BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

94 related articles for article (PubMed ID: 34399789)

  • 21. Four-Week Omega-3 Supplementation in Carriers of the Prosteatotic PNPLA3 p.I148M Genetic Variant: An Open-Label Study.
    Kuttner CS; Mancina R; Wagenpfeil G; Lammert F; Stokes CS
    Lifestyle Genom; 2019; 12(1-6):10-17. PubMed ID: 31454802
    [TBL] [Abstract][Full Text] [Related]  

  • 22. CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians.
    Gragnoli C
    J Cell Physiol; 2008 Nov; 217(2):291-5. PubMed ID: 18680108
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association of the C-344T aldosterone synthase gene variant with essential hypertension: a meta-analysis.
    Sookoian S; Gianotti TF; González CD; Pirola CJ
    J Hypertens; 2007 Jan; 25(1):5-13. PubMed ID: 17143166
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Evaluation of TP53 Pro72Arg and MDM2 SNP285-SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations.
    Ponti F; Corsini S; Gnoli M; Pedrini E; Mordenti M; Sangiorgi L
    Fam Cancer; 2016 Oct; 15(4):635-43. PubMed ID: 26956143
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Association of MTHFR C677T polymorphism with elevated homocysteine level and disease development in vitiligo.
    Bagheri Hamidi A; Namazi N; Mohammad Amoli M; Amani M; Gholami M; Youssefian L; Vahidnezhad H; Abdollahimajd F; Uitto J
    Int J Immunogenet; 2020 Aug; 47(4):342-350. PubMed ID: 32064757
    [TBL] [Abstract][Full Text] [Related]  

  • 26.  GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis.
    Levstik A; Stuart A; Adams PC
    Ann Hepatol; 2016 Nov-Dec 2016; 15(6):907-910. PubMed ID: 27740525
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association between XRCC3 Thr241Met Polymorphism and Risk of Breast Cancer: Meta-Analysis of 23 Case-Control Studies.
    Chai F; Liang Y; Chen L; Zhang F; Jiang J
    Med Sci Monit; 2015 Oct; 21():3231-40. PubMed ID: 26498491
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The homozygous ganglioside-induced differentiation-associated protein 1 mutation c.373C > T causes a very early-onset neuropathy: case report and literature review.
    Fusco C; Ucchino V; Barbon G; Bonini E; Mostacciuolo ML; Frattini D; Pisani F; Giustina ED
    J Child Neurol; 2011 Jan; 26(1):49-57. PubMed ID: 21212451
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
    Dhandapani MC; Venkatesan V; Rengaswamy NB; Gowrishankar K; Ekambaram S; Sengutavan P; Perumal V
    Clin Exp Nephrol; 2017 Feb; 21(1):127-133. PubMed ID: 26820844
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The vitamin D receptor (VDR) gene rs11568820 variant is associated with type 2 diabetes and impaired insulin secretion in Italian adult subjects, and associates with increased cardio-metabolic risk in children.
    Sentinelli F; Bertoccini L; Barchetta I; Capoccia D; Incani M; Pani MG; Loche S; Angelico F; Arca M; Morini S; Manconi E; Lenzi A; Cossu E; Leonetti F; Baroni MG; Cavallo MG
    Nutr Metab Cardiovasc Dis; 2016 May; 26(5):407-13. PubMed ID: 27052925
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li-Fraumeni syndrome and related phenotypes.
    Ruijs MW; Schmidt MK; Nevanlinna H; Tommiska J; Aittomäki K; Pruntel R; Verhoef S; Van't Veer LJ
    Eur J Hum Genet; 2007 Jan; 15(1):110-4. PubMed ID: 17003841
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Correlation of the single nucleotide polymorphism rs662 of PON1 with the risk of male infertility].
    Liu HH; Zhao J; Xu J; Zhu PR; Yu MM; Jiang WJ; Zhang J; Li WW; Wu QY; Li ZR; Xia XY
    Zhonghua Nan Ke Xue; 2018 Aug; 24(8):708-712. PubMed ID: 30173430
    [TBL] [Abstract][Full Text] [Related]  

  • 33. IL1RL1 single nucleotide polymorphism predicts sST2 level and mortality in coronary and peripheral artery disease.
    Lin JF; Wu S; Juang JJ; Chiang FT; Hsu LA; Teng MS; Cheng ST; Huang HL; Sun YC; Liu PY; Ko YL
    Atherosclerosis; 2017 Feb; 257():71-77. PubMed ID: 28110258
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Polymorphism in the endoplasmic reticulum mannosidase I (MAN1B1) gene is not associated with liver disease in individuals homozygous for the Z variant of the alpha1-antitrypsin protease inhibitor (PiZZ individuals).
    Chappell S; Guetta-Baranés T; Hadzic N; Stockley R; Kalsheker N
    Hepatology; 2009 Oct; 50(4):1315; author reply 1315-6. PubMed ID: 19739260
    [No Abstract]   [Full Text] [Related]  

  • 35. Meta-analysis of the influence of I148M variant of patatin-like phospholipase domain containing 3 gene (PNPLA3) on the susceptibility and histological severity of nonalcoholic fatty liver disease.
    Sookoian S; Pirola CJ
    Hepatology; 2011 Jun; 53(6):1883-94. PubMed ID: 21381068
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention.
    Kessler T; Wolf B; Eriksson N; Kofink D; Mahmoodi BK; Rai H; Tragante V; Åkerblom A; Becker RC; Bernlochner I; Bopp R; James S; Katus HA; Mayer K; Munz M; Nordio F; O'Donoghue ML; Sager HB; Sibbing D; Solakov L; Storey RF; Wobst J; Asselbergs FW; Byrne RA; Erdmann J; Koenig W; Laugwitz KL; Ten Berg JM; Wallentin L; Kastrati A; Schunkert H
    Cardiovasc Res; 2019 Aug; 115(10):1512-1518. PubMed ID: 30768153
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic polymorphisms in the oxidative stress pathway and susceptibility to non-Hodgkin lymphoma.
    Lan Q; Zheng T; Shen M; Zhang Y; Wang SS; Zahm SH; Holford TR; Leaderer B; Boyle P; Chanock S
    Hum Genet; 2007 Apr; 121(2):161-8. PubMed ID: 17149600
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic mutations potentially cause two novel NCF1 splice variants up-regulated in the mammary gland, blood and neutrophil of cows infected by Escherichia coli.
    Zhang Z; Wang X; Li R; Ju Z; Qi C; Zhang Y; Guo F; Luo G; Li Q; Wang C; Zhong J; Xu Y; Huang J
    Microbiol Res; 2015 May; 174():24-32. PubMed ID: 25946326
    [TBL] [Abstract][Full Text] [Related]  

  • 39. C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition.
    Rueda B; Núñez C; Orozco G; López-Nevot MA; de la Concha EG; Martin J; Urcelay E
    Hum Immunol; 2005 Jul; 66(7):848-52. PubMed ID: 16112033
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetically determined high activities of the TNF-alpha, IL23/IL17, and NFkB pathways were associated with increased risk of ankylosing spondylitis.
    Sode J; Bank S; Vogel U; Andersen PS; Sørensen SB; Bojesen AB; Andersen MR; Brandslund I; Dessau RB; Hoffmann HJ; Glintborg B; Hetland ML; Locht H; Heegaard NH; Andersen V
    BMC Med Genet; 2018 Sep; 19(1):165. PubMed ID: 30208882
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.