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[A neuropeptide at the origin of testicular aging?].
Lacombe A, Lelièvre V, Roselli CE, Salameh W, Lue YH, Lawson G, Muller JM, Waschek JA, Vilain E. Lacombe A, et al. Among authors: vilain e. Med Sci (Paris). 2006 Oct;22(10):809-11. doi: 10.1051/medsci/20062210809. Med Sci (Paris). 2006. PMID: 17026927 Free article. French. No abstract available.
Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans.
Jordan BK, Mohammed M, Ching ST, Délot E, Chen XN, Dewing P, Swain A, Rao PN, Elejalde BR, Vilain E. Jordan BK, et al. Among authors: vilain e. Am J Hum Genet. 2001 May;68(5):1102-9. doi: 10.1086/320125. Epub 2001 Mar 29. Am J Hum Genet. 2001. PMID: 11283799 Free PMC article.
The endless quest for sex determination genes.
Fleming A, Vilain E. Fleming A, et al. Among authors: vilain e. Clin Genet. 2005 Jan;67(1):15-25. doi: 10.1111/j.1399-0004.2004.00376.x. Clin Genet. 2005. PMID: 15617542 Review.
Midkine is expressed early in rat fetal adrenal development.
Dewing P, Ching ST, Zhang YH, Huang BL, Peirce RM, McCabe ER, Vilain E. Dewing P, et al. Among authors: vilain e. Mol Genet Metab. 2000 Dec;71(4):616-22. doi: 10.1006/mgme.2000.3111. Mol Genet Metab. 2000. PMID: 11136554
A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
Schoch K, Meng L, Szelinger S, Bearden DR, Stray-Pedersen A, Busk OL, Stong N, Liston E, Cohn RD, Scaglia F, Rosenfeld JA, Tarpinian J, Skraban CM, Deardorff MA, Friedman JN, Akdemir ZC, Walley N, Mikati MA, Kranz PG, Jasien J, McConkie-Rosell A, McDonald M, Wechsler SB, Freemark M, Kansagra S, Freedman S, Bali D, Millan F, Bale S, Nelson SF, Lee H, Dorrani N; UCLA Clinical Genomics Center; Undiagnosed Diseases Network; Goldstein DB, Xiao R, Yang Y, Posey JE, Martinez-Agosto JA, Lupski JR, Wangler MF, Shashi V. Schoch K, et al. Am J Hum Genet. 2017 Feb 2;100(2):343-351. doi: 10.1016/j.ajhg.2016.12.013. Epub 2017 Jan 26. Am J Hum Genet. 2017. PMID: 28132692 Free PMC article.
235 results