Sigmar Stricker
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BMP signaling controls muscle mass
R Sartori, E Schirwis, B Blaauw, S Bortolanza, J Zhao, E Enzo, A Stantzou, ...
Nature genetics 45 (11), 1309-1318, 2013
Role of Runx genes in chondrocyte differentiation
S Stricker, R Fundele, A Vortkamp, S Mundlos
Developmental biology 245 (1), 95-108, 2002
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
CG Woods, S Stricker, P Seemann, R Stern, J Cox, E Sherridan, ...
The American Journal of Human Genetics 79 (2), 402-408, 2006
Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2
P Seemann, R Schwappacher, KW Kjaer, D Krakow, K Lehmann, ...
The Journal of clinical investigation 115 (9), 2373-2381, 2005
Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation
F Witte, J Dokas, F Neuendorf, S Mundlos, S Stricker
Gene Expression Patterns 9 (4), 215-223, 2009
A molecular pathogenesis for transcription factor associated poly-alanine tract expansions
AN Albrecht, U Kornak, A Böddrich, K Süring, PN Robinson, AC Stiege, ...
Human molecular genetics 13 (20), 2351-2359, 2004
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2
K Lehmann, P Seemann, S Stricker, M Sammar, B Meyer, K Süring, ...
Proceedings of the National Academy of Sciences 100 (21), 12277-12282, 2003
PDE3A mutations cause autosomal dominant hypertension with brachydactyly
PG Maass, A Aydin, FC Luft, C Schaechterle, A Weise, S Stricker, ...
Nature genetics 47 (6), 647-653, 2015
Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal γ subunit
K Hoffmann, JS Müller, S Stricker, A Megarbane, A Rajab, TH Lindner, ...
The American Journal of Human Genetics 79 (2), 303-312, 2006
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders
A Michalk, S Stricker, J Becker, R Rupps, T Pantzar, J Miertus, G Botta, ...
The American Journal of Human Genetics 82 (2), 464-476, 2008
Multiple roles for neurofibromin in skeletal development and growth
M Kolanczyk, N Kossler, J Kühnisch, L Lavitas, S Stricker, U Wilkening, ...
Human molecular genetics 16 (8), 874-886, 2007
Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia
I Kurth, E Klopocki, S Stricker, J van Oosterwijk, S Vanek, J Altmann, ...
Nature genetics 41 (8), 862-863, 2009
Modulation of GDF5/BRI‐b signalling through interaction with the tyrosine kinase receptor Ror2
M Sammar, S Stricker, GC Schwabe, C Sieber, A Hartung, M Hanke, ...
Genes to Cells 9 (12), 1227-1238, 2004
Faulty initiation of proteoglycan synthesis causes cardiac and joint defects
S Baasanjav, L Al-Gazali, T Hashiguchi, S Mizumoto, B Fischer, D Horn, ...
The American Journal of Human Genetics 89 (1), 15-27, 2011
Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN
P Seemann, A Brehm, J König, C Reissner, S Stricker, P Kuss, J Haupt, ...
PLoS genetics 5 (11), e1000747, 2009
A misplaced lncRNA causes brachydactyly in humans
PG Maass, A Rump, H Schulz, S Stricker, L Schulze, K Platzer, A Aydin, ...
The Journal of clinical investigation 122 (11), 3990-4002, 2012
A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range
B Gao, J Hu, S Stricker, M Cheung, G Ma, KF Law, F Witte, J Briscoe, ...
Nature 458 (7242), 1196-1200, 2009
Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis
E Klopocki, S Lohan, F Brancati, R Koll, A Brehm, P Seemann, K Dathe, ...
The American Journal of Human Genetics 88 (1), 70-75, 2011
Expression of galectin-3 in skeletal tissues is controlled by Runx2
M Stock, H Schäfer, S Stricker, G Gross, S Mundlos, F Otto
Journal of Biological Chemistry 278 (19), 17360-17367, 2003
Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome
F Brancati, P Fortugno, I Bottillo, M Lopez, E Josselin, ...
The American Journal of Human Genetics 87 (2), 265-273, 2010
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