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.
152 related articles for article (PubMed ID: 29551503)
1. TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family. Sha YW; Wang X; Su ZY; Wang C; Ji ZY; Mei LB; Zhang L; Deng BB; Huang XJ; Yan W; Chen J; Li P; Cui YQ; Qu QL; Yin C; He XM Gene; 2018 Jun; 659():84-88. PubMed ID: 29551503 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. A novel homozygous frameshift mutation in Li Y; Wang WL; Tu CF; Meng LL; Hu TY; Du J; Lin G; Nie HC; Tan YQ Asian J Androl; 2021; 23(2):197-204. PubMed ID: 33037173 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Loss-of-function variant in TDRD6 cause male infertility with severe oligo-astheno-teratozoospermia in human and mice. Bi X; Jin H; Wan F; Xia Y; Guo H; Chen S; Wang B J Cell Mol Med; 2024 Sep; 28(18):e18580. PubMed ID: 39331689 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. A novel homozygous missense mutation in AK7 causes multiple morphological anomalies of the flagella and oligoasthenoteratozoospermia. Xiang M; Wang Y; Xu W; Zheng N; Deng H; Zhang J; Duan Z; Zha X; Zhang W; Song G; Shi X; Wang F; Cao Y; Zhu F J Assist Reprod Genet; 2022 Jan; 39(1):261-266. PubMed ID: 34854019 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Luo C; Chen Z; Meng L; Tan C; He W; Tu C; Du J; Lu GX; Lin G; Tan YQ; Hu TY Clin Genet; 2024 Jul; 106(1):27-36. PubMed ID: 38342987 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. Splicing Mutation in DNALI1 Causes Male Infertility with Severe Oligoasthenoteratozoospermia in Humans. Zhang F; Li J; Liang Z; Chen X; Zheng H; Wu J; Chen W; Li L Reprod Sci; 2024 Jun; 31(6):1610-1616. PubMed ID: 38212584 [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. ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria. Akbari A; Pipitone GB; Anvar Z; Jaafarinia M; Ferrari M; Carrera P; Totonchi M Hum Reprod; 2019 Jun; 34(6):1155-1164. PubMed ID: 31119281 [TBL] [Abstract][Full Text] [Related]
16. A novel mutation of AMHR2 in two brothers with persistent Müllerian duct syndrome and their intracytoplasmic sperm injection outcome. Fang J; Gao G; Liu J; Cai L; Cui Y; Yang X Mol Genet Genomic Med; 2021 Oct; 9(10):e1801. PubMed ID: 34480531 [TBL] [Abstract][Full Text] [Related]
17. Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family. Okutman O; Muller J; Baert Y; Serdarogullari M; Gultomruk M; Piton A; Rombaut C; Benkhalifa M; Teletin M; Skory V; Bakircioglu E; Goossens E; Bahceci M; Viville S Hum Mol Genet; 2015 Oct; 24(19):5581-8. PubMed ID: 26199321 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF). Sha YW; Xu X; Mei LB; Li P; Su ZY; He XQ; Li L Gene; 2017 Oct; 633():48-53. PubMed ID: 28866084 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]