BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 33517345)

  • 1. A loss-of-function variant in DNA mismatch repair gene MLH3 underlies severe oligozoospermia.
    Nawaz S; Ullah MI; Hamid BS; Nargis J; Nawaz M; Hussain S; Ahmad W
    J Hum Genet; 2021 Jul; 66(7):725-730. PubMed ID: 33517345
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
    Chen S; Wang G; Zheng X; Ge S; Dai Y; Ping P; Chen X; Liu G; Zhang J; Yang Y; Zhang X; Zhong A; Zhu Y; Chu Q; Huang Y; Zhang Y; Shen C; Yuan Y; Yuan Q; Pei X; Cheng CY; Sun F
    Hum Mol Genet; 2020 Aug; 29(14):2451-2459. PubMed ID: 32469048
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.
    Tu C; Meng L; Nie H; Yuan S; Wang W; Du J; Lu G; Lin G; Tan YQ
    Fertil Steril; 2020 Mar; 113(3):561-568. PubMed ID: 32111475
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The association of four SNPs in DNA mismatch repair genes with idiopathic male infertility in northwest China.
    Zhao X; Mu C; Ma J; Dai X; Jiao H
    Int J Immunogenet; 2019 Dec; 46(6):451-458. PubMed ID: 31342644
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition.
    Olkinuora A; Nieminen TT; Mårtensson E; Rohlin A; Ristimäki A; Koskenvuo L; Lepistö A; ; Gebre-Medhin S; Nordling M; Peltomäki P
    Genet Med; 2019 Aug; 21(8):1868-1873. PubMed ID: 30573798
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.
    Tu C; Wang Y; Nie H; Meng L; Wang W; Li Y; Li D; Zhang H; Lu G; Lin G; Tan YQ; Du J
    Clin Genet; 2020 May; 97(5):741-746. PubMed ID: 32017041
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
    Okutman O; Muller J; Skory V; Garnier JM; Gaucherot A; Baert Y; Lamour V; Serdarogullari M; Gultomruk M; Röpke A; Kliesch S; Herbepin V; Aknin I; Benkhalifa M; Teletin M; Bakircioglu E; Goossens E; Charlet-Berguerand N; Bahceci M; Tüttelmann F; Viville S
    J Assist Reprod Genet; 2017 May; 34(5):683-694. PubMed ID: 28401488
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A homozygous FANCM frameshift pathogenic variant causes male infertility.
    Yin H; Ma H; Hussain S; Zhang H; Xie X; Jiang L; Jiang X; Iqbal F; Bukhari I; Jiang H; Ali A; Zhong L; Li T; Fan S; Zhang B; Gao J; Li Y; Nazish J; Khan T; Khan M; Zubair M; Hao Q; Fang H; Huang J; Huleihel M; Sha J; Pandita TK; Zhang Y; Shi Q
    Genet Med; 2019 Jan; 21(1):62-70. PubMed ID: 29895858
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The role of MSH5 C85T and MLH3 C2531T polymorphisms in the risk of male infertility with azoospermia or severe oligozoospermia.
    Xu K; Lu T; Zhou H; Bai L; Xiang Y
    Clin Chim Acta; 2010 Jan; 411(1-2):49-52. PubMed ID: 19808033
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Single-nucleotide polymorphism rs 175080 in the MLH3 gene and its relation to male infertility.
    Markandona O; Dafopoulos K; Anifandis G; Messini CI; Dimitraki M; Tsezou A; Georgoulias P; Messinis IE
    J Assist Reprod Genet; 2015 Dec; 32(12):1795-9. PubMed ID: 26520453
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A rare frameshift mutation in SYCP1 is associated with human male infertility.
    Nabi S; Askari M; Rezaei-Gazik M; Salehi N; Almadani N; Tahamtani Y; Totonchi M
    Mol Hum Reprod; 2022 Apr; 28(4):. PubMed ID: 35377450
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exonic sequencing and MLH3 gene expression analysis of breast cancer patients.
    Khailany RA; Ozaslan M
    Cell Mol Biol (Noisy-le-grand); 2021 Nov; 67(3):35-43. PubMed ID: 34933735
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse.
    Chen PC; Dudley S; Hagen W; Dizon D; Paxton L; Reichow D; Yoon SR; Yang K; Arnheim N; Liskay RM; Lipkin SM
    Cancer Res; 2005 Oct; 65(19):8662-70. PubMed ID: 16204034
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
    Wu Y; Li Y; Murtaza G; Zhou J; Jiao Y; Gong C; Hu C; Han Q; Zhang H; Zhang Y; Shi B; Ma H; Jiang X; Shi Q
    Hum Reprod; 2021 Sep; 36(10):2793-2804. PubMed ID: 34392356
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
    Okutman O; Muller J; Baert Y; Serdarogullari M; Gultomruk M; Piton A; Rombaut C; Benkhalifa M; Teletin M; Skory V; Bakircioglu E; Goossens E; Bahceci M; Viville S
    Hum Mol Genet; 2015 Oct; 24(19):5581-8. PubMed ID: 26199321
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis-2 with impaired intellectual development.
    Zaka A; Shahzad S; Rao HZ; Hashim Y; Basit S
    Am J Med Genet A; 2021 Feb; 185(2):355-361. PubMed ID: 33141514
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.
    Li L; Sha YW; Su ZY; Mei LB; Ji ZY; Zhang Q; Lin SB; Wang X; Qiu PP; Li P; Yin C
    Gene; 2018 Jan; 639():106-110. PubMed ID: 29017965
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of UHRF1 gene polymorphisms with oligospermia in Chinese males.
    Zhu W; Du J; Chen Q; Zhang Z; Wu B; Xu J; Li T; Bi Y; Shi H; Li R
    J Assist Reprod Genet; 2019 Dec; 36(12):2563-2573. PubMed ID: 31802345
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility.
    Ji G; Long Y; Zhou Y; Huang C; Gu A; Wang X
    BMC Med; 2012 May; 10():49. PubMed ID: 22594646
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expression analysis of MLH3, MLH1, and MSH4 in maturation arrest.
    Ferrás C; Fernandes S; Silva J; Barros A; Sousa M
    Reprod Sci; 2012 Jun; 19(6):587-96. PubMed ID: 22344730
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.