245 related articles for article (PubMed ID: 21559371)
1. Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.
Tüttelmann F; Simoni M; Kliesch S; Ledig S; Dworniczak B; Wieacker P; Röpke A
PLoS One; 2011 Apr; 6(4):e19426. PubMed ID: 21559371
[TBL] [Abstract][Full Text] [Related]
2. High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.
Krausz C; Giachini C; Lo Giacco D; Daguin F; Chianese C; Ars E; Ruiz-Castane E; Forti G; Rossi E
PLoS One; 2012; 7(10):e44887. PubMed ID: 23056185
[TBL] [Abstract][Full Text] [Related]
3. Identification of genomic imbalances (CNVs as well as LOH) in sertoli cell only syndrome cases through cytoscan microarray.
Sharma A; Jain M; Halder A; Kaushal S
Gene; 2021 Oct; 801():145851. PubMed ID: 34274474
[TBL] [Abstract][Full Text] [Related]
4. Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia.
Dong Y; Pan Y; Wang R; Zhang Z; Xi Q; Liu RZ
Genet Mol Res; 2015 Dec; 14(4):16041-9. PubMed ID: 26662397
[TBL] [Abstract][Full Text] [Related]
5. Chromosomal microarray analysis of infertile men with azoospermia factor microdeletions.
Zhu Y; Hu L; Cao D; Ou X; Jiang M
Gene; 2020 Apr; 735():144389. PubMed ID: 31982552
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Duplications in 19p13.3 are associated with male infertility.
Singh V; Bala R; Chakraborty A; Rajender S; Trivedi S; Singh K
J Assist Reprod Genet; 2019 Oct; 36(10):2171-2179. PubMed ID: 31418107
[TBL] [Abstract][Full Text] [Related]
8. Associations of Y-chromosome subdeletion gr/gr with the prevalence of Y-chromosome haplogroups in infertile patients.
Shahid M; Dhillon VS; Khalil HS; Sexana A; Husain SA
Eur J Hum Genet; 2011 Jan; 19(1):23-9. PubMed ID: 20823911
[TBL] [Abstract][Full Text] [Related]
9. Identification and Functional Investigation of Novel Heterozygous
Murtaza G; Yang L; Khan I; Unar A; Khan M; Huan Z; Khan R; Shi Q
Genet Test Mol Biomarkers; 2021 Oct; 25(10):654-659. PubMed ID: 34672775
[No Abstract] [Full Text] [Related]
10. Genome-wide screening of severe male factor infertile patients using BAC-array comparative genomic hybridization (CGH).
Song SH; Shim SH; Bang JK; Park JE; Sung SR; Cha DH
Gene; 2012 Sep; 506(1):248-52. PubMed ID: 22750321
[TBL] [Abstract][Full Text] [Related]
11. Y-chromosome genes associated with sertoli cell-only syndrome identified by array comparative genome hybridization.
Lan KC; Wang HJ; Wang TJ; Lin HJ; Chang YC; Kang HY
Biomed J; 2023 Apr; 46(2):100524. PubMed ID: 35358715
[TBL] [Abstract][Full Text] [Related]
12. Androgen receptor gene CAG and GGN repeat polymorphisms in Chilean men with primary severe spermatogenic failure.
Castro-Nallar E; Bacallao K; Parada-Bustamante A; Lardone MC; López PV; Madariaga M; Valdevenito R; Piottante A; Ebensperger M; Castro A
J Androl; 2010; 31(6):552-9. PubMed ID: 20378930
[TBL] [Abstract][Full Text] [Related]
13. Sertoli cell-only syndrome: advances, challenges, and perspectives in genetics and mechanisms.
Wang X; Liu X; Qu M; Li H
Cell Mol Life Sci; 2023 Feb; 80(3):67. PubMed ID: 36814036
[TBL] [Abstract][Full Text] [Related]
14. Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility.
Lo Giacco D; Chianese C; Ars E; Ruiz-Castañé E; Forti G; Krausz C
J Med Genet; 2014 May; 51(5):340-4. PubMed ID: 24421283
[TBL] [Abstract][Full Text] [Related]
15. MECHANISMS IN ENDOCRINOLOGY: Aberrations of the X chromosome as cause of male infertility.
Röpke A; Tüttelmann F
Eur J Endocrinol; 2017 Nov; 177(5):R249-R259. PubMed ID: 28611019
[TBL] [Abstract][Full Text] [Related]
16. Copy number variants within AZF region of Y chromosome and their association with idiopathic male infertility in Serbian population.
Vučić N; Kotarac N; Matijašević S; Radenković L; Vuković I; Budimirović B; Djordjević M; Savić-Pavićević D; Brajušković G
Andrologia; 2022 Feb; 54(1):e14297. PubMed ID: 34716599
[TBL] [Abstract][Full Text] [Related]
17. The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study.
Li HG; Fan LH; Liu B; Qian YQ; Chen M; Sun YX; Dong MY
Asian J Androl; 2020; 22(6):642-648. PubMed ID: 32362598
[TBL] [Abstract][Full Text] [Related]
18. [Detection of Y chromosome microdeletions in patients with severe oligozoospermia and azoospermia].
Song NH; Wu HF; Zhang W; Hua LX; Zhou ZM; Feng NH; Zhang J; Qiao D; Zhang JX
Zhonghua Yi Xue Za Zhi; 2006 May; 86(20):1376-80. PubMed ID: 16796918
[TBL] [Abstract][Full Text] [Related]
19. Genomic testing for copy number and single nucleotide variants in spermatogenic failure.
Hardy J; Pollock N; Gingrich T; Sweet P; Ramesh A; Kuong J; Basar A; Jiang H; Hwang K; Vukina J; Jaffe T; Olszewska M; Kurpisz M; Yatsenko AN
J Assist Reprod Genet; 2022 Sep; 39(9):2103-2114. PubMed ID: 35849255
[TBL] [Abstract][Full Text] [Related]
20. Genetic variants in meiotic program initiation pathway genes are associated with spermatogenic impairment in a Han Chinese population.
Lu C; Xu M; Wang Y; Qin Y; Du G; Wu W; Han X; Ji C; Yang Y; Gu A; Xia Y; Song L; Wang S; Wang X
PLoS One; 2013; 8(1):e53443. PubMed ID: 23320086
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]