Mundlos 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: mundlos 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: mundlos 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. Among authors: mundlos s. 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: mundlos 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. Among authors: mundlos s. Dev Comp Immunol. 2003 Sep;27(8):673-84. doi: 10.1016/s0145-305x(03)00037-5. Dev Comp Immunol. 2003. PMID: 12798364

6

Genetic disorders of the skeleton: a developmental approach.

Kornak U, Mundlos S. Kornak U, et al. Among authors: mundlos s. Am J Hum Genet. 2003 Sep;73(3):447-74. doi: 10.1086/377110. Epub 2003 Jul 31. Am J Hum Genet. 2003. PMID: 12900795 Free PMC article. Review.

7

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: mundlos 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.

8

Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome.

Schwabe GC, Trepczik B, Süring K, Brieske N, Tucker AS, Sharpe PT, Minami Y, Mundlos S. Schwabe GC, et al. Among authors: mundlos s. Dev Dyn. 2004 Feb;229(2):400-10. doi: 10.1002/dvdy.10466. Dev Dyn. 2004. PMID: 14745966 Free article.

9

Gene-Ontology analysis reveals association of tissue-specific 5' CpG-island genes with development and embryogenesis.

Robinson PN, Böhme U, Lopez R, Mundlos S, Nürnberg P. Robinson PN, et al. Among authors: mundlos s. Hum Mol Genet. 2004 Sep 1;13(17):1969-78. doi: 10.1093/hmg/ddh207. Epub 2004 Jul 14. Hum Mol Genet. 2004. PMID: 15254011

10

RGD-containing fibrillin-1 fragments upregulate matrix metalloproteinase expression in cell culture: a potential factor in the pathogenesis of the Marfan syndrome.

Booms P, Pregla R, Ney A, Barthel F, Reinhardt DP, Pletschacher A, Mundlos S, Robinson PN. Booms P, et al. Among authors: mundlos s. Hum Genet. 2005 Jan;116(1-2):51-61. doi: 10.1007/s00439-004-1194-7. Epub 2004 Oct 23. Hum Genet. 2005. PMID: 15517394

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