Witte F - Search Results

1

A Novel Role for the BMP Antagonist Noggin in Sensitizing Cells to Non-canonical Wnt-5a/Ror2/Disheveled Pathway Activation.

Bernatik O, Radaszkiewicz T, Behal M, Dave Z, Witte F, Mahl A, Cernohorsky NH, Krejci P, Stricker S, Bryja V. Bernatik O, et al. Among authors: witte f. Front Cell Dev Biol. 2017 May 4;5:47. doi: 10.3389/fcell.2017.00047. eCollection 2017. Front Cell Dev Biol. 2017. PMID: 28523267 Free PMC article.

2

Negative regulation of Wnt signaling mediated by CK1-phosphorylated Dishevelled via Ror2.

Witte F, Bernatik O, Kirchner K, Masek J, Mahl A, Krejci P, Mundlos S, Schambony A, Bryja V, Stricker S. Witte F, et al. FASEB J. 2010 Jul;24(7):2417-26. doi: 10.1096/fj.09-150615. Epub 2010 Mar 9. FASEB J. 2010. PMID: 20215527

3

The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling.

van Wijk NV, Witte F, Feike AC, Schambony A, Birchmeier W, Mundlos S, Stricker S. van Wijk NV, et al. Among authors: witte f. Biochem Biophys Res Commun. 2009 Dec 11;390(2):211-6. doi: 10.1016/j.bbrc.2009.09.086. Epub 2009 Sep 26. Biochem Biophys Res Commun. 2009. PMID: 19785987

4

Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region.

Witte F, Chan D, Economides AN, Mundlos S, Stricker S. Witte F, et al. Proc Natl Acad Sci U S A. 2010 Aug 10;107(32):14211-6. doi: 10.1073/pnas.1009314107. Epub 2010 Jul 26. Proc Natl Acad Sci U S A. 2010. PMID: 20660756 Free PMC article.

5

A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.

Schwarzer W, Witte F, Rajab A, Mundlos S, Stricker S. Schwarzer W, et al. Among authors: witte f. Hum Mol Genet. 2009 Nov 1;18(21):4013-21. doi: 10.1093/hmg/ddp345. Epub 2009 Jul 29. Hum Mol Genet. 2009. PMID: 19640924

6

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. Among authors: witte f. Dev Dyn. 2006 Dec;235(12):3456-65. doi: 10.1002/dvdy.20993. Dev Dyn. 2006. PMID: 17061261 Free article.

7

Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation.

Witte F, Dokas J, Neuendorf F, Mundlos S, Stricker S. Witte F, et al. Gene Expr Patterns. 2009 Apr;9(4):215-23. doi: 10.1016/j.gep.2008.12.009. Epub 2009 Jan 13. Gene Expr Patterns. 2009. PMID: 19185060

8

A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range.

Gao B, Hu J, Stricker S, Cheung M, Ma G, Law KF, Witte F, Briscoe J, Mundlos S, He L, Cheah KS, Chan D. Gao B, et al. Among authors: witte f. Nature. 2009 Apr 30;458(7242):1196-200. doi: 10.1038/nature07862. Epub 2009 Mar 1. Nature. 2009. PMID: 19252479

9

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.

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, Valenzuela DM, Economides AN. Raz R, et al. Among authors: witte f. Development. 2008 May;135(9):1713-23. doi: 10.1242/dev.015149. Epub 2008 Mar 19. Development. 2008. PMID: 18353862

10

Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis.

Kuss P, Villavicencio-Lorini P, Witte F, Klose J, Albrecht AN, Seemann P, Hecht J, Mundlos S. Kuss P, et al. Among authors: witte f. J Clin Invest. 2009 Jan;119(1):146-56. doi: 10.1172/JCI36851. Epub 2008 Dec 15. J Clin Invest. 2009. PMID: 19075394 Free PMC article.

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