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 *

75 related articles for article (PubMed ID: 30351207)

  • 21. Association of the cytotoxic T lymphocyte-associated antigen 4 gene with type 1 diabetes: evidence for independent effects of two polymorphisms on the same haplotype block.
    Anjos SM; Tessier MC; Polychronakos C
    J Clin Endocrinol Metab; 2004 Dec; 89(12):6257-65. PubMed ID: 15579786
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Statistical estimation and pedigree analysis of CCR2-CCR5 haplotypes.
    Clark VJ; Metheny N; Dean M; Peterson RJ
    Hum Genet; 2001 Jun; 108(6):484-93. PubMed ID: 11499673
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China.
    Abudoukelimu M; Fu ZY; Maimaiti A; Ma YT; Abudu M; Zhu Q; Adi D; Yang YN; Li XM; Xie X; Liu F; Chen BD
    Lipids Health Dis; 2015 Sep; 14():120. PubMed ID: 26415596
    [TBL] [Abstract][Full Text] [Related]  

  • 24. FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women.
    Rull K; Grigorova M; Ehrenberg A; Vaas P; Sekavin A; Nõmmemees D; Adler M; Hanson E; Juhanson P; Laan M
    Hum Reprod; 2018 May; 33(5):954-966. PubMed ID: 29617818
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Common polymorphisms of ATP binding cassette transporter A1, including a functional promoter polymorphism, associated with plasma high density lipoprotein cholesterol levels in Turks.
    Hodoğlugil U; Williamson DW; Huang Y; Mahley RW
    Atherosclerosis; 2005 Dec; 183(2):199-212. PubMed ID: 15935359
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Using DNA pools for genotyping trios.
    Beckman KB; Abel KJ; Braun A; Halperin E
    Nucleic Acids Res; 2006; 34(19):e129. PubMed ID: 17020923
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 3'UTR SNPs and Haplotypes in the GATA4 Gene Contribute to the Genetic Risk of Congenital Heart Disease.
    Pulignani S; Vecoli C; Sabina S; Foffa I; Ait-Ali L; Andreassi MG
    Rev Esp Cardiol (Engl Ed); 2016 Aug; 69(8):760-5. PubMed ID: 27118528
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Effect of donor CTLA-4 alleles and haplotypes on graft-versus-host disease occurrence in Tunisian patients receiving a human leukocyte antigen-identical sibling hematopoietic stem cell transplant.
    Sellami MH; Bani M; Torjemane L; Kaabi H; Ladeb S; Ben Othmane T; Hmida S
    Hum Immunol; 2011 Feb; 72(2):139-43. PubMed ID: 21081144
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Alleles and haplotypes of the interleukin 10 gene polymorphisms are associated with risk of developing acute coronary syndrome in Mexican patients.
    Fragoso JM; Vallejo M; Alvarez-León E; Delgadillo H; Peña-Duque MA; Cardoso-Saldaña G; Posadas-Romero C; Martínez-Ríos MA; Vargas-Alarcón G
    Cytokine; 2011 Jul; 55(1):29-33. PubMed ID: 21481602
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The KPNB3 locus is associated with schizophrenia.
    Wei J; Hemmings GP
    Neurosci Lett; 2004 Sep; 368(3):323-6. PubMed ID: 15364420
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Determination of ABCB1 polymorphisms and haplotypes frequencies in a French population.
    Jeannesson E; Albertini L; Siest G; Gomes AM; Ribeiro V; Aslanidis C; Schmitz G; Visvikis-Siest S
    Fundam Clin Pharmacol; 2007 Aug; 21(4):411-8. PubMed ID: 17635180
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism?
    Løvlie R; Daly AK; Matre GE; Molven A; Steen VM
    Pharmacogenetics; 2001 Feb; 11(1):45-55. PubMed ID: 11207030
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
    Kocabas NA; Faghel C; Barreto M; Kasper S; Linotte S; Mendlewicz J; Noro M; Oswald P; Souery D; Zohar J; Massat I
    Int Clin Psychopharmacol; 2010 Jul; 25(4):218-27. PubMed ID: 20531207
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Common variants in glucuronidation enzymes and membrane transporters as potential risk factors for colorectal cancer: a case control study.
    Falkowski S; Woillard JB; Postil D; Tubiana-Mathieu N; Terrebonne E; Pariente A; Smith D; Guimbaud R; Thalamas C; Rouguieg-Malki K; Marquet P; Picard N
    BMC Cancer; 2017 Dec; 17(1):901. PubMed ID: 29282011
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Promoter polymorphism in the MS4A2 gene and asthma in the Indian population.
    Sharma S; Ghosh B
    Int Arch Allergy Immunol; 2009; 149(3):208-18. PubMed ID: 19218813
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Detection of β-Thalassemia Mutations Using TaqMan Single Nucleotide Polymorphism Genotyping Assays.
    Alwazani WA; Zahid R; Elaimi A; Bajouh O; Hindawi S; Arab B; Damanhouri G; Saka MY; Turki R; Khan JA; Dallol A; Abuzenadah AM
    Genet Test Mol Biomarkers; 2016 Mar; 20(3):154-7. PubMed ID: 26890443
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Major histocompatibility complex class I chain-related gene polymorphisms: associated with susceptibility to Kawasaki disease and coronary artery aneurysms.
    Hsieh YY; Chang CC; Hsu CM; Chen SY; Lin WH; Tsai FJ
    Genet Test Mol Biomarkers; 2011 Nov; 15(11):755-63. PubMed ID: 21815799
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association of NKG2D gene variants with susceptibility and severity of rheumatoid arthritis.
    Mariaselvam CM; Tamouza R; Krishnamoorthy R; Charron D; Misra DP; Jain VK; Negi VS
    Clin Exp Immunol; 2017 Mar; 187(3):369-375. PubMed ID: 27783394
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Association of the polymorphisms 292 C>T and 1304 G>A in the SLC38A4 gene with hyperglycaemia.
    González-Renteria SM; Loera-Castañeda V; Chairez-Hernández I; Sosa-Macias M; Paniagua-Castro N; Lares-Aseff I; Rodríguez-Moran M; Guerrero-Romero F; Galaviz-Hernández C
    Diabetes Metab Res Rev; 2013 Jan; 29(1):39-43. PubMed ID: 22945694
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The genetic variants in 3' untranslated region of voltage-gated sodium channel alpha 1 subunit gene affect the mRNA-microRNA interactions and associate with epilepsy.
    Li T; Kuang Y; Li B
    BMC Genet; 2016 Jul; 17(1):111. PubMed ID: 27473590
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.