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Journal Abstract Search

242 related items for PubMed ID: 21769819

  • 41. Angiotensin converting enzyme gene polymorphisms and coronary risk in a Portuguese population.
    Mendonça I, Freitas IA, Sousa CA, Gomes S, Faria P, Drumond A, Silva G, Araújo JJ, Freitas S, Ornelas I, Andrade G, Coelho AP, Silva PM, Cardoso A, Brehm AA, dos Reis RP.
    Rev Port Cardiol; 2004 Dec; 23(12):1593-601. PubMed ID: 15732660
    [Abstract] [Full Text] [Related]

  • 42. Tetra primer ARMS-PCR relates folate/homocysteine pathway genes and ACE gene polymorphism with coronary artery disease.
    Masud R, Qureshi IZ.
    Mol Cell Biochem; 2011 Sep; 355(1-2):289-97. PubMed ID: 21567207
    [Abstract] [Full Text] [Related]

  • 43. Angiotensin-I converting enzyme genotype DD is a risk factor for coronary artery disease.
    Beohar N, Damaraju S, Prather A, Yu QT, Raizner A, Kleiman NS, Roberts R, Marian AJ.
    J Investig Med; 1995 Jun; 43(3):275-80. PubMed ID: 7614074
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  • 44. Interaction of MTHFR 1298C with ACE D allele augments the risk of diabetic nephropathy in Western Iran.
    Rahimi Z, Hasanvand A, Felehgari V.
    DNA Cell Biol; 2012 Apr; 31(4):553-9. PubMed ID: 21942443
    [Abstract] [Full Text] [Related]

  • 45. The methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and cancer risk: the Croatian case-control study.
    Reljic A, Simundic AM, Topic E, Nikolac N, Justinic D, Stefanovic M.
    Clin Biochem; 2007 Sep; 40(13-14):981-5. PubMed ID: 17573062
    [Abstract] [Full Text] [Related]

  • 46. Association study of ACE2 (angiotensin I-converting enzyme 2) gene polymorphisms with coronary heart disease and myocardial infarction in a Chinese Han population.
    Yang W, Huang W, Su S, Li B, Zhao W, Chen S, Gu D.
    Clin Sci (Lond); 2006 Nov; 111(5):333-40. PubMed ID: 16822235
    [Abstract] [Full Text] [Related]

  • 47. Methylenetetrahydrofolate reductase polymorphisms and breast cancer risk: a meta-analysis from 41 studies with 16,480 cases and 22,388 controls.
    Qi X, Ma X, Yang X, Fan L, Zhang Y, Zhang F, Chen L, Zhou Y, Jiang J.
    Breast Cancer Res Treat; 2010 Sep; 123(2):499-506. PubMed ID: 20135343
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  • 48. The relationship of ACE and CETP gene polymorphisms with cardiovascular disease in a cohort of Asian Indian patients with and those without type 2 diabetes.
    Ganesan M, Bhaskar S, Mani R, Idris MM, Khaja N, Gulla S, Kumar U, Moova S, Vattam KK, Eppa K, Hasan Q, Pulakurthy UR.
    J Diabetes Complications; 2011 Sep; 25(5):303-8. PubMed ID: 21185205
    [Abstract] [Full Text] [Related]

  • 49. Association between genetic polymorphisms and sites of cervicocerebral artery atherosclerosis.
    Chutinet A, Suwanwela NC, Snabboon T, Chaisinanunkul N, Furie KL, Phanthumchinda K.
    J Stroke Cerebrovasc Dis; 2012 Jul; 21(5):379-85. PubMed ID: 21296594
    [Abstract] [Full Text] [Related]

  • 50. Genetic polymorphisms and the risk of progressive renal failure in elderly Hungarian patients.
    Zsom M, Fülöp T, Zsom L, Baráth A, Maróti Z, Endreffy E.
    Hemodial Int; 2011 Oct; 15(4):501-8. PubMed ID: 22111818
    [Abstract] [Full Text] [Related]

  • 51. Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677-->T transition in the MTHFR gene.
    Zak I, Niemiec P, Sarecka B, Balcerzyk A, Ciemniewski Z, Rudowska E, Dylag S.
    Acta Biochim Pol; 2003 Oct; 50(2):527-34. PubMed ID: 12833177
    [Abstract] [Full Text] [Related]

  • 52. Genetic predisposition for development of nephropathy in type 2 diabetes mellitus.
    Kumar R, Sharma RK, Agarwal S.
    Biochem Genet; 2013 Dec; 51(11-12):865-75. PubMed ID: 23846111
    [Abstract] [Full Text] [Related]

  • 53. Angiotensin converting enzyme insertion/deletion (I/D) (rs4646994) and Vegf polymorphism (+405G/C; rs2010963) in type II diabetic patients: Association with the risk of coronary artery disease.
    Moradzadegan A, Vaisi-Raygani A, Nikzamir A, Rahimi Z.
    J Renin Angiotensin Aldosterone Syst; 2015 Sep; 16(3):672-80. PubMed ID: 24505095
    [Abstract] [Full Text] [Related]

  • 54. Common variants of the ACE gene and aneurysmal subarachnoid hemorrhage in a Danish population: a case-control study.
    Staalsø JM, Nielsen M, Edsen T, Koefoed P, Springborg JB, Moltke FB, Laursen H, Nielsen HB, Olsen NV.
    J Neurosurg Anesthesiol; 2011 Oct; 23(4):304-9. PubMed ID: 21709586
    [Abstract] [Full Text] [Related]

  • 55. Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease.
    Vaisi-Raygani A, Rahimi Z, Tavilani H, Vaisi-Raygani H, Kiani A, Aminian M, Shakiba E, Shakiba Y, Pourmotabbed T.
    Mol Biol Rep; 2012 Mar; 39(3):2723-31. PubMed ID: 21681430
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  • 56. Association of caspases with an increased prostate cancer risk in north Indian population.
    Mittal RD, Mittal T, Singh AK, Mandal RK.
    DNA Cell Biol; 2012 Jan; 31(1):67-73. PubMed ID: 21668377
    [Abstract] [Full Text] [Related]

  • 57. Interactions of lymphotoxin alpha (TNF-beta), angiotensin-converting enzyme (ACE), and endothelin-1 (ET-1) gene polymorphisms in adult periodontitis.
    Hollá LI, Fassmann A, Vasků A, Znojil V, Vanek J, Vácha J.
    J Periodontol; 2001 Jan; 72(1):85-9. PubMed ID: 11210078
    [Abstract] [Full Text] [Related]

  • 58. Association between rs4673 (C/T) and rs13306294 (A/G) haplotypes of NAD(P)H oxidase p22phox gene and severity of stenosis in coronary arteries.
    Najafi M, Alipoor B, Shabani M, Amirfarhangi A, Ghasemi H.
    Gene; 2012 May 10; 499(1):213-7. PubMed ID: 22410402
    [Abstract] [Full Text] [Related]

  • 59. Lack of association between the C677T single nucleotide polymorphism of the MTHFR gene and glaucoma in Iranian patients.
    Nilforoushan N, Aghapour S, Raoofian R, Saee Rad S, Greene WK, Fakhraie G, Heidari M.
    Acta Med Iran; 2012 May 10; 50(3):208-12. PubMed ID: 22418991
    [Abstract] [Full Text] [Related]

  • 60. Prevalence of MTHFR, Factor V, ACE and APOE gene polymorphisms among Muslims of Manipur, India.
    Asghar M, Kabita S, Kalla L, Murry B, Saraswathy KN.
    Ann Hum Biol; 2013 Jan 10; 40(1):83-7. PubMed ID: 23110422
    [Abstract] [Full Text] [Related]

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