178 related articles for article (PubMed ID: 19342699)
1. Phenotypic expression of partial AZFc deletions is independent of the variations in DAZL and BOULE in a Han population.
Chen P; Ma M; Li L; Zhang S; Su D; Ma Y; Liu Y; Tao D; Lin L; Yang Y
J Androl; 2010; 31(2):163-8. PubMed ID: 19342699
[TBL] [Abstract][Full Text] [Related]
2. Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment.
Yang Y; Ma M; Li L; Zhang W; Chen P; Ma Y; Liu Y; Tao D; Lin L; Zhang S
Hum Reprod; 2008 Sep; 23(9):2167-72. PubMed ID: 18579508
[TBL] [Abstract][Full Text] [Related]
3. Expression profiles of the DAZ gene family in human testis with and without spermatogenic failure.
Kuo PL; Wang ST; Lin YM; Lin YH; Teng YN; Hsu CC
Fertil Steril; 2004 Apr; 81(4):1034-40. PubMed ID: 15066460
[TBL] [Abstract][Full Text] [Related]
4. Association of partial AZFc region deletions with spermatogenic impairment and male infertility.
Ferlin A; Tessari A; Ganz F; Marchina E; Barlati S; Garolla A; Engl B; Foresta C
J Med Genet; 2005 Mar; 42(3):209-13. PubMed ID: 15744033
[TBL] [Abstract][Full Text] [Related]
5. DAZL polymorphisms and susceptibility to spermatogenic failure: an example of remarkable ethnic differences.
Becherini L; Guarducci E; Degl'Innocenti S; Rotondi M; Forti G; Krausz C
Int J Androl; 2004 Dec; 27(6):375-81. PubMed ID: 15595957
[TBL] [Abstract][Full Text] [Related]
6. Survey of the two polymorphisms in DAZL, an autosomal candidate for the azoospermic factor, in Japanese infertile men and implications for male infertility.
Yang XJ; Shinka T; Nozawa S; Yan HT; Yoshiike M; Umeno M; Sato Y; Chen G; Iwamoto T; Nakahori Y
Mol Hum Reprod; 2005 Jul; 11(7):513-5. PubMed ID: 16123080
[TBL] [Abstract][Full Text] [Related]
7. Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan.
Lin YW; Hsu LC; Kuo PL; Huang WJ; Chiang HS; Yeh SD; Hsu TY; Yu YH; Hsiao KN; Cantor RM; Yen PH
Hum Mutat; 2007 May; 28(5):486-94. PubMed ID: 17285591
[TBL] [Abstract][Full Text] [Related]
8. Y-chromosome AZFc structural architecture and relationship to male fertility.
Ravel C; Chantot-Bastaraud S; El Houate B; Rouba H; Legendre M; Lorenço D; Mandelbaum J; Siffroi JP; McElreavey K
Fertil Steril; 2009 Dec; 92(6):1924-33. PubMed ID: 18990391
[TBL] [Abstract][Full Text] [Related]
9. A to G transitions at 260, 386 and 437 in DAZL gene are not associated with spermatogenic failure in Indian population.
Thangaraj K; Deepa SR; Pavani K; Gupta NJ; Reddy P; Reddy AG; Chakravarty BN; Singh L
Int J Androl; 2006 Oct; 29(5):510-14. PubMed ID: 16573709
[TBL] [Abstract][Full Text] [Related]
10. Additional genomic duplications in AZFc underlie the b2/b3 deletion-associated risk of spermatogenic impairment in Han Chinese population.
Lu C; Zhang F; Yang H; Xu M; Du G; Wu W; An Y; Qin Y; Ji G; Han X; Gu A; Xia Y; Song L; Wang S; Jin L; Wang X
Hum Mol Genet; 2011 Nov; 20(22):4411-21. PubMed ID: 21852246
[TBL] [Abstract][Full Text] [Related]
11. Differential effect of specific gr/gr deletion subtypes on spermatogenesis in the Chinese Han population.
Yang Y; Ma M; Li L; Su D; Chen P; Ma Y; Liu Y; Tao D; Lin L; Zhang S
Int J Androl; 2010 Oct; 33(5):745-54. PubMed ID: 20039973
[TBL] [Abstract][Full Text] [Related]
12. A single-nucleotide polymorphism of the DAZL gene promoter confers susceptibility to spermatogenic failure in the Taiwanese Han.
Teng YN; Chang YP; Tseng JT; Kuo PH; Lee IW; Lee MS; Kuo PL
Hum Reprod; 2012 Sep; 27(9):2857-65. PubMed ID: 22752612
[TBL] [Abstract][Full Text] [Related]
13. Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility.
Machev N; Saut N; Longepied G; Terriou P; Navarro A; Levy N; Guichaoua M; Metzler-Guillemain C; Collignon P; Frances AM; Belougne J; Clemente E; Chiaroni J; Chevillard C; Durand C; Ducourneau A; Pech N; McElreavey K; Mattei MG; Mitchell MJ
J Med Genet; 2004 Nov; 41(11):814-25. PubMed ID: 15520406
[TBL] [Abstract][Full Text] [Related]
14. Yfm1, a multicopy marker specific for the Y chromosome and beneficial for forensic, population, genetic, and spermatogenesis-related studies.
Ewis AA; Lee JW; Kuroki Y; Shinka T; Nakahori Y
J Hum Genet; 2002; 47(10):523-8. PubMed ID: 12376741
[TBL] [Abstract][Full Text] [Related]
15. Analysis of partial azoospermia factor c deletion and DAZ copy number in azoospermia and severe oligozoospermia.
Alimardanian L; Saliminejad K; Razi S; Ahani A
Andrologia; 2016 Nov; 48(9):890-894. PubMed ID: 27739146
[TBL] [Abstract][Full Text] [Related]
16. A frequent Y chromosome b2/b3 subdeletion shows strong association with male infertility in Han-Chinese population.
Wu B; Lu NX; Xia YK; Gu AH; Lu CC; Wang W; Song L; Wang SL; Shen HB; Wang XR
Hum Reprod; 2007 Apr; 22(4):1107-13. PubMed ID: 17204527
[TBL] [Abstract][Full Text] [Related]
17. Combined deletion of DAZ2 and DAZ4 copies of Y chromosome DAZ gene is associated with male infertility in Tunisian men.
Ghorbel M; Baklouti-Gargouri S; Keskes R; Chakroun N; Sellami A; Fakhfakh F; Ammar-Keskes L
Gene; 2014 Sep; 547(2):191-4. PubMed ID: 24878370
[TBL] [Abstract][Full Text] [Related]
18. Gene copy number alterations in the azoospermia-associated AZFc region and their effect on spermatogenic impairment.
Lu C; Jiang J; Zhang R; Wang Y; Xu M; Qin Y; Lin Y; Guo X; Ni B; Zhao Y; Diao N; Chen F; Shen H; Sha J; Xia Y; Hu Z; Wang X
Mol Hum Reprod; 2014 Sep; 20(9):836-43. PubMed ID: 24935076
[TBL] [Abstract][Full Text] [Related]
19. Association of DAZ1/DAZ2 deletion with spermatogenic impairment and male infertility in the South Chinese population.
Li Q; Qiao D; Song NH; Ding Y; Wang ZJ; Yang J; Wang W; Yin CJ
World J Urol; 2013 Dec; 31(6):1403-9. PubMed ID: 23512232
[TBL] [Abstract][Full Text] [Related]
20. Partial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility.
Zhang F; Lu C; Li Z; Xie P; Xia Y; Zhu X; Wu B; Cai X; Wang X; Qian J; Wang X; Jin L
J Med Genet; 2007 Jul; 44(7):437-44. PubMed ID: 17412880
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
