| Year |
Citation |
Score |
| 2023 |
Melo US, Jatzlau J, Prada-Medina CA, Flex E, Hartmann S, Ali S, Schöpflin R, Bernardini L, Ciolfi A, Moeinzadeh MH, Klever MK, Altay A, Vallecillo-García P, Carpentieri G, Delledonne M, ... ... Stricker S, et al. Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation. Nature Communications. 14: 6301. PMID 37813867 DOI: 10.1038/s41467-023-42123-7 |
0.427 |
|
| 2023 |
Asfour H, Hirsinger E, Rouco R, Zarrouki F, Hayashi S, Swist S, Braun T, Patel K, Relaix F, Andrey G, Stricker S, Duprez D, Stantzou A, Amthor H. Inhibitory SMAD6 interferes with BMP-dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles. Development (Cambridge, England). 150. PMID 37272529 DOI: 10.1242/dev.201504 |
0.7 |
|
| 2023 |
Melo US, Jatzlau J, Prada-Medina CA, Flex E, Hartmann S, Ali S, Schöpflin R, Bernardini L, Ciolfi A, Moeinzadeh MH, Klever MK, Altay A, Vallecillo-García P, Carpentieri G, Delledonne M, ... ... Stricker S, et al. Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation. Nature Communications. 14: 2034. PMID 37041138 DOI: 10.1038/s41467-023-37585-8 |
0.517 |
|
| 2020 |
Helmbacher F, Stricker S. Tissue cross talks governing limb muscle development and regeneration. Seminars in Cell & Developmental Biology. 104: 14-30. PMID 32517852 DOI: 10.1016/J.Semcdb.2020.05.005 |
0.324 |
|
| 2019 |
Feng C, Chan WCW, Lam Y, Wang X, Chen P, Niu B, Ng VCW, Yeo JC, Stricker S, Cheah KSE, Koch M, Mundlos S, Ng HH, Chan D. Lgr5 and Col22a1 Mark Progenitor Cells in the Lineage toward Juvenile Articular Chondrocytes. Stem Cell Reports. PMID 31522976 DOI: 10.1016/J.Stemcr.2019.08.006 |
0.548 |
|
| 2018 |
Stumm J, Vallecillo-García P, Vom Hofe-Schneider S, Ollitrault D, Schrewe H, Economides AN, Marazzi G, Sassoon DA, Stricker S. Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury. Stem Cell Research. 32: 8-16. PMID 30149291 DOI: 10.1016/J.Scr.2018.08.010 |
0.368 |
|
| 2018 |
Murgai A, Altmeyer S, Wiegand S, Tylzanowski P, Stricker S. Cooperation of BMP and IHH signaling in interdigital cell fate determination. Plos One. 13: e0197535. PMID 29771958 DOI: 10.1371/Journal.Pone.0197535 |
0.443 |
|
| 2018 |
Orgeur M, Martens M, Leonte G, Nassari S, Bonnin MA, Börno ST, Timmermann B, Hecht J, Duprez D, Stricker S. Genome-wide strategies identify downstream target genes of connective tissue-associated transcription factors. Development (Cambridge, England). PMID 29511024 DOI: 10.1242/Dev.161208 |
0.348 |
|
| 2017 |
Nassari S, Blavet C, Bonnin MA, Stricker S, Duprez D, Fournier-Thibault C. The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development. Scientific Reports. 7: 17279. PMID 29222527 DOI: 10.1038/S41598-017-17490-Z |
0.31 |
|
| 2017 |
Vallecillo-García P, Orgeur M, Vom Hofe-Schneider S, Stumm J, Kappert V, Ibrahim DM, Börno ST, Hayashi S, Relaix F, Hildebrandt K, Sengle G, Koch M, Timmermann B, Marazzi G, Sassoon DA, ... ... Stricker S, et al. Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development. Nature Communications. 8: 1218. PMID 29084951 DOI: 10.1038/S41467-017-01120-3 |
0.737 |
|
| 2017 |
Sanz-Ezquerro JJ, Münsterberg AE, Stricker S. Editorial: Signaling Pathways in Embryonic Development. Frontiers in Cell and Developmental Biology. 5: 76. PMID 28913334 DOI: 10.3389/Fcell.2017.00076 |
0.306 |
|
| 2017 |
Dörpholz G, Murgai A, Jatzlau J, Horbelt D, Belverdi MP, Heroven C, Schreiber I, Wendel G, Ruschke K, Stricker S, Knaus P. IRS4, a novel modulator of BMP/Smad and Akt signalling during early muscle differentiation. Scientific Reports. 7: 8778. PMID 28821740 DOI: 10.1038/S41598-017-08676-6 |
0.423 |
|
| 2017 |
Bernatik O, Radaszkiewicz T, Behal M, Dave Z, Witte F, Mahl A, Cernohorsky NH, Krejci P, Stricker S, Bryja V. A Novel Role for the BMP Antagonist Noggin in Sensitizing Cells to Non-canonical Wnt-5a/Ror2/Disheveled Pathway Activation. Frontiers in Cell and Developmental Biology. 5: 47. PMID 28523267 DOI: 10.3389/Fcell.2017.00047 |
0.415 |
|
| 2017 |
Stricker S, Rauschenberger V, Schambony A. ROR-Family Receptor Tyrosine Kinases. Current Topics in Developmental Biology. 123: 105-142. PMID 28236965 DOI: 10.1016/Bs.Ctdb.2016.09.003 |
0.412 |
|
| 2016 |
Knierim E, Hirata H, Wolf NI, Morales-Gonzalez S, Schottmann G, Tanaka Y, Rudnik-Schöneborn S, Orgeur M, Zerres K, Vogt S, van Riesen A, Gill E, Seifert F, Zwirner A, Kirschner J, ... ... Stricker S, et al. Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures. American Journal of Human Genetics. PMID 26924529 DOI: 10.1016/J.Ajhg.2016.01.006 |
0.434 |
|
| 2015 |
Bourgeois A, Esteves de Lima J, Charvet B, Kawakami K, Stricker S, Duprez D. Stable and bicistronic expression of two genes in somite- and lateral plate-derived tissues to study chick limb development. Bmc Developmental Biology. 15: 39. PMID 26518454 DOI: 10.1186/S12861-015-0088-3 |
0.404 |
|
| 2015 |
Berkholz J, Orgeur M, Stricker S, Munz B. skNAC and Smyd1 in transcriptional control. Experimental Cell Research. 336: 182-91. PMID 26162853 DOI: 10.1016/J.Yexcr.2015.06.019 |
0.323 |
|
| 2015 |
Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, et al. PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature Genetics. 47: 647-53. PMID 25961942 DOI: 10.1038/Ng.3302 |
0.545 |
|
| 2015 |
Pfirrmann T, Emmerich D, Ruokonen P, Quandt D, Buchen R, Fischer-Zirnsak B, Hecht J, Krawitz P, Meyer P, Klopocki E, Stricker S, Lausch E, Seliger B, Hollemann T, Reinhard T, et al. Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model. Human Molecular Genetics. 24: 3119-32. PMID 25712132 DOI: 10.1093/Hmg/Ddv063 |
0.445 |
|
| 2014 |
Yang T, Bassuk AG, Stricker S, Fritzsch B. Prickle1 is necessary for the caudal migration of murine facial branchiomotor neurons. Cell and Tissue Research. 357: 549-61. PMID 24927917 DOI: 10.1007/S00441-014-1925-6 |
0.334 |
|
| 2014 |
Kuss P, Kraft K, Stumm J, Ibrahim D, Vallecillo-Garcia P, Mundlos S, Stricker S. Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A. Developmental Biology. 385: 83-93. PMID 24161848 DOI: 10.1016/J.Ydbio.2013.10.013 |
0.75 |
|
| 2013 |
Sartori R, Schirwis E, Blaauw B, Bortolanza S, Zhao J, Enzo E, Stantzou A, Mouisel E, Toniolo L, Ferry A, Stricker S, Goldberg AL, Dupont S, Piccolo S, Amthor H, et al. BMP signaling controls muscle mass. Nature Genetics. 45: 1309-18. PMID 24076600 DOI: 10.1038/Ng.2772 |
0.409 |
|
| 2013 |
Jamsheer A, Zemojtel T, Kolanczyk M, Stricker S, Hecht J, Krawitz P, Doelken SC, Glazar R, Socha M, Mundlos S. Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion. Journal of Medical Genetics. 50: 579-84. PMID 23709756 DOI: 10.1136/Jmedgenet-2013-101659 |
0.517 |
|
| 2013 |
Amthor H, Sartori R, Schirwis E, Blaauw B, Bortolanza S, Zhao J, Enzo E, Stantzou A, Mouisel E, Toniolo L, Ferry A, Stricker S, Goldberg AL, Dupont S, Piccolo S, et al. O.20 BMP signalling controls muscle mass Neuromuscular Disorders. 23: 850-851. DOI: 10.1016/J.Nmd.2013.06.730 |
0.398 |
|
| 2012 |
Maass PG, Rump A, Schulz H, Stricker S, Schulze L, Platzer K, Aydin A, Tinschert S, Goldring MB, Luft FC, Bähring S. A misplaced lncRNA causes brachydactyly in humans. The Journal of Clinical Investigation. 122: 3990-4002. PMID 23093776 DOI: 10.1172/Jci65508 |
0.315 |
|
| 2012 |
Ott CE, Hein H, Lohan S, Hoogeboom J, Foulds N, Grünhagen J, Stricker S, Villavicencio-Lorini P, Klopocki E, Mundlos S. Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia. Journal of Medical Genetics. 49: 437-41. PMID 22717651 DOI: 10.1136/Jmedgenet-2012-100825 |
0.532 |
|
| 2012 |
Klopocki E, Lohan S, Doelken SC, Stricker S, Ockeloen CW, Soares Thiele de Aguiar R, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordass U, et al. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics. 49: 119-25. PMID 22147889 DOI: 10.1136/Jmedgenet-2011-100409 |
0.563 |
|
| 2012 |
Stricker S, Mathia S, Haupt J, Seemann P, Meier J, Mundlos S. Odd-skipped related genes regulate differentiation of embryonic limb mesenchyme and bone marrow mesenchymal stromal cells. Stem Cells and Development. 21: 623-33. PMID 21671783 DOI: 10.1089/Scd.2011.0154 |
0.581 |
|
| 2011 |
Stricker S, Mundlos S. FGF and ROR2 receptor tyrosine kinase signaling in human skeletal development. Current Topics in Developmental Biology. 97: 179-206. PMID 22074606 DOI: 10.1016/B978-0-12-385975-4.00013-9 |
0.569 |
|
| 2011 |
Baasanjav S, Al-Gazali L, Hashiguchi T, Mizumoto S, Fischer B, Horn D, Seelow D, Ali BR, Aziz SA, Langer R, Saleh AA, Becker C, Nürnberg G, Cantagrel V, Gleeson JG, ... ... Stricker S, et al. Faulty initiation of proteoglycan synthesis causes cardiac and joint defects. American Journal of Human Genetics. 89: 15-27. PMID 21763480 DOI: 10.1016/J.Ajhg.2011.05.021 |
0.539 |
|
| 2011 |
Kossler N, Stricker S, Rödelsperger C, Robinson PN, Kim J, Dietrich C, Osswald M, Kühnisch J, Stevenson DA, Braun T, Mundlos S, Kolanczyk M. Neurofibromin (Nf1) is required for skeletal muscle development. Human Molecular Genetics. 20: 2697-709. PMID 21478499 DOI: 10.1093/Hmg/Ddr149 |
0.559 |
|
| 2011 |
Stricker S, Mundlos S. Mechanisms of digit formation: Human malformation syndromes tell the story. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 990-1004. PMID 21337664 DOI: 10.1002/Dvdy.22565 |
0.578 |
|
| 2011 |
Klopocki E, Lohan S, Brancati F, Koll R, Brehm A, Seemann P, Dathe K, Stricker S, Hecht J, Bosse K, Betz RC, Garaci FG, Dallapiccola B, Jain M, Muenke M, et al. Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. American Journal of Human Genetics. 88: 70-5. PMID 21167467 DOI: 10.1016/J.Ajhg.2010.11.006 |
0.59 |
|
| 2010 |
Clayton P, Fischer B, Mann A, Mansour S, Rossier E, Veen M, Lang C, Baasanjav S, Kieslich M, Brossuleit K, Gravemann S, Schnipper N, Karbasyian M, Demuth I, Zwerger M, ... ... Stricker S, et al. Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein. Nucleus (Austin, Tex.). 1: 354-66. PMID 21327084 DOI: 10.4161/Nucl.1.4.12435 |
0.565 |
|
| 2010 |
Brancati F, Fortugno P, Bottillo I, Lopez M, Josselin E, Boudghene-Stambouli O, Agolini E, Bernardini L, Bellacchio E, Iannicelli M, Rossi A, Dib-Lachachi A, Stuppia L, Palka G, Mundlos S, ... Stricker S, et al. Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. American Journal of Human Genetics. 87: 265-73. PMID 20691405 DOI: 10.1016/J.Ajhg.2010.07.003 |
0.567 |
|
| 2010 |
Witte F, Chan D, Economides AN, Mundlos S, Stricker S. Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region. Proceedings of the National Academy of Sciences of the United States of America. 107: 14211-6. PMID 20660756 DOI: 10.1073/Pnas.1009314107 |
0.569 |
|
| 2010 |
Witte F, Bernatik O, Kirchner K, Masek J, Mahl A, Krejci P, Mundlos S, Schambony A, Bryja V, Stricker S. Negative regulation of Wnt signaling mediated by CK1-phosphorylated Dishevelled via Ror2. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 24: 2417-26. PMID 20215527 DOI: 10.1096/Fj.09-150615 |
0.512 |
|
| 2010 |
Jensen LR, Bartenschlager H, Rujirabanjerd S, Tzschach A, Nümann A, Janecke AR, Spörle R, Stricker S, Raynaud M, Nelson J, Hackett A, Fryns JP, Chelly J, de Brouwer AP, Hamel B, et al. A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. Pathogenetics. 3: 2. PMID 20181063 DOI: 10.1186/1755-8417-3-2 |
0.395 |
|
| 2010 |
Maass PG, Wirth J, Aydin A, Rump A, Stricker S, Tinschert S, Otero M, Tsuchimochi K, Goldring MB, Luft FC, Bähring S. A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E. Human Molecular Genetics. 19: 848-60. PMID 20015959 DOI: 10.1093/Hmg/Ddp553 |
0.307 |
|
| 2009 |
Seemann P, Brehm A, König J, Reissner C, Stricker S, Kuss P, Haupt J, Renninger S, Nickel J, Sebald W, Groppe JC, Plöger F, Pohl J, Schmidt-von Kegler M, Walther M, et al. Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN. Plos Genetics. 5: e1000747. PMID 19956691 DOI: 10.1371/Journal.Pgen.1000747 |
0.603 |
|
| 2009 |
van Wijk NV, Witte F, Feike AC, Schambony A, Birchmeier W, Mundlos S, Stricker S. The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling. Biochemical and Biophysical Research Communications. 390: 211-6. PMID 19785987 DOI: 10.1016/J.Bbrc.2009.09.086 |
0.561 |
|
| 2009 |
Stricker S, Prüss H, Horvath R, Baruffini E, Lodi T, Siebert E, Endres M, Zschenderlein R, Meisel A. A variable neurodegenerative phenotype with polymerase gamma mutation. Journal of Neurology, Neurosurgery, and Psychiatry. 80: 1181-2. PMID 19762913 DOI: 10.1136/Jnnp.2008.166066 |
0.326 |
|
| 2009 |
Schwarzer W, Witte F, Rajab A, Mundlos S, Stricker S. A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes. Human Molecular Genetics. 18: 4013-21. PMID 19640924 DOI: 10.1093/Hmg/Ddp345 |
0.542 |
|
| 2009 |
Kurth I, Klopocki E, Stricker S, van Oosterwijk J, Vanek S, Altmann J, Santos HG, van Harssel JJ, de Ravel T, Wilkie AO, Gal A, Mundlos S. Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia. Nature Genetics. 41: 862-3. PMID 19639023 DOI: 10.1038/Ng0809-862 |
0.441 |
|
| 2009 |
Gao B, Hu J, Stricker S, Cheung M, Ma G, Law KF, Witte F, Briscoe J, Mundlos S, He L, Cheah KS, Chan D. A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range. Nature. 458: 1196-200. PMID 19252479 DOI: 10.1038/Nature07862 |
0.569 |
|
| 2009 |
Witte F, Dokas J, Neuendorf F, Mundlos S, Stricker S. Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation. Gene Expression Patterns : Gep. 9: 215-23. PMID 19185060 DOI: 10.1016/J.Gep.2008.12.009 |
0.613 |
|
| 2008 |
Winkel A, Stricker S, Tylzanowski P, Seiffart V, Mundlos S, Gross G, Hoffmann A. Wnt-ligand-dependent interaction of TAK1 (TGF-beta-activated kinase-1) with the receptor tyrosine kinase Ror2 modulates canonical Wnt-signalling. Cellular Signalling. 20: 2134-44. PMID 18762249 DOI: 10.1016/J.Cellsig.2008.08.009 |
0.496 |
|
| 2008 |
Steichen-Gersdorf E, Gassner I, Superti-Furga A, Ullmann R, Stricker S, Klopocki E, Mundlos S. Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4. Clinical Genetics. 74: 560-5. PMID 18616733 DOI: 10.1111/J.1399-0004.2008.01050.X |
0.54 |
|
| 2008 |
Hecht J, Stricker S, Wiecha U, Stiege A, Panopoulou G, Podsiadlowski L, Poustka AJ, Dieterich C, Ehrich S, Suvorova J, Mundlos S, Seitz V. Evolution of a core gene network for skeletogenesis in chordates. Plos Genetics. 4: e1000025. PMID 18369444 DOI: 10.1371/Journal.Pgen.1000025 |
0.575 |
|
| 2008 |
Raz R, Stricker S, Gazzerro E, Clor JL, Witte F, Nistala H, Zabski S, Pereira RC, Stadmeyer L, Wang X, Gowen L, Sleeman MW, Yancopoulos GD, Canalis E, Mundlos S, et al. The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome. Development (Cambridge, England). 135: 1713-23. PMID 18353862 DOI: 10.1242/Dev.015149 |
0.559 |
|
| 2008 |
Michalk A, Stricker S, Becker J, Rupps R, Pantzar T, Miertus J, Botta G, Naretto VG, Janetzki C, Yaqoob N, Ott CE, Seelow D, Wieczorek D, Fiebig B, Wirth B, et al. Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. American Journal of Human Genetics. 82: 464-76. PMID 18252226 DOI: 10.1016/J.Ajhg.2007.11.006 |
0.583 |
|
| 2007 |
Reijntjes S, Stricker S, Mankoo BS. A comparative analysis of Meox1 and Meox2 in the developing somites and limbs of the chick embryo. The International Journal of Developmental Biology. 51: 753-9. PMID 17939123 DOI: 10.1387/Ijdb.072332Sr |
0.386 |
|
| 2007 |
Kolanczyk M, Kossler N, Kühnisch J, Lavitas L, Stricker S, Wilkening U, Manjubala I, Fratzl P, Spörle R, Herrmann BG, Parada LF, Kornak U, Mundlos S. Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics. 16: 874-86. PMID 17317783 DOI: 10.1093/Hmg/Ddm032 |
0.561 |
|
| 2007 |
Hecht J, Seitz V, Urban M, Wagner F, Robinson PN, Stiege A, Dieterich C, Kornak U, Wilkening U, Brieske N, Zwingman C, Kidess A, Stricker S, Mundlos S. Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2(-/-) mouse model. Gene Expression Patterns : Gep. 7: 102-12. PMID 16829211 DOI: 10.1016/J.Modgep.2006.05.014 |
0.575 |
|
| 2007 |
Zemojtel T, Kolanczyk M, Kossler N, Stricker S, Lurz R, Mikula I, Duchniewicz M, Schuelke M, Ghafourifar P, Martasek P, Vingron M, Mundlos S. Corrigendum to "Mammalian mitochondrial nitric oxide synthase: Characterization of a novel candidate" [FEBS Lett. 580 (2006) 455-462] (DOI:10.1016/j.febslet.2005.12.038) Febs Letters. 581: 2072-2073. DOI: 10.1016/J.Febslet.2007.04.006 |
0.433 |
|
| 2006 |
Stricker S, Verhey van Wijk N, Witte F, Brieske N, Seidel K, Mundlos S. Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 235: 3456-65. PMID 17061261 DOI: 10.1002/Dvdy.20993 |
0.586 |
|
| 2006 |
Guo G, Booms P, Halushka M, Dietz HC, Ney A, Stricker S, Hecht J, Mundlos S, Robinson PN. Induction of macrophage chemotaxis by aortic extracts of the mgR Marfan mouse model and a GxxPG-containing fibrillin-1 fragment. Circulation. 114: 1855-62. PMID 17030689 DOI: 10.1161/Circulationaha.105.601674 |
0.455 |
|
| 2006 |
Woods CG, Stricker S, Seemann P, Stern R, Cox J, Sherridan E, Roberts E, Springell K, Scott S, Karbani G, Sharif SM, Toomes C, Bond J, Kumar D, Al-Gazali L, et al. Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome. American Journal of Human Genetics. 79: 402-8. PMID 16826533 DOI: 10.1086/506332 |
0.562 |
|
| 2006 |
Hoffmann K, Muller JS, Stricker S, Megarbane A, Rajab A, Lindner TH, Cohen M, Chouery E, Adaimy L, Ghanem I, Delague V, Boltshauser E, Talim B, Horvath R, Robinson PN, et al. Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit. American Journal of Human Genetics. 79: 303-12. PMID 16826520 DOI: 10.1086/506257 |
0.559 |
|
| 2006 |
Koch M, Veit G, Stricker S, Bhatt P, Kutsch S, Zhou P, Reinders E, Hahn RA, Song R, Burgeson RE, Gerecke DR, Mundlos S, Gordon MK. Expression of type XXIII collagen mRNA and protein. The Journal of Biological Chemistry. 281: 21546-57. PMID 16728390 DOI: 10.1074/Jbc.M604131200 |
0.502 |
|
| 2006 |
Stricker S, Brieske N, Haupt J, Mundlos S. Comparative expression pattern of Odd-skipped related genes Osr1 and Osr2 in chick embryonic development. Gene Expression Patterns : Gep. 6: 826-34. PMID 16554187 DOI: 10.1016/J.Modgep.2006.02.003 |
0.55 |
|
| 2006 |
Zemojtel T, Kolanczyk M, Kossler N, Stricker S, Lurz R, Mikula I, Duchniewicz M, Schuelke M, Ghafourifar P, Martasek P, Vingron M, Mundlos S. Mammalian mitochondrial nitric oxide synthase: characterization of a novel candidate. Febs Letters. 580: 455-62. PMID 16380119 DOI: 10.1016/J.Febslet.2005.12.038 |
0.482 |
|
| 2005 |
Seemann P, Schwappacher R, Kjaer KW, Krakow D, Lehmann K, Dawson K, Stricker S, Pohl J, Plöger F, Staub E, Nickel J, Sebald W, Knaus P, Mundlos S. Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2. The Journal of Clinical Investigation. 115: 2373-81. PMID 16127465 DOI: 10.1172/Jci25118 |
0.536 |
|
| 2005 |
Niedermaier M, Schwabe GC, Fees S, Helmrich A, Brieske N, Seemann P, Hecht J, Seitz V, Stricker S, Leschik G, Schrock E, Selby PB, Mundlos S. An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression. The Journal of Clinical Investigation. 115: 900-9. PMID 15841179 DOI: 10.1172/Jci200523675 |
0.574 |
|
| 2005 |
Sieber C, Sammar M, Stricker S, Schwabe GC, Hartung A, Pohl J, Minami Y, Sebald W, Mundlos S, Knaus P. Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2 Gbm Annual Fall Meeting Berlin/Potsdam 2005. 2005. DOI: 10.1240/sav_gbm_2005_h_001246 |
0.407 |
|
| 2005 |
Niedermaier M, Schwabe GC, Fees S, Helmrich A, Brieske N, Seemann P, Hecht J, Seitz V, Stricker S, Leschik G, Schrock E, Selby PB, Mundlos S. An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression Journal of Clinical Investigation. 115: 900-909. DOI: 10.1172/JCI200523675 |
0.483 |
|
| 2004 |
Sammar M, Stricker S, Schwabe GC, Sieber C, Hartung A, Hanke M, Oishi I, Pohl J, Minami Y, Sebald W, Mundlos S, Knaus P. Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. 9: 1227-38. PMID 15569154 DOI: 10.1111/J.1365-2443.2004.00799.X |
0.541 |
|
| 2004 |
Albrecht AN, Kornak U, Böddrich A, Süring K, Robinson PN, Stiege AC, Lurz R, Stricker S, Wanker EE, Mundlos S. A molecular pathogenesis for transcription factor associated poly-alanine tract expansions. Human Molecular Genetics. 13: 2351-9. PMID 15333588 DOI: 10.1093/Hmg/Ddh277 |
0.466 |
|
| 2003 |
Lehmann K, Seemann P, Stricker S, Sammar M, Meyer B, Süring K, Majewski F, Tinschert S, Grzeschik KH, Müller D, Knaus P, Nürnberg P, Mundlos S. Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2. Proceedings of the National Academy of Sciences of the United States of America. 100: 12277-82. PMID 14523231 DOI: 10.1073/Pnas.2133476100 |
0.571 |
|
| 2003 |
Stricker S, Poustka AJ, Wiecha U, Stiege A, Hecht J, Panopoulou G, Vilcinskas A, Mundlos S, Seitz V. A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution. Developmental and Comparative Immunology. 27: 673-84. PMID 12798364 DOI: 10.1016/S0145-305X(03)00037-5 |
0.554 |
|
| 2003 |
Stock M, Schäfer H, Stricker S, Gross G, Mundlos S, Otto F. Expression of galectin-3 in skeletal tissues is controlled by Runx2. The Journal of Biological Chemistry. 278: 17360-7. PMID 12604608 DOI: 10.1074/Jbc.M207631200 |
0.574 |
|
| 2002 |
Stricker S, Fundele R, Vortkamp A, Mundlos S. Role of Runx genes in chondrocyte differentiation. Developmental Biology. 245: 95-108. PMID 11969258 DOI: 10.1006/Dbio.2002.0640 |
0.587 |
|
| 2002 |
Albrecht AN, Schwabe GC, Stricker S, Böddrich A, Wanker EE, Mundlos S. The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements. Mechanisms of Development. 112: 53-67. PMID 11850178 DOI: 10.1016/S0925-4773(01)00639-6 |
0.618 |
|
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