186 related articles for article (PubMed ID: 33169450)
1. Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility.
Hu TY; Zhang H; Meng LL; Yuan SM; Tu CF; Du J; Lu GX; Lin G; Nie HC; Tan YQ
Hum Mutat; 2021 Jan; 42(1):31-36. PubMed ID: 33169450
[TBL] [Abstract][Full Text] [Related]
2. From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the
Kherraf ZE; Cazin C; Lestrade F; Muronova J; Coutton C; Arnoult C; Thierry-Mieg N; Ray PF
Asian J Androl; 2022; 24(3):243-247. PubMed ID: 35017390
[TBL] [Abstract][Full Text] [Related]
3. A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.
Tu C; Meng L; Nie H; Yuan S; Wang W; Du J; Lu G; Lin G; Tan YQ
Fertil Steril; 2020 Mar; 113(3):561-568. PubMed ID: 32111475
[TBL] [Abstract][Full Text] [Related]
4. Sequencing of the
Wen Y; Wang X; Zheng R; Dai S; Li J; Yang Y; Shen Y
J Med Genet; 2023 Apr; 60(4):380-390. PubMed ID: 35973810
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
Okutman O; Muller J; Skory V; Garnier JM; Gaucherot A; Baert Y; Lamour V; Serdarogullari M; Gultomruk M; Röpke A; Kliesch S; Herbepin V; Aknin I; Benkhalifa M; Teletin M; Bakircioglu E; Goossens E; Charlet-Berguerand N; Bahceci M; Tüttelmann F; Viville S
J Assist Reprod Genet; 2017 May; 34(5):683-694. PubMed ID: 28401488
[TBL] [Abstract][Full Text] [Related]
7. Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia.
Yi S; Wang W; Su L; Meng L; Li Y; Tan C; Liu Q; Zhang H; Fan L; Lu G; Hu L; Du J; Lin G; Tan YQ; Tu C; Zhang Q
Mol Hum Reprod; 2024 Feb; 30(2):. PubMed ID: 38258527
[TBL] [Abstract][Full Text] [Related]
8. [Analysis of Y chromosome microdeletion in non-obstructive male infertile patients with azoospermia and severe oligozoospermia].
Ting-Ting H; Xian-Ping D; Xia W; Jing R; Li-Yuan Z
Sichuan Da Xue Xue Bao Yi Xue Ban; 2013 Mar; 44(2):188-92. PubMed ID: 23745252
[TBL] [Abstract][Full Text] [Related]
9. Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Wyrwoll MJ; Temel ŞG; Nagirnaja L; Oud MS; Lopes AM; van der Heijden GW; Heald JS; Rotte N; Wistuba J; Wöste M; Ledig S; Krenz H; Smits RM; Carvalho F; Gonçalves J; Fietz D; Türkgenç B; Ergören MC; Çetinkaya M; Başar M; Kahraman S; McEleny K; Xavier MJ; Turner H; Pilatz A; Röpke A; Dugas M; Kliesch S; Neuhaus N; ; Aston KI; Conrad DF; Veltman JA; Friedrich C; Tüttelmann F
Am J Hum Genet; 2020 Aug; 107(2):342-351. PubMed ID: 32673564
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest.
van der Bijl N; Röpke A; Biswas U; Wöste M; Jessberger R; Kliesch S; Friedrich C; Tüttelmann F
Hum Reprod; 2019 Nov; 34(11):2112-2119. PubMed ID: 31682730
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
Chen S; Wang G; Zheng X; Ge S; Dai Y; Ping P; Chen X; Liu G; Zhang J; Yang Y; Zhang X; Zhong A; Zhu Y; Chu Q; Huang Y; Zhang Y; Shen C; Yuan Y; Yuan Q; Pei X; Cheng CY; Sun F
Hum Mol Genet; 2020 Aug; 29(14):2451-2459. PubMed ID: 32469048
[TBL] [Abstract][Full Text] [Related]
13. The association of testis-specific hTAF7L gene variants with idiopathic azoospermic and severe oligozoospermic male infertility.
Ambulkar PS; Waghmare JE; Verma Shivkumar P; Chaudhari AR; Gangane NM; Narang P; Pal AK
Andrologia; 2022 Dec; 54(11):e14581. PubMed ID: 36068176
[TBL] [Abstract][Full Text] [Related]
14. An association study of four candidate loci for human male fertility traits with male infertility.
Sato Y; Tajima A; Tsunematsu K; Nozawa S; Yoshiike M; Koh E; Kanaya J; Namiki M; Matsumiya K; Tsujimura A; Komatsu K; Itoh N; Eguchi J; Imoto I; Yamauchi A; Iwamoto T
Hum Reprod; 2015 Jun; 30(6):1510-4. PubMed ID: 25908656
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia].
Hu LP; Liu NH; Pan Q; Liang DS; Long ZG; Hu H; Zhu HY; Dai HP; Cai F; Wu LQ; Xia K; Xia JH
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):241-5. PubMed ID: 17478930
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.
Aston KI; Carrell DT
J Androl; 2009; 30(6):711-25. PubMed ID: 19478329
[TBL] [Abstract][Full Text] [Related]
18. Chromosomal abnormalities in patients with oligozoospermia and non-obstructive azoospermia.
Pylyp LY; Spinenko LO; Verhoglyad NV; Zukin VD
J Assist Reprod Genet; 2013 Jun; 30(5):729-32. PubMed ID: 23575767
[TBL] [Abstract][Full Text] [Related]
19. A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.
Li L; Sha YW; Su ZY; Mei LB; Ji ZY; Zhang Q; Lin SB; Wang X; Qiu PP; Li P; Yin C
Gene; 2018 Jan; 639():106-110. PubMed ID: 29017965
[TBL] [Abstract][Full Text] [Related]
20. [Association of FASL-844 polymorphism with the risk of idiopathic azoospermia and severe oligozoospermia].
Wang W; Lu NX; Xia YA; Wang XR; Zhang W; Song NH; Wei M; Su JT
Zhonghua Nan Ke Xue; 2007 Apr; 13(4):302-5. PubMed ID: 17491259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
