These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 35973810)

  • 21. Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility.
    Liu R; Yan Z; Fan Y; Qu R; Chen B; Li B; Wu L; Wu H; Mu J; Zhao L; Wang W; Dong J; Zeng Y; Li Q; Wang L; Sang Q; Zhang Z; Kuang Y
    Hum Reprod; 2022 Jun; 37(7):1394-1405. PubMed ID: 35551387
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of biallelic variations of
    Ruan T; Yang Y; Jiang C; Shen G; Li D; Shen Y
    Front Endocrinol (Lausanne); 2023; 14():1133222. PubMed ID: 36967801
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family.
    Ma Y; Xie N; Xie D; Sun L; Li S; Li P; Li Y; Li J; Dong Z; Xie X
    Fertil Steril; 2019 May; 111(5):909-917.e1. PubMed ID: 30878252
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Biallelic mutations in
    Tian S; Tu C; He X; Meng L; Wang J; Tang S; Gao Y; Liu C; Wu H; Zhou Y; Lv M; Lin G; Jin L; Cao Y; Tang D; Zhang F; Tan YQ
    J Med Genet; 2023 Aug; 60(8):827-834. PubMed ID: 36593121
    [TBL] [Abstract][Full Text] [Related]  

  • 27.
    Zheng R; Wang Y; Li Y; Guo J; Wen Y; Jiang C; Yang Y; Shen Y
    J Med Genet; 2023 Mar; 60(3):254-264. PubMed ID: 35654582
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia.
    Hua J; Wan YY
    J Assist Reprod Genet; 2019 Mar; 36(3):529-534. PubMed ID: 30594972
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome.
    Zhu F; Liu C; Wang F; Yang X; Zhang J; Wu H; Zhang Z; He X; Zhang Z; Zhou P; Wei Z; Shang Y; Wang L; Zhang R; Ouyang YC; Sun QY; Cao Y; Li W
    Am J Hum Genet; 2018 Aug; 103(2):188-199. PubMed ID: 30032984
    [TBL] [Abstract][Full Text] [Related]  

  • 31. IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3.
    Zhang Z; Zhou H; Deng X; Zhang R; Qu R; Mu J; Liu R; Zeng Y; Chen B; Wang L; Sang Q; Bao S
    Hum Reprod; 2023 Jan; 38(1):168-179. PubMed ID: 36355624
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome.
    Zhu F; Wang F; Yang X; Zhang J; Wu H; Zhang Z; Zhang Z; He X; Zhou P; Wei Z; Gecz J; Cao Y
    Am J Hum Genet; 2016 Oct; 99(4):942-949. PubMed ID: 27640305
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.
    Celse T; Cazin C; Mietton F; Martinez G; Martinez D; Thierry-Mieg N; Septier A; Guillemain C; Beurois J; Clergeau A; Mustapha SFB; Kharouf M; Zoghmar A; Chargui A; Papaxanthos A; Dorphin B; Foliguet B; Triki C; Sifer C; Lauton D; Tachdjian G; Schuler G; Lejeune H; Puechberty J; Bessonnat J; Pasquier L; Mery L; Poulain M; Chaabouni M; Sermondade N; Cabry R; Benbouhadja S; Veau S; Frapsauce C; Mitchell V; Achard V; Satre V; Hennebicq S; Zouari R; Arnoult C; Kherraf ZE; Coutton C; Ray PF
    Hum Genet; 2021 Jan; 140(1):43-57. PubMed ID: 33108537
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetics of teratozoospermia: Back to the head.
    Beurois J; Cazin C; Kherraf ZE; Martinez G; Celse T; Touré A; Arnoult C; Ray PF; Coutton C
    Best Pract Res Clin Endocrinol Metab; 2020 Dec; 34(6):101473. PubMed ID: 33183966
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Biallelic
    Hu T; Meng L; Tan C; Luo C; He WB; Tu C; Zhang H; Du J; Nie H; Lu GX; Lin G; Tan YQ
    J Med Genet; 2023 Feb; 60(2):144-153. PubMed ID: 35387802
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10.
    Xiang M; Wang Y; Xu W; Zheng N; Zhang J; Duan Z; Zha X; Shi X; Wang F; Cao Y; Zhu F
    J Assist Reprod Genet; 2021 Oct; 38(10):2791-2799. PubMed ID: 34409526
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.
    Li Y; Li Y; Wang Y; Meng L; Tan C; Du J; Tan YQ; Nie H; Zhang Q; Lu G; Lin G; Li H; Zhang H; Tu C
    J Assist Reprod Genet; 2023 Jan; 40(1):41-51. PubMed ID: 36515799
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Mutations in CCIN cause teratozoospermia and male infertility.
    Fan Y; Huang C; Chen J; Chen Y; Wang Y; Yan Z; Yu W; Wu H; Yang Y; Nie L; Huang S; Wang F; Wang H; Hua Y; Lyu Q; Kuang Y; Lei M
    Sci Bull (Beijing); 2022 Oct; 67(20):2112-2123. PubMed ID: 36546111
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.