198 related articles for article (PubMed ID: 35387802)
1. Biallelic
Hu T; Meng L; Tan C; Luo C; He WB; Tu C; Zhang H; Du J; Nie H; Lu GX; Lin G; Tan YQ
J Med Genet; 2023 Feb; 60(2):144-153. PubMed ID: 35387802
[TBL] [Abstract][Full Text] [Related]
2. TENT5D disruption causes oligoasthenoteratozoospermia and male infertility.
Sha Y; Liu W; Tang S; Zhang X; Xiao Z; Xiao Y; Deng H; Zhou H; Wei X
Andrology; 2023 Sep; 11(6):1121-1131. PubMed ID: 36746179
[TBL] [Abstract][Full Text] [Related]
3. Novel biallelic variants in DNAH1 cause multiple morphological abnormalities of sperm flagella with favorable outcomes of fertility after ICSI in Han Chinese males.
Long S; Fu L; Ma J; Yu H; Tang X; Hu T; Han W; Liu W; Liao H; Fu T; Huang G; Lu W; Lin T
Andrology; 2024 Feb; 12(2):349-364. PubMed ID: 37302001
[TBL] [Abstract][Full Text] [Related]
4. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.
Wang W; Su L; Meng L; He J; Tan C; Yi D; Cheng D; Zhang H; Lu G; Du J; Lin G; Zhang Q; Tu C; Tan YQ
Hum Reprod; 2023 Jul; 38(7):1399-1411. PubMed ID: 37192818
[TBL] [Abstract][Full Text] [Related]
5. Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans.
Guo R; Wu H; Zhu X; Wang G; Hu K; Li K; Geng H; Xu C; Zu C; Gao Y; Tang D; Cao Y; He X
J Med Genet; 2024 May; 61(6):553-565. PubMed ID: 38341271
[TBL] [Abstract][Full Text] [Related]
6. Biallelic Variants in
Ma A; Zeb A; Ali I; Zhao D; Khan A; Zhang B; Zhou J; Khan R; Zhang H; Zhang Y; Khan I; Shah W; Ali H; Javed AR; Ma H; Shi Q
Front Cell Dev Biol; 2021; 9():803818. PubMed ID: 35174165
[TBL] [Abstract][Full Text] [Related]
7. Homozygous mutations in
Cong J; Wang X; Amiri-Yekta A; Wang L; Kherraf ZE; Liu C; Cazin C; Tang S; Hosseini SH; Tian S; Daneshipour A; Wang J; Zhou Y; Zeng Y; Yang S; He X; Li J; Cao Y; Jin L; Ray PF; Zhang F
J Med Genet; 2022 Jul; 59(7):710-718. PubMed ID: 34348960
[TBL] [Abstract][Full Text] [Related]
8. Deleterious variants in TAF7L cause human oligoasthenoteratozoospermia and its impairing histone to protamine exchange inducing reduced
Bai H; Sha Y; Tan Y; Li P; Zhang Y; Xu J; Xu S; Ji Z; Wang X; Chen W; Zhang J; Yao C; Li Z; Zhi E
Front Endocrinol (Lausanne); 2022; 13():1099270. PubMed ID: 36714566
[TBL] [Abstract][Full Text] [Related]
9. Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.
Ferreux L; Bourdon M; Chargui A; Schmitt A; Stouvenel L; Lorès P; Ray P; Lousqui J; Pocate-Cheriet K; Santulli P; Dulioust E; Toure A; Patrat C
Hum Reprod; 2021 Oct; 36(11):2848-2860. PubMed ID: 34529793
[TBL] [Abstract][Full Text] [Related]
10. Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.
Liu C; Miyata H; Gao Y; Sha Y; Tang S; Xu Z; Whitfield M; Patrat C; Wu H; Dulioust E; Tian S; Shimada K; Cong J; Noda T; Li H; Morohoshi A; Cazin C; Kherraf ZE; Arnoult C; Jin L; He X; Ray PF; Cao Y; Touré A; Zhang F; Ikawa M
Am J Hum Genet; 2020 Aug; 107(2):330-341. PubMed ID: 32619401
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A novel CCDC39 mutation causes multiple morphological abnormalities of the flagella in a primary ciliary dyskinesia patient.
Chen D; Liang Y; Li J; Zhang X; Zheng R; Wang X; Zhang H; Shen Y
Reprod Biomed Online; 2021 Nov; 43(5):920-930. PubMed ID: 34674941
[TBL] [Abstract][Full Text] [Related]
13. Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella.
Huang T; Yin Y; Liu C; Li M; Yu X; Wang X; Zhang H; Muhammad T; Gao F; Li W; Chen ZJ; Liu H; Ma J
Sci Bull (Beijing); 2020 May; 65(10):854-864. PubMed ID: 36659204
[TBL] [Abstract][Full Text] [Related]
14. Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia.
Wei X; Liu W; Zhu X; Li Y; Zhang X; Chen J; Isachenko V; Sha Y; Lu Z
Clin Genet; 2021 Oct; 100(4):376-385. PubMed ID: 34096614
[TBL] [Abstract][Full Text] [Related]
15. Homozygous variants in
Liu C; Shen Y; Tang S; Wang J; Zhou Y; Tian S; Wu H; Cong J; He X; Jin L; Cao Y; Yang Y; Zhang F
J Med Genet; 2023 Feb; 60(2):137-143. PubMed ID: 35228300
[TBL] [Abstract][Full Text] [Related]
16. Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.
Liu Y; Li Y; Meng L; Li K; Gao Y; Lv M; Guo R; Xu Y; Zhou P; Wei Z; He X; Cao Y; Wu H; Tan Y; Hua R
Hum Mol Genet; 2023 May; 32(10):1730-1740. PubMed ID: 36708031
[TBL] [Abstract][Full Text] [Related]
17. CCDC157 is essential for sperm differentiation and shows oligoasthenoteratozoospermia-related mutations in men.
Zheng H; Gong C; Li J; Hou J; Gong X; Zhu X; Deng H; Wu H; Zhang F; Shi Q; Zhou J; Shi B; Yang X; Xi Y
J Cell Mol Med; 2024 Apr; 28(7):e18215. PubMed ID: 38509755
[TBL] [Abstract][Full Text] [Related]
18. The impact of RABL2B gene (rs144944885) on human male infertility in patients with oligoasthenoteratozoospermia and immotile short tail sperm defects.
Hosseini SH; Sadighi Gilani MA; Meybodi AM; Sabbaghian M
J Assist Reprod Genet; 2017 Apr; 34(4):505-510. PubMed ID: 28138870
[TBL] [Abstract][Full Text] [Related]
19. Homozygous frameshift variant in POC1B causes male infertility with oligoasthenoteratozoospermia in human and mice.
Hua J; Xu B; Liu W; Shi J; Jiang H; Zha X; Zhang X; Wan Y
Hum Mol Genet; 2023 Jul; 32(14):2307-2317. PubMed ID: 37070736
[TBL] [Abstract][Full Text] [Related]
20. Biallelic variants in
Martinez G; Beurois J; Dacheux D; Cazin C; Bidart M; Kherraf ZE; Robinson DR; Satre V; Le Gac G; Ka C; Gourlaouen I; Fichou Y; Petre G; Dulioust E; Zouari R; Thierry-Mieg N; Touré A; Arnoult C; Bonhivers M; Ray P; Coutton C
J Med Genet; 2020 Oct; 57(10):708-716. PubMed ID: 32161152
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
