BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 34657236)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Novel biallelic variants in DNAH1 cause multiple morphological abnormalities of sperm flagella with favorable outcomes of fertility after ICSI in Han Chinese males.
    Long S; Fu L; Ma J; Yu H; Tang X; Hu T; Han W; Liu W; Liao H; Fu T; Huang G; Lu W; Lin T
    Andrology; 2024 Feb; 12(2):349-364. PubMed ID: 37302001
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella.
    Gao Y; Tian S; Sha Y; Zha X; Cheng H; Wang A; Liu C; Lv M; Ni X; Li Q; Wu H; Tan Q; Tang D; Song B; Ding D; Cong J; Xu Y; Zhou P; Wei Z; Cao Y; Xu Y; Zhang F; He X
    Reprod Biomed Online; 2021 May; 42(5):963-972. PubMed ID: 33771466
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
    Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
    Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF.
    Xu C; Tang D; Shao Z; Geng H; Gao Y; Li K; Tan Q; Wang G; Wang C; Wu H; Li G; Lv M; He X; Cao Y
    Reprod Biol Endocrinol; 2022 Mar; 20(1):41. PubMed ID: 35232447
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injection.
    Wambergue C; Zouari R; Fourati Ben Mustapha S; Martinez G; Devillard F; Hennebicq S; Satre V; Brouillet S; Halouani L; Marrakchi O; Makni M; Latrous H; Kharouf M; Amblard F; Arnoult C; Ray PF; Coutton C
    Hum Reprod; 2016 Jun; 31(6):1164-72. PubMed ID: 27094479
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.
    Ferreux L; Bourdon M; Chargui A; Schmitt A; Stouvenel L; Lorès P; Ray P; Lousqui J; Pocate-Cheriet K; Santulli P; Dulioust E; Toure A; Patrat C
    Hum Reprod; 2021 Oct; 36(11):2848-2860. PubMed ID: 34529793
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homozygous DNAH1 frameshift mutation causes multiple morphological anomalies of the sperm flagella in Chinese.
    Wang X; Jin H; Han F; Cui Y; Chen J; Yang C; Zhu P; Wang W; Jiao G; Wang W; Hao C; Gao Z
    Clin Genet; 2017 Feb; 91(2):313-321. PubMed ID: 27573432
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.
    Liu C; Tu C; Wang L; Wu H; Houston BJ; Mastrorosa FK; Zhang W; Shen Y; Wang J; Tian S; Meng L; Cong J; Yang S; Jiang Y; Tang S; Zeng Y; Lv M; Lin G; Li J; Saiyin H; He X; Jin L; Touré A; Ray PF; Veltman JA; Shi Q; O'Bryan MK; Cao Y; Tan YQ; Zhang F
    Am J Hum Genet; 2021 Feb; 108(2):309-323. PubMed ID: 33472045
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel compound heterozygous mutations in
    Wang M; Yang QY; Zhou JP; Tan HP; Hu J; Jin L; Zhu LX
    Asian J Androl; 2023; 25(4):512-519. PubMed ID: 36510862
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.
    Martinez G; Kherraf ZE; Zouari R; Fourati Ben Mustapha S; Saut A; Pernet-Gallay K; Bertrand A; Bidart M; Hograindleur JP; Amiri-Yekta A; Kharouf M; Karaouzène T; Thierry-Mieg N; Dacheux-Deschamps D; Satre V; Bonhivers M; Touré A; Arnoult C; Ray PF; Coutton C
    Hum Reprod; 2018 Oct; 33(10):1973-1984. PubMed ID: 30137358
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation in DNAH17 is present in a patient with multiple morphological abnormalities of the flagella.
    Zheng R; Sun Y; Jiang C; Chen D; Yang Y; Shen Y
    Reprod Biomed Online; 2021 Sep; 43(3):532-541. PubMed ID: 34373205
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review.
    Tang X; Ma J; Wang X; Long S; Wan L; Yu H; Yang J; Huang G; Lin T
    J Assist Reprod Genet; 2023 Sep; 40(9):2175-2184. PubMed ID: 37392306
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.