106 related articles for article (PubMed ID: 25439847)
1. Copy number variation associated with meiotic arrest in idiopathic male infertility.
Eggers S; DeBoer KD; van den Bergen J; Gordon L; White SJ; Jamsai D; McLachlan RI; Sinclair AH; O'Bryan MK
Fertil Steril; 2015 Jan; 103(1):214-9. PubMed ID: 25439847
[TBL] [Abstract][Full Text] [Related]
2. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C
Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047
[TBL] [Abstract][Full Text] [Related]
3. Genetic variants in the ETV5 gene in fertile and infertile men with nonobstructive azoospermia associated with Sertoli cell-only syndrome.
O'Bryan MK; Grealy A; Stahl PJ; Schlegel PN; McLachlan RI; Jamsai D
Fertil Steril; 2012 Oct; 98(4):827-35.e1-3. PubMed ID: 22771031
[TBL] [Abstract][Full Text] [Related]
4. Meiotic arrest occurs most frequently at metaphase and is often incomplete in azoospermic men.
Enguita-Marruedo A; Sleddens-Linkels E; Ooms M; de Geus V; Wilke M; Blom E; Dohle GR; Looijenga LHJ; van Cappellen W; Baart EB; Baarends WM
Fertil Steril; 2019 Dec; 112(6):1059-1070.e3. PubMed ID: 31767154
[TBL] [Abstract][Full Text] [Related]
5. Copy number variations in testicular maturation arrest.
Halder A; Kumar P; Jain M; Iyer VK
Andrology; 2017 May; 5(3):460-472. PubMed ID: 28217965
[TBL] [Abstract][Full Text] [Related]
6. Genomic and genetic variation in E2F transcription factor-1 in men with nonobstructive azoospermia.
Jorgez CJ; Wilken N; Addai JB; Newberg J; Vangapandu HV; Pastuszak AW; Mukherjee S; Rosenfeld JA; Lipshultz LI; Lamb DJ
Fertil Steril; 2015 Jan; 103(1):44-52.e1. PubMed ID: 25439843
[TBL] [Abstract][Full Text] [Related]
7. Single nucleotide polymorphism array analysis in men with idiopathic azoospermia or oligoasthenozoospermia syndrome.
Frühmesser A; Vogt PH; Zimmer J; Witsch-Baumgartner M; Fauth C; Zschocke J; Pinggera GM; Kotzot D
Fertil Steril; 2013 Jul; 100(1):81-7. PubMed ID: 23579007
[TBL] [Abstract][Full Text] [Related]
8. Analysis of copy number variation in men with non-obstructive azoospermia.
Wyrwoll MJ; Wabschke R; Röpke A; Wöste M; Ruckert C; Perrey S; Rotte N; Hardy J; Astica L; Lupiáñez DG; Wistuba J; Westernströer B; Schlatt S; Berman AJ; Müller AM; Kliesch S; Yatsenko AN; Tüttelmann F; Friedrich C
Andrology; 2022 Nov; 10(8):1593-1604. PubMed ID: 36041235
[TBL] [Abstract][Full Text] [Related]
9. Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men.
Miyamoto T; Tsujimura A; Miyagawa Y; Koh E; Namiki M; Horikawa M; Saijo Y; Sengoku K
J Assist Reprod Genet; 2012 Jan; 29(1):47-51. PubMed ID: 22116646
[TBL] [Abstract][Full Text] [Related]
10. Novel bi-allelic variants in KASH5 are associated with meiotic arrest and non-obstructive azoospermia.
Yang C; Lin X; Ji Z; Huang Y; Zhang L; Luo J; Chen H; Li P; Tian R; Zhi E; Hong Y; Zhou Z; Zhang F; Li Z; Yao C
Mol Hum Reprod; 2022 Jun; 28(7):. PubMed ID: 35674372
[TBL] [Abstract][Full Text] [Related]
11. A new
Yu XC; Li MJ; Cai FF; Yang SJ; Liu HB; Zhang HB
Asian J Androl; 2021; 23(5):510-515. PubMed ID: 33762476
[TBL] [Abstract][Full Text] [Related]
12. Potential biomarkers of nonobstructive azoospermia identified in microarray gene expression analysis.
Malcher A; Rozwadowska N; Stokowy T; Kolanowski T; Jedrzejczak P; Zietkowiak W; Kurpisz M
Fertil Steril; 2013 Dec; 100(6):1686-94.e1-7. PubMed ID: 24012201
[TBL] [Abstract][Full Text] [Related]
13. Decreased expression of SAM68 in human testes with spermatogenic defects.
Li LJ; Zhang FB; Liu SY; Tian YH; Le F; Lou HY; Huang HF; Jin F
Fertil Steril; 2014 Jul; 102(1):61-67.e3. PubMed ID: 24794312
[TBL] [Abstract][Full Text] [Related]
14. Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification.
Du R; Lu C; Jiang Z; Li S; Ma R; An H; Xu M; An Y; Xia Y; Jin L; Wang X; Zhang F
J Hum Genet; 2012 Aug; 57(8):545-51. PubMed ID: 22673690
[TBL] [Abstract][Full Text] [Related]
15. Methylation defects of imprinted genes in human testicular spermatozoa.
Marques CJ; Francisco T; Sousa S; Carvalho F; Barros A; Sousa M
Fertil Steril; 2010 Jul; 94(2):585-94. PubMed ID: 19338988
[TBL] [Abstract][Full Text] [Related]
16. A Screen for Genomic Disorders of Infertility Identifies MAST2 Duplications Associated with Nonobstructive Azoospermia in Humans.
Huang N; Wen Y; Guo X; Li Z; Dai J; Ni B; Yu J; Lin Y; Zhou W; Yao B; Jiang Y; Sha J; Conrad DF; Hu Z
Biol Reprod; 2015 Sep; 93(3):61. PubMed ID: 26203179
[TBL] [Abstract][Full Text] [Related]
17. Status of the executioner step of apoptosis in human with normal spermatogenesis and azoospermia.
Bozec A; Amara S; Guarmit B; Selva J; Albert M; Rollet J; El Sirkasi M; Vialard F; Bailly M; Benahmed M; Mauduit C
Fertil Steril; 2008 Nov; 90(5):1723-31. PubMed ID: 18177647
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. SPANX gene variation in fertile and infertile males.
Hansen S; Eichler EE; Fullerton SM; Carrell D
Syst Biol Reprod Med; 2010 Feb; 55():18-26. PubMed ID: 20073942
[TBL] [Abstract][Full Text] [Related]
20. Stuffer-free multiplex ligation-dependent probe amplification based on conformation-sensitive capillary electrophoresis: a novel technology for robust multiplex determination of copy number variation.
Shin GW; Jung SH; Yim SH; Chung B; Yeol Jung G; Chung YJ
Electrophoresis; 2012 Oct; 33(19-20):3052-61. PubMed ID: 22965760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]