Sigmar Stricker, PhD - Publications

Biochemistry Free University of Berlin 

55 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
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  0.64
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  0.4
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  0.32
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  0.4
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  0.56
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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/JCI23675  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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