These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 31613733)

  • 21. [Association between 1019C/T polymorphism of Connexin 37 gene and restenosis after coronary stenting].
    Yang Y; Guo SX; Yang ZY; Zhang T; Cao HM; Wang RX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):456-60. PubMed ID: 23926016
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population.
    Kashyap S; Kumar S; Agarwal V; Misra DP; Rai MK; Kapoor A
    Gene; 2018 Mar; 648():89-96. PubMed ID: 29309886
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Apolipoprotein isoform E4 does not increase coronary heart disease risk in carriers of low-density lipoprotein receptor mutations.
    Versmissen J; Oosterveer DM; Hoekstra M; Out R; Berbée JF; Blommesteijn-Touw AC; van Vark-van der Zee L; Vongpromek R; Vanmierlo T; Defesche JC; Mulder M; Kastelein JJ; Sijbrands EJ
    Circ Cardiovasc Genet; 2011 Dec; 4(6):655-60. PubMed ID: 22010136
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular Evaluation of PROGINS Mutation in Progesterone Receptor Gene and Determination of its Frequency, Distribution Pattern and Association with Breast Cancer Susceptibility in Saudi Arabia.
    Albalawi IA; Mir R; Abu-Duhier FM
    Endocr Metab Immune Disord Drug Targets; 2020; 20(5):760-770. PubMed ID: 31763970
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Impact of polymorphism rs7041 and rs4588 of Vitamin D Binding Protein on the extent of coronary artery disease.
    Daffara V; Verdoia M; Rolla R; Nardin M; Marino P; Bellomo G; Carriero A; De Luca G;
    Nutr Metab Cardiovasc Dis; 2017 Sep; 27(9):775-783. PubMed ID: 28779988
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association of rs1122608 with Coronary Artery Disease and Lipid Profile: A Meta-analysis.
    Liu S; Xiu B; Liu J; Xue A; Tang Q; Shen Y; Xie J
    Arch Med Res; 2016 May; 47(4):315-20. PubMed ID: 27664493
    [TBL] [Abstract][Full Text] [Related]  

  • 27. There is an association between a genetic polymorphism in the ZNF259 gene involved in lipid metabolism and coronary artery disease.
    Mirhafez SR; Avan A; Khatamianfar S; Ghasemi F; Moohebati M; Ebrahimi M; Ghazizadeh H; Ghayour-Mobarhan M; Pasdar A
    Gene; 2019 Jul; 704():80-85. PubMed ID: 30902787
    [TBL] [Abstract][Full Text] [Related]  

  • 28. IKZF1 gene polymorphisms increased the risk of childhood acute lymphoblastic leukemia in an Iranian population.
    Bahari G; Hashemi M; Naderi M; Taheri M
    Tumour Biol; 2016 Jul; 37(7):9579-86. PubMed ID: 26790447
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular analysis of the LDLR gene in coronary artery disease patients from the Indian population.
    ArulJothi KN; Whitthall RA; Futema M; Humphries SE; George M; Elangovan S; Nair DR; Devi A
    Clin Biochem; 2016 Jun; 49(9):669-674. PubMed ID: 26927322
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
    Do R; Stitziel NO; Won HH; Jørgensen AB; Duga S; Angelica Merlini P; Kiezun A; Farrall M; Goel A; Zuk O; Guella I; Asselta R; Lange LA; Peloso GM; Auer PL; ; Girelli D; Martinelli N; Farlow DN; DePristo MA; Roberts R; Stewart AF; Saleheen D; Danesh J; Epstein SE; Sivapalaratnam S; Hovingh GK; Kastelein JJ; Samani NJ; Schunkert H; Erdmann J; Shah SH; Kraus WE; Davies R; Nikpay M; Johansen CT; Wang J; Hegele RA; Hechter E; Marz W; Kleber ME; Huang J; Johnson AD; Li M; Burke GL; Gross M; Liu Y; Assimes TL; Heiss G; Lange EM; Folsom AR; Taylor HA; Olivieri O; Hamsten A; Clarke R; Reilly DF; Yin W; Rivas MA; Donnelly P; Rossouw JE; Psaty BM; Herrington DM; Wilson JG; Rich SS; Bamshad MJ; Tracy RP; Cupples LA; Rader DJ; Reilly MP; Spertus JA; Cresci S; Hartiala J; Tang WH; Hazen SL; Allayee H; Reiner AP; Carlson CS; Kooperberg C; Jackson RD; Boerwinkle E; Lander ES; Schwartz SM; Siscovick DS; McPherson R; Tybjaerg-Hansen A; Abecasis GR; Watkins H; Nickerson DA; Ardissino D; Sunyaev SR; O'Donnell CJ; Altshuler D; Gabriel S; Kathiresan S
    Nature; 2015 Feb; 518(7537):102-6. PubMed ID: 25487149
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Susceptible gene polymorphism in patients with three-vessel coronary artery disease.
    Liu R; Song L; Jiang L; Tang X; Xu L; Gao Z; Zhao X; Xu J; Gao R; Yuan J
    BMC Cardiovasc Disord; 2020 Apr; 20(1):172. PubMed ID: 32293292
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Associations Between
    Qiu H; Chen Z; Lv L; Tang W; Hu R
    DNA Cell Biol; 2020 Jan; 39(1):25-36. PubMed ID: 31692368
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dab2 gene variant is associated with increased coronary artery disease risk in Chinese Han population.
    Wang Y; Wang Y; Adi D; He X; Liu F; Abudesimu A; Fu Z; Ma Y
    Medicine (Baltimore); 2020 Jul; 99(27):e20924. PubMed ID: 32629690
    [TBL] [Abstract][Full Text] [Related]  

  • 34. ENPP1 121Q functional variant enhances susceptibility to coronary artery disease in South Indian patients with type 2 diabetes mellitus.
    Sumi S; Ramachandran S; RamanKutty V; Patel MM; Anand TN; Mullasari AS; Kartha CC
    Mol Cell Biochem; 2017 Nov; 435(1-2):67-72. PubMed ID: 28497367
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Familial hypercholesterolemia and familial defective apolipoprotein B-100: comparison of the phenotypic expression In 116 cases.
    Brugger D; Schuster H; Zöllner N
    Eur J Med Res; 1996 May; 1(8):383-6. PubMed ID: 9360938
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The 3'-UTR C>T polymorphism of the oxidized LDL-receptor 1 (OLR1) gene does not associate with coronary artery disease in Italian CAD patients or with the severity of coronary disease.
    Sentinelli F; Filippi E; Fallarino M; Romeo S; Fanelli M; Buzzetti R; Berni A; Baroni MG
    Nutr Metab Cardiovasc Dis; 2006 Jul; 16(5):345-52. PubMed ID: 16829343
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Chemokine receptor 5 (CCR5) deletion polymorphism in North Indian patients with coronary artery disease.
    Sharda S; Gilmour A; Harris V; Singh VP; Sinha N; Tewari S; Ramesh V; Agrawal S; Mastana S
    Int J Cardiol; 2008 Feb; 124(2):254-8. PubMed ID: 17383752
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Polymorphisms of TGFβ-1 and TGFBR2 in relation to coronary artery disease in a Chinese population.
    Yang M; Zhu M; Tang L; Zhu H; Lu Y; Xu B; Jiang J; Chen X
    Clin Biochem; 2016 Aug; 49(12):873-8. PubMed ID: 27234600
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Association of C1019T polymorphism in the connexin 37 gene and coronary artery disease in Chinese Han population].
    Han YL; Xi SY; Zhang XL; Yan CH; Yang Y; Kang J
    Zhonghua Yi Xue Za Zhi; 2007 Jan; 87(2):100-4. PubMed ID: 17418016
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Age and hypertension related changes in genotypes of MTHFR 677C>T, 1298A>C and PON1 -108C>T SNPs in men with coronary artery disease (CAD).
    Strauss E; Głuszek J; Pawlak AL
    J Physiol Pharmacol; 2005 Mar; 56 Suppl 2():65-75. PubMed ID: 16077191
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.