Polymorphism of CYP2D6, CYP2C19, CYP2C9 and CYP2C8 in the Faroese population
Halling J, et al.
Eur J Clin Pharmacol 2005 Jul
GNB3 C825T polymorphism and response to interferon-alfa/ribavirin treatment in patients with hepatitis C virus genotype 1 (HCV-1) infection
Sarrazin C, et al.
J Hepatol 2005 Jul
Genetic polymorphisms of eosinophil-derived neurotaxin and eosinophil cationic protein in tropical pulmonary eosinophilia
Kim YJ, et al.
Am J Trop Med Hyg 2005 Jul;73(1):125-30
Polymorphisms in the DNA methyltransferase 3b gene and prostate cancer risk
Singal R, et al.
Oncol Rep 2005 Aug;14(2):569-73
A single nucleotide polymorphism in the extracellular domain of TRAIL receptor DR4 at nucleotide 626 in gastric cancer patients in Japan
Kuraoka K, et al.
Oncol Rep 2005 Aug;14(2):465-70
FGFR4 Gly388Arg polymorphism and prognosis of breast and colorectal cancer
Spinola M, et al.
Oncol Rep 2005 Aug;14(2):415-9
Metabolic gene polymorphisms and lung cancer risk in non-smokers An update of the GSEC study
Raimondi S, et al.
Mutat Res 2005 Jul
G-308A TNF-alpha polymorphism is associated with an increased risk of invasive cervical cancer
Duarte I, et al.
Biochem Biophys Res Commun 2005 Jul
Polymorphism of the p53 tumor suppressor gene is associated with susceptibility to uterine leiomyoma
Denschlag D, et al.
Fertil Steril 2005 Jul;84(1):162-6
Mutations in the tyrosine kinase domain of the EGFR gene associated with gefitinib response in non-small-cell lung cancer
Rosell R, et al.
Lung Cancer 2005 Jul
Mutations in the ATM gene lead to impaired overall and treatment free survival of patients with B-CLL that is independent of IGVH mutation status
Austen B, et al.
Blood 2005 Jul
Mutation screen and association study of EZH2 as a susceptibility gene for aggressive prostate cancer
Bachmann N, et al.
Prostate 2005 Jul
BRAF mutations in colorectal carcinoma suggest two entities of microsatellite-unstable tumors
Lubomierski N, et al.
Cancer 2005 Jul
Genetic polymorphisms of N-acetyltransferase 2 and colorectal cancer risk
He LJ, et al.
World J Gastroenterol 2005 Jul;11(27):4268-71
Glutathione S-transferase M1 gene but not insulin-like growth factor-2 gene or epidermal growth factor gene is associated with prostate cancer()
Lai MT, et al.
Urol Oncol 2005 Jul-2005 Aug;23(4):225-9
Associations between polymorphisms in the steroid 5-alpha reductase type II (SRD5A2) gene and benign prostatic hyperplasia and prostate cancer()
Salam MT , et al.
Urol Oncol 2005 Jul-2005 Aug;23(4):246-53
Allele 2 of the interleukin-1 receptor antagonist gene (IL1RN*2) is associated with a decreased risk of primary lung cancer
Hu Z, et al.
Cancer Lett 2005 Jul
Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk
Park K, et al.
Cancer Lett 2005 Jul
MGMT genotype modulates the associations between cigarette smoking, dietary antioxidants and breast cancer risk
Shen J, et al.
Carcinogenesis 2005 Jul
Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism
Festa F, et al.
Mutat Res 2005 Jul;574(1-2):105-11
The possible role of TP53 mutation status in the treatment of squamous cell carcinomas of the head and neck (HNSCC) with radiotherapy with different overall treatment times
Eriksen JG, et al.
Radiother Oncol 2005 Jul
Polymorphisms associated with asthma are inversely related to glioblastoma multiforme
Schwartzbaum J, et al.
Cancer Res 2005 Jul;65(14):6459-65
Poor Survival Associated with the BRAF V600E Mutation in Microsatellite-Stable Colon Cancers
Samowitz WS, et al.
Cancer Res 2005 Jul;65(14):6063-9
Genotype of inflammatory cytokines in limbal stem cell graft in Italian patients
Lescai F, et al.
Biochem Biophys Res Commun 2005 Jun;332(1):95-100
Tobacco smoking, estrogen receptor {alpha} gene variation, and small low-density lipoprotein level
Shearman AM, et al.
Hum Mol Genet 2005 Jul
Association of endothelial lipase gene (LIPG) haplotypes with high-density lipoprotein cholesterol subfractions and apolipoprotein AI plasma levels in Japanese Americans
Hutter CM, et al.
Atherosclerosis 2005 Jul
A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians
Dastani Z, et al.
Atherosclerosis 2005 Jul
Polymorphism of the AHSG gene is associated with increased adipocyte beta2-adrenoceptor function
Lavebratt C, et al.
J Lipid Res 2005 Jul
Impact of the introduction of a guideline on the targeted detection of hereditary haemochromatosis
Jacobs EM, et al.
Neth J Med 2005 Jun;63(6):205-14
Glutathione-S-transferase M1, Obesity, Statins, and Autonomic Effects of Particles
Schwartz J, et al.
Am J Respir Crit Care Med 2005 Jul
Interleukin-1-beta gene, but not the interleukin-1 receptor antagonist gene, is associated with graves' disease
Chen RH, et al.
J Clin Lab Anal 2005 Jul;19(4):133-8
CTLA4 is differentially associated with autoimmune diseases in the Dutch population
Zhernakova A, et al.
Hum Genet 2005 Jul:1-9
Effect of the APOC3 Sst I SNP on fasting triglyceride levels in men heterozygous for the LPL P207L deficiency
Garenc C, et al.
Eur J Hum Genet 2005 Jul
The effect of HLA class II, insulin and CTLA4 gene regions on the development of humoral beta cell autoimmunity
Hermann R, et al.
Diabetologia 2005 Jul
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes
Meyre D, et al.
Nat Genet 2005 Jul
Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype?
Tessier MC, et al.
J Med Genet 2005 Jul
Introducing Genetic Testing for Adult-Type Hypolactasia
Buning C, et al.
Digestion 2005 Jul;71(4):245-50
Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions
Heijmans BT, et al.
Eur J Hum Genet 2005 Jul
The Serotonin Transporter Length Polymorphism, Neuroticism, and Depression: A Comprehensive Assessment of Association
Willis-Owen SA, et al.
Biol Psychiatry 2005 Jul
A Cluster of Cholesterol-Related Genes Confers Susceptibility for Alzheimer's Disease
Papassotiropoulos A, et al.
J Clin Psychiatry 2005 Jul;66(7):940-7
APOE polymorphism, socioeconomic status and cognitive function in mid-life The Whitehall II longitudinal study
Zhao JH, et al.
Soc Psychiatry Psychiatr Epidemiol 2005 Jul
Interaction between CYP19 Aromatase and Butyrylcholinesterase Genes Increases Alzheimer's Disease Risk
Combarros O, et al.
Dement Geriatr Cogn Disord 2005 Jul;20(2-3):153-7
Are cytokine gene polymorphisms associated with outcome in patients with idiopathic intermediate uveitis in the United Kingdom?
Stanford MR, et al.
Br J Ophthalmol 2005 Aug;89(8):1013-6
Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy
Lenzen KP, et al.
Epilepsy Res 2005 Jul
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes
Bonifati V, et al.
Neurology 2005 Jul;65(1):87-95
Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases
Santangelo SL, et al.
Ophthalmic Genet 2005 Jun;26(2):85-9
Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: A two-stage study
Myllykangas L, et al.
J Neurol Sci 2005 Jul
Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis
Vogler S, et al.
J Mol Med 2005 Jul
Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease
Ide M, et al.
Hum Genet 2005 Jul
The Role of Factor V Leiden and Prothrombin G20210a Mutations in Sudden Sensorineural Hearing Loss
Gorur K, et al.
Otol Neurotol 2005 Jul;26(4):599-601
Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease
Sinha R, et al.
Parkinsonism Relat Disord 2005 Jul
Prothrombin g20210a mutation in Turkish children with thrombosis and the frequency of prothrombin c20209t
Gurgey A, et al.
Pediatr Hematol Oncol 2005 Jun;22(4):309-14
Atherosclerotic risk genotypes and recurrent coronary events after myocardial infarction
Moss AJ, et al.
Am J Cardiol 2005 Jul;96(2):177-82
Clinical Restenosis after Coronary Stent Implantation Is Associated with the Heme Oxygenase-1 Gene Promoter Polymorphism and the Heme Oxygenase-1 +99G/C Variant
Gulesserian T, et al.
Clin Chem 2005 Jul
Factor v leiden mutation in cerebrovascular disease
Buyru N, et al.
Clin Appl Thromb Hemost 2005 Jul;11(3):339-42
Linkage of Ischemic Stroke to the PDE4D Region on 5q in a Swedish Population
Nilsson-Ardnor S, et al.
Stroke 2005 Jul
Plasminogen Activator Inhibitor-1 4G/5G Polymorphism and Risk of Stroke. Replicated Findings in Two Nested Case-Control Studies Based on Independent Cohorts
Wiklund PG, et al.
Stroke 2005 Jul
Candidate genes of cerebral infarction and traditional classification in koreans with cerebral infarction
Um JY, et al.
Int J Neurosci 2005 Jun;115(6):743-56
Influence of Alcohol Dehydrogenase 1C Polymorphism on the Alcohol-Cardiovascular Disease Association (from the Framingham Offspring Study)
Djousse L, et al.
Am J Cardiol 2005 Jul;96(2):227-32
Allelic variation in the serotonin transporter (5HTT) gene contributes to idiopathic pulmonary hypertension in children
Vachharajani A & Saunders S
Biochem Biophys Res Commun 2005 Jul
Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
Peters N, et al.
Arch Neurol 2005 Jul;62(7):1091-4
Association of improved cardiac function in donors with C34T mutation of the amp deaminase 1 gene
Yuen AH, et al.
Nucleosides Nucleotides Nucleic Acids 2005;24(4):275-7
Association between the GNB3 Polymorphism and Blood Pressure in Young Korean Men
Lee J, et al.
Med Sci Sports Exerc 2005 Jul;37(7):1138-43
Association between TNF-alpha -308G>A polymorphism and the development of acute coronary syndromes in Greek subjects: The CARDIO2000-GENE Study
Dedoussis GV, et al.
Genet Med 2005 Jul-2005 Aug;7(6):411-6
ABO/secretor genetic complex is associated with the susceptibility of childhood asthma in Taiwan
Chen YL, et al.
Clin Exp Allergy 2005 Jul;35(7):926-32
Interleukin-10 promoter polymorphisms and atopic asthma in North Indians
Chatterjee R, et al.
Clin Exp Allergy 2005 Jul;35(7):914-9
Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults
Weidinger S, et al.
Clin Exp Allergy 2005 Jul;35(7):866-72
Association of IL-13, RANTES, and leukotriene C4 synthase gene promoter polymorphisms with asthma and/or atopy in African Americans
Moissidis I, et al.
Genet Med 2005 Jul-2005 Aug;7(6):406-10
Consequence of functional Nod2 and Tlr4 mutations on gene transcription in Crohn's disease patients
Braat H, et al.
J Mol Med 2005 Jul
Association of polymorphic alleles of CTLA4 with inflammatory bowel disease in the Japanese
Machida H, et al.
World J Gastroenterol 2005 Jul;11(27):4188-93
Genetic variations in the human gelatinase a (matrix metalloproteinase-2) promoter are not associated with susceptibility to, and severity of, chronic periodontitis
Holla LI, et al.
J Periodontol 2005 Jul;76(7):1056-60
Galactose-1-phosphate uridyl transferase gene mutations in women with premature ovarian failure
Mlinar B, et al.
Fertil Steril 2005 Jul;84(1):253-5
Effects of estrogen-only therapy on LDL oxidation in women with hysterectomy: Does paraoxonase genotype play a role?
Akcay YD, et al.
Maturitas 2005 Jul
Association between allelic variants in cytokine genes and preeclampsia
Haggerty CL, et al.
Am J Obstet Gynecol 2005 Jul;193(1):209-15
Genetic prothrombotic risk factors in women with unexplained pregnancy loss
Sottilotta G, et al.
Thromb Res 2005 Jul
Roles of Methylenetetrahydrofolate Reductase C677T Polymorphism in Repeated Pregnancy Loss
Wiwanitkit V
Clin Appl Thromb Hemost 2005 Jul;11(3):343-5
A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo
Canton I, et al.
Genes Immun 2005 Jul
Is GST Gene Polymorphism a Risk Factor in Developing Exfoliation Syndrome?
Yilmaz A, et al.
Curr Eye Res 2005 Jul;30(7):575-81
HLA-Cw*0602 associates more strongly to psoriasis in the Swedish population than variants of the novel 6p21.3 gene PSORS1C3
Holm SJ, et al.
Acta Derm Venereol 2005;85(1):2-8
Extensive polymorphisms of LILRB1 (ILT2, LIR1) and their association with HLA-DRB1 shared epitope negative rheumatoid arthritis
Kuroki K, et al.
Hum Mol Genet 2005 Jul
Smoking is a risk factor for anti-CCP antibodies only in RA patients that carry HLA-DRB1 Shared Epitope alleles
Linn-Rasker SP, et al.
Ann Rheum Dis 2005 Jul
The influence of IL6, COL1A1 and VDR gene polymorphisms on bone mineral density in Crohn's disease
Todhunter CE, et al.
Gut 2005 Jul
Influence of VEGF gene polymorphisms on the severity of ankylosing spondylitis
Seo JS, et al.
Rheumatology ( Oxford ) 2005 Jul
Genetic Variation of Infant Reduced Folate Carrier (A80G) and Risk of Orofacial Defects and Congenital Heart Defects in China
Pei L, et al.
Ann Epidemiol 2005 Jul
Angiotensin converting enzyme gene, smoking and mortality in a population-based study
Arias-Vasquez A, et al.
Eur J Clin Invest 2005 Jul;35(7):444-9
No evidence for an association between extreme longevity and Microsomal Transfer Protein polymorphisms in a longitudinal study of 1651 nonagenarians
Bathum L, et al.
Eur J Hum Genet 2005 Jul
The CYP2C19 genotype and the use of oral contraceptives influence the pharmacokinetics of carisoprodol in healthy human subjects
Bramness JG, et al.
Eur J Clin Pharmacol 2005 Jul
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