BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 18248681)

  • 21. Interleukin-4 genetic variants correlate with its transcript and protein levels in patients with vitiligo.
    Imran M; Laddha NC; Dwivedi M; Mansuri MS; Singh J; Rani R; Gokhale RS; Sharma VK; Marfatia YS; Begum R
    Br J Dermatol; 2012 Aug; 167(2):314-23. PubMed ID: 22512783
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age-related macular degeneration in Hungarian patients.
    Losonczy G; Fekete Á; Vokó Z; Takács L; Káldi I; Ajzner É; Kasza M; Vajas A; Berta A; Balogh I
    Acta Ophthalmol; 2011 May; 89(3):255-62. PubMed ID: 19845562
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Relationship between age-related macular degeneration-associated variants of complement factor H and LOC387715 with coronary artery disease.
    Pulido JS; McConnell JP; Lennon RJ; Bryant SC; Peterson LM; Berger PB; Somers V; Highsmith WE
    Mayo Clin Proc; 2007 Mar; 82(3):301-7. PubMed ID: 17352366
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Different hereditary contribution of the CFH gene between polypoidal choroidal vasculopathy and age-related macular degeneration in Chinese Han people.
    Huang L; Li Y; Guo S; Sun Y; Zhang C; Bai Y; Li S; Yang F; Zhao M; Wang B; Yu W; Zhao M; Khor CC; Li X
    Invest Ophthalmol Vis Sci; 2014 Apr; 55(4):2534-8. PubMed ID: 24692129
    [TBL] [Abstract][Full Text] [Related]  

  • 25. PLEKHA1-LOC387715-HTRA1 polymorphisms and exudative age-related macular degeneration in the French population.
    Leveziel N; Souied EH; Richard F; Barbu V; Zourdani A; Morineau G; Zerbib J; Coscas G; Soubrane G; Benlian P
    Mol Vis; 2007 Nov; 13():2153-9. PubMed ID: 18079691
    [TBL] [Abstract][Full Text] [Related]  

  • 26. DNA repair gene polymorphisms at XRCC1, XRCC3, XPD, and OGG1 loci in Maharashtrian population of central India.
    Pramanik S; Devi S; Chowdhary S; Surendran ST; Krishnamurthi K; Chakrabarti T
    Chemosphere; 2011 Feb; 82(7):941-6. PubMed ID: 21183201
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutation in the beta3 subunit of Guanine nucleotide-binding protein (GNB3) gene is not associated with Type II diabetes mellitus risk: a case-control study of a North Indian population.
    Rizvi S; Raza ST; Rahman Q; Mahdi F; Zaidi ZH; Zaidi A
    Biomarkers; 2017 Dec; 22(8):782-789. PubMed ID: 28602143
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Single nucleotide polymorphisms of the ALDH2 gene in six Indian populations.
    Bhaskar LV; Thangaraj K; Osier M; Reddy AG; Rao AP; Singh L; Rao VR
    Ann Hum Biol; 2007; 34(6):607-19. PubMed ID: 17952709
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Distinct haplotype profiles and strong linkage disequilibrium at the MDR1 multidrug transporter gene locus in three ethnic Asian populations.
    Tang K; Ngoi SM; Gwee PC; Chua JM; Lee EJ; Chong SS; Lee CG
    Pharmacogenetics; 2002 Aug; 12(6):437-50. PubMed ID: 12172212
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Age-related macular degeneration and association of CFH Y402H and LOC387715 A69S polymorphisms in a Turkish population.
    Soysal Y; Inan UÜ; Küsbeci T; Imirzalioğlu N
    DNA Cell Biol; 2012 Mar; 31(3):323-30. PubMed ID: 21790300
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Characterizing the genetic differences between two distinct migrant groups from Indo-European and Dravidian speaking populations in India.
    Ali M; Liu X; Pillai EN; Chen P; Khor CC; Ong RT; Teo YY
    BMC Genet; 2014 Jul; 15():86. PubMed ID: 25053360
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Risk conferred by tagged SNPs of AGT gene in causing susceptibility to essential hypertension.
    Padma G; Swapna N; Mamata M; Charita B; Padma T
    Clin Exp Hypertens; 2014; 36(8):579-85. PubMed ID: 24490766
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hypertension genetics, single nucleotide polymorphisms, and the common disease:common variant hypothesis.
    Doris PA
    Hypertension; 2002 Feb; 39(2 Pt 2):323-31. PubMed ID: 11882567
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Influence of protein tyrosine phosphatase gene (PTPN22) polymorphisms on rheumatic heart disease susceptibility in North Indian population.
    Gupta U; Mir SS; Chauhan T; Garg N; Agarwal SK; Pande S; Mittal B
    Tissue Antigens; 2014 Nov; 84(5):492-6. PubMed ID: 25273327
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic polymorphisms of drug-metabolizing phase I enzymes CYP2E1, CYP2A6 and CYP3A5 in South Indian population.
    Krishnakumar D; Gurusamy U; Dhandapani K; Surendiran A; Baghel R; Kukreti R; Gangadhar R; Prayaga U; Manjunath S; Adithan C
    Fundam Clin Pharmacol; 2012 Apr; 26(2):295-306. PubMed ID: 21265876
    [TBL] [Abstract][Full Text] [Related]  

  • 36. APOE polymorphism and lipid profile in three ethnic groups in the Singapore population.
    Tan CE; Tai ES; Tan CS; Chia KS; Lee J; Chew SK; Ordovas JM
    Atherosclerosis; 2003 Oct; 170(2):253-60. PubMed ID: 14612205
    [TBL] [Abstract][Full Text] [Related]  

  • 37. GLUT4 gene polymorphisms and their association with type 2 diabetes in south Indians.
    Bodhini D; Radha V; Ghosh S; Majumder PP; Rao MR; Mohan V
    Diabetes Technol Ther; 2011 Sep; 13(9):913-20. PubMed ID: 21668369
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cardiac Troponin T (TNNT2) mutations are less prevalent in Indian hypertrophic cardiomyopathy patients.
    Rani DS; Nallari P; Dhandapany PS; Tamilarasi S; Shah A; Archana V; AshokKumar M; Narasimhan C; Singh L; Thangaraj K
    DNA Cell Biol; 2012 Apr; 31(4):616-24. PubMed ID: 22017532
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genotype distribution-based inference of collective effects in genome-wide association studies: insights to age-related macular degeneration disease mechanism.
    Woo HJ; Yu C; Kumar K; Gold B; Reifman J
    BMC Genomics; 2016 Aug; 17(1):695. PubMed ID: 27576376
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Neovascular age-related macular degeneration and its association with LOC387715 and complement factor H polymorphism.
    Shuler RK; Hauser MA; Caldwell J; Gallins P; Schmidt S; Scott WK; Agarwal A; Haines JL; Pericak-Vance MA; Postel EA
    Arch Ophthalmol; 2007 Jan; 125(1):63-7. PubMed ID: 17210853
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.