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Items: 1 to 20 of 102

1.

Ikbkap/Elp1 deficiency causes male infertility by disrupting meiotic progression.

Lin FJ, Shen L, Jang CW, Falnes PØ, Zhang Y.

PLoS Genet. 2013 May;9(5):e1003516. doi: 10.1371/journal.pgen.1003516. Epub 2013 May 23.

2.

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.

J Cell Biol. 2008 Feb 25;180(4):673-9. doi: 10.1083/jcb.200709057. Epub 2008 Feb 18.

3.

Mouse pachytene checkpoint 2 (trip13) is required for completing meiotic recombination but not synapsis.

Li XC, Schimenti JC.

PLoS Genet. 2007 Aug;3(8):e130. Epub 2007 Jun 21. Erratum in: PLoS Genet. 2007 Sep 7;3(9):e168. Li, Xin [corrected to Li, Xin Chenglin].

4.

Disruption of pairing and synapsis of chromosomes causes stage-specific apoptosis of male meiotic cells.

Hamer G, Novak I, Kouznetsova A, Höög C.

Theriogenology. 2008 Feb;69(3):333-9. Epub 2007 Nov 7.

PMID:
17997150
5.

Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis.

Shin YH, Choi Y, Erdin SU, Yatsenko SA, Kloc M, Yang F, Wang PJ, Meistrich ML, Rajkovic A.

PLoS Genet. 2010 Nov 4;6(11):e1001190. doi: 10.1371/journal.pgen.1001190. Erratum in: PLoS Genet. 2011;7(2). doi: 10.1371/annotation/8aa656b6-55f7-4795-a441-cf243ea62175.

6.

Impairment of pachytene spermatogenesis in Dmrt7 deficient mice, possibly causing meiotic arrest.

Date S, Nozawa O, Inoue H, Hidema S, Nishimori K.

Biosci Biotechnol Biochem. 2012;76(9):1621-6. Epub 2012 Sep 7.

7.

[Molecular and cellular characterization ion of IKAP protein and the Elongator complex. Implications for familial dysautonomia].

Close P, Creppe C, Cornez I, Chariot A.

Bull Mem Acad R Med Belg. 2007;162(5-6):315-22. French. Erratum in: Bull Mem Acad R Med Belg. 2008;163(1-2):159. Close, P [added].

PMID:
18405001
8.

Disruption of CHTF18 causes defective meiotic recombination in male mice.

Berkowitz KM, Sowash AR, Koenig LR, Urcuyo D, Khan F, Yang F, Wang PJ, Jongens TA, Kaestner KH.

PLoS Genet. 2012;8(11):e1002996. doi: 10.1371/journal.pgen.1002996. Epub 2012 Nov 1.

9.

Meiotic recombination and male infertility: from basic science to clinical reality?

Hann MC, Lau PE, Tempest HG.

Asian J Androl. 2011 Mar;13(2):212-8. doi: 10.1038/aja.2011.1. Epub 2011 Feb 7. Review.

10.

CDK2 is required for proper homologous pairing, recombination and sex-body formation during male mouse meiosis.

Viera A, Rufas JS, Martínez I, Barbero JL, Ortega S, Suja JA.

J Cell Sci. 2009 Jun 15;122(Pt 12):2149-59. doi: 10.1242/jcs.046706.

11.

Cloning, characterization, and genomic structure of the mouse Ikbkap gene.

Cuajungco MP, Leyne M, Mull J, Gill SP, Gusella JF, Slaugenhaupt SA.

DNA Cell Biol. 2001 Sep;20(9):579-86.

PMID:
11747609
12.

A mutation in the nuclear pore complex gene Tmem48 causes gametogenesis defects in skeletal fusions with sterility (sks) mice.

Akiyama K, Noguchi J, Hirose M, Kajita S, Katayama K, Khalaj M, Tsuji T, Fairfield H, Byers C, Reinholdt L, Ogura A, Kunieda T.

J Biol Chem. 2013 Nov 1;288(44):31830-41. doi: 10.1074/jbc.M113.492306. Epub 2013 Sep 17.

13.

Disrupting Cyclin Dependent Kinase 1 in Spermatocytes Causes Late Meiotic Arrest and Infertility in Mice.

Clement TM, Inselman AL, Goulding EH, Willis WD, Eddy EM.

Biol Reprod. 2015 Dec;93(6):137. doi: 10.1095/biolreprod.115.134940. Epub 2015 Oct 21.

14.

[Meiotic recombination in unexplained human male infertility: an updated review].

Sun F.

Zhonghua Nan Ke Xue. 2007 Sep;13(9):773-6. Review. Chinese.

PMID:
17929549
15.

Cohesin SMC1 beta is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination.

Revenkova E, Eijpe M, Heyting C, Hodges CA, Hunt PA, Liebe B, Scherthan H, Jessberger R.

Nat Cell Biol. 2004 Jun;6(6):555-62. Epub 2004 May 16.

PMID:
15146193
16.
17.

Matefin/SUN-1 phosphorylation is part of a surveillance mechanism to coordinate chromosome synapsis and recombination with meiotic progression and chromosome movement.

Woglar A, Daryabeigi A, Adamo A, Habacher C, Machacek T, La Volpe A, Jantsch V.

PLoS Genet. 2013;9(3):e1003335. doi: 10.1371/journal.pgen.1003335. Epub 2013 Mar 7.

18.

Familial dysautonomia (FD) patients have reduced levels of the modified wobble nucleoside mcm(5)s(2)U in tRNA.

Karlsborn T, Tükenmez H, Chen C, Byström AS.

Biochem Biophys Res Commun. 2014 Nov 21;454(3):441-5. doi: 10.1016/j.bbrc.2014.10.116. Epub 2014 Oct 30.

19.

Rectifier of aberrant mRNA splicing recovers tRNA modification in familial dysautonomia.

Yoshida M, Kataoka N, Miyauchi K, Ohe K, Iida K, Yoshida S, Nojima T, Okuno Y, Onogi H, Usui T, Takeuchi A, Hosoya T, Suzuki T, Hagiwara M.

Proc Natl Acad Sci U S A. 2015 Mar 3;112(9):2764-9. doi: 10.1073/pnas.1415525112. Epub 2015 Feb 9.

20.

Loss of mouse Ikbkap, a subunit of elongator, leads to transcriptional deficits and embryonic lethality that can be rescued by human IKBKAP.

Chen YT, Hims MM, Shetty RS, Mull J, Liu L, Leyne M, Slaugenhaupt SA.

Mol Cell Biol. 2009 Feb;29(3):736-44. doi: 10.1128/MCB.01313-08. Epub 2008 Nov 17.

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