| Year |
Citation |
Score |
| 2016 |
Pawlik B, Schlüter T, Hartwich H, Breuel S, Heepmann L, Nothwang HG. Comparative Analysis of Gene Regulatory Network Components in the Auditory Hindbrain of Mice and Chicken. Brain, Behavior and Evolution. PMID 27866201 DOI: 10.1159/000449447 |
0.321 |
|
| 2015 |
Ebbers L, Satheesh SV, Janz K, Rüttiger L, Blosa M, Hofmann F, Morawski M, Griesemer D, Knipper M, Friauf E, Nothwang HG. L-type Calcium Channel Cav1.2 Is Required for Maintenance of Auditory Brainstem Nuclei. The Journal of Biological Chemistry. 290: 23692-710. PMID 26242732 DOI: 10.1074/Jbc.M115.672675 |
0.636 |
|
| 2014 |
Nothwang HG, Engel J, Knipper M, Friauf E. L-Typ-Kalzium-Kanäle im Hörsystem E-Neuroforum. 20. DOI: 10.1515/nf-2014-0304 |
0.527 |
|
| 2014 |
Nothwang HG, Engel J, Knipper M, Friauf E. L-type calcium channels in the auditory system | L-Typ-Kalzium-Kanäle im Hörsystem Neuroforum. 20: 8545-8553. |
0.518 |
|
| 2013 |
Ehmann H, Hartwich H, Salzig C, Hartmann N, Clément-Ziza M, Ushakov K, Avraham KB, Bininda-Emonds OR, Hartmann AK, Lang P, Friauf E, Nothwang HG. Time-dependent gene expression analysis of the developing superior olivary complex. The Journal of Biological Chemistry. 288: 25865-79. PMID 23893414 DOI: 10.1074/Jbc.M113.490508 |
0.594 |
|
| 2012 |
Satheesh SV, Kunert K, Rüttiger L, Zuccotti A, Schönig K, Friauf E, Knipper M, Bartsch D, Nothwang HG. Retrocochlear function of the peripheral deafness gene Cacna1d. Human Molecular Genetics. 21: 3896-909. PMID 22678062 DOI: 10.1093/hmg/dds217 |
0.599 |
|
| 2011 |
Hirtz JJ, Boesen M, Braun N, Deitmer JW, Kramer F, Lohr C, Müller B, Nothwang HG, Striessnig J, Löhrke S, Friauf E. Cav1.3 calcium channels are required for normal development of the auditory brainstem. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 8280-94. PMID 21632949 DOI: 10.1523/Jneurosci.5098-10.2011 |
0.694 |
|
| 2010 |
Hartmann AM, Wenz M, Mercado A, Störger C, Mount DB, Friauf E, Nothwang HG. Differences in the large extracellular loop between the K(+)-Cl(-) cotransporters KCC2 and KCC4. The Journal of Biological Chemistry. 285: 23994-4002. PMID 20516068 DOI: 10.1074/jbc.M110.144063 |
0.591 |
|
| 2009 |
Hartmann AM, Blaesse P, Kranz T, Wenz M, Schindler J, Kaila K, Friauf E, Nothwang HG. Opposite effect of membrane raft perturbation on transport activity of KCC2 and NKCC1. Journal of Neurochemistry. 111: 321-31. PMID 19686239 DOI: 10.1111/J.1471-4159.2009.06343.X |
0.736 |
|
| 2009 |
Wenz M, Hartmann AM, Friauf E, Nothwang HG. CIP1 is an activator of the K+-Cl- cotransporter KCC2. Biochemical and Biophysical Research Communications. 381: 388-92. PMID 19232517 DOI: 10.1016/j.bbrc.2009.02.057 |
0.64 |
|
| 2008 |
Friauf E, Wenz M, Oberhofer M, Nothwang HG, Balakrishnan V, Knipper M, Löhrke S. Hypothyroidism impairs chloride homeostasis and onset of inhibitory neurotransmission in developing auditory brainstem and hippocampal neurons. The European Journal of Neuroscience. 28: 2371-80. PMID 19087168 DOI: 10.1111/j.1460-9568.2008.06528.x |
0.682 |
|
| 2008 |
Ehmann H, Salzig C, Lang P, Friauf E, Nothwang HG. Minimal sex differences in gene expression in the rat superior olivary complex. Hearing Research. 245: 65-72. PMID 18793710 DOI: 10.1016/j.heares.2008.08.008 |
0.547 |
|
| 2008 |
Becker M, Nothwang HG, Friauf E. Different protein profiles in inferior colliculus and cerebellum: a comparative proteomic study. Neuroscience. 154: 233-44. PMID 18400408 DOI: 10.1016/j.neuroscience.2008.02.017 |
0.568 |
|
| 2008 |
Blaesse P, Nothwang HG. Neuronale Chloridhomöostase: entwicklungs- und aktivitätsabhängige Regulation von Chloridtransportern E-Neuroforum. 14. DOI: 10.1515/Nf-2008-0102 |
0.667 |
|
| 2008 |
Blaesse P, Nothwang HG. Neuronal chloride homeostasis: Development and activity-dependent regulation of cation-chloride cotransporters | Neuronale Chloridhomöstase: Entwicklungs- und aktivitätsabhängige Regulation von Chloridtransportern Neuroforum. 14: 148-158. |
0.694 |
|
| 2006 |
Blaesse P, Guillemin I, Schindler J, Schweizer M, Delpire E, Khiroug L, Friauf E, Nothwang HG. Oligomerization of KCC2 correlates with development of inhibitory neurotransmission. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10407-19. PMID 17035525 DOI: 10.1523/Jneurosci.3257-06.2006 |
0.765 |
|
| 2006 |
Schindler J, Jung S, Niedner-Schatteburg G, Friauf E, Nothwang HG. Enrichment of integral membrane proteins from small amounts of brain tissue. Journal of Neural Transmission (Vienna, Austria : 1996). 113: 995-1013. PMID 16835696 DOI: 10.1007/S00702-006-0508-4 |
0.569 |
|
| 2006 |
Nothwang HG, Koehl A, Friauf E. Comparative gene expression analysis reveals a characteristic molecular profile of the superior olivary complex. The Anatomical Record. Part a, Discoveries in Molecular, Cellular, and Evolutionary Biology. 288: 409-23. PMID 16550588 DOI: 10.1002/ar.a.20301 |
0.593 |
|
| 2006 |
Schindler J, Lewandrowski U, Sickmann A, Friauf E, Nothwang HG. Proteomic analysis of brain plasma membranes isolated by affinity two-phase partitioning. Molecular & Cellular Proteomics : McP. 5: 390-400. PMID 16249173 DOI: 10.1074/mcp.T500017-MCP200 |
0.579 |
|
| 2005 |
Blaesse P, Ehrhardt S, Friauf E, Nothwang HG. Developmental pattern of three vesicular glutamate transporters in the rat superior olivary complex. Cell and Tissue Research. 320: 33-50. PMID 15714284 DOI: 10.1007/S00441-004-1054-8 |
0.74 |
|
| 2005 |
Guillemin I, Becker M, Ociepka K, Friauf E, Nothwang HG. A subcellular prefractionation protocol for minute amounts of mammalian cell cultures and tissue. Proteomics. 5: 35-45. PMID 15602774 DOI: 10.1002/pmic.200400892 |
0.558 |
|
| 2004 |
Koehl A, Schmidt N, Rieger A, Pilgram SM, Letunic I, Bork P, Soto F, Friauf E, Nothwang HG. Gene expression profiling of the rat superior olivary complex using serial analysis of gene expression. The European Journal of Neuroscience. 20: 3244-58. PMID 15610157 DOI: 10.1111/J.1460-9568.2004.03791.X |
0.623 |
|
| 2003 |
Nothwang HG, Becker M, Ociepka K, Friauf E. Protein analysis in the rat auditory brainstem by two-dimensional gel electrophoresis and mass spectrometry. Brain Research. Molecular Brain Research. 116: 59-69. PMID 12941461 DOI: 10.1016/S0169-328X(03)00234-1 |
0.573 |
|
| 2003 |
Balakrishnan V, Becker M, Löhrke S, Nothwang HG, Güresir E, Friauf E. Expression and function of chloride transporters during development of inhibitory neurotransmission in the auditory brainstem. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 4134-45. PMID 12764101 DOI: 10.1523/JNEUROSCI.23-10-04134.2003 |
0.713 |
|
| 2003 |
Becker M, Nothwang HG, Friauf E. Differential expression pattern of chloride transporters NCC, NKCC2, KCC1, KCC3, KCC4, and AE3 in the developing rat auditory brainstem. Cell and Tissue Research. 312: 155-65. PMID 12712325 DOI: 10.1007/s00441-003-0713-5 |
0.665 |
|
| 2003 |
Koehl A, Friauf E, Nothwang HG. Efficient cloning of SAGE tags by blunt-end ligation of polished concatemers. Biotechniques. 34: 692-4. PMID 12703289 DOI: 10.2144/03344bm01 |
0.479 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2015 |
Mahadevan V, Dargaei Z, Ivakine EA, Hartmann AM, Ng D, Chevrier J, Ormond J, Nothwang HG, McInnes RR, Woodin MA. Neto2-null mice have impaired GABAergic inhibition and are susceptible to seizures. Frontiers in Cellular Neuroscience. 9: 368. PMID 26441539 DOI: 10.3389/Fncel.2015.00368 |
0.299 |
|
| 2023 |
Radulovic T, Rajaram E, Ebbers L, Pagella S, Winklhofer M, Kopp-Scheinpflug C, Nothwang HG, Milenkovic I, Hartmann AM. Serine 937 phosphorylation enhances KCC2 activity and strengthens synaptic inhibition. Scientific Reports. 13: 21660. PMID 38066086 DOI: 10.1038/s41598-023-48884-x |
0.287 |
|
| 2016 |
Hartwich H, Rosengauer E, Rüttiger L, Wilms V, Waterholter SK, Nothwang HG. Functional Role of γ-Crystallin N in the Auditory Hindbrain. Plos One. 11: e0161140. PMID 27517863 DOI: 10.1371/journal.pone.0161140 |
0.284 |
|
| 2023 |
Saleh AJ, Ahmed Y, Peters LO, Nothwang HG. Comparative expression analysis of the Atoh7 gene regulatory network in the mouse and chicken auditory hindbrain. Cell and Tissue Research. PMID 36961563 DOI: 10.1007/s00441-023-03763-9 |
0.283 |
|
| 2015 |
Llano O, Smirnov S, Soni S, Golubtsov A, Guillemin I, Hotulainen P, Medina I, Nothwang HG, Rivera C, Ludwig A. KCC2 regulates actin dynamics in dendritic spines via interaction with β-PIX. The Journal of Cell Biology. 209: 671-86. PMID 26056138 DOI: 10.1083/jcb.201411008 |
0.272 |
|
| 2014 |
Hartmann AM, Nothwang HG. Molecular and evolutionary insights into the structural organization of cation chloride cotransporters. Frontiers in Cellular Neuroscience. 8: 470. PMID 25653592 DOI: 10.3389/fncel.2014.00470 |
0.265 |
|
| 2012 |
Döding A, Hartmann AM, Beyer T, Nothwang HG. KCC2 transport activity requires the highly conserved L₆₇₅ in the C-terminal β1 strand. Biochemical and Biophysical Research Communications. 420: 492-7. PMID 22414695 DOI: 10.1016/j.bbrc.2012.02.147 |
0.264 |
|
| 2017 |
Ebbers L, Weber M, Nothwang HG. Activity-dependent formation of a vesicular inhibitory amino acid transporter gradient in the superior olivary complex of NMRI mice. Bmc Neuroscience. 18: 75. PMID 29073893 DOI: 10.1186/s12868-017-0393-9 |
0.248 |
|
| 2012 |
Rosengauer E, Hartwich H, Hartmann AM, Rudnicki A, Satheesh SV, Avraham KB, Nothwang HG. Egr2::cre mediated conditional ablation of dicer disrupts histogenesis of mammalian central auditory nuclei. Plos One. 7: e49503. PMID 23152916 DOI: 10.1371/Journal.Pone.0049503 |
0.247 |
|
| 2011 |
Hartmann AM, Nothwang HG. Opposite temperature effect on transport activity of KCC2/KCC4 and N(K)CCs in HEK-293 cells. Bmc Research Notes. 4: 526. PMID 22152068 DOI: 10.1186/1756-0500-4-526 |
0.241 |
|
| 2013 |
Kullmann L, Schlüter T, Wagner H, Nothwang HG. Evolutionary conservation of Kv3.1 in the barn owl Tyto alba. Brain, Behavior and Evolution. 81: 187-93. PMID 23615168 DOI: 10.1159/000350196 |
0.232 |
|
| 2013 |
Zuccotti A, Lee SC, Campanelli D, Singer W, Satheesh SV, Patriarchi T, Geisler HS, Köpschall I, Rohbock K, Nothwang HG, Hu J, Hell JW, Schimmang T, Rüttiger L, Knipper M. L-type CaV1.2 deletion in the cochlea but not in the brainstem reduces noise vulnerability: implication for CaV1.2-mediated control of cochlear BDNF expression. Frontiers in Molecular Neuroscience. 6: 20. PMID 23950737 DOI: 10.3389/Fnmol.2013.00020 |
0.229 |
|
| 2014 |
Hartmann AM, Tesch D, Nothwang HG, Bininda-Emonds OR. Evolution of the cation chloride cotransporter family: ancient origins, gene losses, and subfunctionalization through duplication. Molecular Biology and Evolution. 31: 434-47. PMID 24273324 DOI: 10.1093/Molbev/Mst225 |
0.227 |
|
| 2014 |
Weber M, Hartmann AM, Beyer T, Ripperger A, Nothwang HG. A novel regulatory locus of phosphorylation in the C terminus of the potassium chloride cotransporter KCC2 that interferes with N-ethylmaleimide or staurosporine-mediated activation. The Journal of Biological Chemistry. 289: 18668-79. PMID 24849604 DOI: 10.1074/jbc.M114.567834 |
0.226 |
|
| 2022 |
Hartmann AM, Nothwang HG. NKCC1 and KCC2: Structural insights into phospho-regulation. Frontiers in Molecular Neuroscience. 15: 964488. PMID 35935337 DOI: 10.3389/fnmol.2022.964488 |
0.222 |
|
| 2021 |
Schinzel F, Seyfer H, Ebbers L, Nothwang HG. The Lbx1 lineage differentially contributes to inhibitory cell types of the dorsal cochlear nucleus, a cerebellum-like structure, and the cerebellum. The Journal of Comparative Neurology. PMID 33786818 DOI: 10.1002/cne.25147 |
0.221 |
|
| 2018 |
Schlüter T, Berger C, Rosengauer E, Fieth P, Krohs C, Ushakov K, Steel KP, Avraham KB, Hartmann A, Felmy F, Nothwang HG. miR-96 is required for normal development of the auditory hindbrain. Human Molecular Genetics. PMID 29325119 DOI: 10.1093/Hmg/Ddy007 |
0.218 |
|
| 2016 |
Ebbers L, Runge K, Nothwang HG. Differential patterns of histone methylase EHMT2 and its catalyzed histone modifications H3K9me1 and H3K9me2 during maturation of central auditory system. Cell and Tissue Research. PMID 27083448 DOI: 10.1007/s00441-016-2401-2 |
0.215 |
|
| 2014 |
Willaredt MA, Ebbers L, Nothwang HG. Central auditory function of deafness genes. Hearing Research. 312: 9-20. PMID 24566090 DOI: 10.1016/j.heares.2014.02.004 |
0.214 |
|
| 2000 |
Scheer MP, van der Maarel S, Kübart S, Schulz A, Wirth J, Schweiger S, Ropers H, Nothwang HG. DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner. Genomics. 63: 123-32. PMID 10662551 DOI: 10.1006/geno.1999.6027 |
0.212 |
|
| 2020 |
Krohs C, Bordeynik-Cohen M, Messika-Gold N, Elkon R, Avraham KB, Nothwang HG. Expression pattern of cochlear microRNAs in the mammalian auditory hindbrain. Cell and Tissue Research. PMID 33156384 DOI: 10.1007/s00441-020-03290-x |
0.204 |
|
| 2021 |
Hartmann AM, Fu L, Ziegler C, Winklhofer M, Nothwang HG. Structural changes in the extracellular loop 2 of the murine KCC2 potassium chloride cotransporter modulate ion transport. The Journal of Biological Chemistry. 100793. PMID 34019872 DOI: 10.1016/j.jbc.2021.100793 |
0.203 |
|
| 2017 |
Hartmann AM, Pisella LI, Medina I, Nothwang HG. Molecular cloning and biochemical characterization of two cation chloride cotransporter subfamily members of Hydra vulgaris. Plos One. 12: e0179968. PMID 28662098 DOI: 10.1371/journal.pone.0179968 |
0.199 |
|
| 2000 |
Thiesen S, Kübart S, Ropers HH, Nothwang HG. Isolation of two novel human RhoGEFs, ARHGEF3 and ARHGEF4, in 3p13-21 and 2q22. Biochemical and Biophysical Research Communications. 273: 364-9. PMID 10873612 DOI: 10.1006/bbrc.2000.2925 |
0.198 |
|
| 2009 |
Schindler J, Nothwang HG. Isolation of plasma membranes from the nervous system by countercurrent distribution in aqueous polymer two-phase systems. Methods in Molecular Biology (Clifton, N.J.). 564: 335-40. PMID 19544032 DOI: 10.1007/978-1-60761-157-8_19 |
0.198 |
|
| 2018 |
Köppl C, Wilms V, Russell IJ, Nothwang HG. Evolution of Endolymph Secretion and Endolymphatic Potential Generation in the Vertebrate Inner Ear. Brain, Behavior and Evolution. 1-31. PMID 30415265 DOI: 10.1159/000494050 |
0.193 |
|
| 2013 |
Schindler J, Ye J, Jensen ON, Nothwang HG. Monitoring the native phosphorylation state of plasma membrane proteins from a single mouse cerebellum. Journal of Neuroscience Methods. 213: 153-64. PMID 23246975 DOI: 10.1016/j.jneumeth.2012.10.003 |
0.193 |
|
| 2001 |
Nothwang HG, Kim HG, Aoki J, Geisterfer M, Kübart S, Wegner RD, van Moers A, Ashworth LK, Haaf T, Bell J, Arai H, Tommerup N, Ropers HH, Wirth J. Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain. Human Molecular Genetics. 10: 797-806. PMID 11285245 DOI: 10.1093/hmg/10.8.797 |
0.19 |
|
| 2024 |
Lessle S, Ebbers L, Dörflinger Y, Hoppe S, Kaiser M, Nothwang HG, Körber C. Maintenance of a central high frequency synapse in the absence of synaptic activity. Frontiers in Cellular Neuroscience. 18: 1404206. PMID 39624646 DOI: 10.3389/fncel.2024.1404206 |
0.189 |
|
| 2021 |
Saleh AJ, Nothwang HG. Differential expression of microRNAs in the developing avian auditory hindbrain. The Journal of Comparative Neurology. PMID 34180540 DOI: 10.1002/cne.25205 |
0.187 |
|
| 2017 |
Wilms V, Söffgen C, Nothwang HG. Differences in molecular mechanisms of K(+) clearance in the auditory sensory epithelium of birds and mammals. The Journal of Experimental Biology. PMID 28526685 DOI: 10.1242/jeb.158030 |
0.184 |
|
| 1999 |
Caubit X, Thangarajah R, Theil T, Wirth J, Nothwang HG, Rüther U, Krauss S. Mouse Dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 214: 66-80. PMID 9915577 DOI: 10.1002/(SICI)1097-0177(199901)214:1<66::AID-DVDY7>3.0.CO;2-7 |
0.181 |
|
| 2021 |
Krohs C, Körber C, Ebbers L, Altaf F, Hollje G, Hoppe S, Dörflinger Y, Prosser HM, Nothwang HG. Loss of miR-183/96 alters synaptic strength via pre- and postsynaptic mechanisms at a central synapse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 34193555 DOI: 10.1523/JNEUROSCI.0139-20.2021 |
0.18 |
|
| 2021 |
Krohs C, Körber C, Ebbers L, Altaf F, Hollje G, Hoppe S, Dörflinger Y, Prosser HM, Nothwang HG. Loss of miR-183/96 alters synaptic strength via pre- and postsynaptic mechanisms at a central synapse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 34193555 DOI: 10.1523/JNEUROSCI.0139-20.2021 |
0.18 |
|
| 2016 |
Wilms V, Köppl C, Söffgen C, Hartmann AM, Nothwang HG. Molecular bases of K(+) secretory cells in the inner ear: shared and distinct features between birds and mammals. Scientific Reports. 6: 34203. PMID 27680950 DOI: 10.1038/srep34203 |
0.18 |
|
| 2009 |
Nothwang HG, Schindler J. Two-dimensional separation of membrane proteins by 16-BAC-SDS-PAGE. Methods in Molecular Biology (Clifton, N.J.). 528: 269-77. PMID 19153699 DOI: 10.1007/978-1-60327-310-7_19 |
0.176 |
|
| 2009 |
Schindler J, Nothwang HG. Enrichment of brain plasma membranes by affinity two-phase partitioning. Methods in Molecular Biology (Clifton, N.J.). 528: 119-26. PMID 19153688 DOI: 10.1007/978-1-60327-310-7_8 |
0.175 |
|
| 2000 |
Vollmer M, Kremer M, Ruf R, Miot S, Nothwang HG, Wirth J, Otto E, Krapf R, Hildebrandt F. Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes. Genomics. 68: 127-35. PMID 10964510 DOI: 10.1006/geno.2000.6292 |
0.172 |
|
| 1999 |
Schröer A, Schneider S, Ropers HH, Nothwang HG. Cloning and characterization of UXT, a novel gene in human Xp11, which is widely and abundantly expressed in tumor tissue Genomics. 56: 340-343. PMID 10087202 DOI: 10.1006/geno.1998.5712 |
0.17 |
|
| 2015 |
Willaredt MA, Schlüter T, Nothwang HG. The gene regulatory networks underlying formation of the auditory hindbrain. Cellular and Molecular Life Sciences : Cmls. 72: 519-35. PMID 25332098 DOI: 10.1007/s00018-014-1759-0 |
0.168 |
|
| 2018 |
Cordshagen A, Busch W, Winklhofer M, Nothwang HG, Hartmann AM. Phospho-regulation of the intracellular termini of K-Cl cotransporter 2 (KCC2) enables flexible control of its activity. The Journal of Biological Chemistry. PMID 30201606 DOI: 10.1074/jbc.RA118.004349 |
0.164 |
|
| 2023 |
Bordeynik-Cohen M, Sperber M, Ebbers L, Messika-Gold N, Krohs C, Koffler-Brill T, Noy Y, Elkon R, Nothwang HG, Avraham KB. Shared and organ-specific gene-expression programs during the development of the cochlea and the superior olivary complex. Rna Biology. 20: 629-640. PMID 37602850 DOI: 10.1080/15476286.2023.2247628 |
0.162 |
|
| 2006 |
Becker M, Schindler J, Nothwang HG. Neuroproteomics - the tasks lying ahead. Electrophoresis. 27: 2819-29. PMID 16739225 DOI: 10.1002/elps.200500892 |
0.161 |
|
| 1993 |
Bey F, Silva Pereira I, Coux O, Viegas-Péquignot E, Recillas Targa F, Nothwang HG, Dutrillaux B, Scherrer K. The prosomal RNA-binding protein p27K is a member of the alpha-type human prosomal gene family. Molecular & General Genetics : Mgg. 237: 193-205. PMID 7681138 DOI: 10.1007/Bf00282801 |
0.157 |
|
| 2020 |
Cordshagen A, Busch W, Winklhofer M, Nothwang HG, Hartmann AM. Correction: Phosphoregulation of the intracellular termini of K-Cl cotransporter 2 (KCC2) enables flexible control of its activity. The Journal of Biological Chemistry. 295: 11948. PMID 32817128 DOI: 10.1074/jbc.AAC120.015318 |
0.154 |
|
| 2020 |
Zhang J, Cordshagen A, Medina I, Nothwang HG, Wisniewski JR, Winklhofer M, Hartmann AM. Staurosporine and NEM mainly impair WNK-SPAK/OSR1 mediated phosphorylation of KCC2 and NKCC1. Plos One. 15: e0232967. PMID 32413057 DOI: 10.1371/Journal.Pone.0232967 |
0.154 |
|
| 2006 |
Schindler J, Nothwang HG. Aqueous polymer two-phase systems: effective tools for plasma membrane proteomics. Proteomics. 6: 5409-17. PMID 16972286 DOI: 10.1002/pmic.200600243 |
0.15 |
|
| 1994 |
Tamura T, Osaka F, Kawamura Y, Higuti T, Ishida N, Nothwang HG, Tsurumi C, Tanaka K, Ichihara A. Isolation and characterization of alpha-type HC3 and beta-type HC5 subunit genes of human proteasomes. Journal of Molecular Biology. 244: 117-24. PMID 7966316 DOI: 10.1006/jmbi.1994.1710 |
0.148 |
|
| 1998 |
Nothwang HG, Rensing C, Kübler M, Denich D, Brandl B, Stubanus M, Haaf T, Kurnit D, Hildebrandt F. Identification of a novel Ran binding protein 2 related gene (RANBP2L1) and detection of a gene cluster on human chromosome 2q11-q12. Genomics. 47: 383-92. PMID 9480752 DOI: 10.1006/geno.1997.5119 |
0.148 |
|
| 2015 |
Nothwang HG, Ebbers L, Schlüter T, Willaredt MA. The emerging framework of mammalian auditory hindbrain development. Cell and Tissue Research. 361: 33-48. PMID 25636588 DOI: 10.1007/s00441-014-2110-7 |
0.139 |
|
| 2015 |
Nothwang HG, Ebbers L, Schlüter T, Willaredt MA. Erratum to: The emerging framework of mammalian auditory hindbrain development. Cell and Tissue Research. PMID 25762307 DOI: 10.1007/s00441-015-2161-4 |
0.137 |
|
| 2014 |
Nothwang H, Engel J, Knipper M, Friauf E. L-type calcium channels in the auditory system E-Neuroforum. 5: 60-66. DOI: 10.1007/s13295-014-0059-3 |
0.132 |
|
| 2012 |
Hartwich H, Satheesh SV, Nothwang HG. A pink mouse reports the switch from red to green fluorescence upon Cre-mediated recombination. Bmc Research Notes. 5: 296. PMID 22697046 DOI: 10.1186/1756-0500-5-296 |
0.129 |
|
| 1994 |
Nothwang HG, Tamura T, Tanaka K, Ichihara A. Sequence analyses and inter-species comparisons of three novel human proteasomal subunits, HsN3, HsC7-I and HsC10-II, confine potential proteolytic active-site residues. Biochimica Et Biophysica Acta. 1219: 361-8. PMID 7918633 DOI: 10.1016/0167-4781(94)90060-4 |
0.126 |
|
| 1994 |
Akiyama K, Yokota K, Kagawa S, Shimbara N, Tamura T, Akioka H, Nothwang HG, Noda C, Tanaka K, Ichihara A. cDNA cloning and interferon gamma down-regulation of proteasomal subunits X and Y. Science (New York, N.Y.). 265: 1231-4. PMID 8066462 DOI: 10.1126/science.8066462 |
0.12 |
|
| 1992 |
Nothwang HG, Coux O, Bey F, Scherrer K. Prosomes and their multicatalytic proteinase activity. European Journal of Biochemistry / Febs. 207: 621-30. PMID 1633813 DOI: 10.1111/J.1432-1033.1992.Tb17089.X |
0.117 |
|
| 1997 |
Hildebrandt F, Otto E, Rensing C, Nothwang HG, Vollmer M, Adolphs J, Hanusch H, Brandis M. A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1. Nature Genetics. 17: 149-53. PMID 9326933 DOI: 10.1038/ng1097-149 |
0.115 |
|
| 2001 |
Omran H, Häffner K, Burth S, Fernandez C, Fargier B, Villaquiran A, Nothwang HG, Schnittger S, Lehrach H, Woo D, Brandis M, Sudbrak R, Hildebrandt F. Human adolescent nephronophthisis: gene locus synteny with polycystic kidney disease in pcy mice. Journal of the American Society of Nephrology : Jasn. 12: 107-13. PMID 11134256 |
0.111 |
|
| 2000 |
Kutsche K, Yntema H, Brandt A, Jantke I, Nothwang HG, Orth U, Boavida MG, David D, Chelly J, Fryns JP, Moraine C, Ropers HH, Hamel BC, van Bokhoven H, Gal A. Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation. Nature Genetics. 26: 247-50. PMID 11017088 DOI: 10.1038/80002 |
0.109 |
|
| 1997 |
Nothwang HG, Wirth J, Brandl B, Haaf T, Nielsen KB, Tommerup N, Ropers HH. Identification of positional candidates for neurological disorders on chromsome 13q14-->q22. Cytogenetics and Cell Genetics. 79: 293-7. PMID 9605876 DOI: 10.1159/000134747 |
0.107 |
|
| 2009 |
Apweiler R, Aslanidis C, Deufel T, Gerstner A, Hansen J, Hochstrasser D, Kellner R, Kubicek M, Lottspeich F, Maser E, Mewes HW, Meyer HE, Müllner S, Mutter W, Neumaier M, ... ... Nothwang HG, et al. Approaching clinical proteomics: current state and future fields of application in cellular proteomics. Cytometry. Part a : the Journal of the International Society For Analytical Cytology. 75: 816-32. PMID 19739086 DOI: 10.1002/Cyto.A.20779 |
0.103 |
|
| 2001 |
Wirth J, Back E, Hüttenhofer A, Nothwang HG, Lich C, Gross S, Menzel C, Schinzel A, Kioschis P, Tommerup N, Ropers HH, Horsthemke B, Buiting K. A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15. Human Molecular Genetics. 10: 201-10. PMID 11159938 DOI: 10.1093/hmg/10.3.201 |
0.101 |
|
| 1998 |
Nothwang HG, Stubanus M, Adolphs J, Hanusch H, Vossmerbäumer U, Denich D, Kübler M, Mincheva A, Lichter P, Hildebrandt F. Construction of a gene map of the nephronophthisis type 1 (NPHP1) region on human chromosome 2q12-q13. Genomics. 47: 276-85. PMID 9479500 DOI: 10.1006/geno.1997.5102 |
0.1 |
|
| 2009 |
Apweiler R, Aslanidis C, Deufel T, Gerstner A, Hansen J, Hochstrasser D, Kellner R, Kubicek M, Lottspeich F, Maser E, Mewes HW, Meyer HE, Müllner S, Mutter W, Neumaier M, ... ... Nothwang HG, et al. Approaching clinical proteomics: current state and future fields of application in fluid proteomics. Clinical Chemistry and Laboratory Medicine : Cclm / Fescc. 47: 724-44. PMID 19527139 DOI: 10.1515/Cclm.2009.167 |
0.099 |
|
| 1994 |
Coux O, Nothwang HG, Silva Pereira I, Recillas Targa F, Bey F, Scherrer K. Phylogenic relationships of the amino acid sequences of prosome (proteasome, MCP) subunits. Molecular & General Genetics : Mgg. 245: 769-80. PMID 7830725 DOI: 10.1007/Bf00297284 |
0.098 |
|
| 2001 |
Bolz H, von Brederlow B, RamÃrez A, Bryda EC, Kutsche K, Nothwang HG, Seeliger M, del C-Salcedó Cabrera M, Vila MC, Molina OP, Gal A, Kubisch C. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nature Genetics. 27: 108-12. PMID 11138009 DOI: 10.1038/83667 |
0.097 |
|
| 2020 |
Claußen M, Schulze J, Nothwang HG. Loss of inner hair cell ribbon synapses and auditory nerve fiber regression in Cldn14 knockout mice. Hearing Research. 391: 107950. PMID 32251970 DOI: 10.1016/j.heares.2020.107950 |
0.097 |
|
| 1992 |
Coux O, Camoin L, Nothwang HG, Bey F, Silva Pereira I, Keith G, Strosberg AD, Scherrer K. The protein of M(r) 21,000 constituting the prosome-like particle of duck erythroblasts is homologous to apoferritin. European Journal of Biochemistry / Febs. 207: 823-32. PMID 1499559 DOI: 10.1111/J.1432-1033.1992.Tb17113.X |
0.096 |
|
| 1992 |
Nothwang HG, Coux O, Bey F, Scherrer K. Disruption of prosomes by some bivalent metal ions results in the loss of their multicatalytic proteinase activity and cancels the nuclease resistance of prosomal RNA. The Biochemical Journal. 287: 733-9. PMID 1445237 DOI: 10.1042/Bj2870733 |
0.094 |
|
| 2000 |
Kutsche K, Glauner E, Knauf S, Pomarino A, Schmidt M, Schröder B, Nothwang HG, Schüler HM, Goecke TO, Kersten AJ, Althaus C, Gal A. Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium Cytogenetics and Cell Genetics. 91: 141-147. PMID 11173847 |
0.094 |
|
| 1997 |
Nothwang HG, Strahm B, Denich D, Kübler M, Schwabe J, Gingrich JC, Jauch A, Cox A, Nicklin MJ, Kurnit DM, Hildebrandt F. Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13. Genomics. 41: 370-8. PMID 9169134 DOI: 10.1006/geno.1997.4654 |
0.089 |
|
| 2016 |
Nothwang HG. Evolution of mammalian sound localization circuits: a developmental perspective. Progress in Neurobiology. PMID 27032475 DOI: 10.1016/j.pneurobio.2016.02.003 |
0.085 |
|
| 2000 |
Nothwang HG, Schröer A, van der Maarel S, Kübart S, Schneider S, Riesselmann L, Menzel C, Hinzmann B, Vogt D, Rosenthal A, Fryns J, Tommerup N, Haaf T, Ropers HH, Wirth J. Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations. Cytogenetics and Cell Genetics. 90: 126-33. PMID 11060462 |
0.082 |
|
| 1996 |
Hildebrandt F, Cybulla M, Strahm B, Nothwang HG, Singh-Sawhney I, Berz K, Nicklin M, Reiner O, Brandis M. Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13. Cytogenetics and Cell Genetics. 73: 235-9. PMID 8697815 DOI: 10.1159/000134346 |
0.079 |
|
| 2012 |
Hartwich H, Nothwang HG. An easy and versatile 2-step protocol for targeted modification and subcloning of DNA from bacterial artificial chromosomes using non-commercial plasmids. Bmc Research Notes. 5: 156. PMID 22433714 DOI: 10.1186/1756-0500-5-156 |
0.076 |
|
| 1997 |
Hildebrandt F, Strahm B, Nothwang HG, Gretz N, Schnieders B, Singh-Sawhney I, Kutt R, Vollmer M, Brandis M. Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie. Kidney International. 51: 261-9. PMID 8995741 DOI: 10.1038/ki.1997.31 |
0.076 |
|
| 2017 |
Nolte L, Tinne N, Schulze J, Heinemann D, Antonopoulos GC, Meyer H, Nothwang HG, Lenarz T, Heisterkamp A, Warnecke A, Ripken T. Scanning laser optical tomography for in toto imaging of the murine cochlea. Plos One. 12: e0175431. PMID 28388662 DOI: 10.1371/journal.pone.0175431 |
0.074 |
|
| 2019 |
Schulze J, Nolte L, Lyutenski S, Tinne N, Heinemann D, Ripken T, Willaredt MA, Nothwang HG, Lenarz T, Warnecke A. [Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version]. Hno. PMID 30963223 DOI: 10.1007/s00106-019-0652-4 |
0.073 |
|
| 2019 |
Schulze J, Nolte L, Lyutenski S, Tinne N, Heinemann D, Ripken T, Willaredt MA, Nothwang HG, Lenarz T, Warnecke A. Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. Hno. PMID 31065762 DOI: 10.1007/s00106-019-0654-2 |
0.073 |
|
| 1999 |
Wirth J, Nothwang HG, van der Maarel S, Menzel C, Borck G, Lopez-Pajares I, Brøndum-Nielsen K, Tommerup N, Bugge M, Ropers HH, Haaf T. Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes. Journal of Medical Genetics. 36: 271-8. PMID 10227392 |
0.048 |
|
| 1992 |
Nothwang HG, Coux O, Keith G, Silva-Pereira I, Scherrer K. The major RNA in prosomes of HeLa cells and duck erythroblasts is tRNA(Lys,3). Nucleic Acids Research. 20: 1959-65. PMID 1579498 DOI: 10.1093/Nar/20.8.1959 |
0.046 |
|
| 1998 |
Hildebrandt F, Nothwang HG, Vossmerbäumer U, Springer C, Strahm B, Hoppe B, Keuth B, Fuchshuber A, Querfeld U, Neuhaus TJ, Brandis M. Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie. Pediatric Nephrology (Berlin, Germany). 12: 16-9. PMID 9502560 DOI: 10.1007/s004670050394 |
0.043 |
|
| 1990 |
Scherrer K, Nothwang HG, Pereira IS, Bey F, Olink-Coux M, Huesca M, Coux O, Arcangeletti C, Chezzi C, Buri JF. The prosomes: molecular and cellular biology. Molecular Biology Reports. 14: 75. PMID 1694565 DOI: 10.1007/Bf00360422 |
0.041 |
|
| 1992 |
Coux O, Nothwang HG, Scherrer K, Bergsma-Schutter W, Arnberg AC, Timmins PA, Langowski J, Cohen-Addad C. Structure and RNA content of the prosomes. Febs Letters. 300: 49-55. PMID 1372271 DOI: 10.1016/0014-5793(92)80162-A |
0.034 |
|
| 2017 |
Schlüter T, Ebbers L, Nothwang HG. Mehr als das Ohr — die Evolution des Hörsinns Biospektrum. 23: 638-640. DOI: 10.1007/s12268-017-0849-6 |
0.03 |
|
| 1996 |
Spur NK, Bashir R, Bushby K, Cox A, Cox S, Hilde Brandt F, Hill N, Kao FT, Krols L, Marzella R, Miller N, Nothwang HG, Rocchi M, Sarfarazi M, Stratakis CA, et al. Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996. Cytogenetics and Cell Genetics. 73: 255-73. PMID 8751373 DOI: 10.1159/000134352 |
0.028 |
|
| 2001 |
Borck G, Wirth J, Hardt T, Tönnies H, Brøndum-Nielsen K, Bugge M, Tommerup N, Nothwang HG, Ropers HH, Haaf T. Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome. Journal of Medical Genetics. 38: 117-21. PMID 11288711 DOI: 10.1136/jmg.38.2.117 |
0.025 |
|
| 2002 |
Maróti Z, Kutsche K, Sutajova M, Gal A, Nothwang HG, Czeizel AE, TÃmár L, Sólyom E. Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome. American Journal of Medical Genetics. 109: 234-7. PMID 11977185 DOI: 10.1002/ajmg.10314 |
0.015 |
|
| 2000 |
Schröer A, Scheer MP, Zacharias S, Schneider S, Ropers HH, Nothwang HG, Chelly J, Hamel B, Fryns JP, Shaw P, Moraine C. Cosegregation of T108A Elk-1 with mental retardation. American Journal of Medical Genetics. 95: 404-5. PMID 11186900 DOI: 10.1002/1096-8628(20001211)95:4<404::AID-AJMG21>3.0.CO;2-G |
0.01 |
|
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