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 *

39 related articles for article (PubMed ID: 20022652)

  • 1. Identification of two novel variants in PRKAG2 gene in Tunisian type 2 diabetic patients with family history of cardiovascular disease.
    Nouira S; Arfa I; Kammoun I; Abid A; Ouragini H; Dorboz I; Ghazouani W; Fadhel SB; Zorgati MM; Ammar SB; Blousa-Chabchoub S; Kachboura S; Abdelhak S
    Diabetes Res Clin Pract; 2010 Feb; 87(2):e7-10. PubMed ID: 20022652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a single nucleotide polymorphism showing no insulin-mediated suppression of the promoter activity in the human insulin receptor substrate 2 gene.
    Iwamoto K; Mori H; Okazawa H; Hashiramoto M; Kasuga M
    Diabetologia; 2002 Aug; 45(8):1182-95. PubMed ID: 12189449
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human calcium/calmodulin-dependent protein kinase II gamma gene (CAMK2G): cloning, genomic structure and detection of variants in subjects with type II diabetes.
    Gloyn AL; Desai M; Clark A; Levy JC; Holman RR; Frayling TM; Hattersley AT; Ashcroft SJ
    Diabetologia; 2002 Apr; 45(4):580-3. PubMed ID: 12032636
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association of calpain-10 polymorphisms with type 2 diabetes in the Tunisian population.
    Kifagi C; Makni K; Mnif F; Boudawara M; Hamza N; Rekik N; Abid M; Rebaï A; Granier C; Jarraya F; Ayadi H
    Diabetes Metab; 2008 Jun; 34(3):273-8. PubMed ID: 18487065
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of seven novel nucleotide variants in the hepatocyte nuclear factor-1alpha (TCF1) promoter region in MODY patients.
    Godart F; Bellanné-Chantelot C; Clauin S; Gragnoli C; Abderrahmani A; Blanché H; Boutin P; Chèvre JC; Froguel P; Bailleul B
    Hum Mutat; 2000; 15(2):173-80. PubMed ID: 10649494
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L; Wang H; Chen J; Jin W; Liu L; Ban B; Shen J; Hua Z; Chai J
    Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene.
    Li W; Detter JC; Weiss HJ; Cramer EM; Zhang Q; Novak EK; Favier R; Kingsmore SF; Swank RT
    Mol Genet Metab; 2000 Dec; 71(4):599-608. PubMed ID: 11136552
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of specific angiotensin-converting enzyme variants and haplotypes that confer risk and protection against type 2 diabetic nephropathy.
    Ezzidi I; Mtiraoui N; Kacem M; Chaieb M; Mahjoub T; Almawi WY
    Diabetes Metab Res Rev; 2009 Nov; 25(8):717-24. PubMed ID: 19787680
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Effect of parental hypertension and/or parental diabetes on hypertension in Taiwanese diabetic patients.
    Tseng CH
    Eur J Clin Invest; 2007 Nov; 37(11):870-7. PubMed ID: 17973782
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association study of the genetic polymorphisms of the transcription factor 7-like 2 (TCF7L2) gene and type 2 diabetes in the Chinese population.
    Chang YC; Chang TJ; Jiang YD; Kuo SS; Lee KC; Chiu KC; Chuang LM
    Diabetes; 2007 Oct; 56(10):2631-7. PubMed ID: 17579206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Leu262Val polymorphism of presenilin associated rhomboid like protein (PARL) is associated with earlier onset of type 2 diabetes and increased urinary microalbumin creatinine ratio in an Irish case-control population.
    Hatunic M; Stapleton M; Hand E; DeLong C; Crowley VE; Nolan JJ
    Diabetes Res Clin Pract; 2009 Mar; 83(3):316-9. PubMed ID: 19185381
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diabetic retinopathy, PAI-1 4G/5G and -844G/A polymorphisms, and changes in circulating PAI-1 levels in Tunisian type 2 diabetes patients.
    Ezzidi I; Mtiraoui N; Chaieb M; Kacem M; Mahjoub T; Almawi WY
    Diabetes Metab; 2009 Jun; 35(3):214-9. PubMed ID: 19419896
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Single Nucleotide Polymorphisms in exon 3 of the adiponectin gene in subjects with type 2 diabetes mellitus.
    Kretowski A; Gugała K; Okruszko A; Wawrusiewicz-Kurylonek N; Górska M
    Rocz Akad Med Bialymst; 2005; 50():148-50. PubMed ID: 16358955
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genomic organization and structure of the 5'-flanking region of the TEX101 gene: alternative promoter usage and splicing generate transcript variants with distinct 5'-untranslated region.
    Tsukamoto H; Takizawa T; Takamori K; Ogawa H; Araki Y
    Mol Reprod Dev; 2007 Feb; 74(2):154-62. PubMed ID: 16941676
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exon/intron boundaries, novel polymorphisms, and association analysis with schizophrenia of the human synaptic vesicle monoamine transporter (SVMT) gene.
    Kunugi H; Ishida S; Akahane A; Nanko S
    Mol Psychiatry; 2001 Jul; 6(4):456-60. PubMed ID: 11443533
    [TBL] [Abstract][Full Text] [Related]  

  • 16. VEGF polymorphisms are associated with severity of diabetic retinopathy.
    Churchill AJ; Carter JG; Ramsden C; Turner SJ; Yeung A; Brenchley PE; Ray DW
    Invest Ophthalmol Vis Sci; 2008 Aug; 49(8):3611-6. PubMed ID: 18441306
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association between the -634C/G polymorphisms of the vascular endothelial growth factor and retinopathy in type 2 diabetes: a meta-analysis.
    Zhao T; Zhao J
    Diabetes Res Clin Pract; 2010 Oct; 90(1):45-53. PubMed ID: 20591524
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variation in the yak dectin-1 gene (CLEC7A).
    Yang G; Zhou H; Hu J; Luo Y; Hickford JG
    DNA Cell Biol; 2011 Dec; 30(12):1069-71. PubMed ID: 21612412
    [TBL] [Abstract][Full Text] [Related]  

  • 19. PPARGC1A variation associated with DNA damage, diabetes, and cardiovascular diseases: the Boston Puerto Rican Health Study.
    Lai CQ; Tucker KL; Parnell LD; Adiconis X; García-Bailo B; Griffith J; Meydani M; Ordovás JM
    Diabetes; 2008 Apr; 57(4):809-16. PubMed ID: 18162502
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel polymorphism in the 5' flanking region of the glucose transporter (GLUT1) gene is strongly associated with diabetic nephropathy in patients with Type 1 diabetes mellitus.
    Hodgkinson AD; Page T; Millward BA; Demaine AG
    J Diabetes Complications; 2005; 19(2):65-9. PubMed ID: 15745834
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 2.