161 related articles for article (PubMed ID: 35863052)
1. Pathogenic variant in ACTL7A causes severe teratozoospermia characterized by bubble-shaped acrosomes and male infertility.
Dai J; Chen Y; Li Q; Zhang T; Zhou Q; Gong F; Lu G; Zheng W; Lin G
Mol Hum Reprod; 2022 Jul; 28(8):. PubMed ID: 35863052
[TBL] [Abstract][Full Text] [Related]
2. Novel bi-allelic variants in ACTL7A are associated with male infertility and total fertilization failure.
Wang J; Zhang J; Sun X; Lin Y; Cai L; Cui Y; Liu J; Liu M; Yang X
Hum Reprod; 2021 Nov; 36(12):3161-3169. PubMed ID: 34727571
[TBL] [Abstract][Full Text] [Related]
3. Loss of SPACA1 function causes autosomal recessive globozoospermia by damaging the acrosome-acroplaxome complex.
Chen P; Saiyin H; Shi R; Liu B; Han X; Gao Y; Ye X; Zhang X; Sun Y
Hum Reprod; 2021 Aug; 36(9):2587-2596. PubMed ID: 34172998
[TBL] [Abstract][Full Text] [Related]
4. Loss of ACTL7A causes small head sperm by defective acrosome-acroplaxome-manchette complex.
Zhang Y; Tang J; Wang X; Sun Y; Yang T; Shen X; Yang X; Shi H; Sun X; Xin A
Reprod Biol Endocrinol; 2023 Sep; 21(1):82. PubMed ID: 37667331
[TBL] [Abstract][Full Text] [Related]
5. Testis-specific actin-like 7A (ACTL7A) is an indispensable protein for subacrosomal-associated F-actin formation, acrosomal anchoring, and male fertility.
Ferrer P; Upadhyay S; Ikawa M; Clement TM
Mol Hum Reprod; 2023 Feb; 29(3):. PubMed ID: 36734600
[TBL] [Abstract][Full Text] [Related]
6. Novel variants in ACTL7A and PLCZ1 are associated with male infertility and total fertilization failure.
Zhao S; Cui Y; Guo S; Liu B; Bian Y; Zhao S; Chen Z; Zhao H
Clin Genet; 2023 May; 103(5):603-608. PubMed ID: 36593593
[TBL] [Abstract][Full Text] [Related]
7. Novel ACTL7A variants in males lead to fertilization failure and male infertility.
Wang M; Zhou J; Long R; Jin H; Gao L; Zhu L; Jin L
Andrology; 2023 Nov; ():. PubMed ID: 37991128
[TBL] [Abstract][Full Text] [Related]
8. Actl7a deficiency in mice leads to male infertility and fertilization failure.
Zhou X; Liu Z; Jia W; Hou M; Zhang X
Biochem Biophys Res Commun; 2022 Oct; 623():154-161. PubMed ID: 35921706
[TBL] [Abstract][Full Text] [Related]
9. A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns.
Zhou J; Zhang B; Zeb A; Ma A; Chen J; Zhao D; Rahim F; Khan R; Zhang H; Zhang Y; Khan I; Kakakhel MBS; Khan A; Shah W; Jiang X; Zhang F; Yang X; Xiao J; Xu B; Ma H; Shi Q
Clin Genet; 2023 Nov; 104(5):564-570. PubMed ID: 37286336
[TBL] [Abstract][Full Text] [Related]
10. Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and mice.
Dai J; Zhang T; Guo J; Zhou Q; Gu Y; Zhang J; Hu L; Zong Y; Song J; Zhang S; Dai C; Gong F; Lu G; Zheng W; Lin G
Am J Hum Genet; 2021 Mar; 108(3):469-481. PubMed ID: 33626338
[TBL] [Abstract][Full Text] [Related]
11. Loss of perinuclear theca ACTRT1 causes acrosome detachment and severe male subfertility in mice.
Zhang XZ; Wei LL; Zhang XH; Jin HJ; Chen SR
Development; 2022 Jun; 149(12):. PubMed ID: 35616329
[TBL] [Abstract][Full Text] [Related]
12. Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human.
Zhang Q; Jin H; Long S; Tang X; Li J; Liu W; Han W; Liao H; Fu T; Huang G; Chen S; Lin T
Hum Reprod; 2024 May; 39(5):880-891. PubMed ID: 38414365
[TBL] [Abstract][Full Text] [Related]
13. Disruption in
Xin A; Qu R; Chen G; Zhang L; Chen J; Tao C; Fu J; Tang J; Ru Y; Chen Y; Peng X; Shi H; Zhang F; Sun X
Sci Adv; 2020 Aug; 6(35):eaaz4796. PubMed ID: 32923619
[TBL] [Abstract][Full Text] [Related]
14. A novel homozygous mutation in ACTL7A leads to male infertility.
Zhou X; Xi Q; Jia W; Li Z; Liu Z; Luo G; Xing C; Zhang D; Hou M; Liu H; Yang X; Luo Y; Peng X; Wang G; Zou T; Zhu L; Jin L; Zhang X
Mol Genet Genomics; 2023 Mar; 298(2):353-360. PubMed ID: 36574082
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A loss-of-function variant in SSFA2 causes male infertility with globozoospermia and failed oocyte activation.
Huang G; Zhang X; Yao G; Huang L; Wu S; Li X; Guo J; Wen Y; Wang Y; Shang L; Li N; Xu W
Reprod Biol Endocrinol; 2022 Jul; 20(1):103. PubMed ID: 35836265
[TBL] [Abstract][Full Text] [Related]
17. AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice.
Guidi LG; Holloway ZG; Arnoult C; Ray PF; Monaco AP; Molnár Z; Velayos-Baeza A
Sci Rep; 2018 Jul; 8(1):10379. PubMed ID: 29991750
[TBL] [Abstract][Full Text] [Related]
18. Loss of the Na
Oberheide K; Puchkov D; Jentsch TJ
J Biol Chem; 2017 Jun; 292(26):10845-10854. PubMed ID: 28476888
[TBL] [Abstract][Full Text] [Related]
19. Dynamic of contribution of UBPy-sorted cargo to acrosome biogenesis: effects of its derailment in a mouse model of globozoospermia, the infertile Vps54 (L967Q) mutant.
Gioria M; Pasini ME; Berruti G
Cell Tissue Res; 2017 Aug; 369(2):413-427. PubMed ID: 28299521
[TBL] [Abstract][Full Text] [Related]
20. Phospholipase C zeta (PLCζ) and male infertility: Clinical update and topical developments.
Amdani SN; Yeste M; Jones C; Coward K
Adv Biol Regul; 2016 May; 61():58-67. PubMed ID: 26700242
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
