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Page 1
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome.
Schorderet DF, Nichini O, Boisset G, Polok B, Tiab L, Mayeur H, Raji B, de la Houssaye G, Abitbol MM, Munier FL. Schorderet DF, et al. Among authors: polok b. Am J Hum Genet. 2008 May;82(5):1178-84. doi: 10.1016/j.ajhg.2008.03.007. Am J Hum Genet. 2008. PMID: 18423520 Free PMC article.
Bigh3 is upregulated in regenerating zebrafish fin.
Page L, Polok B, Bustamante M, Schorderet DF. Page L, et al. Among authors: polok b. Zebrafish. 2013 Mar;10(1):36-42. doi: 10.1089/zeb.2012.0759. Epub 2013 Mar 28. Zebrafish. 2013. PMID: 23536989
Essential role for Pbx1 in corneal morphogenesis.
Murphy MJ, Polok BK, Schorderet DF, Cleary ML. Murphy MJ, et al. Among authors: polok bk. Invest Ophthalmol Vis Sci. 2010 Feb;51(2):795-803. doi: 10.1167/iovs.08-3327. Epub 2009 Sep 24. Invest Ophthalmol Vis Sci. 2010. PMID: 19797217 Free PMC article.
[TDF system in cobalt radioisotope teletherapy].
Szymczyk W, Kowalczyk M, Lesiak J, Korzeniowski S, Polok B. Szymczyk W, et al. Among authors: polok b. Nowotwory. 1987 Jan-Mar;37(1):77-88. Nowotwory. 1987. PMID: 3628034 Polish. No abstract available.
15 results