Stricker S - Search Results

1

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

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

A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution.

Stricker S, Poustka AJ, Wiecha U, Stiege A, Hecht J, Panopoulou G, Vilcinskas A, Mundlos S, Seitz V. Stricker S, et al. Dev Comp Immunol. 2003 Sep;27(8):673-84. doi: 10.1016/s0145-305x(03)00037-5. Dev Comp Immunol. 2003. PMID: 12798364

6

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.

7

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.

8

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.

9

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.

10

Mammalian mitochondrial nitric oxide synthase: characterization of a novel candidate.

Zemojtel T, Kolanczyk M, Kossler N, Stricker S, Lurz R, Mikula I, Duchniewicz M, Schuelke M, Ghafourifar P, Martasek P, Vingron M, Mundlos S. Zemojtel T, et al. Among authors: stricker s. FEBS Lett. 2006 Jan 23;580(2):455-62. doi: 10.1016/j.febslet.2005.12.038. Epub 2005 Dec 20. FEBS Lett. 2006. PMID: 16380119 Free article.

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