BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

308 related articles for article (PubMed ID: 38650655)

  • 1. Effects of
    Olszewska M; Malcher A; Stokowy T; Pollock N; Berman AJ; Budkiewicz S; Kamieniczna M; Jackowiak H; Suszynska-Zajczyk J; Jedrzejczak P; Yatsenko AN; Kurpisz M
    Hum Reprod Open; 2024; 2024(2):hoae020. PubMed ID: 38650655
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects.
    Li Y; Wang Y; Wen Y; Zhang T; Wang X; Jiang C; Zheng R; Zhou F; Chen D; Yang Y; Shen Y
    Hum Reprod; 2021 Dec; 37(1):152-177. PubMed ID: 34791246
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Systematic characterization of human testis-specific actin capping protein β3 as a possible biomarker for male infertility.
    Soda T; Miyagawa Y; Ueda N; Takezawa K; Okuda H; Fukuhara S; Fujita K; Kiuchi H; Uemura M; Okamoto Y; Tsujimura A; Tanaka H; Nonomura N
    Hum Reprod; 2017 Mar; 32(3):514-522. PubMed ID: 28104696
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nexin-Dynein regulatory complex component DRC7 but not FBXL13 is required for sperm flagellum formation and male fertility in mice.
    Morohoshi A; Miyata H; Shimada K; Nozawa K; Matsumura T; Yanase R; Shiba K; Inaba K; Ikawa M
    PLoS Genet; 2020 Jan; 16(1):e1008585. PubMed ID: 31961863
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.
    Oud MS; Houston BJ; Volozonoka L; Mastrorosa FK; Holt GS; Alobaidi BKS; deVries PF; Astuti G; Ramos L; Mclachlan RI; O'Bryan MK; Veltman JA; Chemes HE; Sheth H
    Hum Reprod; 2021 Aug; 36(9):2597-2611. PubMed ID: 34089056
    [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. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
    Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C
    Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia.
    Yan Y; Yang X; Liu Y; Shen Y; Tu W; Dong Q; Yang D; Ma Y; Yang Y
    Hum Reprod; 2017 Jul; 32(7):1521-1531. PubMed ID: 28498920
    [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. TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa.
    Castaneda JM; Hua R; Miyata H; Oji A; Guo Y; Cheng Y; Zhou T; Guo X; Cui Y; Shen B; Wang Z; Hu Z; Zhou Z; Sha J; Prunskaite-Hyyrylainen R; Yu Z; Ramirez-Solis R; Ikawa M; Matzuk MM; Liu M
    Proc Natl Acad Sci U S A; 2017 Jul; 114(27):E5370-E5378. PubMed ID: 28630322
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.
    Wang W; Su L; Meng L; He J; Tan C; Yi D; Cheng D; Zhang H; Lu G; Du J; Lin G; Zhang Q; Tu C; Tan YQ
    Hum Reprod; 2023 Jul; 38(7):1399-1411. PubMed ID: 37192818
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biallelic mutations in RNA-binding protein ADAD2 cause spermiogenic failure and non-obstructive azoospermia in humans.
    Shi B; Shah W; Liu L; Gong C; Zhou J; Abbas T; Ma H; Zhang H; Yang M; Zhang Y; Ullah N; Mahammad Z; Khan M; Murtaza G; Ali A; Khan R; Sha J; Yuan Y; Shi Q
    Hum Reprod Open; 2023; 2023(3):hoad022. PubMed ID: 37325547
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility.
    Zhou S; Wu H; Zhang J; He X; Liu S; Zhou P; Hua R; Cao Y; Liu M
    Eur J Hum Genet; 2022 Jun; 30(6):721-729. PubMed ID: 35388187
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest.
    van der Bijl N; Röpke A; Biswas U; Wöste M; Jessberger R; Kliesch S; Friedrich C; Tüttelmann F
    Hum Reprod; 2019 Nov; 34(11):2112-2119. PubMed ID: 31682730
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Long-chain fatty acid triglyceride (TG) metabolism disorder impairs male fertility: a study using adipose triglyceride lipase deficient mice.
    Masaki H; Kim N; Nakamura H; Kumasawa K; Kamata E; Hirano KI; Kimura T
    Mol Hum Reprod; 2017 Jul; 23(7):452-460. PubMed ID: 28510703
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sperm acquire epididymis-derived proteins through epididymosomes.
    Barrachina F; Battistone MA; Castillo J; Mallofré C; Jodar M; Breton S; Oliva R
    Hum Reprod; 2022 Apr; 37(4):651-668. PubMed ID: 35137089
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human.
    Zhang Q; Jin H; Long S; Tang X; Li J; Liu W; Han W; Liao H; Fu T; Huang G; Chen S; Lin T
    Hum Reprod; 2024 May; 39(5):880-891. PubMed ID: 38414365
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.