These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
135 related articles for article (PubMed ID: 37713809)
1. Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis. Sha Y; Liu W; Li S; Osadchuk LV; Chen Y; Nie H; Gao S; Xie L; Qin W; Zhou H; Li L EBioMedicine; 2023 Oct; 96():104798. PubMed ID: 37713809 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
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. IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3. Zhang Z; Zhou H; Deng X; Zhang R; Qu R; Mu J; Liu R; Zeng Y; Chen B; Wang L; Sang Q; Bao S Hum Reprod; 2023 Jan; 38(1):168-179. PubMed ID: 36355624 [TBL] [Abstract][Full Text] [Related]
6. Bi-allelic variants in Meng GQ; Wang Y; Luo C; Tan YM; Li Y; Tan C; Tu C; Zhang QJ; Hu L; Zhang H; Meng LL; Liu CY; Deng L; Lu GX; Lin G; Du J; Tan YQ; Sha Y; Wang L; He WB Hum Reprod Open; 2024; 2024(1):hoae003. PubMed ID: 38312775 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF. Xu C; Tang D; Shao Z; Geng H; Gao Y; Li K; Tan Q; Wang G; Wang C; Wu H; Li G; Lv M; He X; Cao Y Reprod Biol Endocrinol; 2022 Mar; 20(1):41. PubMed ID: 35232447 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertility. Nawaz S; Hussain S; Bilal M; Syed N; Liaqat K; Ullah I; Akil AA; Fakhro KA; Ahmad W J Gene Med; 2024 Jan; 26(1):e3583. PubMed ID: 37640479 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injection. Wambergue C; Zouari R; Fourati Ben Mustapha S; Martinez G; Devillard F; Hennebicq S; Satre V; Brouillet S; Halouani L; Marrakchi O; Makni M; Latrous H; Kharouf M; Amblard F; Arnoult C; Ray PF; Coutton C Hum Reprod; 2016 Jun; 31(6):1164-72. PubMed ID: 27094479 [TBL] [Abstract][Full Text] [Related]
16. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility. Liu C; Tu C; Wang L; Wu H; Houston BJ; Mastrorosa FK; Zhang W; Shen Y; Wang J; Tian S; Meng L; Cong J; Yang S; Jiang Y; Tang S; Zeng Y; Lv M; Lin G; Li J; Saiyin H; He X; Jin L; Touré A; Ray PF; Veltman JA; Shi Q; O'Bryan MK; Cao Y; Tan YQ; Zhang F Am J Hum Genet; 2021 Feb; 108(2):309-323. PubMed ID: 33472045 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice. Tu C; Cong J; Zhang Q; He X; Zheng R; Yang X; Gao Y; Wu H; Lv M; Gu Y; Lu S; Liu C; Tian S; Meng L; Wang W; Tan C; Nie H; Li D; Zhang H; Gong F; Hu L; Lu G; Xu W; Lin G; Zhang F; Cao Y; Tan YQ Am J Hum Genet; 2021 Aug; 108(8):1466-1477. PubMed ID: 34237282 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia. Yan Y; Yang X; Liu Y; Shen Y; Tu W; Dong Q; Yang D; Ma Y; Yang Y Hum Reprod; 2017 Jul; 32(7):1521-1531. PubMed ID: 28498920 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]