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.
178 related articles for article (PubMed ID: 35166991)
1. A novel homozygous mutation in DNAJB13-a gene associated with the sperm axoneme-leads to teratozoospermia. Liu M; Li J; Jiang C; Zhou Y; Sun Y; Yang Y; Shen Y J Assist Reprod Genet; 2022 Mar; 39(3):757-764. PubMed ID: 35166991 [TBL] [Abstract][Full Text] [Related]
2. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects. Li Y; Wang Y; Wen Y; Zhang T; Wang X; Jiang C; Zheng R; Zhou F; Chen D; Yang Y; Shen Y Hum Reprod; 2021 Dec; 37(1):152-177. PubMed ID: 34791246 [TBL] [Abstract][Full Text] [Related]
3. Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility. El Khouri E; Thomas L; Jeanson L; Bequignon E; Vallette B; Duquesnoy P; Montantin G; Copin B; Dastot-Le Moal F; Blanchon S; Papon JF; Lorès P; Yuan L; Collot N; Tissier S; Faucon C; Gacon G; Patrat C; Wolf JP; Dulioust E; Crestani B; Escudier E; Coste A; Legendre M; Touré A; Amselem S Am J Hum Genet; 2016 Aug; 99(2):489-500. PubMed ID: 27486783 [TBL] [Abstract][Full Text] [Related]
4. Missense mutation in DNAJB13 gene correlated with male fertility in asthenozoospermia. Li WN; Zhu L; Jia MM; Yin SL; Lu GX; Liu G Andrology; 2020 Mar; 8(2):299-306. PubMed ID: 31342671 [TBL] [Abstract][Full Text] [Related]
5. PRSS55 is a novel potential causative gene for human male infertility. Liu M; Jiang C; Zhang X; Zhang G; Liu M; Zheng R; Yang Y; Shen Y Reprod Biomed Online; 2022 Sep; 45(3):553-562. PubMed ID: 35821214 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella. Martinez G; Kherraf ZE; Zouari R; Fourati Ben Mustapha S; Saut A; Pernet-Gallay K; Bertrand A; Bidart M; Hograindleur JP; Amiri-Yekta A; Kharouf M; Karaouzène T; Thierry-Mieg N; Dacheux-Deschamps D; Satre V; Bonhivers M; Touré A; Arnoult C; Ray PF; Coutton C Hum Reprod; 2018 Oct; 33(10):1973-1984. PubMed ID: 30137358 [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. Mechanistic insights into acephalic spermatozoa syndrome-associated mutations in the human Shang Y; Yan J; Tang W; Liu C; Xiao S; Guo Y; Yuan L; Chen L; Jiang H; Guo X; Qiao J; Li W J Biol Chem; 2018 Feb; 293(7):2395-2407. PubMed ID: 29298896 [TBL] [Abstract][Full Text] [Related]
10. Sequencing of the Wen Y; Wang X; Zheng R; Dai S; Li J; Yang Y; Shen Y J Med Genet; 2023 Apr; 60(4):380-390. PubMed ID: 35973810 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Novel variations in TENT5D lead to teratozoospermia in infertile patients. Zhang YT; Shen G; Zhuo LC; Yang X; Wang SY; Ruan TC; Jiang C; Wang X; Wang Y; Yang YH; Shen Y Andrology; 2024 Sep; 12(6):1336-1346. PubMed ID: 38228861 [TBL] [Abstract][Full Text] [Related]
13. Biallelic mutations in Hua J; Guo L; Yao Y; Hu W; Wan YY; Xu B Asian J Androl; 2023; 25(3):398-403. PubMed ID: 36178131 [TBL] [Abstract][Full Text] [Related]
14. Deleterious genetic changes in AGTPBP1 result in teratozoospermia with sperm head and flagella defects. Lin YH; Wang YY; Lai TH; Teng JL; Lin CW; Ke CC; Yu IS; Lee HL; Chan CC; Tung CH; Conrad DF; O'Bryan MK; Lin YH J Cell Mol Med; 2024 Jan; 28(2):e18031. PubMed ID: 37937809 [TBL] [Abstract][Full Text] [Related]
15. Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa. Cazin C; Boumerdassi Y; Martinez G; Fourati Ben Mustapha S; Whitfield M; Coutton C; Thierry-Mieg N; Di Pizio P; Rives N; Arnoult C; Touré A; Ray PF; Zouari R; Sifer C; Kherraf ZE Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33671757 [TBL] [Abstract][Full Text] [Related]
16. Mutations in CCIN cause teratozoospermia and male infertility. Fan Y; Huang C; Chen J; Chen Y; Wang Y; Yan Z; Yu W; Wu H; Yang Y; Nie L; Huang S; Wang F; Wang H; Hua Y; Lyu Q; Kuang Y; Lei M Sci Bull (Beijing); 2022 Oct; 67(20):2112-2123. PubMed ID: 36546111 [TBL] [Abstract][Full Text] [Related]
17. A heat-shock protein 40, DNAJB13, is an axoneme-associated component in mouse spermatozoa. Guan J; Yuan L Mol Reprod Dev; 2008 Sep; 75(9):1379-86. PubMed ID: 18247331 [TBL] [Abstract][Full Text] [Related]
18. DNAJB13, a type II HSP40 family member, localizes to the spermatids and spermatozoa during mouse spermatogenesis. Li W; Liu G BMC Dev Biol; 2014 Sep; 14():38. PubMed ID: 25233908 [TBL] [Abstract][Full Text] [Related]
19. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Oud MS; Okutman Ö; Hendricks LAJ; de Vries PF; Houston BJ; Vissers LELM; O'Bryan MK; Ramos L; Chemes HE; Viville S; Veltman JA Hum Reprod; 2020 Jan; 35(1):240-252. PubMed ID: 31985809 [TBL] [Abstract][Full Text] [Related]
20. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations. Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]