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Items: 1 to 20 of 71

1.

A comprehensive gene mutation screen in men with asthenozoospermia.

Visser L, Westerveld GH, Xie F, van Daalen SK, van der Veen F, Lombardi MP, Repping S.

Fertil Steril. 2011 Mar 1;95(3):1020-4.e1-9. doi: 10.1016/j.fertnstert.2010.11.067. Epub 2011 Jan 21.

PMID:
21255775
2.

Association between the apolipoprotein B signal peptide gene insertion/deletion polymorphism and male infertility.

Peterlin B, Zorn B, Volk M, Kunej T.

Mol Hum Reprod. 2006 Dec;12(12):777-9. Epub 2006 Oct 27.

PMID:
17071710
3.

Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure.

Westerveld GH, Korver CM, van Pelt AM, Leschot NJ, van der Veen F, Repping S, Lombardi MP.

Hum Reprod. 2006 Dec;21(12):3178-84. Epub 2006 Aug 24.

PMID:
16931801
4.

Asthenoteratozoospermia in mice lacking testis expressed gene 18 (Tex18).

Jaroszynski L, Dev A, Li M, Meinhardt A, de Rooij DG, Mueller C, Böhm D, Wolf S, Adham IM, Wulf G, Engel W, Nayernia K.

Mol Hum Reprod. 2007 Mar;13(3):155-63. Epub 2007 Jan 5.

PMID:
17208930
5.

Single nucleotide polymorphism (SNP) of the endothelial nitric oxide synthase (eNOS) gene (Glu298Asp variant) in infertile men with asthenozoospermia.

Buldreghini E, Mahfouz RZ, Vignini A, Mazzanti L, Ricciardo-Lamonica G, Lenzi A, Agarwal A, Balercia G.

J Androl. 2010 Sep-Oct;31(5):482-8. doi: 10.2164/jandrol.109.008979. Epub 2010 May 13.

PMID:
20467051
6.

Association of polymorphisms in tektin-t gene with idiopathic asthenozoospermia in Sichuan, China.

Zhang SH, Zhang JH, Ding XP, Zhang S, Chen HH, Jing YL.

J Assist Reprod Genet. 2016 Feb;33(2):181-7. doi: 10.1007/s10815-015-0617-9. Epub 2015 Nov 19.

7.

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y.

Sun C, Skaletsky H, Birren B, Devon K, Tang Z, Silber S, Oates R, Page DC.

Nat Genet. 1999 Dec;23(4):429-32.

PMID:
10581029
8.

[UBE2B gene and male infertility: an update].

Zhang Q, Mou LS, Gui YT, Cai ZM.

Zhonghua Nan Ke Xue. 2014 Apr;20(4):367-71. Review. Chinese.

PMID:
24873167
9.

[Mutation of MTCYB and MTATP6 is associated with asthenospermia].

Feng CQ, Song YB, Zou YG, Mao XM.

Zhonghua Nan Ke Xue. 2008 Apr;14(4):321-3. Chinese.

PMID:
18481423
10.

A case of severe asthenozoospermia: a novel sperm tail defect of possible genetic origin identified by electron microscopy and immunocytochemistry.

Collodel G, Federico MG, Pascarelli NA, Geminiani M, Renieri T, Moretti E.

Fertil Steril. 2011 Jan;95(1):289.e11-6. doi: 10.1016/j.fertnstert.2010.05.029. Epub 2010 Jun 25.

PMID:
20579639
11.

[Mutation of KLHL-10 in idiopathic infertile males with azoospermia, oligospermia or asthenospermia].

Qiu QM, Liu G, Li WN, Shi QW, Zhu FX, Lu GX.

Zhonghua Nan Ke Xue. 2009 Nov;15(11):974-9. Chinese.

PMID:
20218307
12.

Heterogeneous nuclear ribonucleoprotein G-T (HNRNP G-T) mutations in men with impaired spermatogenesis.

Westerveld GH, Gianotten J, Leschot NJ, van der Veen F, Repping S, Lombardi MP.

Mol Hum Reprod. 2004 Apr;10(4):265-9. Epub 2004 Mar 2.

PMID:
14996998
13.

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect.

Buiting K, Gross S, Lich C, Gillessen-Kaesbach G, el-Maarri O, Horsthemke B.

Am J Hum Genet. 2003 Mar;72(3):571-7. Epub 2003 Jan 23.

14.

The role of the testis-specific gene hTAF7L in the aetiology of male infertility.

Stouffs K, Willems A, Lissens W, Tournaye H, Van Steirteghem A, Liebaers I.

Mol Hum Reprod. 2006 Apr;12(4):263-7. Epub 2006 Apr 5.

PMID:
16597641
15.
16.

Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosa.

Clark GR, Crowe P, Muszynska D, O'Prey D, O'Neill J, Alexander S, Willoughby CE, McKay GJ, Silvestri G, Simpson DA.

Ophthalmology. 2010 Nov;117(11):2169-77.e3. doi: 10.1016/j.ophtha.2010.02.029. Epub 2010 Jun 29.

PMID:
20591486
17.
18.

Mutation screening in the human epsilon-globin gene using single-strand conformation polymorphism analysis.

Papachatzopoulou A, Menounos PG, Kolonelou C, Patrinos GP.

Am J Hematol. 2006 Feb;81(2):136-8.

19.

Increased frequency of mutations in DNA from infertile men with meiotic arrest.

Nudell D, Castillo M, Turek PJ, Pera RR.

Hum Reprod. 2000 Jun;15(6):1289-94.

PMID:
10831557
20.

Mouse models for genes involved in impaired spermatogenesis.

O'Bryan MK, de Kretser D.

Int J Androl. 2006 Feb;29(1):76-89; discussion 105-8. Review.

PMID:
16466527

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