Saut N - Search Results

1

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility.

Machev N, Saut N, Longepied G, Terriou P, Navarro A, Levy N, Guichaoua M, Metzler-Guillemain C, Collignon P, Frances AM, Belougne J, Clemente E, Chiaroni J, Chevillard C, Durand C, Ducourneau A, Pech N, McElreavey K, Mattei MG, Mitchell MJ. Machev N, et al. Among authors: saut n. J Med Genet. 2004 Nov;41(11):814-25. doi: 10.1136/jmg.2004.022111. J Med Genet. 2004. PMID: 15520406 Free PMC article.

2

Complete deletion of the AZFb interval from the Y chromosome in an oligozoospermic man.

Longepied G, Saut N, Aknin-Seifer I, Levy R, Frances AM, Metzler-Guillemain C, Guichaoua MR, Mitchell MJ. Longepied G, et al. Among authors: saut n. Hum Reprod. 2010 Oct;25(10):2655-63. doi: 10.1093/humrep/deq209. Epub 2010 Aug 17. Hum Reprod. 2010. PMID: 20716563

3

The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility.

Saut N, Terriou P, Navarro A, Lévy N, Mitchell MJ. Saut N, et al. Mol Hum Reprod. 2000 Sep;6(9):789-93. doi: 10.1093/molehr/6.9.789. Mol Hum Reprod. 2000. PMID: 10956550

4

The mouse Y chromosome interval necessary for spermatogonial proliferation is gene dense with syntenic homology to the human AZFa region.

Mazeyrat S, Saut N, Sargent CA, Grimmond S, Longepied G, Ehrmann IE, Ellis PS, Greenfield A, Affara NA, Mitchell MJ. Mazeyrat S, et al. Among authors: saut n. Hum Mol Genet. 1998 Oct;7(11):1713-24. doi: 10.1093/hmg/7.11.1713. Hum Mol Genet. 1998. PMID: 9736773

5

RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene.

Mazeyrat S, Saut N, Mattei MG, Mitchell MJ. Mazeyrat S, et al. Among authors: saut n. Nat Genet. 1999 Jul;22(3):224-6. doi: 10.1038/10282. Nat Genet. 1999. PMID: 10391207 No abstract available.

6

The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences.

Sargent CA, Boucher CA, Kirsch S, Brown G, Weiss B, Trundley A, Burgoyne P, Saut N, Durand C, Levy N, Terriou P, Hargreave T, Cooke H, Mitchell M, Rappold GA, Affara NA. Sargent CA, et al. Among authors: saut n. J Med Genet. 1999 Sep;36(9):670-7. J Med Genet. 1999. PMID: 10507722 Free PMC article.

7

Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study.

Fontaine-Bisson B, Alessi MC, Saut N, Fumeron F, Marre M, Dutour A, Badens C, Levy N, Tichet J, Juhan-Vague I, Trégouët DA, Balkau B, Morange PE. Fontaine-Bisson B, et al. Among authors: saut n. J Mol Med (Berl). 2010 Feb;88(2):193-201. doi: 10.1007/s00109-009-0548-y. Epub 2009 Oct 16. J Mol Med (Berl). 2010. PMID: 19841875

8

A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.

Morange PE, Bezemer I, Saut N, Bare L, Burgos G, Brocheton J, Durand H, Biron-Andreani C, Schved JF, Pernod G, Galan P, Drouet L, Zelenika D, Germain M, Nicaud V, Heath S, Ninio E, Delluc A, Münzel T, Zeller T, Brand-Herrmann SM, Alessi MC, Tiret L, Lathrop M, Cambien F, Blankenberg S, Emmerich J, Trégouët DA, Rosendaal FR. Morange PE, et al. Among authors: saut n. Am J Hum Genet. 2010 Apr 9;86(4):592-5. doi: 10.1016/j.ajhg.2010.02.011. Epub 2010 Mar 11. Am J Hum Genet. 2010. PMID: 20226436 Free PMC article.

9

A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis.

Mazeyrat S, Saut N, Grigoriev V, Mahadevaiah SK, Ojarikre OA, Rattigan A, Bishop C, Eicher EM, Mitchell MJ, Burgoyne PS. Mazeyrat S, et al. Among authors: saut n. Nat Genet. 2001 Sep;29(1):49-53. doi: 10.1038/ng717. Nat Genet. 2001. PMID: 11528390

10

Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: the Athero Gene study.

Kallel C, Cohen W, Saut N, Blankenberg S, Schnabel R, Rupprecht HJ, Bickel C, Munzel T, Tregouet DA, Morange PE. Kallel C, et al. Among authors: saut n. BMC Med Genet. 2012 Nov 8;13:103. doi: 10.1186/1471-2350-13-103. BMC Med Genet. 2012. PMID: 23136988 Free PMC article.

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