BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 36068176)

  • 1. The association of testis-specific hTAF7L gene variants with idiopathic azoospermic and severe oligozoospermic male infertility.
    Ambulkar PS; Waghmare JE; Verma Shivkumar P; Chaudhari AR; Gangane NM; Narang P; Pal AK
    Andrologia; 2022 Dec; 54(11):e14581. PubMed ID: 36068176
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The role of the testis-specific gene hTAF7L in the aetiology of male infertility.
    Stouffs K; Willems A; Lissens W; Tournaye H; Van Steirteghem A; Liebaers I
    Mol Hum Reprod; 2006 Apr; 12(4):263-7. PubMed ID: 16597641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy.
    Najmabadi H; Huang V; Yen P; Subbarao MN; Bhasin D; Banaag L; Naseeruddin S; de Kretser DM; Baker HW; McLachlan RI
    J Clin Endocrinol Metab; 1996 Apr; 81(4):1347-52. PubMed ID: 8636331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure.
    Akinloye O; Gromoll J; Callies C; Nieschlag E; Simoni M
    Andrologia; 2007 Oct; 39(5):190-5. PubMed ID: 17714218
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel variations in spermatogenic transcription regulators RFX2 and TAF7 increase risk of azoospermia.
    Pal S; Paladhi P; Dutta S; Bose G; Ghosh P; Chattopadhyay R; Chakravarty B; Saha I; Ghosh S
    J Assist Reprod Genet; 2021 Dec; 38(12):3195-3212. PubMed ID: 34762273
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Varicocele and male infertility in Northeast China: Y chromosome microdeletion as an underlying cause.
    Dai RL; Hou Y; Li FB; Yue JM; Xi Q; Liu RZ
    Genet Mol Res; 2015 Jun; 14(2):6583-90. PubMed ID: 26125865
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association study of single-nucleotide polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR, and TAS2R38 genes with male infertility.
    Plaseski T; Noveski P; Popeska Z; Efremov GD; Plaseska-Karanfilska D
    J Androl; 2012; 33(4):675-83. PubMed ID: 22016351
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia.
    Ayhan Ö; Balkan M; Guven A; Hazan R; Atar M; Tok A; Tolun A
    J Med Genet; 2014 Apr; 51(4):239-44. PubMed ID: 24431330
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of AZF microdeletions and reproductive hormonal profile analysis of infertile sudanese men pursuing assisted reproductive approaches.
    Elsaid HOA; Gadkareim T; Abobakr T; Mubarak E; Abdelrhem MA; Abu D; Alhassan EA; Abushama H
    BMC Urol; 2021 Apr; 21(1):69. PubMed ID: 33892694
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic variants in meiotic program initiation pathway genes are associated with spermatogenic impairment in a Han Chinese population.
    Lu C; Xu M; Wang Y; Qin Y; Du G; Wu W; Han X; Ji C; Yang Y; Gu A; Xia Y; Song L; Wang S; Wang X
    PLoS One; 2013; 8(1):e53443. PubMed ID: 23320086
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Relationship of SNP of H2BFWT gene to male infertility in a Chinese population with idiopathic spermatogenesis impairment.
    Ying HQ; Scott MB; Zhou-Cun A
    Biomarkers; 2012 Aug; 17(5):402-6. PubMed ID: 22509975
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of G/T(rs222859) polymorphism in Exon 1 of YBX2 gene with azoospermia, among Iranian infertile males.
    Najafipour R; Rashvand Z; Alizadeh A; Aleyasin A; Moghbelinejad S
    Andrologia; 2016 Nov; 48(9):956-960. PubMed ID: 26804374
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of partial azoospermia factor c deletion and DAZ copy number in azoospermia and severe oligozoospermia.
    Alimardanian L; Saliminejad K; Razi S; Ahani A
    Andrologia; 2016 Nov; 48(9):890-894. PubMed ID: 27739146
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo mutations in idiopathic male infertility-A pilot study.
    Hodžić A; Maver A; Plaseska-Karanfilska D; Ristanović M; Noveski P; Zorn B; Terzic M; Kunej T; Peterlin B
    Andrology; 2021 Jan; 9(1):212-220. PubMed ID: 32860660
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High frequency of TTTY2-like gene-related deletions in patients with idiopathic oligozoospermia and azoospermia.
    Yapijakis C; Serefoglou Z; Papadimitriou K; Makrinou E
    Andrologia; 2015 Jun; 47(5):536-44. PubMed ID: 24919818
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cytogenetic and molecular analysis of the Y chromosome: absence of a significant relationship between CAG repeat length in exon 1 of the androgen receptor gene and infertility in Indian men.
    Dhillon VS; Husain SA
    Int J Androl; 2003 Oct; 26(5):286-95. PubMed ID: 14511217
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia].
    Kusić J; Radojković D; Maletić V; Branković S; Savić A
    Srp Arh Celok Lek; 2002; 130(1-2):1-6. PubMed ID: 12073281
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic variants of eNOS gene may modify the susceptibility to idiopathic male infertility.
    Ying HQ; Pu XY; Liu SR; A ZC
    Biomarkers; 2013 Aug; 18(5):412-7. PubMed ID: 23756085
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic anomalies in patients with severe oligozoospermia and azoospermia in eastern Turkey: a prospective study.
    Ceylan GG; Ceylan C; Elyas H
    Genet Mol Res; 2009 Aug; 8(3):915-22. PubMed ID: 19731213
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic characterization of a missense mutation in the X-linked TAF7L gene identified in an oligozoospermic man†.
    Ling L; Li F; Yang P; Oates RD; Silber S; Kurischko C; Luca FC; Leu NA; Zhang J; Yue Q; Skaletsky H; Brown LG; Rozen SG; Page DC; Wang PJ; Zheng K
    Biol Reprod; 2022 Jul; 107(1):157-167. PubMed ID: 35554494
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.