Association of MMP-9 gene polymorphisms with Behçet's disease risk
Keywords: پلیمورفیسم تک نوکلئوتیدی; Behçet's disease; Matrix metalloproteinases-9; Single nucleotide polymorphism
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Identifying the similarities and differences between single nucleotide polymorphism array (SNPa) analysis and karyotyping in acute myeloid leukemia and myelodysplastic syndromes
Keywords: پلیمورفیسم تک نوکلئوتیدی; Acute myeloid leukemia; Myelodysplastic syndromes; Loss of heterozygosity; Single nucleotide polymorphism; Karyotype
Mode of dendritic cell activation: The decisive hand in Th2/Th17 cell differentiation. Implications in asthma severity?
Keywords: پلیمورفیسم تک نوکلئوتیدی; Asthma; Dendritic cells; T helper 2 cells; T helper 17 cells; Eosinophils; Neutrophils; Ag; antigen; AHR; airway hyper responsiveness; APC; antigen presenting cell; ATS; American Thoracic Society; BAL; bronchoalveolar lavage; Bcl-6; B-cell lymphoma; C; co
Cloning of porcine GPIHBP1 gene and its tissue expression pattern and genetic effect on adipose traits
Keywords: پلیمورفیسم تک نوکلئوتیدی; ACTB; β-actin; BFT; back fat thickness; Ï2; chi-square; GPIHBP1; glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1; HWE; Hardy-Weinberg equilibrium; IMF; intramuscular fat; LPL; lipoprotein lipase; Ly6; lymphocyte antige
Genome-wide SNP discovery and identification of QTL associated with agronomic traits in oil palm using genotyping-by-sequencing (GBS)
Keywords: پلیمورفیسم تک نوکلئوتیدی; SNP; single nucleotide polymorphism; GBS; genotyping-by-sequencing; QTL; quantitative trait loci; Single nucleotide polymorphisms; Oil palm; Genetic linkage mapping; Quantitative trait loci; Genotyping-by-sequencing;
A common variant near BDNF is associated with dietary calcium intake in adolescents
Keywords: پلیمورفیسم تک نوکلئوتیدی; Adolescence; Obesity; Dietary intake; Single nucleotide polymorphism; FTO; BDNF; BDNF; brain-derived neurotrophic factor; BMI; body mass index; FTO; fat mass and obesity associated; GWAS; genomewide association study; KCTD15; potassium channel tetrameriza
CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies
Keywords: پلیمورفیسم تک نوکلئوتیدی; Asthma; exacerbation; genome-wide association study; expression quantitative trait locus; CTNNA3; SEMA3D; biobank; childhood asthma; ABRIDGE; Asthma BioRepository for Integrative Genomic Exploration; ASM; Airway smooth muscle; BioVU; Biobank of Vanderbilt
A haplotype of the norepinephrine transporter gene (SLC6A2) is associated with visual memory in attention-deficit/hyperactivity disorder
Keywords: پلیمورفیسم تک نوکلئوتیدی; ADHD; attention-deficit/hyperactivity disorder; CANTAB; Cambridge Neuropsychological Test Automated Battery; HB; haplotype block; LD; linkage disequilibrium; SLC6A2; norepinephrine transporter gene; SNP; single nucleotide polymorphism; Attention-deficit/h
Research ArticleHepatic steatosis in Wilson disease - Role of copper and PNPLA3 mutations
Keywords: پلیمورفیسم تک نوکلئوتیدی; NAFLD; non-alcoholic fatty liver disease; NAS; NAFLD-activity score; NASH; non-alcoholic steatohepatitis; PNPLA3; patatin-like phospholipase domain-containing protein 3; SNP; single nucleotide polymorphism; WD; Wilson disease; Wilson disease; PNPLA3; Stea
Genome analysis of rice-blast fungus Magnaporthe oryzae field isolates from southern India
Keywords: پلیمورفیسم تک نوکلئوتیدی; Genome comparison; Next generation sequencing; Magnaporthe; Single nucleotide polymorphism; Isolate specific genes
Five functional polymorphisms of B7/CD28 co-signaling molecules alter susceptibility to colorectal cancer
Keywords: پلیمورفیسم تک نوکلئوتیدی; Co-signaling molecules; Single nucleotide polymorphism; microRNA; Colorectal cancer
Common type 2 diabetes risk variant in MTNR1B worsens the deleterious effect of melatonin on glucose tolerance in humans
Keywords: پلیمورفیسم تک نوکلئوتیدی; AUC; area under the curve; CIR; corrected insulin response; C120; concentration 120Â min after the start of the OGTT; DI; disposition index; GWAS; genome-wide-association studies; ISI; Insulin Sensitivity Index; MAF; minor allele frequency; MT2; melatonin
Toll-like receptor 1 variations influence susceptibility and immune response to Mycobacterium tuberculosis
Keywords: پلیمورفیسم تک نوکلئوتیدی; Toll-like receptor 1; Mycobacterium tuberculosis; Single nucleotide polymorphism; India; Modeling; Functional analysisBCG, bacterium Calmette-Guérin; CI, Confidence interval; DNA, Deoxyribonucleic acid; ELISA, Enzyme-linked immunosorbent assay; HEK, Human
Increased mesolimbic cue-reactivity in carriers of the mu-opioid-receptor gene OPRM1 A118G polymorphism predicts drinking outcome: A functional imaging study in alcohol dependent subjects
Keywords: پلیمورفیسم تک نوکلئوتیدی; OPRM1; Single nucleotide polymorphism; Endogenous opioids; Alcoholism; Relapse; fMRI;
Single nucleotide polymorphisms of the NF-κB and STAT3 signaling pathway genes predict lung cancer prognosis in a Chinese Han population
Keywords: پلیمورفیسم تک نوکلئوتیدی; Single nucleotide polymorphism; lung cancer; prognosis; NF-κB; STAT3
The inducible E3 ubiquitin ligases SIAH1 and SIAH2 perform critical roles in breast and prostate cancers
Keywords: پلیمورفیسم تک نوکلئوتیدی; Cytokine; Estrogen; Sex hormone; SIAH1; SIAH2; ACK1/TNK2; activated CDC42-associated kinase 1; AR; androgen receptor; ATM; ataxia telangiectasia mutated; ATR; ataxia telangiectasia mutated related; BF; biochemical failure; DCC; deleted in colorectal cance
Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin
Keywords: پلیمورفیسم تک نوکلئوتیدی; Atopy; skin barrier; atopic dermatitis; desmosome; desmoplakin; atopic sensitization; eosinophilic esophagitis; aCGH; Array comparative genome hybridization; AD; Atopic dermatitis; DSG1; Desmoglein 1 gene; DSP; Desmoplakin gene; PPK; Palmoplantar keratode
Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos
Keywords: پلیمورفیسم تک نوکلئوتیدی; IgE; genome-wide association study; admixture mapping; allergy; asthma; next-generation sequencing; Latinos; Hispanics; minority populations; eQTL; Expression quantitative trait locus; GALA I; Genetics of Asthma in Latino Americans; GALA II; Genes-environ
Variant of BCL3 gene is strongly associated with five-year survival of non-small-cell lung cancer patients
Keywords: پلیمورفیسم تک نوکلئوتیدی; BCL3; B-cell CLL/lymphoma 3; NSCLC; non-small-cell lung cancer; RelA; v-rel avian reticuloendotheliosis viral oncogene homolog A; RelB; v-rel avian reticuloendotheliosis viral oncogene homolog B; c-Rel; v-rel avian reticuloendotheliosis viral oncogene hom
Research ArticleGenome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
Keywords: پلیمورفیسم تک نوکلئوتیدی; HH; hereditary hemochromatosis; GWAS; genome-wide association study; SNP; single nucleotide polymorphism; HAS; Haute Autorité de santé; HFE-hemochromatosis; GWAS; Transferrin;
CYP3A5 and ABCB1 Polymorphisms as Predictors for Sunitinib Outcome in Metastatic Renal Cell Carcinoma
Keywords: پلیمورفیسم تک نوکلئوتیدی; Sunitinib; Pharmacogenetics; Metastatic renal cell carcinoma; Single nucleotide polymorphism; Biomarker; Association analysis;
Aggregate Effects of Intraocular Pressure and Cup-to-Disc Ratio Genetic Variants on Glaucoma in a Multiethnic Asian Population
Keywords: پلیمورفیسم تک نوکلئوتیدی; AUC; area under the curve; CI; confidence interval; GRS; genetic risk score; IGGC; International Glaucoma Genetics Consortium; IOP; intraocular pressure; ISGEO; International Society of Geographical and Epidemiological Ophthalmology; OR; odds ratio; PACG;
Common Sequence Variation in the VEGFC Gene Is Associated with Diabetic Retinopathy and Diabetic Macular Edema
Keywords: پلیمورفیسم تک نوکلئوتیدی; CI; confidence interval; DM; diabetes mellitus; DME; diabetic macular edema; DR; diabetic retinopathy; HbA1c; hemoglobin A1c; HREC; Human Research Ethics Committees; NPDR; nonproliferative diabetic retinopathy; OR; odds ratio; PDR; proliferative diabetic
Association of specific language impairment candidate genes CMIP and ATP2C2 with developmental dyslexia in Chinese population
Keywords: پلیمورفیسم تک نوکلئوتیدی; Developmental dyslexia; Specific language impairment; CMIP; ATP2C2; Single nucleotide polymorphism;
Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group
Keywords: پلیمورفیسم تک نوکلئوتیدی; CM; cardiomyopathy; DCM; dilated cardiomyopathy; HCM; hypertrophic cardiomyopathy; NGS; next-generation sequencing; indels; insertion and/or deletion; SNP; single nucleotide polymorphism; MNP; multiple nucleotide polymorphism; Mutations; SNP; Cardiomyopat
Allelic variations in the CYBA gene of NADPH oxidase and risk of kidney complications in patients with type 1 diabetes
Keywords: پلیمورفیسم تک نوکلئوتیدی; ACE; angiotensin converting enzyme; ANCOVA; analysis of covariance; ANOVA; analysis of variance; AOPP; advanced oxidation protein products; CI; confidence intervals; eGFR; estimated glomerular filtration rate; ESRD; end-stage renal disease; GENEDIAB; Gén
Joint Associations of Diet, Lifestyle, and Genes with Age-Related Macular Degeneration
Keywords: پلیمورفیسم تک نوکلئوتیدی; AMD; age-related macular degeneration; AREDS; Age-Related Eye Disease Study; ARMS2; age-related maculopathy susceptibility locus 2; CAREDS; Carotenoids in Age-Related Eye Disease Study; CFH; complement factor H; CFI; complement factor I; CI; confidence in
Functional importance of a peripheral pocket in mammalian cytochrome P450 2B enzymes
Keywords: پلیمورفیسم تک نوکلئوتیدی; Cytochrome P450; Structure-function relationship; Site-directed mutagenesis; Monooxygenase coupling; CYP; cytochrome P450; ITC; isothermal titration calorimetry; H/D; hydrogen deuterium; DXMS; H/D exchange coupled to mass spectrometry; SNP; single nucle
Patatin-like phospholipase domain containing-3 gene (PNPLA3) I148M polymorphism and liver damage in chronic hepatitis C Egyptian patients
Keywords: پلیمورفیسم تک نوکلئوتیدی; Chronic hepatitis C infection; Steatosis; Liver fibrosis; Genetics; Single nucleotide polymorphism; Patatin-like phospholipase domain-containing protein 3 (PNPLA3)
Identification of a Serum amyloid A gene and the association of SNPs with Vibrio-resistance and growth traits in the clam Meretrix meretrix
Keywords: پلیمورفیسم تک نوکلئوتیدی; Meretrix meretrix; Serum amyloid A; Single nucleotide polymorphism; Vibrio-resistance; Growth trait
SNPs in APOBEC3 cytosine deaminases and their association with Visna/Maedi disease progression
Keywords: پلیمورفیسم تک نوکلئوتیدی; APOBEC3 genes; Single nucleotide polymorphism; Visna/Maedi; MicroRNA target sites; Association analysis
La modulación de la expresión de IL-10 por el polimorfismo IL-10-592C/A (rs1800872) es independiente de la presencia y carga bacteriana de los periodontopatógenos clásicos
Keywords: پلیمورفیسم تک نوکلئوتیدی; Periodontitis crónica; Polimorfismo de nucleótido simple; Interleucina 10; Interacción hospedero patógeno; InfectogenómicaChronic periodontitis; Single nucleotide polymorphism; Interleukin-10, Host pathogen interaction, Infectogenomics
The expression of CD39 on regulatory T cells is genetically driven and further upregulated at sites of inflammation
Keywords: پلیمورفیسم تک نوکلئوتیدی; Regulatory T cells; CD39; IFN-γ; IL-17; Suppression; Single nucleotide polymorphism
Chronic Central Serous Chorioretinopathy Is Associated with Genetic Variants Implicated in Age-Related Macular Degeneration
Keywords: پلیمورفیسم تک نوکلئوتیدی; AMD; age-related macular degeneration; AP; alternative complement pathway; CFH; complement factor H; cCSC; chronic central serous chorioretinopathy; CSC; central serous chorioretinopathy; EUGENDA; European Genetic Database; FA; fluorescein angiography; IC
Novel SNPs in the Ankyrin 1 gene and their association with beef quality traits
Keywords: پلیمورفیسم تک نوکلئوتیدی; ANK1; Ankyrin 1 gene; SNP; Single nucleotide polymorphism; LTL; Longissimus thoracis et lumborum muscle; SM; M. semimembranosus muscle; Cattle; Meat; Polymorphism; Tenderness; Colour;
Aryl hydrocarbon receptor SNP -130 C/T associates with dioxins susceptibility through regulating its receptor activity and downstream effectors including interleukin 24
Keywords: پلیمورفیسم تک نوکلئوتیدی; Aryl hydrocarbon receptor; Single nucleotide polymorphism; Genetic susceptibility; Dioxins; Interleukin 24; Yusho;
Modulation of C-reactive protein and plasma omega-6 fatty acid levels by phospholipase A2 gene polymorphisms following a 6-week supplementation with fish oil
Keywords: پلیمورفیسم تک نوکلئوتیدی; (EPA); eicosapentaenoic acid; (DHA); docosahexaenoic acid; (AA); arachidonic acid; (CRP); C-reactive protein; (PLA2); phospholipase A2; (SNP); single nucleotide polymorphism; (Î total n-6 FAs); changes in total n-6 FAs; (Î CRP); changes in plasma CRP le
Linkage and association analysis of obesity traits reveals novel loci and interactions with dietary n-3 fatty acids in an Alaska Native (Yup'ik) population
Keywords: پلیمورفیسم تک نوکلئوتیدی; BMI; body mass index; GWAS; genome-wide association study; n-3 PUFA; omega-3 polyunsaturated fatty acids; CANHR; Center for Alaska Native Health Research; HDL; high density lipoprotein; LDL; low density lipoprotein; VLDL; very low density lipoprotein; δ1
Mouse model of OPRM1 (A118G) polymorphism has altered hippocampal function
Keywords: پلیمورفیسم تک نوکلئوتیدی; Mu-opioid receptor; Single nucleotide polymorphism; OPRM1; A112G; A118G; N40D; Mice; Sex; Genotype; Hippocampus;
Implication of HLA-G 5â² upstream regulatory region polymorphisms in idiopathic recurrent spontaneous abortions
Keywords: پلیمورفیسم تک نوکلئوتیدی; 5â² upstream regulatory region; HLA-G; idiopathic recurrent miscarriages; pregnancy outcome; single nucleotide polymorphism;
MMP20 and ARMS2/HTRA1 Are Associated with Neovascular Lesion Size in Age-Related Macular Degeneration
Keywords: پلیمورفیسم تک نوکلئوتیدی; AMD; age-related macular degeneration; cDNA; complementary DNA; CNV; choroidal neovascularization; GLD; greatest linear dimension; GWAS; genome-wide association study; LD; linkage disequilibrium; MMP; matrix metalloprotease; PCV; polypoidal choroidal vasc
RNA-Seq SSRs and small RNA-Seq SSRs: New approaches in cancer biomarker discovery
Keywords: پلیمورفیسم تک نوکلئوتیدی; BPC; Benign pancreatic cancer; CNVs; Copy number variations; DE; Differentially expressed; ESTs; Expressed sequence tags; ncRNAs; Non-coding RNAs; NGS; Next generation sequencing; PBMCs; Peripheral blood mononuclear cells; PC; Pancreatic cancer; RNA-seq;
Identification of Canadian wheat varieties using OpenArray genotyping technology
Keywords: پلیمورفیسم تک نوکلئوتیدی; Wheat; Single nucleotide polymorphism; Variety identification; Cultivar identification; CPSR; Canada Prairie Spring Red; CWGP; Canada Western General Purpose; CWRS; Canada Western Red Spring; CWRW; Canada Western Red Winter; KVD; kernel visual distinguish
Human FABP1 T94A variant enhances cholesterol uptake
Keywords: پلیمورفیسم تک نوکلئوتیدی; C/EBPα; CCAAT/enhancer binding protein alpha; CETP; cholesteryl ester transfer protein; CPT1A; carnitine palmitoyl transferase IA, liver; CPT2; carnitine palmitoyl-CoA transferase II; CVD; cardiovascular disease; FABP1; human liver fatty acid binding pro
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism: Epidemiology, metabolism and the associated diseases
Keywords: پلیمورفیسم تک نوکلئوتیدی; C677T polymorphism; Folic acid; Methylenetetrahydrofolate reductase (MTHFR) gene; Diseases; Single nucleotide polymorphism; Vitamin B12
Can survival of European flat oysters following experimental infection with Bonamia ostreae be predicted using QTLs?
Keywords: پلیمورفیسم تک نوکلئوتیدی; Ostrea edulis; Single Nucleotide Polymorphism; Disease resistance; Genetic and QTL mapping; Candidate genes;
Structure-function relationships in human d-amino acid oxidase variants corresponding to known SNPs
Keywords: پلیمورفیسم تک نوکلئوتیدی; ALS; amyotrophic lateral sclerosis; CBIO; 6-chloro-benzo(d)isoxazol-3-ol; CD; circular dichroism; CNS; central nervous system; CPZ; chlorpromazine; DAAO; d-amino acid oxidase (EC 1.4.3.3); EYFP; enhanced yellow fluorescent protein; hDAAO; human d-amino ac
CT Scan Findings of Probable Usual Interstitial Pneumonitis Have a High Predictive Value for Histologic Usual Interstitial Pneumonitis
Keywords: پلیمورفیسم تک نوکلئوتیدی; IPF; idiopathic pulmonary fibrosis; SNP; single nucleotide polymorphism; UIP; usual interstitial pneumonitis;
Assessing host-specificity of Escherichia coli using a supervised learning logic-regression-based analysis of single nucleotide polymorphisms in intergenic regions
Keywords: پلیمورفیسم تک نوکلئوتیدی; SNP; single nucleotide polymorphism; PFGE; pulsed field gel electrophoresis; rep-PCR; repetitive sequence-based polymerase chain reaction; AFLP; amplified fragment length polymorphism; MLST; multilocus sequence typing; MSST; multi-spacer sequence typing;
Hydroxymethylation and its potential implication in DNA repair system: A review and future perspectives
Keywords: پلیمورفیسم تک نوکلئوتیدی; C; Cytosine; DNMT; DNA methyl transferase; BER; Base Excision Repair; NER; Nucleotide Excision Repair; TET; Ten Eleven Translocation protein; 5mC; 5methylcytosine; 5hmC; 5-hydroxymethylcytosine; 5fC; 5-formylcytosine; 5caC; 5-carboxylcytosine; ESC; Embryo