BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 25792652)

  • 1. The effects of PON1 gene Q192R variant on the development of uterine leiomyoma in Turkish patients.
    Attar R; Atasoy H; İnal-Gültekin G; Timirci-Kahraman Ö; Güleç-Yilmaz S; Dalan AB; Yildirim G; Ergen A; Isbir T
    In Vivo; 2015; 29(2):243-6. PubMed ID: 25792652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Q192R variant in paraoxonase 1 gene confers susceptibility to leiomyoma.
    Shahbazi S; Zarei S; Torfeh M; Fatahi N
    J Cancer Res Ther; 2020; 16(4):884-887. PubMed ID: 32930135
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of paraoxonase 1 (PON1) L55M and PON1 Q192R gene polymorphisms and risk of psoriasis.
    Kalkan G; Seçkin HY; Benli İ; Akbaş A; Ateş Ö; Özyurt H; Baş Y; Oğrum A; Pancar GŞ
    G Ital Dermatol Venereol; 2019 Jun; 154(3):321-326. PubMed ID: 28399619
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lack of influence of the ACE1 gene I/D polymorphism on the formation and growth of benign uterine leiomyoma in Turkish patients.
    Gultekin GI; Yilmaz SG; Kahraman OT; Atasoy H; Dalan AB; Attar R; Buyukoren A; Ucunoglu N; Isbir T
    Asian Pac J Cancer Prev; 2015; 16(3):1123-7. PubMed ID: 25735342
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Relationship between the paraoxonase 1 gene glutamine 192 to arginine polymorphism and gestational diabetes mellitus in Saudi women.
    Al-Hakeem MM; Abotalib Z; Alharbi KK; Khan IA
    Clin Biochem; 2014 Oct; 47(15):122-5. PubMed ID: 25036896
    [TBL] [Abstract][Full Text] [Related]  

  • 6. G-protein-coupled estrogen receptor-30 gene polymorphisms are associated with uterine leiomyoma risk.
    Kasap B; Öztürk Turhan N; Edgünlü T; Duran M; Akbaba E; Öner G
    Bosn J Basic Med Sci; 2016 Jan; 16(1):39-45. PubMed ID: 26773178
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Q192R and L55M Polymorphisms of Paraoxonase 1 Gene in Chronic Myelogenous Leukemia and Chronic Lymphocytic Leukemia.
    Tomatir AG; Pehlivan S; Sahin HH; Balci SO; Budeyri S; Pehlivan M
    Anticancer Res; 2015 Sep; 35(9):4807-12. PubMed ID: 26254371
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lack of association between paraoxonase-1 Q192R polymorphism and rheumatoid arthritis in southeast Iran.
    Hashemi M; Moazeni-Roodi AK; Fazaeli A; Sandoughi M; Bardestani GR; Kordi-Tamandani DM; Ghavami S
    Genet Mol Res; 2010 Feb; 9(1):333-9. PubMed ID: 20198589
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polymorphism of catechol-o-methyltransferase and uterine leiomyoma.
    Ates O; Demirturk F; Toprak M; Sezer S
    Mol Cell Biochem; 2013 Mar; 375(1-2):179-83. PubMed ID: 23238870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lack of association between paraoxonase 1 Q192R polymorphism and multiple sclerosis in relapse phase: A case-control study.
    Moghtaderi A; Hashemi M; Sharafaddinzadeh N; Dabiri S; Moazeni-Roodi A; Ramroodi N; Zolfaghari M
    Clin Biochem; 2011 Jul; 44(10-11):795-8. PubMed ID: 21545792
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Serum paraoxonase-1 (PON1) activities (PONase/AREase) and polymorphisms in patients with type 2 diabetes mellitus in a North-West Indian population.
    Gupta N; Binukumar BK; Singh S; Sunkaria A; Kandimalla R; Bhansali A; Gill KD
    Gene; 2011 Nov; 487(1):88-95. PubMed ID: 21803130
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The evaluation of two genetic polymorphisms of paraoxonase 1 in patients with pulmonary embolism.
    Basol N; Karakus N; Savas AY; Karakus K; Kaya İ; Karaman S; Yigit S
    J Clin Lab Anal; 2018 Sep; 32(7):e22455. PubMed ID: 29682786
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Q192R polymorphism in the PON1 gene and nasal polyp in a Turkish population.
    Solmaz Avcikurt A; Gencer N; Yazici H
    J Biochem Mol Toxicol; 2021 Jan; 35(1):e22628. PubMed ID: 32905659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Investigating paraoxonase-1 gene Q192R and L55M polymorphism in patients with renal cell cancer.
    Uyar OA; Kara M; Erol D; Ardicoglu A; Yuce H
    Genet Mol Res; 2011 Feb; 10(1):133-9. PubMed ID: 21308654
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Is paraoxonase 192 gene polymorphism a risk factor for membranoproliferative glomerulonephritis in children?
    Bilge I; Sirin A; Agachan B; Emre S; Sadikoglu B; Yilmaz H; Sucu A; Isbir T
    Cell Biochem Funct; 2007; 25(2):159-65. PubMed ID: 16175651
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigation of the common paraoxonase 1 variants with paraoxonase activity on bone fragility in Turkish patients.
    Toptaş B; Kurt Ö; Aydoğan HY; Yaylim I; Zeybek Ü; Can A; Agachan B; Uyar M; Özyavuz MK; Isbir T
    Mol Biol Rep; 2013 Nov; 40(11):6519-24. PubMed ID: 24057271
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 192R allele of paraoxanase 1 (PON1) gene as a new marker for susceptibility to bladder cancer.
    Oztürk O; Kağnici OF; Oztürk T; Durak H; Tüzüner BM; Kisakesen HI; Cakalir C; Isbir T
    Anticancer Res; 2009 Oct; 29(10):4041-6. PubMed ID: 19846948
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluation of paraoxonase 1 polymorphisms in patients with bipolar disorder.
    Küçükali CI; Ulusoy C; Özkan Ö; Orhan N; Güleç H; Erdağ E; Buker S; Tüzün E
    In Vivo; 2015; 29(1):103-8. PubMed ID: 25600537
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polymorphism of the p53 tumor suppressor gene is associated with susceptibility to uterine leiomyoma.
    Denschlag D; Bettendorf H; Watermann D; Keck C; Tempfer C; Pietrowski D
    Fertil Steril; 2005 Jul; 84(1):162-6. PubMed ID: 16009172
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effect of PON1 Q192R genetic polymorphism on clopidogrel efficacy and cardiovascular events in the Clopidogrel in the Unstable Angina to Prevent Recurrent Events trial and the Atrial Fibrillation Clopidogrel Trial with Irbesartan for Prevention of Vascular Events.
    Paré G; Ross S; Mehta SR; Yusuf S; Anand SS; Connolly SJ; Fox KA; Eikelboom JW
    Circ Cardiovasc Genet; 2012 Apr; 5(2):250-6. PubMed ID: 22368149
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.