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 *

207 related articles for article (PubMed ID: 35534203)

  • 1. Biallelic mutations in
    Liu W; Wei X; Liu X; Chen G; Zhang X; Liang X; Isachenko V; Sha Y; Wang Y
    J Med Genet; 2023 Feb; 60(2):154-162. PubMed ID: 35534203
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ARMC12 regulates spatiotemporal mitochondrial dynamics during spermiogenesis and is required for male fertility.
    Shimada K; Park S; Miyata H; Yu Z; Morohoshi A; Oura S; Matzuk MM; Ikawa M
    Proc Natl Acad Sci U S A; 2021 Feb; 118(6):. PubMed ID: 33536340
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis.
    Sha Y; Liu W; Li S; Osadchuk LV; Chen Y; Nie H; Gao S; Xie L; Qin W; Zhou H; Li L
    EBioMedicine; 2023 Oct; 96():104798. PubMed ID: 37713809
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.
    Wang G; Zhu X; Gao Y; Lv M; Li K; Tang D; Wu H; Xu C; Geng H; Shen Q; Zha X; Duan Z; Zhang J; Hua R; Tao F; Zhou P; Wei Z; Cao Y; Guo R; He X
    Hum Mutat; 2022 Dec; 43(12):2079-2090. PubMed ID: 36135717
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertility.
    Nawaz S; Hussain S; Bilal M; Syed N; Liaqat K; Ullah I; Akil AA; Fakhro KA; Ahmad W
    J Gene Med; 2024 Jan; 26(1):e3583. PubMed ID: 37640479
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.
    Gao Y; Wu H; Xu Y; Shen Q; Xu C; Geng H; Lv M; Tan Q; Li K; Tang D; Song B; Zhou P; Wei Z; He X; Cao Y
    Hum Mutat; 2022 Mar; 43(3):434-443. PubMed ID: 34923715
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. TENT5D disruption causes oligoasthenoteratozoospermia and male infertility.
    Sha Y; Liu W; Tang S; Zhang X; Xiao Z; Xiao Y; Deng H; Zhou H; Wei X
    Andrology; 2023 Sep; 11(6):1121-1131. PubMed ID: 36746179
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel homozygous LRRC6 mutation causes male infertility with asthenozoospermia and primary ciliary dyskinesia in humans.
    Shi S; Tang X; Long S; Yang J; Wang T; Wang H; Hu T; Shi J; Huang G; Qiao S; Lin T
    Andrology; 2024 Jun; ():. PubMed ID: 38934611
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.
    Liu Y; Li Y; Meng L; Li K; Gao Y; Lv M; Guo R; Xu Y; Zhou P; Wei Z; He X; Cao Y; Wu H; Tan Y; Hua R
    Hum Mol Genet; 2023 May; 32(10):1730-1740. PubMed ID: 36708031
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homozygous mutations in
    Cong J; Wang X; Amiri-Yekta A; Wang L; Kherraf ZE; Liu C; Cazin C; Tang S; Hosseini SH; Tian S; Daneshipour A; Wang J; Zhou Y; Zeng Y; Yang S; He X; Li J; Cao Y; Jin L; Ray PF; Zhang F
    J Med Genet; 2022 Jul; 59(7):710-718. PubMed ID: 34348960
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family.
    Rahim F; Tao L; Khan K; Ali I; Zeb A; Khan I; Dil S; Abbas T; Hussain A; Zubair M; Zhang H; Hui M; Khan MA; Shah W; Shi Q
    Clin Genet; 2024 Oct; 106(4):437-447. PubMed ID: 39221575
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Homozygous mutation in
    Sha Y; Liu W; Nie H; Han L; Ma C; Zhang X; Xiao Z; Qin W; Jiang X; Wei X
    Front Endocrinol (Lausanne); 2022; 13():1058651. PubMed ID: 36726469
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations.
    Lv M; Liu C; Ma C; Yu H; Shao Z; Gao Y; Liu Y; Wu H; Tang D; Tan Q; Zhang J; Li K; Xu C; Geng H; Zhang J; Li H; Mao X; Ge L; Fu F; Zhong K; Xu Y; Tao F; Zhou P; Wei Z; He X; Zhang F; Cao Y
    Reprod Biol Endocrinol; 2022 Jan; 20(1):5. PubMed ID: 34980136
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.