Levy N - Search Results

1

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: levy n. J Med Genet. 1999 Sep;36(9):670-7. J Med Genet. 1999. PMID: 10507722 Free PMC article.

2

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: levy 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.

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. Among authors: levy n. Mol Hum Reprod. 2000 Sep;6(9):789-93. doi: 10.1093/molehr/6.9.789. Mol Hum Reprod. 2000. PMID: 10956550

4

Low-frequency protamine 1 gene transversions c.102G->T and c.-107G->C do not correlate with male infertility.

Kichine E, Msaidie S, Bokilo AD, Ducourneau A, Navarro A, Levy N, Terriou P, Collignon P, Boetsch G, Chiaroni J, Mitchell MJ. Kichine E, et al. Among authors: levy n. J Med Genet. 2008 Apr;45(4):255-6. J Med Genet. 2008. PMID: 18381856 No abstract available.

5

The ubiquitin-activating enzyme E1 homologous genes on the mouse Y chromosome (Ube1y) represent one functional gene and six partial pseudogenes.

Lévy N, Navarro A, Bishop CE, Mitchell MJ. Lévy N, et al. Mamm Genome. 2000 Feb;11(2):164-8. doi: 10.1007/s003350010031. Mamm Genome. 2000. PMID: 10656933 No abstract available.

6

Molecular analysis of an isoYq chromosome in a sterile male mouse.

Levy N, de Boer P, Mattei J, Mitchell MJ. Levy N, et al. Mamm Genome. 1996 Aug;7(8):608-9. doi: 10.1007/s003359900180. Mamm Genome. 1996. PMID: 8678984 No abstract available.

7

Abnormal retention of nuclear lamina and disorganization of chromatin-related proteins in spermatozoa from DPY19L2-deleted globozoospermic patients.

Paci M, Elkhatib R, Longepied G, Hennebicq S, Bessonat J, Courbière B, Bourgeois P, Levy N, Mitchell MJ, Metzler-Guillemain C. Paci M, et al. Among authors: levy n. Reprod Biomed Online. 2017 Nov;35(5):562-570. doi: 10.1016/j.rbmo.2017.07.013. Epub 2017 Aug 4. Reprod Biomed Online. 2017. PMID: 28882431

8

Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases.

Kerr B, Delrue MA, Sigaudy S, Perveen R, Marche M, Burgelin I, Stef M, Tang B, Eden OB, O'Sullivan J, De Sandre-Giovannoli A, Reardon W, Brewer C, Bennett C, Quarell O, M'Cann E, Donnai D, Stewart F, Hennekam R, Cavé H, Verloes A, Philip N, Lacombe D, Levy N, Arveiler B, Black G. Kerr B, et al. Among authors: levy n. J Med Genet. 2006 May;43(5):401-5. doi: 10.1136/jmg.2005.040352. Epub 2006 Jan 27. J Med Genet. 2006. PMID: 16443854 Free PMC article.

9

LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome.

Gaudy-Marqueste C, Roll P, Esteves-Vieira V, Weiller PJ, Grob JJ, Cau P, Lévy N, De Sandre-Giovannoli A. Gaudy-Marqueste C, et al. Among authors: levy n. J Med Genet. 2010 Jun;47(6):361-70. doi: 10.1136/jmg.2009.071696. J Med Genet. 2010. PMID: 20522425

10

Homozygous deletion of SUN5 in three men with decapitated spermatozoa.

Elkhatib RA, Paci M, Longepied G, Saias-Magnan J, Courbière B, Guichaoua MR, Lévy N, Metzler-Guillemain C, Mitchell MJ. Elkhatib RA, et al. Among authors: levy n. Hum Mol Genet. 2017 Aug 15;26(16):3167-3171. doi: 10.1093/hmg/ddx200. Hum Mol Genet. 2017. PMID: 28541472

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