Stricker S - Search Results

1

Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2.

Sammar M, Stricker S, Schwabe GC, Sieber C, Hartung A, Hanke M, Oishi I, Pohl J, Minami Y, Sebald W, Mundlos S, Knaus P. Sammar M, et al. Among authors: stricker s. Genes Cells. 2004 Dec;9(12):1227-38. doi: 10.1111/j.1365-2443.2004.00799.x. Genes Cells. 2004. PMID: 15569154 Free article.

2

The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements.

Albrecht AN, Schwabe GC, Stricker S, Böddrich A, Wanker EE, Mundlos S. Albrecht AN, et al. Among authors: stricker s. Mech Dev. 2002 Mar;112(1-2):53-67. doi: 10.1016/s0925-4773(01)00639-6. Mech Dev. 2002. PMID: 11850178 Free article.

3

Role of Runx genes in chondrocyte differentiation.

Stricker S, Fundele R, Vortkamp A, Mundlos S. Stricker S, et al. Dev Biol. 2002 May 1;245(1):95-108. doi: 10.1006/dbio.2002.0640. Dev Biol. 2002. PMID: 11969258 Free article.

4

Expression of galectin-3 in skeletal tissues is controlled by Runx2.

Stock M, Schäfer H, Stricker S, Gross G, Mundlos S, Otto F. Stock M, et al. Among authors: stricker s. J Biol Chem. 2003 May 9;278(19):17360-7. doi: 10.1074/jbc.M207631200. Epub 2003 Feb 25. J Biol Chem. 2003. PMID: 12604608 Free article.

5

Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2.

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. Lehmann K, et al. Among authors: stricker s. Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12277-82. doi: 10.1073/pnas.2133476100. Epub 2003 Oct 1. Proc Natl Acad Sci U S A. 2003. PMID: 14523231 Free PMC article.

6

A molecular pathogenesis for transcription factor associated poly-alanine tract expansions.

Albrecht AN, Kornak U, Böddrich A, Süring K, Robinson PN, Stiege AC, Lurz R, Stricker S, Wanker EE, Mundlos S. Albrecht AN, et al. Among authors: stricker s. Hum Mol Genet. 2004 Oct 15;13(20):2351-9. doi: 10.1093/hmg/ddh277. Epub 2004 Aug 27. Hum Mol Genet. 2004. PMID: 15333588

7

An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression.

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. Niedermaier M, et al. Among authors: stricker s. J Clin Invest. 2005 Apr;115(4):900-9. doi: 10.1172/JCI23675. J Clin Invest. 2005. PMID: 15841179 Free PMC article.

8

Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2.

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. Seemann P, et al. Among authors: stricker s. J Clin Invest. 2005 Sep;115(9):2373-81. doi: 10.1172/JCI25118. Epub 2005 Aug 25. J Clin Invest. 2005. PMID: 16127465 Free PMC article.

9

Comparative expression pattern of Odd-skipped related genes Osr1 and Osr2 in chick embryonic development.

Stricker S, Brieske N, Haupt J, Mundlos S. Stricker S, et al. Gene Expr Patterns. 2006 Oct;6(8):826-34. doi: 10.1016/j.modgep.2006.02.003. Epub 2006 Mar 22. Gene Expr Patterns. 2006. PMID: 16554187

10

Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome.

Stricker S, Verhey van Wijk N, Witte F, Brieske N, Seidel K, Mundlos S. Stricker S, et al. Dev Dyn. 2006 Dec;235(12):3456-65. doi: 10.1002/dvdy.20993. Dev Dyn. 2006. PMID: 17061261 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

263 results

Search Page