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.
198 related articles for article (PubMed ID: 38992144)
1. A novel homozygous missense TTC12 variant identified in an infertile Pakistani man with severe oligoasthenoteratozoospermia and primary ciliary dyskinesia. Ali I; Ali H; Unar A; Rahim F; Khan K; Dil S; Abbas T; Hussain A; Zeb A; Zubair M; Zhang H; Ma H; Jiang X; Khan MA; Xu B; Shah W; Shi Q Mol Genet Genomics; 2024 Jul; 299(1):69. PubMed ID: 38992144 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes. Liu Z; Wang C; Ni F; Li T; Yang F; Wei H; Li T; Huang C; Wang J; Wang B Genet Test Mol Biomarkers; 2024 Aug; 28(8):337-341. PubMed ID: 38837151 [No Abstract] [Full Text] [Related]
4. 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]
5. TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella. Thomas L; Bouhouche K; Whitfield M; Thouvenin G; Coste A; Louis B; Szymanski C; Bequignon E; Papon JF; Castelli M; Lemullois M; Dhalluin X; Drouin-Garraud V; Montantin G; Tissier S; Duquesnoy P; Copin B; Dastot F; Couvet S; Barbotin AL; Faucon C; Honore I; Maitre B; Beydon N; Tamalet A; Rives N; Koll F; Escudier E; Tassin AM; Touré A; Mitchell V; Amselem S; Legendre M Am J Hum Genet; 2020 Feb; 106(2):153-169. PubMed ID: 31978331 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia. Guo T; Tu CF; Yang DH; Ding SZ; Lei C; Wang RC; Liu L; Kang X; Shen XQ; Yang YF; Tan ZP; Tan YQ; Luo H Hum Genet; 2021 May; 140(5):761-773. PubMed ID: 33389130 [TBL] [Abstract][Full Text] [Related]
8. A novel stop-gain mutation in ARMC2 is associated with multiple morphological abnormalities of the sperm flagella. Khan I; Dil S; Zhang H; Zhang B; Khan T; Zeb A; Zhou J; Nawaz S; Zubair M; Khan K; Ma H; Shi Q Reprod Biomed Online; 2021 Nov; 43(5):913-919. PubMed ID: 34493464 [TBL] [Abstract][Full Text] [Related]
9. Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice. Zhang B; Khan I; Liu C; Ma A; Khan A; Zhang Y; Zhang H; Kakakhel MBS; Zhou J; Zhang W; Li Y; Ali A; Jiang X; Murtaza G; Khan R; Zubair M; Yuan L; Khan M; Wang L; Zhang F; Wang X; Ma H; Shi Q Clin Genet; 2021 Jan; 99(1):176-186. PubMed ID: 33070343 [TBL] [Abstract][Full Text] [Related]
10. A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella. Ali A; Unar A; Muhammad Z; Dil S; Zhang B; Sadaf H; Khan M; Ali M; Khan R; Shah KMB; Ma A; Jiang X; Zhang Y; Zhang H; Shi Q J Assist Reprod Genet; 2024 Jan; 41(1):109-120. PubMed ID: 37831349 [TBL] [Abstract][Full Text] [Related]
11. Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia. Wang Y; Tu C; Nie H; Meng L; Li D; Wang W; Zhang H; Lu G; Lin G; Tan YQ; Du J J Assist Reprod Genet; 2020 Apr; 37(4):811-820. PubMed ID: 32170493 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family. Rahim F; Tao L; Khan K; Ali I; Zeb A; Khan I; Dil S; Abbas T; Hussain A; Zubair M; Zhang H; Hui M; Khan MA; Shah W; Shi Q Clin Genet; 2024 Oct; 106(4):437-447. PubMed ID: 39221575 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. A novel homozygous frameshift variant in Dil S; Khan A; Unar A; Yang ML; Ali I; Zeb A; Zhang H; Zhou JT; Zubair M; Khan K; Bai S; Shi QH Asian J Androl; 2023; 25(3):350-355. PubMed ID: 36308074 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
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. 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]
20. A recurrent homozygous missense mutation in Zubair M; Khan R; Ma A; Hameed U; Khan M; Abbas T; Ahmad R; Zhou JT; Shah W; Hussain A; Ahmed N; Khan I; Khan K; Zhang YW; Zhang H; Wu LM; Shi QH Asian J Androl; 2022; 24(3):255-259. PubMed ID: 35259782 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]