BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

432 related articles for article (PubMed ID: 31658987)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 6. A novel splicing variant in DNAH8 causes asthenozoospermia.
    Zhou Z; Mao X; Chen B; Mu J; Wang W; Li B; Yan Z; Dong J; Li Q; Kuang Y; Wang L; Wu L; Sang Q
    J Assist Reprod Genet; 2021 Jun; 38(6):1545-1550. PubMed ID: 33611675
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella.
    Ali A; Unar A; Muhammad Z; Dil S; Zhang B; Sadaf H; Khan M; Ali M; Khan R; Shah KMB; Ma A; Jiang X; Zhang Y; Zhang H; Shi Q
    J Assist Reprod Genet; 2024 Jan; 41(1):109-120. PubMed ID: 37831349
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Novel compound heterozygous variants in dynein axonemal heavy chain 17 cause asthenoteratospermia with sperm flagellar defects.
    Song B; Liu C; Gao Y; Marley JL; Li W; Ni X; Liu W; Chen Y; Wang J; Wang C; Zhou P; Wei Z; He X; Zhang F; Cao Y
    J Genet Genomics; 2020 Nov; 47(11):713-717. PubMed ID: 33423959
    [No Abstract]   [Full Text] [Related]  

  • 12. Novel homozygous
    He X; Li W; Wu H; Lv M; Liu W; Liu C; Zhu F; Li C; Fang Y; Yang C; Cheng H; Zhang J; Tan J; Chen T; Tang D; Song B; Wang X; Zha X; Wang H; Wei Z; Yang S; Saiyin H; Zhou P; Jin L; Wang J; Zhang Z; Zhang F; Cao Y
    J Med Genet; 2019 Feb; 56(2):96-103. PubMed ID: 30415212
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Disruption of the murine dynein light chain gene Tcte3-3 results in asthenozoospermia.
    Rashid S; Grzmil P; Drenckhahn JD; Meinhardt A; Adham I; Engel W; Neesen J
    Reproduction; 2010 Jan; 139(1):99-111. PubMed ID: 19778998
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia.
    Ni X; Wang J; Lv M; Liu C; Zhong Y; Tian S; Wu H; Cheng H; Gao Y; Tan Q; Chen B; Li Q; Song B; Wei Z; Zhou P; He X; Zhang F; Cao Y
    J Assist Reprod Genet; 2020 Jun; 37(6):1431-1439. PubMed ID: 32323121
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Homozygous mutations in
    Lv M; Liu W; Chi W; Ni X; Wang J; Cheng H; Li WY; Yang S; Wu H; Zhang J; Gao Y; Liu C; Li C; Yang C; Tan Q; Tang D; Zhang J; Song B; Chen YJ; Li Q; Zhong Y; Zhang Z; Saiyin H; Jin L; Xu Y; Zhou P; Wei Z; Zhang C; He X; Zhang F; Cao Y
    J Med Genet; 2020 Jul; 57(7):445-453. PubMed ID: 32051257
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
    Lorès P; Kherraf ZE; Amiri-Yekta A; Whitfield M; Daneshipour A; Stouvenel L; Cazin C; Cavarocchi E; Coutton C; Llabador MA; Arnoult C; Thierry-Mieg N; Ferreux L; Patrat C; Hosseini SH; Mustapha SFB; Zouari R; Dulioust E; Ray PF; Touré A
    Hum Genet; 2021 Jul; 140(7):1031-1043. PubMed ID: 33689014
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report.
    Beurois J; Martinez G; Cazin C; Kherraf ZE; Amiri-Yekta A; Thierry-Mieg N; Bidart M; Petre G; Satre V; Brouillet S; Touré A; Arnoult C; Ray PF; Coutton C
    Hum Reprod; 2019 Oct; 34(10):2071-2079. PubMed ID: 31621862
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.