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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. Development. 2008 May;135(9):1713-23. doi: 10.1242/dev.015149. Epub 2008 Mar 19. Development. 2008. PMID: 18353862
Essential role of STAT3 for embryonic stem cell pluripotency.
Raz R, Lee CK, Cannizzaro LA, d'Eustachio P, Levy DE. Raz R, et al. Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2846-51. doi: 10.1073/pnas.96.6.2846. Proc Natl Acad Sci U S A. 1999. PMID: 10077599 Free PMC article.
Cooperation between STAT3 and c-jun suppresses Fas transcription.
Ivanov VN, Bhoumik A, Krasilnikov M, Raz R, Owen-Schaub LB, Levy D, Horvath CM, Ronai Z. Ivanov VN, et al. Among authors: raz r. Mol Cell. 2001 Mar;7(3):517-28. doi: 10.1016/s1097-2765(01)00199-x. Mol Cell. 2001. PMID: 11463377 Free article.
341 results