the C-terminal region of connexin43. Molecular Biology of the Cell. 15: 4597-608. PMID 15282340 DOI: 10.1091/Mbc.E04-04-0324  0.445
2004 Gellhaus A, Dong X, Propson S, Maass K, Klein-Hitpass L, Kibschull M, Traub O, Willecke K, Perbal B, Lye SJ, Winterhager E. Connexin43 interacts with NOV: a possible mechanism for negative regulation of cell growth in choriocarcinoma cells. The Journal of Biological Chemistry. 279: 36931-42. PMID 15181016 DOI: 10.1074/jbc.M404073200  0.395
2004 Nakase T, Söhl G, Theis M, Willecke K, Naus CC. Increased apoptosis and inflammation after focal brain ischemia in mice lacking connexin43 in astrocytes. The American Journal of Pathology. 164: 2067-75. PMID 15161641 DOI: 10.1016/S0002-9440(10)63765-0  0.43
2004 Hombach S, Janssen-Bienhold U, Söhl G, Schubert T, Büssow H, Ott T, Weiler R, Willecke K. Functional expression of connexin57 in horizontal cells of the mouse retina. The European Journal of Neuroscience. 19: 2633-40. PMID 15147297 DOI: 10.1111/J.0953-816X.2004.03360.X  0.842
2004 Degen J, Meier C, Van Der Giessen RS, Söhl G, Petrasch-Parwez E, Urschel S, Dermietzel R, Schilling K, De Zeeuw CI, Willecke K. Expression pattern of lacZ reporter gene representing connexin36 in transgenic mice. The Journal of Comparative Neurology. 473: 511-25. PMID 15116387 DOI: 10.1002/Cne.20085  0.6
2004 Söhl G, Willecke K. Gap junctions and the connexin protein family. Cardiovascular Research. 62: 228-32. PMID 15094343 DOI: 10.1016/J.Cardiores.2003.11.013  0.481
2004 Eckardt D, Theis M, Döring B, Speidel D, Willecke K, Ott T. Spontaneous ectopic recombination in cell-type-specific Cre mice removes loxP-flanked marker cassettes in vivo. Genesis (New York, N.Y. : 2000). 38: 159-65. PMID 15083516 DOI: 10.1002/gene.20011  0.423
2004 Feigenspan A, Janssen-Bienhold U, Hormuzdi S, Monyer H, Degen J, Söhl G, Willecke K, Ammermüller J, Weiler R. Expression of connexin36 in cone pedicles and OFF-cone bipolar cells of the mouse retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 3325-34. PMID 15056712 DOI: 10.1523/Jneurosci.5598-03.2004  0.424
2004 Theis M, Speidel D, Willecke K. Astrocyte cultures from conditional connexin43-deficient mice. Glia. 46: 130-41. PMID 15042581 DOI: 10.1002/glia.10350  0.461
2004 Bry C, Maass K, Miyoshi K, Willecke K, Ott T, Robinson GW, Hennighausen L. Loss of connexin 26 in mammary epithelium during early but not during late pregnancy results in unscheduled apoptosis and impaired development. Developmental Biology. 267: 418-29. PMID 15013803 DOI: 10.1016/j.ydbio.2003.11.022  0.415
2004 Cohen-Salmon M, Maxeiner S, Krüger O, Theis M, Willecke K, Petit C. Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear. Cell and Tissue Research. 316: 15-22. PMID 14986102 DOI: 10.1007/S00441-004-0861-2  0.69
2004 Theis M, Mas C, Döring B, Degen J, Brink C, Caille D, Charollais A, Krüger O, Plum A, Nepote V, Herrera P, Meda P, Willecke K. Replacement by a lacZ reporter gene assigns mouse connexin36, 45 and 43 to distinct cell types in pancreatic islets. Experimental Cell Research. 294: 18-29. PMID 14980497 DOI: 10.1016/j.yexcr.2003.09.031  0.475
2004 van Rijen HV, Eckardt D, Degen J, Theis M, Ott T, Willecke K, Jongsma HJ, Opthof T, de Bakker JM. Slow conduction and enhanced anisotropy increase the propensity for ventricular tachyarrhythmias in adult mice with induced deletion of connexin43. Circulation. 109: 1048-55. PMID 14967725 DOI: 10.1161/01.Cir.0000117402.70689.75  0.382
2004 Eckardt D, Theis M, Degen J, Ott T, van Rijen HV, Kirchhoff S, Kim JS, de Bakker JM, Willecke K. Functional role of connexin43 gap junction channels in adult mouse heart assessed by inducible gene deletion. Journal of Molecular and Cellular Cardiology. 36: 101-10. PMID 14734052 DOI: 10.1016/j.yjmcc.2003.10.006  0.506
2004 Yoon BI, Hirabayashi Y, Kawasaki Y, Tsuboi I, Ott T, Kodama Y, Kanno J, Kim DY, Willecke K, Inoue T. Exacerbation of benzene pneumotoxicity in connexin 32 knockout mice: enhanced proliferation of CYP2E1-immunoreactive alveolar epithelial cells. Toxicology. 195: 19-29. PMID 14698565 DOI: 10.1016/J.Tox.2003.08.014  0.399
2003 Araya R, Eckardt D, Riquelme MA, Willecke K, Sáez JC. Presence and importance of connexin43 during myogenesis. Cell Communication & Adhesion. 10: 451-6. PMID 14681056 DOI: 10.1080/Cac.10.4-6.451.456  0.628
2003 Castro CH, Stains JP, Sheikh S, Szejnfeld VL, Willecke K, Theis M, Civitelli R. Development of mice with osteoblast-specific connexin43 gene deletion. Cell Communication & Adhesion. 10: 445-50. PMID 14681055 DOI: 10.1080/Cac.10.4-6.445.450  0.496
2003 Nakase T, Fushiki S, Söhl G, Theis M, Willecke K, Naus CC. Neuroprotective role of astrocytic gap junctions in ischemic stroke. Cell Communication & Adhesion. 10: 413-7. PMID 14681050 DOI: 10.1080/Cac.10.4-6.413.417  0.399
2003 Söhl G, Willecke K. An update on connexin genes and their nomenclature in mouse and man. Cell Communication & Adhesion. 10: 173-80. PMID 14681012 DOI: 10.1080/Cac.10.4-6.173.180  0.39
2003 Frisch C, Theis M, De Souza Silva MA, Dere E, Söhl G, Teubner B, Namestkova K, Willecke K, Huston JP. Mice with astrocyte-directed inactivation of connexin43 exhibit increased exploratory behaviour, impaired motor capacities, and changes in brain acetylcholine levels. The European Journal of Neuroscience. 18: 2313-8. PMID 14622192 DOI: 10.1046/J.1460-9568.2003.02971.X  0.814
2003 Bedner P, Niessen H, Odermatt B, Willecke K, Harz H. A method to determine the relative cAMP permeability of connexin channels. Experimental Cell Research. 291: 25-35. PMID 14597405 DOI: 10.1016/S0014-4827(03)00323-9  0.579
2003 Dere E, De Souza-Silva MA, Frisch C, Teubner B, Söhl G, Willecke K, Huston JP. Connexin30-deficient mice show increased emotionality and decreased rearing activity in the open-field along with neurochemical changes. The European Journal of Neuroscience. 18: 629-38. PMID 12911759 DOI: 10.1046/J.1460-9568.2003.02784.X  0.819
2003 Theis M, Söhl G, Speidel D, Kühn R, Willecke K. Connexin43 is not expressed in principal cells of mouse cortex and hippocampus. The European Journal of Neuroscience. 18: 267-74. PMID 12887408 DOI: 10.1046/J.1460-9568.2003.02740.X  0.485
2003 Söhl G, Nielsen PA, Eiberger J, Willecke K. Expression profiles of the novel human connexin genes hCx30.2, hCx40.1, and hCx62 differ from their putative mouse orthologues. Cell Communication & Adhesion. 10: 27-36. PMID 12881038 DOI: 10.1080/15419060302063  0.372
2003 Sakai R, Elfgang C, Vogel R, Willecke K, Weingart R. The electrical behaviour of rat connexin46 gap junction channels expressed in transfected HeLa cells. Pflã¼Gers Archiv : European Journal of Physiology. 446: 714-27. PMID 12861414 DOI: 10.1007/S00424-003-1129-5  0.307
2003 Kretz M, Euwens C, Hombach S, Eckardt D, Teubner B, Traub O, Willecke K, Ott T. Altered connexin expression and wound healing in the epidermis of connexin-deficient mice. Journal of Cell Science. 116: 3443-52. PMID 12840073 DOI: 10.1242/Jcs.00638  0.433
2003 Maxeiner S, Krüger O, Schilling K, Traub O, Urschel S, Willecke K. Spatiotemporal transcription of connexin45 during brain development results in neuronal expression in adult mice. Neuroscience. 119: 689-700. PMID 12809690 DOI: 10.1016/S0306-4522(03)00077-0  0.747
2003 De Zeeuw CI, Chorev E, Devor A, Manor Y, Van Der Giessen RS, De Jeu MT, Hoogenraad CC, Bijman J, Ruigrok TJ, French P, Jaarsma D, Kistler WM, Meier C, Petrasch-Parwez E, Dermietzel R, ... ... Willecke K, et al. Deformation of network connectivity in the inferior olive of connexin 36-deficient mice is compensated by morphological and electrophysiological changes at the single neuron level. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 4700-11. PMID 12805309 DOI: 10.1523/Jneurosci.23-11-04700.2003  0.803
2003 Odermatt B, Wellershaus K, Wallraff A, Seifert G, Degen J, Euwens C, Fuss B, Büssow H, Schilling K, Steinhäuser C, Willecke K. Connexin 47 (Cx47)-deficient mice with enhanced green fluorescent protein reporter gene reveal predominant oligodendrocytic expression of Cx47 and display vacuolized myelin in the CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 4549-59. PMID 12805295 DOI: 10.1523/Jneurosci.23-11-04549.2003  0.721
2003 Theis M, Jauch R, Zhuo L, Speidel D, Wallraff A, Döring B, Frisch C, Söhl G, Teubner B, Euwens C, Huston J, Steinhäuser C, Messing A, Heinemann U, Willecke K. Accelerated hippocampal spreading depression and enhanced locomotory activity in mice with astrocyte-directed inactivation of connexin43. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 766-76. PMID 12574405 DOI: 10.1523/Jneurosci.23-03-00766.2003  0.475
2003 Frossard JL, Rubbia-Brandt L, Wallig MA, Benathan M, Ott T, Morel P, Hadengue A, Suter S, Willecke K, Chanson M. Severe acute pancreatitis and reduced acinar cell apoptosis in the exocrine pancreas of mice deficient for the Cx32 gene. Gastroenterology. 124: 481-93. PMID 12557153 DOI: 10.1053/gast.2003.50052  0.396
2003 Lin JH, Yang J, Liu S, Takano T, Wang X, Gao Q, Willecke K, Nedergaard M. Connexin mediates gap junction-independent resistance to cellular injury. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 430-41. PMID 12533603 DOI: 10.1523/Jneurosci.23-02-00430.2003  0.399
2003 Teubner B, Michel V, Pesch J, Lautermann J, Cohen-Salmon M, Söhl G, Jahnke K, Winterhager E, Herberhold C, Hardelin JP, Petit C, Willecke K. Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential. Human Molecular Genetics. 12: 13-21. PMID 12490528 DOI: 10.1093/Hmg/Ddg001  0.425
2002 Kistler WM, De Jeu MT, Elgersma Y, Van Der Giessen RS, Hensbroek R, Luo C, Koekkoek SK, Hoogenraad CC, Hamers FP, Gueldenagel M, Sohl G, Willecke K, De Zeeuw CI. Analysis of Cx36 knockout does not support tenet that olivary gap junctions are required for complex spike synchronization and normal motor performance. Annals of the New York Academy of Sciences. 978: 391-404. PMID 12582068 DOI: 10.1111/J.1749-6632.2002.Tb07582.X  0.792
2002 Thönnissen E, Rabionet R, Arbonès ML, Estivill X, Willecke K, Ott T. Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression. Human Genetics. 111: 190-7. PMID 12189493 DOI: 10.1007/S00439-002-0750-2  0.363
2002 Cohen-Salmon M, Ott T, Michel V, Hardelin JP, Perfettini I, Eybalin M, Wu T, Marcus DC, Wangemann P, Willecke K, Petit C. Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death. Current Biology : Cb. 12: 1106-11. PMID 12121617 DOI: 10.1016/S0960-9822(02)00904-1  0.401
2002 Willecke K, Eiberger J, Degen J, Eckardt D, Romualdi A, Güldenagel M, Deutsch U, Söhl G. Structural and functional diversity of connexin genes in the mouse and human genome. Biological Chemistry. 383: 725-37. PMID 12108537 DOI: 10.1515/Bc.2002.076  0.357
2002 Meier C, Petrasch-Parwez E, Habbes HW, Teubner B, Güldenagel M, Degen J, Söhl G, Willecke K, Dermietzel R. Immunohistochemical detection of the neuronal connexin36 in the mouse central nervous system in comparison to connexin36-deficient tissues. Histochemistry and Cell Biology. 117: 461-71. PMID 12107497 DOI: 10.1007/S00418-002-0417-Z  0.438
2002 Maier N, Güldenagel M, Söhl G, Siegmund H, Willecke K, Draguhn A. Reduction of high-frequency network oscillations (ripples) and pathological network discharges in hippocampal slices from connexin 36-deficient mice. The Journal of Physiology. 541: 521-8. PMID 12042356 DOI: 10.1113/Jphysiol.2002.017624  0.799
2002 Lin JH, Takano T, Cotrina ML, Arcuino G, Kang J, Liu S, Gao Q, Jiang L, Li F, Lichtenberg-Frate H, Haubrich S, Willecke K, Goldman SA, Nedergaard M. Connexin 43 enhances the adhesivity and mediates the invasion of malignant glioma cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 4302-11. PMID 12040035 DOI: 10.1523/Jneurosci.22-11-04302.2002  0.433
2002 Evert M, Ott T, Temme A, Willecke K, Dombrowski F. Morphology and morphometric investigation of hepatocellular preneoplastic lesions and neoplasms in connexin32-deficient mice. Carcinogenesis. 23: 697-703. PMID 12016140 DOI: 10.1093/Carcin/23.5.697  0.397
2002 Krüger O, Bény JL, Chabaud F, Traub O, Theis M, Brix K, Kirchhoff S, Willecke K. Altered dye diffusion and upregulation of connexin37 in mouse aortic endothelium deficient in connexin40. Journal of Vascular Research. 39: 160-72. PMID 12011587 DOI: 10.1159/000057764  0.456
2002 Jungbluth S, Willecke K, Champagnat J. Segment-specific expression of connexin31 in the embryonic hindbrain is regulated by Krox20. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 223: 544-51. PMID 11921342 DOI: 10.1002/dvdy.10072  0.403
2002 Romualdi A, Niessen H, Dombrowski F, Willecke K, Ott T. Quantitative analysis of gap-junctional intercellular communication in precision-cut mouse liver slices. Cell and Tissue Research. 307: 315-20. PMID 11904767 DOI: 10.1007/S00441-002-0518-Y  0.371
2002 Walcott B, Moore LC, Birzgalis A, Claros N, Valiunas V, Ott T, Willecke K, Brink PR. Role of gap junctions in fluid secretion of lacrimal glands. American Journal of Physiology. Cell Physiology. 282: C501-7. PMID 11832335 DOI: 10.1152/Ajpcell.00004.2001  0.418
2002 Plum A, Hallas G, Willecke K. Expression of the mouse gap junction gene Gjb3 is regulated by distinct mechanisms in embryonic stem cells and keratinocytes. Genomics. 79: 24-30. PMID 11827454 DOI: 10.1006/geno.2001.6671  0.442
2001 Calabrese A, Güldenagel M, Charollais A, Mas C, Caton D, Bauquis J, Serre-Beinier V, Caille D, Söhl G, Teubner B, Le Gurun S, Trovato-Salinaro A, Condorelli DF, Haefliger JA, Willecke K, et al. Cx36 and the function of endocrine pancreas. Cell Communication & Adhesion. 8: 387-91. PMID 12064624 DOI: 10.3109/15419060109080759  0.424
2001 Theis M, Mas C, Döring B, Krüger O, Herrera P, Meda P, Willecke K. General and conditional replacement of connexin43-coding DNA by a lacZ reporter gene for cell-autonomous analysis of expression. Cell Communication & Adhesion. 8: 383-6. PMID 12064623 DOI: 10.3109/15419060109080758  0.465
2001 Eiberger J, Degen J, Romualdi A, Deutsch U, Willecke K, Söhl G. Connexin genes in the mouse and human genome. Cell Communication & Adhesion. 8: 163-5. PMID 12064582 DOI: 10.3109/15419060109080717  0.321
2001 Temme A, Stümpel F, Söhl G, Rieber EP, Jungermann K, Willecke K, Ott T. Dilated bile canaliculi and attenuated decrease of nerve-dependent bile secretion in connexin32-deficient mouse liver. Pflã¼Gers Archiv : European Journal of Physiology. 442: 961-6. PMID 11680630 DOI: 10.1007/S004240100623  0.38
2001 Zhuo L, Theis M, Alvarez-Maya I, Brenner M, Willecke K, Messing A. hGFAP-cre transgenic mice for manipulation of glial and neuronal function in vivo. Genesis (New York, N.Y. : 2000). 31: 85-94. PMID 11668683 DOI: 10.1002/Gene.10008  0.476
2001 Söhl G, Eiberger J, Jung YT, Kozak CA, Willecke K. The mouse gap junction gene connexin29 is highly expressed in sciatic nerve and regulated during brain development. Biological Chemistry. 382: 973-8. PMID 11501764 DOI: 10.1515/Bc.2001.122  0.405
2001 Güldenagel M, Ammermüller J, Feigenspan A, Teubner B, Degen J, Söhl G, Willecke K, Weiler R. Visual transmission deficits in mice with targeted disruption of the gap junction gene connexin36. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 6036-44. PMID 11487627 DOI: 10.1523/Jneurosci.21-16-06036.2001  0.438
2001 Manthey D, Banach K, Desplantez T, Lee CG, Kozak CA, Traub O, Weingart R, Willecke K. Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels. The Journal of Membrane Biology. 181: 137-48. PMID 11420600 DOI: 10.1007/S00232-001-0017-1  0.414
2001 Söhl G, Theis M, Hallas G, Brambach S, Dahl E, Kidder G, Willecke K. A new alternatively spliced transcript of the mouse connexin32 gene is expressed in embryonic stem cells, oocytes, and liver. Experimental Cell Research. 266: 177-86. PMID 11339836 DOI: 10.1006/Excr.2001.5209  0.403
2001 Eugenín EA, Eckardt D, Theis M, Willecke K, Bennett MV, Saez JC. Microglia at brain stab wounds express connexin 43 and in vitro form functional gap junctions after treatment with interferon-gamma and tumor necrosis factor-alpha. Proceedings of the National Academy of Sciences of the United States of America. 98: 4190-5. PMID 11259646 DOI: 10.1073/Pnas.051634298  0.347
2001 van Rijen HV, van Veen TA, van Kempen MJ, Wilms-Schopman FJ, Potse M, Krueger O, Willecke K, Opthof T, Jongsma HJ, de Bakker JM. Impaired conduction in the bundle branches of mouse hearts lacking the gap junction protein connexin40. Circulation. 103: 1591-8. PMID 11257090 DOI: 10.1161/01.Cir.103.11.1591  0.433
2001 Plum A, Winterhager E, Pesch J, Lautermann J, Hallas G, Rosentreter B, Traub O, Herberhold C, Willecke K. Connexin31-deficiency in mice causes transient placental dysmorphogenesis but does not impair hearing and skin differentiation. Developmental Biology. 231: 334-47. PMID 11237463 DOI: 10.1006/dbio.2000.0148  0.446
2001 Manthey D, Willecke K. Transfection and expression of exogenous connexins in mammalian cells. Methods in Molecular Biology (Clifton, N.J.). 154: 187-99. PMID 11218649 DOI: 10.1385/1-59259-043-8:187  0.429
2001 Teubner B, Odermatt B, Guldenagel M, Sohl G, Degen J, Bukauskas F, Kronengold J, Verselis VK, Jung YT, Kozak CA, Schilling K, Willecke K. Functional expression of the new gap junction gene connexin47 transcribed in mouse brain and spinal cord neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 1117-26. PMID 11160382 DOI: 10.1523/Jneurosci.21-04-01117.2001  0.817
2001 Feigenspan A, Teubner B, Willecke K, Weiler R. Expression of neuronal connexin36 in AII amacrine cells of the mammalian retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 230-9. PMID 11150340 DOI: 10.1523/Jneurosci.21-01-00230.2001  0.415
2001 Theis M, de Wit C, Schlaeger TM, Eckardt D, Krüger O, Döring B, Risau W, Deutsch U, Pohl U, Willecke K. Endothelium-specific replacement of the connexin43 coding region by a lacZ reporter gene. Genesis (New York, N.Y. : 2000). 29: 1-13. PMID 11135457 DOI: 10.1002/1526-968X(200101)29:1<1::AID-GENE1000>3.0.CO;2-0  0.442
2000 Söhl G, Güldenagel M, Beck H, Teubner B, Traub O, Gutiérrez R, Heinemann U, Willecke K. Expression of connexin genes in hippocampus of kainate-treated and kindled rats under conditions of experimental epilepsy. Brain Research. Molecular Brain Research. 83: 44-51. PMID 11072094 DOI: 10.1016/S0169-328X(00)00195-9  0.357
2000 Plum A, Hallas G, Magin T, Dombrowski F, Hagendorff A, Schumacher B, Wolpert C, Kim J, Lamers WH, Evert M, Meda P, Traub O, Willecke K. Unique and shared functions of different connexins in mice. Current Biology : Cb. 10: 1083-91. PMID 10996788 DOI: 10.1016/S0960-9822(00)00690-4  0.478
2000 Krüger O, Plum A, Kim JS, Winterhager E, Maxeiner S, Hallas G, Kirchhoff S, Traub O, Lamers WH, Willecke K. Defective vascular development in connexin 45-deficient mice. Development (Cambridge, England). 127: 4179-93. PMID 10976050  0.636
2000 Kirchhoff S, Kim JS, Hagendorff A, Thönnissen E, Krüger O, Lamers WH, Willecke K. Abnormal cardiac conduction and morphogenesis in connexin40 and connexin43 double-deficient mice. Circulation Research. 87: 399-405. PMID 10969038 DOI: 10.1161/01.Res.87.5.399  0.443
2000 Moennikes O, Buchmann A, Willecke K, Traub O, Schwarz M. Hepatocarcinogenesis in female mice with mosaic expression of connexin32. Hepatology (Baltimore, Md.). 32: 501-6. PMID 10960441 DOI: 10.1053/Jhep.2000.16598  0.439
2000 Güldenagel M, Söhl G, Plum A, Traub O, Teubner B, Weiler R, Willecke K. Expression patterns of connexin genes in mouse retina. The Journal of Comparative Neurology. 425: 193-201. PMID 10954839 DOI: 10.1002/1096-9861(20000918)425:2<193::Aid-Cne3>3.0.Co;2-N  0.493
2000 Teubner B, Degen J, Söhl G, Güldenagel M, Bukauskas FF, Trexler EB, Verselis VK, De Zeeuw CI, Lee CG, Kozak CA, Petrasch-Parwez E, Dermietzel R, Willecke K. Functional expression of the murine connexin 36 gene coding for a neuron-specific gap junctional protein. The Journal of Membrane Biology. 176: 249-62. PMID 10931976 DOI: 10.1007/S00232001094  0.514
2000 Sutor B, Schmolke C, Teubner B, Schirmer C, Willecke K. Myelination defects and neuronal hyperexcitability in the neocortex of connexin 32-deficient mice. Cerebral Cortex (New York, N.Y. : 1991). 10: 684-97. PMID 10906315 DOI: 10.1093/Cercor/10.7.684  0.423
2000 Temme A, Ott T, Haberberger T, Traub O, Willecke K. Acute-phase response and circadian expression of connexin26 are not altered in connexin32-deficient mouse liver. Cell and Tissue Research. 300: 111-7. PMID 10805080 DOI: 10.1007/S004410000177  0.373
2000 Temme A, Ott T, Dombrowski F, Willecke K. The extent of synchronous initiation and termination of DNA synthesis in regenerating mouse liver is dependent on connexin32 expressing gap junctions. Journal of Hepatology. 32: 627-35. PMID 10782912 DOI: 10.1016/S0168-8278(00)80225-1  0.38
2000 Söhl G, Güldenagel M, Traub O, Willecke K. Connexin expression in the retina. Brain Research. Brain Research Reviews. 32: 138-45. PMID 10751663 DOI: 10.1016/S0165-0173(99)00074-0  0.468
2000 de Wit C, Roos F, Bolz SS, Kirchhoff S, Krüger O, Willecke K, Pohl U. Impaired conduction of vasodilation along arterioles in connexin40-deficient mice. Circulation Research. 86: 649-55. PMID 10747000 DOI: 10.1161/01.Res.86.6.649  0.317
2000 Niessen H, Harz H, Bedner P, Krämer K, Willecke K. Selective permeability of different connexin channels to the second messenger inositol 1,4,5-trisphosphate. Journal of Cell Science. 113: 1365-72. PMID 10725220  0.305
2000 Theis M, Magin TM, Plum A, Willecke K. General or cell type-specific deletion and replacement of connexin-coding DNA in the mouse. Methods (San Diego, Calif.). 20: 205-18. PMID 10671314 DOI: 10.1006/meth.1999.0938  0.369
2000 Niessen H, Willecke K. Strongly decreased gap junctional permeability to inositol 1,4, 5-trisphosphate in connexin32 deficient hepatocytes. Febs Letters. 466: 112-4. PMID 10648823 DOI: 10.1016/S0014-5793(99)01770-6  0.373
2000 Beyer EC, Willecke K. Gap junction genes and their regulation Advances in Molecular and Cell Biology. 30: 1-30. DOI: 10.1016/S1569-2558(00)30002-9  0.442
1999 Willecke K, Temme A, Teubner B, Ott T. Characterization of Targeted Connexin32-Deficient Mice: A Model for the Human Charcot-Marie-Tooth (X-Type) Inherited Disease. Annals of the New York Academy of Sciences. 883: 302-309. PMID 29086934 DOI: 10.1111/j.1749-6632.1999.tb08592.x  0.327
1999 Verheule S, van Batenburg CA, Coenjaerts FE, Kirchhoff S, Willecke K, Jongsma HJ. Cardiac conduction abnormalities in mice lacking the gap junction protein connexin40. Journal of Cardiovascular Electrophysiology. 10: 1380-9. PMID 10515563 DOI: 10.1111/J.1540-8167.1999.Tb00194.X  0.379
1999 Valiunas V, Manthey D, Vogel R, Willecke K, Weingart R. Biophysical properties of mouse connexin30 gap junction channels studied in transfected human HeLa cells. The Journal of Physiology. 519: 631-44. PMID 10457079 DOI: 10.1111/J.1469-7793.1999.0631N.X  0.306
1999 Moennikes O, Buchmann A, Ott T, Willecke K, Schwarz M. The effect of connexin32 null mutation on hepatocarcinogenesis in different mouse strains. Carcinogenesis. 20: 1379-1382. PMID 10383916 DOI: 10.1093/Carcin/20.7.1379  0.378
1999 Valiunas V, Niessen H, Willecke K, Weingart R. Electrophysiological properties of gap junction channels in hepatocytes isolated from connexin32-deficient and wild-type mice. Pflã¼Gers Archiv : European Journal of Physiology. 437: 846-56. PMID 10370062 DOI: 10.1007/S004240050854  0.446
1999 Manthey D, Bukauskas F, Lee CG, Kozak CA, Willecke K. Molecular cloning and functional expression of the mouse gap junction gene connexin-57 in human HeLa cells. The Journal of Biological Chemistry. 274: 14716-23. PMID 10329667 DOI: 10.1074/Jbc.274.21.14716  0.338
1999 Willecke K, Kirchhoff S, Plum A, Temme A, Thönnissen E, Ott T. Biological functions of connexin genes revealed by human genetic defects, dominant negative approaches and targeted deletions in the mouse. Novartis Foundation Symposium. 219: 76-88; discussion 88. PMID 10207899 DOI: 10.1002/9780470515587.ch6  0.453
1999 Hagendorff A, Schumacher B, Kirchhoff S, Lüderitz B, Willecke K. Conduction disturbances and increased atrial vulnerability in Connexin40-deficient mice analyzed by transesophageal stimulation. Circulation. 99: 1508-15. PMID 10086977 DOI: 10.1161/01.Cir.99.11.1508  0.341
1999 Houghton FD, Thönnissen E, Kidder GM, Naus CC, Willecke K, Winterhager E. Doubly mutant mice, deficient in connexin32 and -43, show normal prenatal development of organs where the two gap junction proteins are expressed in the same cells. Developmental Genetics. 24: 5-12. PMID 10079506 DOI: 10.1002/(SICI)1520-6408(1999)24:1/2<5::AID-DVG2>3.0.CO;2-F  0.503
1999 Kunzelmann P, Schröder W, Traub O, Steinhäuser C, Dermietzel R, Willecke K. Late onset and increasing expression of the gap junction protein connexin30 in adult murine brain and long-term cultured astrocytes. Glia. 25: 111-9. PMID 9890626 DOI: 10.1002/(SICI)1098-1136(19990115)25:2<111::AID-GLIA2>3.0.CO;2-I  0.433
1998 Traub O, Hertlein B, Kasper M, Eckert R, Krisciukaitis A, Hülser D, Willecke K. Characterization of the gap junction protein connexin37 in murine endothelium, respiratory epithelium, and after transfection in human HeLa cells. European Journal of Cell Biology. 77: 313-22. PMID 9930656 DOI: 10.1016/S0171-9335(98)80090-3  0.397
1998 Stümpel F, Ott T, Willecke K, Jungermann K. Connexin 32 gap junctions enhance stimulation of glucose output by glucagon and noradrenaline in mouse liver. Hepatology (Baltimore, Md.). 28: 1616-20. PMID 9828226 DOI: 10.1002/hep.510280622  0.34
1998 Wenzel K, Manthey D, Willecke K, Grzeschik KH, Traub O. Human gap junction protein connexin31: molecular cloning and expression analysis. Biochemical and Biophysical Research Communications. 248: 910-5. PMID 9704026 DOI: 10.1006/bbrc.1998.9070  0.371
1998 Scherer SS, Xu YT, Nelles E, Fischbeck K, Willecke K, Bone LJ. Connexin32-null mice develop demyelinating peripheral neuropathy. Glia. 24: 8-20. PMID 9700485 DOI: 10.1002/(Sici)1098-1136(199809)24:1<8::Aid-Glia2>3.0.Co;2-3  0.401
1998 Söhl G, Degen J, Teubner B, Willecke K. The murine gap junction gene connexin36 is highly expressed in mouse retina and regulated during brain development. Febs Letters. 428: 27-31. PMID 9645468 DOI: 10.1016/S0014-5793(98)00479-7  0.391
1998 Chanson M, Fanjul M, Bosco D, Nelles E, Suter S, Willecke K, Meda P. Enhanced secretion of amylase from exocrine pancreas of connexin32-deficient mice. The Journal of Cell Biology. 141: 1267-75. PMID 9606217 DOI: 10.1083/jcb.141.5.1267  0.495
1998 Hertlein B, Butterweck A, Haubrich S, Willecke K, Traub O. Phosphorylated carboxy terminal serine residues stabilize the mouse gap junction protein connexin45 against degradation. The Journal of Membrane Biology. 162: 247-57. PMID 9543497 DOI: 10.1007/S002329900362  0.39
1998 Gabriel HD, Jung D, Bützler C, Temme A, Traub O, Winterhager E, Willecke K. Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice. The Journal of Cell Biology. 140: 1453-61. PMID 9508777 DOI: 10.1083/Jcb.140.6.1453  0.381
1998 Kirchhoff S, Nelles E, Hagendorff A, Krüger O, Traub O, Willecke K. Reduced cardiac conduction velocity and predisposition to arrhythmias in connexin40-deficient mice. Current Biology : Cb. 8: 299-302. PMID 9501070 DOI: 10.1016/S0960-9822(98)70114-9  0.496
1998 Cao F, Eckert R, Elfgang C, Nitsche JM, Snyder SA, H-ulser DF, Willecke K, Nicholson BJ. A quantitative analysis of connexin-specific permeability differences of gap junctions expressed in HeLa transfectants and Xenopus oocytes. Journal of Cell Science. 111: 31-43. PMID 9394010  0.319
1997 Dahl E, Willecke K, Balling R. Segment-specific expression of the gap junction gene connexin31 during hindbrain development. Development Genes and Evolution. 207: 359-361. PMID 27747433 DOI: 10.1007/s004270050123  0.409
1997 Temme A, Buchmann A, Gabriel HD, Nelles E, Schwarz M, Willecke K. High incidence of spontaneous and chemically induced liver tumors in mice deficient for connexin32. Current Biology : Cb. 7: 713-6. PMID 9285723 DOI: 10.1016/S0960-9822(06)00302-2  0.436
1997 Delorme B, Dahl E, Jarry-Guichard T, Briand JP, Willecke K, Gros D, Théveniau-Ruissy M. Expression pattern of connexin gene products at the early developmental stages of the mouse cardiovascular system. Circulation Research. 81: 423-37. PMID 9285645 DOI: 10.1161/01.Res.81.3.423  0.455
1997 Kunzelmann P, Blümcke I, Traub O, Dermietzel R, Willecke K. Coexpression of connexin45 and -32 in oligodendrocytes of rat brain. Journal of Neurocytology. 26: 17-22. PMID 9154525 DOI: 10.1023/A:1018555207379  0.425
1997 Anzini P, Neuberg DH-, Schachner M, Nelles E, Willecke K, Zielasek J, Toyka KV, Suter U, Martini R. Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32 The Journal of Neuroscience. 17: 4545-4551. DOI: 10.1523/Jneurosci.17-12-04545.1997  0.384
1996 Haubrich S, Schwarz HJ, Bukauskas F, Lichtenberg-Fraté H, Traub O, Weingart R, Willecke K. Incompatibility of connexin 40 and 43 Hemichannels in gap junctions between mammalian cells is determined by intracellular domains. Molecular Biology of the Cell. 7: 1995-2006. PMID 8970160 DOI: 10.1091/Mbc.7.12.1995  0.417
1996 Willecke K, Haubrich S. Connexin expression systems: to what extent do they reflect the situation in the animal? Journal of Bioenergetics and Biomembranes. 28: 319-26. PMID 8844329 DOI: 10.1007/Bf02110108  0.482
1996 Nelles E, Bützler C, Jung D, Temme A, Gabriel HD, Dahl U, Traub O, Stümpel F, Jungermann K, Zielasek J, Toyka KV, Dermietzel R, Willecke K. Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 93: 9565-70. PMID 8790370 DOI: 10.1073/Pnas.93.18.9565  0.401
1996 Mesnil M, Piccoli C, Tiraby G, Willecke K, Yamasaki H. Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins. Proceedings of the National Academy of Sciences of the United States of America. 93: 1831-5. PMID 8700844 DOI: 10.1073/Pnas.93.5.1831  0.374
1996 Dahl E, Manthey D, Chen Y, Schwarz HJ, Chang YS, Lalley PA, Nicholson BJ, Willecke K. Molecular cloning and functional expression of mouse connexin-30,a gap junction gene highly expressed in adult brain and skin. The Journal of Biological Chemistry. 271: 17903-10. PMID 8663509 DOI: 10.1074/Jbc.271.30.17903  0.429
1996 Mazzoleni G, Camplani A, Telo P, Pozzi A, Tanganelli S, Elfgang C, Willecke K, Ragnotti G. Effect of tumor-promoting and anti-promoting chemicals on the viability and junctional coupling of human HeLa cells transfected with DNAs coding for various murine connexin proteins. Comparative Biochemistry and Physiology. Part C, Pharmacology, Toxicology & Endocrinology. 113: 247-56. PMID 8646616 DOI: 10.1016/0742-8413(95)02094-2  0.393
1995 Delorme B, Dahl E, Jarry-Guichard T, Marics I, Briand JP, Willecke K, Gros D, Théveniau-Ruissy M. Developmental regulation of connexin 40 gene expression in mouse heart correlates with the differentiation of the conduction system. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 204: 358-71. PMID 8601030 DOI: 10.1002/aja.1002040403  0.417
1995 Mesnil M, Krutovskikh V, Piccoli C, Elfgang C, Traub O, Willecke K, Yamasaki H. Negative growth control of HeLa cells by connexin genes: connexin species specificity. Cancer Research. 55: 629-39. PMID 7834634  0.307
1995 Dahl E, Winterhager E, Traub O, Willecke K. Expression of gap junction genes, connexin40 and connexin43, during fetal mouse development. Anatomy and Embryology. 191: 267-78. PMID 7771689 DOI: 10.1007/Bf00187825  0.388
1995 Bukauskas FF, Elfgang C, Willecke K, Weingart R. Heterotypic gap junction channels (connexin26-connexin32) violate the paradigm of unitary conductance. Pflã¼Gers Archiv : European Journal of Physiology. 429: 870-2. PMID 7603841 DOI: 10.1007/Bf00374812  0.388
1995 Elfgang C, Eckert R, Lichtenberg-Fraté H, Butterweck A, Traub O, Klein RA, Hülser DF, Willecke K. Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells. The Journal of Cell Biology. 129: 805-17. PMID 7537274 DOI: 10.1083/Jcb.129.3.805  0.451
1995 Willecke K, Elfgang C, Lichtenberg-Fraté H, Butterweck A, Traub O. Expression of murine connexin DNAs in human HeLa cells: Compatible and incompatible gap junction channels Progress in Cell Research. 4: 337-341. DOI: 10.1016/B978-0-444-81929-1.50069-1  0.397
1995 Bastide B, Neyses L, Ganten D, Paul M, Willecke K, Traub O. Specific expression of connexin40 and connexin43 in normal and hypertensive rat hearts Progress in Cell Research. 4: 217-220. DOI: 10.1016/B978-0-444-81929-1.50044-7  0.346
1995 Mesnil M, Krutovskikh V, Piccoli C, Elfgang C, Traub O, Willecke K, Yamasaki H. Growth inhibition by expression of connexin 26 in HeLa cells Progress in Cell Research. 4: 141-144. DOI: 10.1016/B978-0-444-81929-1.50031-9  0.398
1995 Dahl E, Winterhager E, Traub O, Butterweck A, Reuss B, Willecke K. Expression pattern of different connexins in comparison with communication compartments during early mouse development Progress in Cell Research. 4: 21-25. DOI: 10.1016/B978-0-444-81929-1.50006-X  0.327
1995 Willecke K, Lichtenberg-Fraté H, Butterweck A, Traub O, Elfgang C. Implications of connexin diversity for the function of gap junctions Journal of Cancer Research and Clinical Oncology. 121: A3-A3. DOI: 10.1007/BF02571975  0.324
1994 Traub O, Eckert R, Lichtenberg-Fraté H, Elfgang C, Bastide B, Scheidtmann KH, Hülser DF, Willecke K. Immunochemical and electrophysiological characterization of murine connexin40 and -43 in mouse tissues and transfected human cells. European Journal of Cell Biology. 64: 101-12. PMID 7957300 DOI: 10.18419/Opus-7795  0.465
1994 Schwarz HJ, Chang YS, Lalley PA, Willecke K. Chromosomal assignments of mouse genes for connexin 50 and connexin 33 by somatic cell hybridization. Somatic Cell and Molecular Genetics. 20: 243-7. PMID 7940024 DOI: 10.1007/Bf02254763  0.33
1994 Butterweck A, Elfgang C, Willecke K, Traub O. Differential expression of the gap junction proteins connexin45, -43, -40, -31, and -26 in mouse skin. European Journal of Cell Biology. 65: 152-63. PMID 7889986  0.376
1994 Butterweck A, Gergs U, Elfgang C, Willecke K, Traub O. Immunochemical characterization of the gap junction protein connexin45 in mouse kidney and transfected human HeLa cells. The Journal of Membrane Biology. 141: 247-56. PMID 7807524 DOI: 10.1007/Bf00235134  0.419
1993 Meda P, Pepper MS, Traub O, Willecke K, Gros D, Beyer E, Nicholson B, Paul D, Orci L. Differential expression of gap junction connexins in endocrine and exocrine glands. Endocrinology. 133: 2371-8. PMID 8404689 DOI: 10.1210/Endo.133.5.8404689  0.401
1993 Winterhager E, Grümmer R, Jahn E, Willecke K, Traub O. Spatial and temporal expression of connexin26 and connexin43 in rat endometrium during trophoblast invasion. Developmental Biology. 157: 399-409. PMID 8388816 DOI: 10.1006/dbio.1993.1144  0.327
1993 Bastide B, Neyses L, Ganten D, Paul M, Willecke K, Traub O. Gap junction protein connexin40 is preferentially expressed in vascular endothelium and conductive bundles of rat myocardium and is increased under hypertensive conditions. Circulation Research. 73: 1138-49. PMID 8222085 DOI: 10.1161/01.Res.73.6.1138  0.406
1992 Martin W, Lenz E, Grohé B, Willecke K. Suppression of transformed phenotype in hybrids of v-fgr and v-raf transformed rat-1 cells with rat embryonic fibroblasts is due to transcriptional inactivation of viral oncogenes. Experimental Cell Research. 200: 41-7. PMID 1563491 DOI: 10.1016/S0014-4827(05)80069-2  0.308
1992 Schwarz HJ, Chang YS, Hennemann H, Dahl E, Lalley PA, Willecke K. Chromosomal assignments of mouse connexin genes, coding for gap junctional proteins, by somatic cell hybridization. Somatic Cell and Molecular Genetics. 18: 351-9. PMID 1332196 DOI: 10.1007/Bf01235758  0.376
1992 Stutenkemper R, Geisse S, Schwarz HJ, Look J, Traub O, Nicholson BJ, Willecke K. The hepatocyte-specific phenotype of murine liver cells correlates with high expression of connexin32 and connexin26 but very low expression of connexin43. Experimental Cell Research. 201: 43-54. PMID 1319348 DOI: 10.1016/0014-4827(92)90346-A  0.374
1992 Hennemann H, Suchyna T, Lichtenberg-Fraté H, Jungbluth S, Dahl E, Schwarz J, Nicholson BJ, Willecke K. Molecular cloning and functional expression of mouse connexin40, a second gap junction gene preferentially expressed in lung. The Journal of Cell Biology. 117: 1299-310. PMID 1318884 DOI: 10.1083/Jcb.117.6.1299  0.469
1992 Wilgenbus KK, Kirkpatrick CJ, Knuechel R, Willecke K, Traub O. Expression of Cx26, Cx32 and Cx43 gap junction proteins in normal and neoplastic human tissues. International Journal of Cancer. Journal International Du Cancer. 51: 522-9. PMID 1318266 DOI: 10.1002/Ijc.2910510404  0.34
1991 Martin W, Zempel G, Hülser D, Willecke K. Growth inhibition of oncogene-transformed rat fibroblasts by cocultured normal cells: relevance of metabolic cooperation mediated by gap junctions. Cancer Research. 51: 5348-51. PMID 1913656 DOI: 10.18419/Opus-7790  0.311
1991 Meda P, Chanson M, Pepper M, Giordano E, Bosco D, Traub O, Willecke K, el Aoumari A, Gros D, Beyer EC. In vivo modulation of connexin 43 gene expression and junctional coupling of pancreatic B-cells. Experimental Cell Research. 192: 469-80. PMID 1846336 DOI: 10.1016/0014-4827(91)90066-4  0.414
1991 Willecke K, Heynkes R, Dahl E, Stutenkemper R, Hennemann H, Jungbluth S, Suchyna T, Nicholson BJ. Mouse connexin37: cloning and functional expression of a gap junction gene highly expressed in lung. The Journal of Cell Biology. 114: 1049-57. PMID 1651942 DOI: 10.1083/Jcb.114.5.1049  0.414
1989 Dermietzel R, Traub O, Hwang TK, Beyer E, Bennett MV, Spray DC, Willecke K. Differential expression of three gap junction proteins in developing and mature brain tissues. Proceedings of the National Academy of Sciences of the United States of America. 86: 10148-52. PMID 2557621 DOI: 10.1073/Pnas.86.24.10148  0.345
1989 Traub O, Look J, Dermietzel R, Brümmer F, Hülser D, Willecke K. Comparative characterization of the 21-kD and 26-kD gap junction proteins in murine liver and cultured hepatocytes. The Journal of Cell Biology. 108: 1039-51. PMID 2537831 DOI: 10.1083/Jcb.108.3.1039  0.326
1987 Bruzzone R, Trimble ER, Gjinovci A, Traub O, Willecke K, Meda P. Regulation of pancreatic exocrine function: a role for cell-to-cell communication? Pancreas. 2: 262-71. PMID 3628228 DOI: 10.1097/00006676-198705000-00004  0.35
1987 Dermietzel R, Yancey SB, Traub O, Willecke K, Revel JP. Major loss of the 28-kD protein of gap junction in proliferating hepatocytes. The Journal of Cell Biology. 105: 1925-34. PMID 2822729 DOI: 10.1083/Jcb.105.4.1925  0.37
1986 Abken H, Jungfer H, Albert WH, Willecke K. Immortalization of human lymphocytes by fusion with cytoplasts of transformed mouse L cells. The Journal of Cell Biology. 103: 795-805. PMID 3745269 DOI: 10.1083/Jcb.103.3.795  0.33
1986 Griegel S, Traub O, Willecke K, Schäfer R. Suppression and re-expression of transformed phenotype in hybrids of HA-ras-1-transformed rat-1 cells and early-passage rat embryonic fibroblasts. International Journal of Cancer. Journal International Du Cancer. 38: 697-705. PMID 3533793 DOI: 10.1002/IJC.2910380513  0.307
1986 Janssen-Timmen U, Traub O, Dermietzel R, Rabes HM, Willecke K. Reduced number of gap junctions in rat hepatocarcinomas detected by monoclonal antibody. Carcinogenesis. 7: 1475-82. PMID 3017599 DOI: 10.1093/CARCIN/7.9.1475  0.33
1983 Willecke K, Müller D, Drüge PM, Frixen U, Schäfer R, Dermietzel R, Hülser D. Isolation and characterization of Chinese hamster cells defective in cell-cell coupling via gap junctions. Experimental Cell Research. 144: 95-113. PMID 6840215 DOI: 10.1016/0014-4827(83)90445-7  0.377
1983 Traub O, Willecke K. Cross reaction of antibodies against liver gap junction protein (26K) with lens fiber junction protein (MIP) suggests structural homology between these tissue specific gene products. Biochemical and Biophysical Research Communications. 109: 895-901. PMID 6186254 DOI: 10.1016/0006-291X(82)92024-1  0.305
1982 Bravo R, Schafer R, Willecke K, MacDonald-Bravo H, Fey SJ, Celis JE. More than one-third of the discernible mouse polypeptides are not expressed in a Chinese hamster-mouse embryo fibroblast hybrid that retains all mouse chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 79: 2281-5. PMID 6954539 DOI: 10.1073/PNAS.79.7.2281  0.355
1981 Schäfer R, Doehmer J, Rademacher I, Willecke K. Assignment of the gene for cytoplasmic glutamate-oxaloacetate transaminase to mouse chromosome 19 using chinese hamster x mouse somatic cell hybrids. Somatic Cell Genetics. 6: 709-17. PMID 7444718 DOI: 10.1007/BF01538970  0.38
1980 Doehmer J, Rademacher I, Willecke K. Fusion with mouse thymocytes leads to expression of p30 antigen in fibroblasts of BALB/Mo mice. Virology. 105: 278-81. PMID 6968119 DOI: 10.1016/0042-6822(80)90180-4  0.356
1979 Breindl M, Doehmer J, Willecke K, Dausman J, Jaenisch R. Germ line integration of Moloney leukemia virus: identification of the chromosomal integration site. Proceedings of the National Academy of Sciences of the United States of America. 76: 1938-42. PMID 287034 DOI: 10.1073/Pnas.76.4.1938  0.303
1977 Willecke K, Teber T, Kucherlapati RS, Ruddle FH. Human mitochondrial thymidine kinase is coded for by a gene on chromosome 16 of the nucleus. Somatic Cell Genetics. 3: 237-45. PMID 605384 DOI: 10.1007/Bf01538743  0.552
1976 Wille W, Willecke K. Retention of purified proteins in resealed human erythrocyte ghosts and transfer by fusion into cultured murine recipient cells. Febs Letters. 65: 59-62. PMID 1278411 DOI: 10.1016/0014-5793(76)80621-7  0.305
1976 Willecke K, Reber T, Kucherlapati RS, Ruddle FH. Segregation of human mitochondrial thymidine thymidine kinase activity in human-mouse somatic cell hybrids. Birth Defects Original Article Series. 12: 252-5. PMID 1024620  0.558
1976 Willecke K, Reber T, Kucherlapati RS, Ruddle FH. Segregation of human mitochondrial thymidine kinase activity in human-mouse somatic cell hybrids. Cytogenetics and Cell Genetics. 16: 252-5. PMID 975885 DOI: 10.1159/000130604  0.558
1976 Willecke K, Lange R, Krüger A, Reber T. Cotransfer of two linked human genes into cultured mouse cells. Proceedings of the National Academy of Sciences of the United States of America. 73: 1274-8. PMID 177984 DOI: 10.1073/PNAS.73.4.1274  0.331
1975 Willecke K, Ruddle FH. Transfer of the gene for hypoxanthine-guanine phosphoribosyltransferase of isolated human metaphase chromosomes into murine L-cells. Birth Defects Original Article Series. 11: 288-91. PMID 1239317  0.396
1975 Willecke K, Ruddle FH. Transfer of the gene for hypoxanthine-guanine phosphoribosyltransferase of isolated human metaphase chromosomes into murine L-cells. Cytogenetics and Cell Genetics. 14: 458-61. PMID 1192839  0.396
1975 Willecke K, Ruddle FH. Transfer of the human gene for hypoxanthine-guanine phosphoribosyltransferase via isolated human metaphase chromosomes into mouse L-cells. Proceedings of the National Academy of Sciences of the United States of America. 72: 1792-6. PMID 1057170 DOI: 10.1073/Pnas.72.5.1792  0.486
1975 Elsevier SM, Kucherlapati RS, Nichols EA, Willecke K, Creagan RP, Giles RE, McDougall JK, Ruddle FH. Assignment and regional localization of a gene coding for galactokinase to human chromosome 17q21-22. Birth Defects Original Article Series. 11: 117-9. PMID 173434 DOI: 10.1159/000130365  0.38
1975 Elsevier SM, Kucherlapati RS, Nichols EA, Willecke K, Creagan RP, Giles RE, McDougall JK, Ruddle FH. Assigment and regional localization of a gene coding for galactokinase to human chromosome 17q21-22. Cytogenetics and Cell Genetics. 14: 287-9. PMID 172290 DOI: 10.1159/000130365  0.537
1974 Willecke K, Ruddle FH. Proceedings: Transfer of the human gene (HGPRT) for hypoxanthine phosphoribosyltransferase (EC 2.4.2.8) on isolated human metaphase chromosomes into mouse cells. Hoppe-Seyler's Zeitschrift FüR Physiologische Chemie. 355: 1269. PMID 4461622  0.412
1974 Elsevier SM, Kucherlapati RS, Nichols EA, Creagan RP, Giles RE, Ruddle FH, Willecke K, McDougall JK. Assignment of the gene for galactokinase to human chromosome 17 and its regional localisation to band q21-22. Nature. 251: 633-6. PMID 4371022 DOI: 10.1038/251633A0  0.569
1972 Fournier RE, McKillen MN, Pardee AB, Willecke K. Transport of dicarboxylic acids in Bacillus subtilis. Inducible uptake of L-malate. The Journal of Biological Chemistry. 247: 5587-95. PMID 4626722  0.358
1971 Willecke K, Pardee AB. Fatty acid-requiring mutant of bacillus subtilis defective in branched chain alpha-keto acid dehydrogenase. The Journal of Biological Chemistry. 246: 5264-72. PMID 4999353  0.373
1971 Willecke K, Pardee AB. Inducible transport of citrate in a Gram-positive bacterium, Bacillus subtilis. The Journal of Biological Chemistry. 246: 1032-40. PMID 4993437  0.357
1970 Schweizer E, Willecke K, Winnewisser W, Lynen F. The role of phosphopantetheine in the yeast fatty acid synthetase complex. Vitamins and Hormones. 28: 329-43. PMID 4946805 DOI: 10.1016/S0083-6729(08)60901-2  0.41
1969 Willecke K, Ritter E, Lynen F. Isolation of an acyl carrier protein component from the multienzyme complex of yeast fatty acid synthetase. European Journal of Biochemistry / Febs. 8: 503-9. PMID 5796138 DOI: 10.1111/j.1432-1033.1969.tb00555.x  0.434
1969 Yalpani M, Willecke K, Lynen F. Triacetic acid lactone, a derailment product of fatty acid biosynthesis. European Journal of Biochemistry / Febs. 8: 495-502. PMID 4389576 DOI: 10.1111/j.1432-1033.1969.tb00554.x  0.395
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