129 related articles for article (PubMed ID: 18941885)
21. Association of NR3C1/Glucocorticoid Receptor gene SNP with azoospermia in Japanese men.
Chihara M; Yoshihara K; Ishiguro T; Adachi S; Okada H; Kashima K; Sato T; Tanaka A; Tanaka K; Enomoto T
J Obstet Gynaecol Res; 2016 Jan; 42(1):59-66. PubMed ID: 26556219
[TBL] [Abstract][Full Text] [Related]
22. A histone H3 methyltransferase controls epigenetic events required for meiotic prophase.
Hayashi K; Yoshida K; Matsui Y
Nature; 2005 Nov; 438(7066):374-8. PubMed ID: 16292313
[TBL] [Abstract][Full Text] [Related]
23. A major recombination hotspot in the XqYq pseudoautosomal region gives new insight into processing of human gene conversion events.
Sarbajna S; Denniff M; Jeffreys AJ; Neumann R; Soler Artigas M; Veselis A; May CA
Hum Mol Genet; 2012 May; 21(9):2029-38. PubMed ID: 22291443
[TBL] [Abstract][Full Text] [Related]
24. Rare allelic forms of PRDM9 associated with childhood leukemogenesis.
Hussin J; Sinnett D; Casals F; Idaghdour Y; Bruat V; Saillour V; Healy J; Grenier JC; de Malliard T; Busche S; Spinella JF; Larivière M; Gibson G; Andersson A; Holmfeldt L; Ma J; Wei L; Zhang J; Andelfinger G; Downing JR; Mullighan CG; Awadalla P
Genome Res; 2013 Mar; 23(3):419-30. PubMed ID: 23222848
[TBL] [Abstract][Full Text] [Related]
25. X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
Yatsenko AN; Georgiadis AP; Röpke A; Berman AJ; Jaffe T; Olszewska M; Westernströer B; Sanfilippo J; Kurpisz M; Rajkovic A; Yatsenko SA; Kliesch S; Schlatt S; Tüttelmann F
N Engl J Med; 2015 May; 372(22):2097-107. PubMed ID: 25970010
[TBL] [Abstract][Full Text] [Related]
26. The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutated CFTR alleles.
Steiner B; Truninger K; Sanz J; Schaller A; Gallati S
Hum Mutat; 2004 Aug; 24(2):120-9. PubMed ID: 15241793
[TBL] [Abstract][Full Text] [Related]
27. [Association of single nucleotide polymorphisms of PATZ1 gene with azoospermia].
Huang JX; A ZC
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):393-6. PubMed ID: 20677143
[TBL] [Abstract][Full Text] [Related]
28. Analysis of single nucleotide polymorphisms in the 5'-flanking region of tumor necrosis factor-alpha gene in Japanese patients with early-onset periodontitis.
Endo M; Tai H; Tabeta K; Kobayashi T; Yamazaki K; Yoshie H
J Periodontol; 2001 Nov; 72(11):1554-9. PubMed ID: 11759867
[TBL] [Abstract][Full Text] [Related]
29. [Genetic polymorphism of glutathione S-transferase T1 associated with idiopathic azoospermia and oligospermia].
Wu QF; Xing JP; Sun JH; Xue W; Wang XY; Jin XJ
Zhonghua Nan Ke Xue; 2007 May; 13(5):407-10. PubMed ID: 17569254
[TBL] [Abstract][Full Text] [Related]
30. Polymorphisms in folate-related enzyme genes in idiopathic infertile Brazilian men.
Gava MM; Kayaki EA; Bianco B; Teles JS; Christofolini DM; Pompeo AC; Glina S; Barbosa CP
Reprod Sci; 2011 Dec; 18(12):1267-72. PubMed ID: 21775772
[TBL] [Abstract][Full Text] [Related]
31. Primary Ovarian Insufficiency and Azoospermia in Carriers of a Homozygous PSMC3IP Stop Gain Mutation.
Al-Agha AE; Ahmed IA; Nuebel E; Moriwaki M; Moore B; Peacock KA; Mosbruger T; Neklason DW; Jorde LB; Yandell M; Welt CK
J Clin Endocrinol Metab; 2018 Feb; 103(2):555-563. PubMed ID: 29240891
[TBL] [Abstract][Full Text] [Related]
32. No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency.
Norling A; Hirschberg AL; Karlsson L; Rodriguez-Wallberg KA; Iwarsson E; Wedell A; Barbaro M
Sex Dev; 2014; 8(4):146-50. PubMed ID: 24481226
[TBL] [Abstract][Full Text] [Related]
33. Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment.
Zhang H; Su D; Yang Y; Zhang W; Liu Y; Bai G; Ma M; Ma Y; Zhang S
J Androl; 2010; 31(4):388-92. PubMed ID: 19926886
[TBL] [Abstract][Full Text] [Related]
34. HLA-DR antigen and HLA-DRB1 genotyping with nonobstructive azoospermia in Japan.
Tsujimura A; Takahara S; Kitamura M; Miura H; Koga M; Sada M; Tsuji T; Matsumiya K; Okuyama A
J Androl; 1999; 20(4):545-50. PubMed ID: 10452599
[TBL] [Abstract][Full Text] [Related]
35. Expression of androgen receptor co-regulators in the testes of men with azoospermia.
Lan KC; Hseh CY; Lu SY; Chang SY; Shyr CR; Chen YT; Kang HY; Huang KE
Fertil Steril; 2008 May; 89(5 Suppl):1397-405. PubMed ID: 17919607
[TBL] [Abstract][Full Text] [Related]
36. Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure.
Akinloye O; Gromoll J; Callies C; Nieschlag E; Simoni M
Andrologia; 2007 Oct; 39(5):190-5. PubMed ID: 17714218
[TBL] [Abstract][Full Text] [Related]
37. The poly(A) polymerase beta gene may not be associated with azoospermia caused by Sertoli-cell-only syndrome in Japanese patients by comparing patients and normal controls.
Miyamoto T; Shin T; Iijima M; Minase G; Okada H; Saijo Y; Sengoku K
J Obstet Gynaecol; 2019 Apr; 39(3):434-436. PubMed ID: 30744435
[TBL] [Abstract][Full Text] [Related]
38. Extraordinary molecular evolution in the PRDM9 fertility gene.
Thomas JH; Emerson RO; Shendure J
PLoS One; 2009 Dec; 4(12):e8505. PubMed ID: 20041164
[TBL] [Abstract][Full Text] [Related]
39. Structural basis for human PRDM9 action at recombination hot spots.
Patel A; Horton JR; Wilson GG; Zhang X; Cheng X
Genes Dev; 2016 Feb; 30(3):257-65. PubMed ID: 26833727
[TBL] [Abstract][Full Text] [Related]
40. Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia.
Westerveld GH; Repping S; Lombardi MP; van der Veen F
Mol Hum Reprod; 2005 Sep; 11(9):673-5. PubMed ID: 16227348
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]