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XB-GENEPAGE-483251
Papers associated with sox12
Results 1 - 8 of 8 results
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De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism., Zawerton A, Yao B, Yeager JP, Pippucci T, Haseeb A, Smith JD, Wischmann L, Kühl SJ, Dean JCS, Pilz DT, Holder SE, null null, null null, McNeill A, Graziano C, Lefebvre V., Am J Hum Genet. February 7, 2019; 104 (2): 246-259. |
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Transcriptome analysis identifies genes involved in sex determination and development of Xenopus laevis gonads., Piprek RP, Damulewicz M, Kloc M, Kubiak JZ., Differentiation. January 1, 2018; 100 46-56. ![]() |
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Conservatism and variability of gene expression profiles among homeologous transcription factors in Xenopus laevis., Watanabe M, Yasuoka Y, Mawaribuchi S, Kuretani A, Ito M, Kondo M, Ochi H, Ogino H, Fukui A, Taira M, Kinoshita T., Dev Biol. June 15, 2017; 426 (2): 301-324. ![]() |
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The Sox transcriptional factors: Functions during intestinal development in vertebrates., Fu L, Shi YB., Semin Cell Dev Biol. March 1, 2017; 63 58-67. ![]() |
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Evolutionarily conserved role for SoxC genes in neural crest specification and neuronal differentiation., Uy BR, Simoes-Costa M, Koo DE, Sauka-Spengler T, Bronner ME., Dev Biol. January 15, 2015; 397 (2): 282-92. ![]() |
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sox4 and sox11 function during Xenopus laevis eye development., Cizelsky W, Hempel A, Metzig M, Tao S, Hollemann T, Kühl M, Kühl SJ., PLoS One. July 1, 2013; 8 (7): e69372. ![]() |
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Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL, Park TJ, Woods JO, Cha HJ, Wallingford JB, Marcotte EM., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6544-9. ![]() |
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A novel Xenopus laevis SRY-related gene, xSox33., Hagiuda J, Hiraoka Y, Hasegawa M, Ogawa M, Aiso S., Biochim Biophys Acta. July 28, 2003; 1628 (2): 140-5. ![]() |
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