Detalhe da pesquisa
1.
Strong and weak cross-inheritance of substance use disorders in a nationally representative sample.
Mol Psychiatry
; 27(3): 1742-1753, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34759357
2.
Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitus.
Hum Genomics
; 6: 20, 2012 Sep 25.
Artigo
Inglês
| MEDLINE | ID: mdl-23157875
3.
Thymidylate synthase and methionine synthase polymorphisms are not associated with susceptibility to childhood acute lymphoblastic leukemia in Kurdish population from Western Iran.
Mol Biol Rep
; 39(3): 2195-200, 2012 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21643952
4.
Thrombophilic mutations and susceptibility to preeclampsia in Western Iran.
J Thromb Thrombolysis
; 33(1): 109-15, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22068545
5.
Concomitant presence of endothelial nitric oxide 894T and angiotensin II-converting enzyme D alleles are associated with diabetic nephropathy in a Kurdish population from Western Iran.
Nephrology (Carlton)
; 17(2): 175-81, 2012 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-22026967
6.
Plasma lipids and lipoproteins in children and young adults with major ß-thalassemia from western Iran: influence of genotype.
Mol Biol Rep
; 38(4): 2573-8, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21086180
7.
Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques.
Mol Biol Rep
; 37(1): 149-54, 2010 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-19437135
8.
Haplotype analysis of beta thalassemia patients in Western Iran.
Blood Cells Mol Dis
; 42(2): 140-3, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-19141369
9.
LRRK2 gene G2019S mutation and SNPs [haplotypes] in subtypes of Parkinson's disease.
Parkinsonism Relat Disord
; 15(3): 175-80, 2009 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18752982
10.
Depressive-like behavior and high alcohol drinking co-occur in the FH/WJD rat but appear to be under independent genetic control.
Neurosci Biobehav Rev
; 31(1): 103-14, 2007.
Artigo
Inglês
| MEDLINE | ID: mdl-16982094
11.
Further genetic characterization of the fawn-hooded (FH/Wjd) rat, an animal model of comorbid depression and alcoholism.
Psychiatr Genet
; 17(2): 77-83, 2007 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-17413446
12.
Analysis of alcohol-related phenotypes in F2 progeny derived from FH/Wjd and ACI/N rat strains reveals independent measures and sex differences.
Behav Brain Res
; 177(1): 37-44, 2007 Feb 12.
Artigo
Inglês
| MEDLINE | ID: mdl-17161877
13.
Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
Arch Neurol
; 63(6): 826-32, 2006 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-16769863
14.
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.
JAMA
; 296(6): 661-70, 2006 Aug 09.
Artigo
Inglês
| MEDLINE | ID: mdl-16896109
15.
Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.
Parkinsonism Relat Disord
; 11(6): 341-7, 2005 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-16019250
16.
The Fawn-Hooded (FH/Wjd) rat: a genetic animal model of comorbid depression and alcoholism.
Psychiatr Genet
; 12(1): 1-16, 2002 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-11901354
17.
Association of a variation in the promoter region of the brain-derived neurotrophic factor gene with familial Parkinson's disease.
Parkinsonism Relat Disord
; 10(4): 213-9, 2004 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-15120095
18.
Preeclampsia and angiotensin converting enzyme (ACE) I/D and angiotensin II type-1 receptor (AT1R) A1166C polymorphisms: association with ACE I/D polymorphism.
J Renin Angiotensin Aldosterone Syst
; 14(2): 174-80, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-22719026
19.
MTHFR C677T and eNOS G894T variants in preeclamptic women: Contribution to lipid peroxidation and oxidative stress.
Clin Biochem
; 46(1-2): 143-7, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23103710
20.
Butyrylcholinesterase (BChE) activity is associated with the risk of preeclampsia: influence on lipid and lipoprotein metabolism and oxidative stress.
J Matern Fetal Neonatal Med
; 26(16): 1590-4, 2013 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-23650977