160 related articles for article (PubMed ID: 38597976)
1. Metabolic profiling identifies Qrich2 as a novel glutamine sensor that regulates microtubule glutamylation and mitochondrial function in mouse sperm.
Zhang G; Guo J; Yang H; Li Q; Ye F; Song Y; Xiong D; Zeng J; Zhi W; Yuan S; Lv Y; Li T; Wang Y; Liao L; Deng D; Liu W; Xu W
Cell Mol Life Sci; 2024 Apr; 81(1):170. PubMed ID: 38597976
[TBL] [Abstract][Full Text] [Related]
2. Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella.
Shen Y; Zhang F; Li F; Jiang X; Yang Y; Li X; Li W; Wang X; Cheng J; Liu M; Zhang X; Yuan G; Pei X; Cai K; Hu F; Sun J; Yan L; Tang L; Jiang C; Tu W; Xu J; Wu H; Kong W; Li S; Wang K; Sheng K; Zhao X; Yue H; Yang X; Xu W
Nat Commun; 2019 Jan; 10(1):433. PubMed ID: 30683861
[TBL] [Abstract][Full Text] [Related]
3. A Key regulatory protein QRICH2 governing sperm function with profound antioxidant properties, enhancing sperm viability.
Zhang G; Xiong D; Ye F; Zhao Y; Du X; Zhi W; Liu F; Zeng J; Xu W; Liu W; Shi Y
Reprod Biol; 2024 Jun; 24(2):100881. PubMed ID: 38772286
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations.
Kherraf ZE; Cazin C; Coutton C; Amiri-Yekta A; Martinez G; Boguenet M; Fourati Ben Mustapha S; Kharouf M; Gourabi H; Hosseini SH; Daneshipour A; Touré A; Thierry-Mieg N; Zouari R; Arnoult C; Ray PF
Clin Genet; 2019 Nov; 96(5):394-401. PubMed ID: 31292949
[TBL] [Abstract][Full Text] [Related]
6. LRRC46 Accumulates at the Midpiece of Sperm Flagella and Is Essential for Spermiogenesis and Male Fertility in Mouse.
Yin Y; Mu W; Yu X; Wang Z; Xu K; Wu X; Cai Y; Zhang M; Lu G; Chan WY; Ma J; Huang T; Liu H
Int J Mol Sci; 2022 Jul; 23(15):. PubMed ID: 35955660
[TBL] [Abstract][Full Text] [Related]
7. Biallelic mutations in
Li W; Wu H; Li F; Tian S; Kherraf ZE; Zhang J; Ni X; Lv M; Liu C; Tan Q; Shen Y; Amiri-Yekta A; Cazin C; Zhang J; Liu W; Zheng Y; Cheng H; Wu Y; Wang J; Gao Y; Chen Y; Zha X; Jin L; Liu M; He X; Ray PF; Cao Y; Zhang F
J Med Genet; 2020 Feb; 57(2):89-95. PubMed ID: 31501240
[TBL] [Abstract][Full Text] [Related]
8. Identification of CFAP52 as a novel diagnostic target of male infertility with defects of sperm head-tail connection and flagella development.
Jin HJ; Ruan T; Dai S; Geng XY; Yang Y; Shen Y; Chen SR
Elife; 2023 Dec; 12():. PubMed ID: 38126872
[TBL] [Abstract][Full Text] [Related]
9. Loss of the deglutamylase CCP5 perturbs multiple steps of spermatogenesis and leads to male infertility.
Giordano T; Gadadhar S; Bodakuntla S; Straub J; Leboucher S; Martinez G; Chemlali W; Bosc C; Andrieux A; Bieche I; Arnoult C; Geimer S; Janke C
J Cell Sci; 2019 Feb; 132(3):. PubMed ID: 30635446
[TBL] [Abstract][Full Text] [Related]
10. Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella.
Tang S; Wang X; Li W; Yang X; Li Z; Liu W; Li C; Zhu Z; Wang L; Wang J; Zhang L; Sun X; Zhi E; Wang H; Li H; Jin L; Luo Y; Wang J; Yang S; Zhang F
Am J Hum Genet; 2017 Jun; 100(6):854-864. PubMed ID: 28552195
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
Dong FN; Amiri-Yekta A; Martinez G; Saut A; Tek J; Stouvenel L; Lorès P; Karaouzène T; Thierry-Mieg N; Satre V; Brouillet S; Daneshipour A; Hosseini SH; Bonhivers M; Gourabi H; Dulioust E; Arnoult C; Touré A; Ray PF; Zhao H; Coutton C
Am J Hum Genet; 2018 Apr; 102(4):636-648. PubMed ID: 29606301
[TBL] [Abstract][Full Text] [Related]
13. [Morphological characteristics and phenotypic analysis of multiple morphological abnormalities in sperm flagella].
Wang JX; Yang XY; Cheng HB; Shen LY; Wang GG; Shi YC; Li H; Yang SM
Zhonghua Yi Xue Za Zhi; 2017 Dec; 97(48):3806-3811. PubMed ID: 29325341
[No Abstract] [Full Text] [Related]
14. 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]
15. Structures of sperm flagellar doublet microtubules expand the genetic spectrum of male infertility.
Zhou L; Liu H; Liu S; Yang X; Dong Y; Pan Y; Xiao Z; Zheng B; Sun Y; Huang P; Zhang X; Hu J; Sun R; Feng S; Zhu Y; Liu M; Gui M; Wu J
Cell; 2023 Jun; 186(13):2897-2910.e19. PubMed ID: 37295417
[TBL] [Abstract][Full Text] [Related]
16. Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.
Oud MS; Houston BJ; Volozonoka L; Mastrorosa FK; Holt GS; Alobaidi BKS; deVries PF; Astuti G; Ramos L; Mclachlan RI; O'Bryan MK; Veltman JA; Chemes HE; Sheth H
Hum Reprod; 2021 Aug; 36(9):2597-2611. PubMed ID: 34089056
[TBL] [Abstract][Full Text] [Related]
17. Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice.
Liu W; He X; Yang S; Zouari R; Wang J; Wu H; Kherraf ZE; Liu C; Coutton C; Zhao R; Tang D; Tang S; Lv M; Fang Y; Li W; Li H; Zhao J; Wang X; Zhao S; Zhang J; Arnoult C; Jin L; Zhang Z; Ray PF; Cao Y; Zhang F
Am J Hum Genet; 2019 Apr; 104(4):738-748. PubMed ID: 30929735
[TBL] [Abstract][Full Text] [Related]
18. Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).
Liu W; Sha Y; Li Y; Mei L; Lin S; Huang X; Lu J; Ding L; Kong S; Lu Z
J Med Genet; 2019 Oct; 56(10):678-684. PubMed ID: 31151990
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
