BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (PubMed ID: 33070343)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella.
    Sha Y; Wei X; Ding L; Mei L; Huang X; Lin S; Su Z; Kong L; Zhang Y; Ji Z
    Ann Hum Genet; 2020 May; 84(3):271-279. PubMed ID: 31841227
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagella.
    Liu Z; Wang C; Ni F; Yang F; Wei H; Li T; Wang J; Wang B
    Andrologia; 2022 Nov; 54(10):e14553. PubMed ID: 35932098
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Loss-of-function mutation in DNAH8 induces asthenoteratospermia associated with multiple morphological abnormalities of the sperm flagella.
    Yang Y; Jiang C; Zhang X; Liu X; Li J; Qiao X; Liu H; Shen Y
    Clin Genet; 2020 Oct; 98(4):396-401. PubMed ID: 32681648
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.
    Kherraf ZE; Amiri-Yekta A; Dacheux D; Karaouzène T; Coutton C; Christou-Kent M; Martinez G; Landrein N; Le Tanno P; Fourati Ben Mustapha S; Halouani L; Marrakchi O; Makni M; Latrous H; Kharouf M; Pernet-Gallay K; Gourabi H; Robinson DR; Crouzy S; Blum M; Thierry-Mieg N; Touré A; Zouari R; Arnoult C; Bonhivers M; Ray PF
    Am J Hum Genet; 2018 Sep; 103(3):400-412. PubMed ID: 30122540
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Biallelic variants in
    Martinez G; Beurois J; Dacheux D; Cazin C; Bidart M; Kherraf ZE; Robinson DR; Satre V; Le Gac G; Ka C; Gourlaouen I; Fichou Y; Petre G; Dulioust E; Zouari R; Thierry-Mieg N; Touré A; Arnoult C; Bonhivers M; Ray P; Coutton C
    J Med Genet; 2020 Oct; 57(10):708-716. PubMed ID: 32161152
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Novel mutations in DNAH17 cause sperm flagellum defects and their influence on ICSI outcome.
    Song B; Yang T; Shen Q; Liu Y; Wang C; Li G; Gao Y; Cao Y; He X
    J Assist Reprod Genet; 2023 Oct; 40(10):2485-2492. PubMed ID: 37574497
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia.
    Whitfield M; Thomas L; Bequignon E; Schmitt A; Stouvenel L; Montantin G; Tissier S; Duquesnoy P; Copin B; Chantot S; Dastot F; Faucon C; Barbotin AL; Loyens A; Siffroi JP; Papon JF; Escudier E; Amselem S; Mitchell V; Touré A; Legendre M
    Am J Hum Genet; 2019 Jul; 105(1):198-212. PubMed ID: 31178125
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A DNAH17 missense variant causes flagella destabilization and asthenozoospermia.
    Zhang B; Ma H; Khan T; Ma A; Li T; Zhang H; Gao J; Zhou J; Li Y; Yu C; Bao J; Ali A; Murtaza G; Yin H; Gao Q; Jiang X; Zhang F; Liu C; Khan I; Zubair M; Hussain HMJ; Khan R; Yousaf A; Yuan L; Lu Y; Xu X; Wang Y; Tao Q; Hao Q; Fang H; Cheng H; Zhang Y; Shi Q
    J Exp Med; 2020 Feb; 217(2):. PubMed ID: 31658987
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice.
    Coutton C; Martinez G; Kherraf ZE; Amiri-Yekta A; Boguenet M; Saut A; He X; Zhang F; Cristou-Kent M; Escoffier J; Bidart M; Satre V; Conne B; Fourati Ben Mustapha S; Halouani L; Marrakchi O; Makni M; Latrous H; Kharouf M; Pernet-Gallay K; Bonhivers M; Hennebicq S; Rives N; Dulioust E; Touré A; Gourabi H; Cao Y; Zouari R; Hosseini SH; Nef S; Thierry-Mieg N; Arnoult C; Ray PF
    Am J Hum Genet; 2019 Feb; 104(2):331-340. PubMed ID: 30686508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A novel homozygous frameshift variant in
    Dil S; Khan A; Unar A; Yang ML; Ali I; Zeb A; Zhang H; Zhou JT; Zubair M; Khan K; Bai S; Shi QH
    Asian J Androl; 2023; 25(3):350-355. PubMed ID: 36308074
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 17.