187 related articles for article (PubMed ID: 35388187)
1. Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility.
Zhou S; Wu H; Zhang J; He X; Liu S; Zhou P; Hua R; Cao Y; Liu M
Eur J Hum Genet; 2022 Jun; 30(6):721-729. PubMed ID: 35388187
[TBL] [Abstract][Full Text] [Related]
2. Effects of
Olszewska M; Malcher A; Stokowy T; Pollock N; Berman AJ; Budkiewicz S; Kamieniczna M; Jackowiak H; Suszynska-Zajczyk J; Jedrzejczak P; Yatsenko AN; Kurpisz M
Hum Reprod Open; 2024; 2024(2):hoae020. PubMed ID: 38650655
[TBL] [Abstract][Full Text] [Related]
3. TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa.
Castaneda JM; Hua R; Miyata H; Oji A; Guo Y; Cheng Y; Zhou T; Guo X; Cui Y; Shen B; Wang Z; Hu Z; Zhou Z; Sha J; Prunskaite-Hyyrylainen R; Yu Z; Ramirez-Solis R; Ikawa M; Matzuk MM; Liu M
Proc Natl Acad Sci U S A; 2017 Jul; 114(27):E5370-E5378. PubMed ID: 28630322
[TBL] [Abstract][Full Text] [Related]
4. Nexin-Dynein regulatory complex component DRC7 but not FBXL13 is required for sperm flagellum formation and male fertility in mice.
Morohoshi A; Miyata H; Shimada K; Nozawa K; Matsumura T; Yanase R; Shiba K; Inaba K; Ikawa M
PLoS Genet; 2020 Jan; 16(1):e1008585. PubMed ID: 31961863
[TBL] [Abstract][Full Text] [Related]
5. DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath.
Wu H; Liu Y; Li Y; Li K; Xu C; Gao Y; Lv M; Guo R; Xu Y; Zhou P; Wei Z; Hua R; He X; Cao Y
Cell Death Dis; 2023 Feb; 14(2):127. PubMed ID: 36792588
[TBL] [Abstract][Full Text] [Related]
6. Identification of bi-allelic
Meng Z; Meng Q; Gao T; Zhou H; Xue J; Li H; Wu Y; Lv J
Front Endocrinol (Lausanne); 2022; 13():1091107. PubMed ID: 36686457
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.
Tan C; Meng L; Lv M; He X; Sha Y; Tang D; Tan Y; Hu T; He W; Tu C; Nie H; Zhang H; Du J; Lu G; Fan LQ; Cao Y; Lin G; Tan YQ
Am J Hum Genet; 2022 Jan; 109(1):157-171. PubMed ID: 34932939
[TBL] [Abstract][Full Text] [Related]
9. Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility.
Li K; Wang G; Lv M; Wang J; Gao Y; Tang F; Xu C; Yang W; Yu H; Shao Z; Geng H; Tan Q; Shen Q; Tang D; Ni X; Wang T; Song B; Wu H; Huo R; Zhang Z; Xu Y; Zhou P; Tao F; Wei Z; He X; Cao Y
J Assist Reprod Genet; 2022 Jan; 39(1):251-259. PubMed ID: 34657236
[TBL] [Abstract][Full Text] [Related]
10. Loss of Calmodulin- and Radial-Spoke-Associated Complex Protein CFAP251 Leads to Immotile Spermatozoa Lacking Mitochondria and Infertility in Men.
Auguste Y; Delague V; Desvignes JP; Longepied G; Gnisci A; Besnier P; Levy N; Beroud C; Megarbane A; Metzler-Guillemain C; Mitchell MJ
Am J Hum Genet; 2018 Sep; 103(3):413-420. PubMed ID: 30122541
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure.
Wei X; Sha Y; Wei Z; Zhu X; He F; Zhang X; Liu W; Wang Y; Lu Z
Acta Biochim Biophys Sin (Shanghai); 2021 Oct; 53(10):1300-1309. PubMed ID: 34476482
[TBL] [Abstract][Full Text] [Related]
13. Homozygous variant in DRC3 (LRRC48) gene causes asthenozoospermia and male infertility.
Qin J; Wang J; Chen J; Xu J; Liu S; Deng D; Li F
J Hum Genet; 2024 May; ():. PubMed ID: 38769386
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3.
Zhang Z; Zhou H; Deng X; Zhang R; Qu R; Mu J; Liu R; Zeng Y; Chen B; Wang L; Sang Q; Bao S
Hum Reprod; 2023 Jan; 38(1):168-179. PubMed ID: 36355624
[TBL] [Abstract][Full Text] [Related]
16. Cfap97d1 is important for flagellar axoneme maintenance and male mouse fertility.
Oura S; Kazi S; Savolainen A; Nozawa K; Castañeda J; Yu Z; Miyata H; Matzuk RM; Hansen JN; Wachten D; Matzuk MM; Prunskaite-Hyyryläinen R
PLoS Genet; 2020 Aug; 16(8):e1008954. PubMed ID: 32785227
[TBL] [Abstract][Full Text] [Related]
17. CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.
Jreijiri F; Cavarocchi E; Amiri-Yekta A; Cazin C; Hosseini SH; El Khouri E; Patrat C; Thierry-Mieg N; Ray PF; Dulioust E; Whitfield M; Touré A
Clin Genet; 2024 Mar; 105(3):317-322. PubMed ID: 37975235
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice.
He X; Liu C; Yang X; Lv M; Ni X; Li Q; Cheng H; Liu W; Tian S; Wu H; Gao Y; Yang C; Tan Q; Cong J; Tang D; Zhang J; Song B; Zhong Y; Li H; Zhi W; Mao X; Fu F; Ge L; Shen Q; Zhang M; Saiyin H; Jin L; Xu Y; Zhou P; Wei Z; Zhang F; Cao Y
Am J Hum Genet; 2020 Sep; 107(3):514-526. PubMed ID: 32791035
[TBL] [Abstract][Full Text] [Related]
20. Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.
Liu C; Miyata H; Gao Y; Sha Y; Tang S; Xu Z; Whitfield M; Patrat C; Wu H; Dulioust E; Tian S; Shimada K; Cong J; Noda T; Li H; Morohoshi A; Cazin C; Kherraf ZE; Arnoult C; Jin L; He X; Ray PF; Cao Y; Touré A; Zhang F; Ikawa M
Am J Hum Genet; 2020 Aug; 107(2):330-341. PubMed ID: 32619401
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
