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.
195 related articles for article (PubMed ID: 28548327)
21. LRRC23 deficiency causes male infertility with idiopathic asthenozoospermia by disrupting the assembly of radial spokes. Li Y; Zhang Q; Tan Q; Sha X; Gao Y; Hua R; Zhou P; Wei Z; He X; Cao Y; Li T; Wu H Clin Genet; 2023 Dec; 104(6):694-699. PubMed ID: 37804054 [TBL] [Abstract][Full Text] [Related]
23. Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella. Zhao S; Liu Q; Su L; Meng L; Tan C; Wei C; Zhang H; Luo T; Zhang Q; Tan YQ; Tu C; Chen H; Gao X J Assist Reprod Genet; 2024 May; 41(5):1297-1306. PubMed ID: 38492154 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. Identification of a homozygous GFPT2 variant in a family with asthenozoospermia. Askari M; Kordi-Tamandani DM; Almadani N; McElreavey K; Totonchi M Gene; 2019 May; 699():16-23. PubMed ID: 30849544 [TBL] [Abstract][Full Text] [Related]
26. A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome. Lorès P; Kherraf ZE; Amiri-Yekta A; Whitfield M; Daneshipour A; Stouvenel L; Cazin C; Cavarocchi E; Coutton C; Llabador MA; Arnoult C; Thierry-Mieg N; Ferreux L; Patrat C; Hosseini SH; Mustapha SFB; Zouari R; Dulioust E; Ray PF; Touré A Hum Genet; 2021 Jul; 140(7):1031-1043. PubMed ID: 33689014 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report. Beurois J; Martinez G; Cazin C; Kherraf ZE; Amiri-Yekta A; Thierry-Mieg N; Bidart M; Petre G; Satre V; Brouillet S; Touré A; Arnoult C; Ray PF; Coutton C Hum Reprod; 2019 Oct; 34(10):2071-2079. PubMed ID: 31621862 [TBL] [Abstract][Full Text] [Related]
29. Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Kherraf ZE; Cazin C; Coutton C; Amiri-Yekta A; Martinez G; Boguenet M; Fourati Ben Mustapha S; Kharouf M; Gourabi H; Hosseini SH; Daneshipour A; Touré A; Thierry-Mieg N; Zouari R; Arnoult C; Ray PF Clin Genet; 2019 Nov; 96(5):394-401. PubMed ID: 31292949 [TBL] [Abstract][Full Text] [Related]
30. A novel homozygous mutation in the DNAAF3 gene leads to severe asthenozoospermia and teratospermia. Chen D; Fan G; Xu Y; Luo P; Chen Q; Chen X; Guo Z; Zhu X; Gao Y J Cell Mol Med; 2024 Sep; 28(18):e70092. PubMed ID: 39289782 [TBL] [Abstract][Full Text] [Related]
31. A novel mutation in DNAH17 is present in a patient with multiple morphological abnormalities of the flagella. Zheng R; Sun Y; Jiang C; Chen D; Yang Y; Shen Y Reprod Biomed Online; 2021 Sep; 43(3):532-541. PubMed ID: 34373205 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. Homozygous mutations in Lv M; Liu W; Chi W; Ni X; Wang J; Cheng H; Li WY; Yang S; Wu H; Zhang J; Gao Y; Liu C; Li C; Yang C; Tan Q; Tang D; Zhang J; Song B; Chen YJ; Li Q; Zhong Y; Zhang Z; Saiyin H; Jin L; Xu Y; Zhou P; Wei Z; Zhang C; He X; Zhang F; Cao Y J Med Genet; 2020 Jul; 57(7):445-453. PubMed ID: 32051257 [TBL] [Abstract][Full Text] [Related]
35. EIF4G1 is a novel candidate gene associated with severe asthenozoospermia. Sha Y; Liu W; Huang X; Li Y; Ji Z; Mei L; Lin S; Kong S; Lu J; Kong L; Zhu X; Lu Z; Ding L Mol Genet Genomic Med; 2019 Aug; 7(8):e807. PubMed ID: 31268247 [TBL] [Abstract][Full Text] [Related]
36. Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human. Coutton C; Vargas AS; Amiri-Yekta A; Kherraf ZE; Ben Mustapha SF; Le Tanno P; Wambergue-Legrand C; Karaouzène T; Martinez G; Crouzy S; Daneshipour A; Hosseini SH; Mitchell V; Halouani L; Marrakchi O; Makni M; Latrous H; Kharouf M; Deleuze JF; Boland A; Hennebicq S; Satre V; Jouk PS; Thierry-Mieg N; Conne B; Dacheux D; Landrein N; Schmitt A; Stouvenel L; Lorès P; El Khouri E; Bottari SP; Fauré J; Wolf JP; Pernet-Gallay K; Escoffier J; Gourabi H; Robinson DR; Nef S; Dulioust E; Zouari R; Bonhivers M; Touré A; Arnoult C; Ray PF Nat Commun; 2018 Feb; 9(1):686. PubMed ID: 29449551 [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. Genetic underpinnings of asthenozoospermia. Tu C; Wang W; Hu T; Lu G; Lin G; Tan YQ Best Pract Res Clin Endocrinol Metab; 2020 Dec; 34(6):101472. PubMed ID: 33191078 [TBL] [Abstract][Full Text] [Related]
39. A novel homozygous nonsense variant of AK7 is associated with multiple morphological abnormalities of the sperm flagella. Chang T; Tang H; Zhou X; He J; Liu N; Li Y; Xiang W; Yao Z Reprod Biomed Online; 2024 May; 48(5):103765. PubMed ID: 38492416 [TBL] [Abstract][Full Text] [Related]
40. Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease. Gao Y; Wu H; Xu Y; Shen Q; Xu C; Geng H; Lv M; Tan Q; Li K; Tang D; Song B; Zhou P; Wei Z; He X; Cao Y Hum Mutat; 2022 Mar; 43(3):434-443. PubMed ID: 34923715 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]