183 related articles for article (PubMed ID: 35708642)
1. Homozygous Variant in KASH5 Causes Premature Ovarian Insufficiency by Disordered Meiotic Homologous Pairing.
Zhang Q; Tao C; Gao S; Li S; Xu B; Ke H; Wang Y; Zhang F; Qin Y; Zhang L; Guo T
J Clin Endocrinol Metab; 2022 Aug; 107(9):2589-2597. PubMed ID: 35708642
[TBL] [Abstract][Full Text] [Related]
2. Homozygous missense variant in MEIOSIN causes premature ovarian insufficiency.
Zhang Q; Zhang W; Wu X; Ke H; Qin Y; Zhao S; Guo T
Hum Reprod; 2023 Nov; 38(Supplement_2):ii47-ii56. PubMed ID: 37982418
[TBL] [Abstract][Full Text] [Related]
3. The missing LINC: a mammalian KASH-domain protein coupling meiotic chromosomes to the cytoskeleton.
Stewart CL; Burke B
Nucleus; 2014; 5(1):3-10. PubMed ID: 24637401
[TBL] [Abstract][Full Text] [Related]
4. Novel bi-allelic variants in KASH5 are associated with meiotic arrest and non-obstructive azoospermia.
Yang C; Lin X; Ji Z; Huang Y; Zhang L; Luo J; Chen H; Li P; Tian R; Zhi E; Hong Y; Zhou Z; Zhang F; Li Z; Yao C
Mol Hum Reprod; 2022 Jun; 28(7):. PubMed ID: 35674372
[TBL] [Abstract][Full Text] [Related]
5. Depletion of the LINC complex disrupts cytoskeleton dynamics and meiotic resumption in mouse oocytes.
Luo Y; Lee IW; Jo YJ; Namgoong S; Kim NH
Sci Rep; 2016 Feb; 6():20408. PubMed ID: 26842404
[TBL] [Abstract][Full Text] [Related]
6. Analysis of meiosis in SUN1 deficient mice reveals a distinct role of SUN2 in mammalian meiotic LINC complex formation and function.
Link J; Leubner M; Schmitt J; Göb E; Benavente R; Jeang KT; Xu R; Alsheimer M
PLoS Genet; 2014 Feb; 10(2):e1004099. PubMed ID: 24586178
[TBL] [Abstract][Full Text] [Related]
7. A homozygous
Hou X; Zeb A; Dil S; Zhou J; Zhang H; Shi B; Muhammad Z; Khan I; Zaman Q; Shah WA; Jiang X; Wu L; Ma H; Shi Q
Front Endocrinol (Lausanne); 2023; 14():1128362. PubMed ID: 36864840
[TBL] [Abstract][Full Text] [Related]
8. Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.
Wu H; Zhang X; Hua R; Li Y; Cheng L; Li K; Liu Y; Gao Y; Shen Q; Wang G; Lv M; Xu Y; He X; Cao Y; Liu M
Hum Genet; 2022 Nov; 141(11):1795-1809. PubMed ID: 35587281
[TBL] [Abstract][Full Text] [Related]
9. The meiotic LINC complex component KASH5 is an activating adaptor for cytoplasmic dynein.
Garner KEL; Salter A; Lau CK; Gurusaran M; Villemant CM; Granger EP; McNee G; Woodman PG; Davies OR; Burke BE; Allan VJ
J Cell Biol; 2023 May; 222(5):. PubMed ID: 36946995
[TBL] [Abstract][Full Text] [Related]
10. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S; Jiao Y; Khan R; Jiang X; Javed AR; Ali A; Zhang H; Zhou J; Naeem M; Murtaza G; Li Y; Yang G; Zaman Q; Zubair M; Guan H; Zhang X; Ma H; Jiang H; Ali H; Dil S; Shah W; Ahmad N; Zhang Y; Shi Q
Am J Hum Genet; 2021 Feb; 108(2):324-336. PubMed ID: 33508233
[TBL] [Abstract][Full Text] [Related]
11. A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency.
Carlosama C; Elzaiat M; Patiño LC; Mateus HE; Veitia RA; Laissue P
Hum Mol Genet; 2017 Aug; 26(16):3161-3166. PubMed ID: 28541421
[TBL] [Abstract][Full Text] [Related]
12.
He WB; Tu CF; Liu Q; Meng LL; Yuan SM; Luo AX; He FS; Shen J; Li W; Du J; Zhong CG; Lu GX; Lin G; Fan LQ; Tan YQ
J Med Genet; 2018 Mar; 55(3):198-204. PubMed ID: 29331980
[TBL] [Abstract][Full Text] [Related]
13. A human infertility-associated KASH5 variant promotes mitochondrial localization.
Bentebbal SA; Meqbel BR; Salter A; Allan V; Burke B; Horn HF
Sci Rep; 2021 May; 11(1):10133. PubMed ID: 33980926
[TBL] [Abstract][Full Text] [Related]
14. A mammalian KASH domain protein coupling meiotic chromosomes to the cytoskeleton.
Horn HF; Kim DI; Wright GD; Wong ES; Stewart CL; Burke B; Roux KJ
J Cell Biol; 2013 Sep; 202(7):1023-39. PubMed ID: 24062341
[TBL] [Abstract][Full Text] [Related]
15. Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency.
Wang Y; Guo T; Ke H; Zhang Q; Li S; Luo W; Qin Y
Genet Med; 2021 Dec; 23(12):2309-2315. PubMed ID: 34257419
[TBL] [Abstract][Full Text] [Related]
16. A conserved KASH domain protein associates with telomeres, SUN1, and dynactin during mammalian meiosis.
Morimoto A; Shibuya H; Zhu X; Kim J; Ishiguro K; Han M; Watanabe Y
J Cell Biol; 2012 Jul; 198(2):165-72. PubMed ID: 22826121
[TBL] [Abstract][Full Text] [Related]
17. Homozygous variants in
He WB; Tan C; Zhang YX; Meng LL; Gong F; Lu GX; Lin G; Du J; Tan YQ
J Med Genet; 2021 Mar; 58(3):168-172. PubMed ID: 32303603
[TBL] [Abstract][Full Text] [Related]
18. The KASH5 protein involved in meiotic chromosomal movements is a novel dynein activating adaptor.
Agrawal R; Gillies JP; Zang JL; Zhang J; Garrott SR; Shibuya H; Nandakumar J; DeSantis ME
Elife; 2022 Jun; 11():. PubMed ID: 35703493
[TBL] [Abstract][Full Text] [Related]
19. Pathogenic bi-allelic variants of meiotic ZMM complex gene SPO16 in premature ovarian insufficiency.
Qi Y; Wang Y; Li W; Zhuang S; Li S; Xu K; Qin Y; Guo T
Clin Genet; 2023 Oct; 104(4):486-490. PubMed ID: 37270785
[TBL] [Abstract][Full Text] [Related]
20. STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermia.
Jaillard S; McElreavy K; Robevska G; Akloul L; Ghieh F; Sreenivasan R; Beaumont M; Bashamboo A; Bignon-Topalovic J; Neyroud AS; Bell K; Veron-Gastard E; Launay E; van den Bergen J; Nouyou B; Vialard F; Belaud-Rotureau MA; Ayers KL; Odent S; Ravel C; Tucker EJ; Sinclair AH
Mol Hum Reprod; 2020 Sep; 26(9):665-677. PubMed ID: 32634216
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]