Repping S - Search Results

1

Distinct prophase arrest mechanisms in human male meiosis.

Jan SZ, Jongejan A, Korver CM, van Daalen SKM, van Pelt AMM, Repping S, Hamer G. Jan SZ, et al. Among authors: repping s. Development. 2018 Apr 16;145(16):dev160614. doi: 10.1242/dev.160614. Development. 2018. PMID: 29540502 Free PMC article.

2

Clinical relevance of partial AZFc deletions.

de Vries JW, Repping S, van Daalen SK, Korver CM, Leschot NJ, van der Veen F. de Vries JW, et al. Among authors: repping s. Fertil Steril. 2002 Dec;78(6):1209-14. doi: 10.1016/s0015-0282(02)04390-x. Fertil Steril. 2002. PMID: 12477514 Free article.

3

The use of spermHALO-FISH to determine DAZ gene copy number.

Repping S, de Vries JW, van Daalen SK, Korver CM, Leschot NJ, van der Veen F. Repping S, et al. Mol Hum Reprod. 2003 Apr;9(4):183-8. doi: 10.1093/molehr/gag032. Mol Hum Reprod. 2003. PMID: 12651899

4

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.

Repping S, Skaletsky H, Brown L, van Daalen SK, Korver CM, Pyntikova T, Kuroda-Kawaguchi T, de Vries JW, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Nat Genet. 2003 Nov;35(3):247-51. doi: 10.1038/ng1250. Epub 2003 Oct 5. Nat Genet. 2003. PMID: 14528305

5

A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region.

Repping S, van Daalen SK, Korver CM, Brown LG, Marszalek JD, Gianotten J, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Genomics. 2004 Jun;83(6):1046-52. doi: 10.1016/j.ygeno.2003.12.018. Genomics. 2004. PMID: 15177557

6

Are sequence family variants useful for identifying deletions in the human Y chromosome?

Repping S, Korver CM, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Am J Hum Genet. 2004 Sep;75(3):514-7; author reply 517-9. doi: 10.1086/423394. Am J Hum Genet. 2004. PMID: 15284951 Free PMC article. No abstract available.

7

High mutation rates have driven extensive structural polymorphism among human Y chromosomes.

Repping S, van Daalen SK, Brown LG, Korver CM, Lange J, Marszalek JD, Pyntikova T, van der Veen F, Skaletsky H, Page DC, Rozen S. Repping S, et al. Nat Genet. 2006 Apr;38(4):463-7. doi: 10.1038/ng1754. Epub 2006 Feb 26. Nat Genet. 2006. PMID: 16501575

8

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. Westerveld GH, et al. Among authors: repping s. Hum Reprod. 2006 Dec;21(12):3178-84. doi: 10.1093/humrep/del293. Epub 2006 Aug 24. Hum Reprod. 2006. PMID: 16931801

9

Role for adhesion molecules in the spermatogonial stem cell niche.

de Rooij DG, Repping S, van Pelt AM. de Rooij DG, et al. Among authors: repping s. Cell Stem Cell. 2008 Nov 6;3(5):467-8. doi: 10.1016/j.stem.2008.10.010. Cell Stem Cell. 2008. PMID: 18983958 Free article.

10

Y chromosome gr/gr deletions are a risk factor for low semen quality.

Visser L, Westerveld GH, Korver CM, van Daalen SK, Hovingh SE, Rozen S, van der Veen F, Repping S. Visser L, et al. Among authors: repping s. Hum Reprod. 2009 Oct;24(10):2667-73. doi: 10.1093/humrep/dep243. Epub 2009 Jul 14. Hum Reprod. 2009. PMID: 19602516

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