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Items: 1 to 20 of 86

1.

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.

Dev Dyn. 2006 Dec;235(12):3456-65.

2.

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.

Dev Dyn. 2004 Feb;229(2):400-10.

3.

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome.

van Bokhoven H, Celli J, Kayserili H, van Beusekom E, Balci S, Brussel W, Skovby F, Kerr B, Percin EF, Akarsu N, Brunner HG.

Nat Genet. 2000 Aug;25(4):423-6.

PMID:
10932187
4.

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.

Development. 2008 May;135(9):1713-23. doi: 10.1242/dev.015149. Epub 2008 Mar 19.

5.

ALK2 functions as a BMP type I receptor and induces Indian hedgehog in chondrocytes during skeletal development.

Zhang D, Schwarz EM, Rosier RN, Zuscik MJ, Puzas JE, O'Keefe RJ.

J Bone Miner Res. 2003 Sep;18(9):1593-604.

6.
7.

Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.

Afzal AR, Rajab A, Fenske CD, Oldridge M, Elanko N, Ternes-Pereira E, Tüysüz B, Murday VA, Patton MA, Wilkie AO, Jeffery S.

Nat Genet. 2000 Aug;25(4):419-22.

PMID:
10932186
8.

Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.

Schwabe GC, Tinschert S, Buschow C, Meinecke P, Wolff G, Gillessen-Kaesbach G, Oldridge M, Wilkie AO, Kömec R, Mundlos S.

Am J Hum Genet. 2000 Oct;67(4):822-31. Epub 2000 Sep 12.

10.
11.

The receptor tyrosine kinase Ror2 associates with the melanoma-associated antigen (MAGE) family protein Dlxin-1 and regulates its intracellular distribution.

Matsuda T, Suzuki H, Oishi I, Kani S, Kuroda Y, Komori T, Sasaki A, Watanabe K, Minami Y.

J Biol Chem. 2003 Aug 1;278(31):29057-64. Epub 2003 May 16.

12.

Chicken keratin-19: cloning of cDNA and analysis of expression in the chicken embryonic gut.

Sato K, Yasugi S.

Dev Growth Differ. 1997 Dec;39(6):751-61.

PMID:
9493835
13.

Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.

Oldridge M, Fortuna AM, Maringa M, Propping P, Mansour S, Pollitt C, DeChiara TM, Kimble RB, Valenzuela DM, Yancopoulos GD, Wilkie AO.

Nat Genet. 2000 Mar;24(3):275-8.

PMID:
10700182
15.

Conservation of Sox4 gene structure and expression during chicken embryogenesis.

Maschhoff KL, Anziano PQ, Ward P, Baldwin HS.

Gene. 2003 Nov 27;320:23-30.

PMID:
14597385
16.
17.

Isolation and characterization of a chicken homolog of the c-ret proto-oncogene.

Schuchardt A, Srinivas S, Pachnis V, Costantini F.

Oncogene. 1995 Feb 16;10(4):641-9.

PMID:
7862441
18.

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.

Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12277-82. Epub 2003 Oct 1.

19.

SOX14 is a candidate gene for limb defects associated with BPES and Möbius syndrome.

Wilmore HP, Smith MJ, Wilcox SA, Bell KM, Sinclair AH.

Hum Genet. 2000 Mar;106(3):269-76.

PMID:
10798354
20.

The Ror receptor tyrosine kinase family.

Forrester WC.

Cell Mol Life Sci. 2002 Jan;59(1):83-96. Review.

PMID:
11846036

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