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Year | Number of Results |
---|---|
2001 | 1 |
2008 | 1 |
2015 | 1 |
2017 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 56154
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Page 1
Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.
Gynecol Obstet Invest. 2017;82(3):283-286. doi: 10.1159/000468934. Epub 2017 Mar 30.
Gynecol Obstet Invest. 2017.
PMID: 28355598
Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation.
Wang X, Jin HR, Cui YQ, Chen J, Sha YW, Gao ZL.
Wang X, et al.
Asian J Androl. 2018 Jan-Feb;20(1):101-102. doi: 10.4103/1008-682X.194998.
Asian J Androl. 2018.
PMID: 28303806
Free PMC article.
No abstract available.
Item in Clipboard
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
Okutman O, Muller J, Baert Y, Serdarogullari M, Gultomruk M, Piton A, Rombaut C, Benkhalifa M, Teletin M, Skory V, Bakircioglu E, Goossens E, Bahceci M, Viville S.
Okutman O, et al.
Hum Mol Genet. 2015 Oct 1;24(19):5581-8. doi: 10.1093/hmg/ddv290. Epub 2015 Jul 21.
Hum Mol Genet. 2015.
PMID: 26199321
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Mouse TEX15 is essential for DNA double-strand break repair and chromosomal synapsis during male meiosis.
Yang F, Eckardt S, Leu NA, McLaughlin KJ, Wang PJ.
Yang F, et al.
J Cell Biol. 2008 Feb 25;180(4):673-9. doi: 10.1083/jcb.200709057. Epub 2008 Feb 18.
J Cell Biol. 2008.
PMID: 18283110
Free PMC article.
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An abundance of X-linked genes expressed in spermatogonia.
Wang PJ, McCarrey JR, Yang F, Page DC.
Wang PJ, et al.
Nat Genet. 2001 Apr;27(4):422-6. doi: 10.1038/86927.
Nat Genet. 2001.
PMID: 11279525
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