432 related articles for article (PubMed ID: 31658987)
21. A novel homozygous frameshift variant in
Dil S; Khan A; Unar A; Yang ML; Ali I; Zeb A; Zhang H; Zhou JT; Zubair M; Khan K; Bai S; Shi QH
Asian J Androl; 2023; 25(3):350-355. PubMed ID: 36308074
[TBL] [Abstract][Full Text] [Related]
22. Association of
Zhu D; Zhang H; Wang R; Liu X; Jiang Y; Feng T; Liu R; Zhang G
Biosci Rep; 2019 Jun; 39(6):. PubMed ID: 31160482
[No Abstract] [Full Text] [Related]
23. Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.
Lorès P; Dacheux D; Kherraf ZE; Nsota Mbango JF; Coutton C; Stouvenel L; Ialy-Radio C; Amiri-Yekta A; Whitfield M; Schmitt A; Cazin C; Givelet M; Ferreux L; Fourati Ben Mustapha S; Halouani L; Marrakchi O; Daneshipour A; El Khouri E; Do Cruzeiro M; Favier M; Guillonneau F; Chaudhry M; Sakheli Z; Wolf JP; Patrat C; Gacon G; Savinov SN; Hosseini SH; Robinson DR; Zouari R; Ziyyat A; Arnoult C; Dulioust E; Bonhivers M; Ray PF; Touré A
Am J Hum Genet; 2019 Dec; 105(6):1148-1167. PubMed ID: 31735292
[TBL] [Abstract][Full Text] [Related]
24. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.
Tan C; Meng L; Lv M; He X; Sha Y; Tang D; Tan Y; Hu T; He W; Tu C; Nie H; Zhang H; Du J; Lu G; Fan LQ; Cao Y; Lin G; Tan YQ
Am J Hum Genet; 2022 Jan; 109(1):157-171. PubMed ID: 34932939
[TBL] [Abstract][Full Text] [Related]
25. Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia.
Tang D; Sha Y; Gao Y; Zhang J; Cheng H; Zhang J; Ni X; Wang C; Xu C; Geng H; He X; Cao Y
Reprod Biol Endocrinol; 2021 Feb; 19(1):27. PubMed ID: 33610189
[TBL] [Abstract][Full Text] [Related]
26. Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella.
Ma H; Zhang B; Khan A; Zhao D; Ma A; Zhou J; Khan I; Khan K; Zhang H; Zhang Y; Jiang X; Dil S; Zeb A; Rahim F; Shi Q
Hum Mol Genet; 2021 Oct; 30(21):1977-1984. PubMed ID: 34155512
[TBL] [Abstract][Full Text] [Related]
27. Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure.
Wei X; Sha Y; Wei Z; Zhu X; He F; Zhang X; Liu W; Wang Y; Lu Z
Acta Biochim Biophys Sin (Shanghai); 2021 Oct; 53(10):1300-1309. PubMed ID: 34476482
[TBL] [Abstract][Full Text] [Related]
28. A recurrent homozygous missense mutation in
Zubair M; Khan R; Ma A; Hameed U; Khan M; Abbas T; Ahmad R; Zhou JT; Shah W; Hussain A; Ahmed N; Khan I; Khan K; Zhang YW; Zhang H; Wu LM; Shi QH
Asian J Androl; 2022; 24(3):255-259. PubMed ID: 35259782
[TBL] [Abstract][Full Text] [Related]
29. Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.
Wang Y; Tu C; Nie H; Meng L; Li D; Wang W; Zhang H; Lu G; Lin G; Tan YQ; Du J
J Assist Reprod Genet; 2020 Apr; 37(4):811-820. PubMed ID: 32170493
[TBL] [Abstract][Full Text] [Related]
30. Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella.
Gao Y; Tian S; Sha Y; Zha X; Cheng H; Wang A; Liu C; Lv M; Ni X; Li Q; Wu H; Tan Q; Tang D; Song B; Ding D; Cong J; Xu Y; Zhou P; Wei Z; Cao Y; Xu Y; Zhang F; He X
Reprod Biomed Online; 2021 May; 42(5):963-972. PubMed ID: 33771466
[TBL] [Abstract][Full Text] [Related]
31. A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole-exome sequencing.
Xu X; Sha YW; Mei LB; Ji ZY; Qiu PP; Ji H; Li P; Wang T; Li L
Clin Genet; 2018 Feb; 93(2):345-349. PubMed ID: 28548327
[TBL] [Abstract][Full Text] [Related]
32. Morphological characteristics and initial genetic study of multiple morphological anomalies of the flagella in China.
Yang SM; Li HB; Wang JX; Shi YC; Cheng HB; Wang W; Li H; Hou JQ; Wen DG
Asian J Androl; 2015; 17(3):513-5. PubMed ID: 25652624
[No Abstract] [Full Text] [Related]
33. Biallelic mutations in
Wang W; Tu C; Nie H; Meng L; Li Y; Yuan S; Zhang Q; Du J; Wang J; Gong F; Fan L; Lu GX; Lin G; Tan YQ
J Med Genet; 2019 Nov; 56(11):750-757. PubMed ID: 31413122
[TBL] [Abstract][Full Text] [Related]
34. Homozygous DNAH1 frameshift mutation causes multiple morphological anomalies of the sperm flagella in Chinese.
Wang X; Jin H; Han F; Cui Y; Chen J; Yang C; Zhu P; Wang W; Jiao G; Wang W; Hao C; Gao Z
Clin Genet; 2017 Feb; 91(2):313-321. PubMed ID: 27573432
[TBL] [Abstract][Full Text] [Related]
35. Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations.
Lv M; Liu C; Ma C; Yu H; Shao Z; Gao Y; Liu Y; Wu H; Tang D; Tan Q; Zhang J; Li K; Xu C; Geng H; Zhang J; Li H; Mao X; Ge L; Fu F; Zhong K; Xu Y; Tao F; Zhou P; Wei Z; He X; Zhang F; Cao Y
Reprod Biol Endocrinol; 2022 Jan; 20(1):5. PubMed ID: 34980136
[TBL] [Abstract][Full Text] [Related]
36. Biallelic mutations in
Liu W; Wei X; Liu X; Chen G; Zhang X; Liang X; Isachenko V; Sha Y; Wang Y
J Med Genet; 2023 Feb; 60(2):154-162. PubMed ID: 35534203
[TBL] [Abstract][Full Text] [Related]
37. The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.
Cavarocchi E; Whitfield M; Chargui A; Stouvenel L; Lorès P; Coutton C; Arnoult C; Santulli P; Patrat C; Thierry-Mieg N; Ray PF; Dulioust E; Touré A
Clin Genet; 2021 May; 99(5):684-693. PubMed ID: 33462806
[TBL] [Abstract][Full Text] [Related]
38. A novel homozygous CFAP65 mutation in humans causes male infertility with multiple morphological abnormalities of the sperm flagella.
Zhang X; Shen Y; Wang X; Yuan G; Zhang C; Yang Y
Clin Genet; 2019 Dec; 96(6):541-548. PubMed ID: 31571197
[TBL] [Abstract][Full Text] [Related]
39. Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?
Wang WL; Tu CF; Tan YQ
Asian J Androl; 2020; 22(3):236-245. PubMed ID: 31210147
[TBL] [Abstract][Full Text] [Related]
40. Absence of annulus in human asthenozoospermia: case report.
Lhuillier P; Rode B; Escalier D; Lorès P; Dirami T; Bienvenu T; Gacon G; Dulioust E; Touré A
Hum Reprod; 2009 Jun; 24(6):1296-303. PubMed ID: 19221096
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
