231 related articles for article (PubMed ID: 17714218)
1. 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]
2. The role of the testis-specific gene hTAF7L in the aetiology of male infertility.
Stouffs K; Willems A; Lissens W; Tournaye H; Van Steirteghem A; Liebaers I
Mol Hum Reprod; 2006 Apr; 12(4):263-7. PubMed ID: 16597641
[TBL] [Abstract][Full Text] [Related]
3. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
4. Mutations in SOHLH1 gene associate with nonobstructive azoospermia.
Choi Y; Jeon S; Choi M; Lee MH; Park M; Lee DR; Jun KY; Kwon Y; Lee OH; Song SH; Kim JY; Lee KA; Yoon TK; Rajkovic A; Shim SH
Hum Mutat; 2010 Jul; 31(7):788-93. PubMed ID: 20506135
[TBL] [Abstract][Full Text] [Related]
5. Polymorphisms of the luteinizing hormone/chorionic gonadotropin receptor gene: association with maldescended testes and male infertility.
Simoni M; Tüttelmann F; Michel C; Böckenfeld Y; Nieschlag E; Gromoll J
Pharmacogenet Genomics; 2008 Mar; 18(3):193-200. PubMed ID: 18300940
[TBL] [Abstract][Full Text] [Related]
6. 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
Hum Reprod; 2006 Dec; 21(12):3178-84. PubMed ID: 16931801
[TBL] [Abstract][Full Text] [Related]
7. Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.
Zhang W; Zhang S; Xiao C; Yang Y; Zhoucun A
Reproduction; 2007 Feb; 133(2):511-6. PubMed ID: 17307919
[TBL] [Abstract][Full Text] [Related]
8. Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment.
A Z; Zhang S; Yang Y; Ma Y; Lin L; Zhang W
Hum Reprod; 2006 Mar; 21(3):755-9. PubMed ID: 16293649
[TBL] [Abstract][Full Text] [Related]
9. Basonuclin 1 deficiency causes testicular premature aging: BNC1 cooperates with TAF7L to regulate spermatogenesis.
Li JY; Liu YF; Xu HY; Zhang JY; Lv PP; Liu ME; Ying YY; Qian YQ; Li K; Li C; Huang Y; Xu GF; Ding GL; Mao YC; Xu CM; Liu XM; Sheng JZ; Zhang D; Huang HF
J Mol Cell Biol; 2020 Jan; 12(1):71-83. PubMed ID: 31065688
[TBL] [Abstract][Full Text] [Related]
10. Sequence alterations in the YBX2 gene are associated with male factor infertility.
Hammoud S; Emery BR; Dunn D; Weiss RB; Carrell DT
Fertil Steril; 2009 Apr; 91(4):1090-5. PubMed ID: 18339382
[TBL] [Abstract][Full Text] [Related]
11. Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men.
Deng Y; Zhang W; Su D; Yang Y; Ma Y; Zhang H; Zhang S
Urology; 2008 May; 71(5):878-82. PubMed ID: 18372033
[TBL] [Abstract][Full Text] [Related]
12. Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility.
Tapanainen JS; Aittomäki K; Min J; Vaskivuo T; Huhtaniemi IT
Nat Genet; 1997 Feb; 15(2):205-6. PubMed ID: 9020851
[TBL] [Abstract][Full Text] [Related]
13. Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations.
Ferlin A; Vinanzi C; Garolla A; Selice R; Zuccarello D; Cazzadore C; Foresta C
Clin Endocrinol (Oxf); 2006 Nov; 65(5):606-10. PubMed ID: 17054461
[TBL] [Abstract][Full Text] [Related]
14. Estrogen receptor beta gene mutations in Indian infertile men.
Khattri A; Pandey RK; Gupta NJ; Chakravarty B; Deenadayal M; Singh L; Thangaraj K
Mol Hum Reprod; 2009 Aug; 15(8):513-20. PubMed ID: 19509112
[TBL] [Abstract][Full Text] [Related]
15. Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia.
Ayhan Ö; Balkan M; Guven A; Hazan R; Atar M; Tok A; Tolun A
J Med Genet; 2014 Apr; 51(4):239-44. PubMed ID: 24431330
[TBL] [Abstract][Full Text] [Related]
16. Is there a role for the nuclear export factor 2 gene in male infertility?
Stouffs K; Tournaye H; Van der Elst J; Liebaers I; Lissens W
Fertil Steril; 2008 Nov; 90(5):1787-91. PubMed ID: 18258234
[TBL] [Abstract][Full Text] [Related]
17. UTP14c is a recently acquired retrogene associated with spermatogenesis and fertility in man.
Rohozinski J; Lamb DJ; Bishop CE
Biol Reprod; 2006 Apr; 74(4):644-51. PubMed ID: 16354793
[TBL] [Abstract][Full Text] [Related]
18. An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y.
Sun C; Skaletsky H; Birren B; Devon K; Tang Z; Silber S; Oates R; Page DC
Nat Genet; 1999 Dec; 23(4):429-32. PubMed ID: 10581029
[TBL] [Abstract][Full Text] [Related]
19. Single-nucleotide polymorphisms of the PRDM9 (MEISETZ) gene in patients with nonobstructive azoospermia.
Irie S; Tsujimura A; Miyagawa Y; Ueda T; Matsuoka Y; Matsui Y; Okuyama A; Nishimune Y; Tanaka H
J Androl; 2009; 30(4):426-31. PubMed ID: 19168450
[TBL] [Abstract][Full Text] [Related]
20. Molecular analysis of the PArkin co-regulated gene and association with male infertility.
Wilson GR; Sim ML; Brody KM; Taylor JM; McLachlan RI; O'Bryan MK; Delatycki MB; Lockhart PJ
Fertil Steril; 2010 May; 93(7):2262-8. PubMed ID: 19268936
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
