61 related articles for article (PubMed ID: 34155512)
1. Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella.
Ma H; Zhang B; Khan A; Zhao D; Ma A; Zhou J; Khan I; Khan K; Zhang H; Zhang Y; Jiang X; Dil S; Zeb A; Rahim F; Shi Q
Hum Mol Genet; 2021 Oct; 30(21):1977-1984. PubMed ID: 34155512
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Genetic Defects in
Hwang JY; Nawaz S; Choi J; Wang H; Hussain S; Nawaz M; Lopez-Giraldez F; Jeong K; Dong W; Oh JN; Bilguvar K; Mane S; Lee CK; Bystroff C; Lifton RP; Ahmad W; Chung JJ
Front Cell Dev Biol; 2021; 9():662903. PubMed ID: 33968937
[TBL] [Abstract][Full Text] [Related]
5. 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 Jun; ():. PubMed ID: 38837151
[No Abstract] [Full Text] [Related]
6. Evaluation of The 1499T>C Variant in The
Poursafari Talemi E; Hosseini SH; Gourabi H; Sabbaghian M; Mohseni Meybodi A
Int J Fertil Steril; 2024 Feb; 18(2):180-184. PubMed ID: 38368523
[TBL] [Abstract][Full Text] [Related]
7. Reversible male contraception by targeted inhibition of serine/threonine kinase 33.
Ku AF; Sharma KL; Ta HM; Sutton CM; Bohren KM; Wang Y; Chamakuri S; Chen R; Hakenjos JM; Jimmidi R; Kent K; Li F; Li JY; Ma L; Madasu C; Palaniappan M; Palmer SS; Qin X; Robers MB; Sankaran B; Tan Z; Vasquez YM; Wang J; Wilkinson J; Yu Z; Ye Q; Young DW; Teng M; Kim C; Matzuk MM
Science; 2024 May; 384(6698):885-890. PubMed ID: 38781365
[TBL] [Abstract][Full Text] [Related]
8. A novel homozygous splice variant in
Zhu X; Chen C; Song J; Dong S; Zeng X; Niu Z; Sha Y; Zhang X
Acta Biochim Biophys Sin (Shanghai); 2023 Oct; 55(10):1689-1692. PubMed ID: 37674365
[No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse.
Zhang J; He X; Wu H; Zhang X; Yang S; Liu C; Liu S; Hua R; Zhou S; Zhao S; Hu F; Zhang J; Liu W; Cheng H; Gao Y; Zhang F; Cao Y; Liu M
Hum Mol Genet; 2021 Oct; 30(21):1996-2011. PubMed ID: 34169321
[TBL] [Abstract][Full Text] [Related]
12. Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.
Shen Q; Martinez G; Liu H; Beurois J; Wu H; Amiri-Yekta A; Liang D; Kherraf ZE; Bidart M; Cazin C; Celse T; Satre V; Thierry-Mieg N; Whitfield M; Touré A; Song B; Lv M; Li K; Liu C; Tao F; He X; Zhang F; Arnoult C; Ray PF; Cao Y; Coutton C
Hum Genet; 2021 Sep; 140(9):1367-1377. PubMed ID: 34255152
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.
Wang W; Tian S; Nie H; Tu C; Liu C; Li Y; Li D; Yang X; Meng L; Hu T; Zhang Q; Du J; Fan L; Lu G; Lin G; Zhang F; Tan YQ
Hum Mol Genet; 2021 Nov; 30(23):2240-2254. PubMed ID: 34231842
[TBL] [Abstract][Full Text] [Related]
15. Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development.
Zhang G; Li D; Tu C; Meng L; Tan Y; Ji Z; Cheng J; Lu G; Lin G; Zhang H; Sun J; Wang M; Du J; Xu W
Hum Mol Genet; 2021 Dec; 31(2):219-231. PubMed ID: 34415320
[TBL] [Abstract][Full Text] [Related]
16. CFAP61 is required for sperm flagellum formation and male fertility in human and mouse.
Liu S; Zhang J; Kherraf ZE; Sun S; Zhang X; Cazin C; Coutton C; Zouari R; Zhao S; Hu F; Fourati Ben Mustapha S; Arnoult C; Ray PF; Liu M
Development; 2021 Dec; 148(23):. PubMed ID: 34792097
[TBL] [Abstract][Full Text] [Related]
17. Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly.
Lu S; Gu Y; Wu Y; Yang S; Li C; Meng L; Yuan W; Jiang T; Zhang X; Li Y; Wang C; Liu M; Ye L; Guo X; Shen H; Yang X; Tan Y; Hu Z
Cell Discov; 2021 Nov; 7(1):110. PubMed ID: 34782613
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
Wu Y; Li Y; Murtaza G; Zhou J; Jiao Y; Gong C; Hu C; Han Q; Zhang H; Zhang Y; Shi B; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Sep; 36(10):2793-2804. PubMed ID: 34392356
[TBL] [Abstract][Full Text] [Related]
20. Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.
Zhang X; Li M; Jiang X; Ma H; Fan S; Li Y; Yu C; Xu J; Khan R; Jiang H; Shi Q
PLoS Genet; 2021 Aug; 17(8):e1009753. PubMed ID: 34388164
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
