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Items: 5

1.

CATSPER2, a human autosomal nonsyndromic male infertility gene.

Avidan N, Tamary H, Dgany O, Cattan D, Pariente A, Thulliez M, Borot N, Moati L, Barthelme A, Shalmon L, Krasnov T, Ben-Asher E, Olender T, Khen M, Yaniv I, Zaizov R, Shalev H, Delaunay J, Fellous M, Lancet D, Beckmann JS.

Eur J Hum Genet. 2003 Jul;11(7):497-502.

2.

Insights into sperm cell motility signaling through sNHE and the CatSpers.

Quill TA, Wang D, Garbers DL.

Mol Cell Endocrinol. 2006 May 16;250(1-2):84-92. Epub 2006 Jan 18. Review.

PMID:
16413670
3.

[Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].

Sandström H, Wahlin A.

Lakartidningen. 1999 Jan 27;96(4):343-7. Review. Swedish.

PMID:
10024825
4.

Genetic male infertility and mutation of CATSPER ion channels.

Hildebrand MS, Avenarius MR, Fellous M, Zhang Y, Meyer NC, Auer J, Serres C, Kahrizi K, Najmabadi H, Beckmann JS, Smith RJ.

Eur J Hum Genet. 2010 Nov;18(11):1178-84. doi: 10.1038/ejhg.2010.108. Epub 2010 Jul 21. Review.

5.

Genetic mutation as a cause of male infertility in two brothers.

Fisher LM.

Urol Nurs. 2002 Apr;22(2):112, 123. Review.

PMID:
11993238

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