Keywords: بیماری پیچیده; Natural products; Complex disease; Hybrid; Multi-targeted;
مقالات ISI بیماری پیچیده (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: بیماری پیچیده; complex disease; genetic diagnosis; phenotypic characterization; ACY1; Aminoacylase 1; JHF; Juvenile hyaline fibromatosis; PROVEAN; Protein Variation Effect Analyzer; SMALED2; Spinal muscular atrophy, lower extremity-predominant type 2; SNP; Single-nucleo
Keywords: بیماری پیچیده; USA; Gene-environment interactions; Molecularization; Environment; Genomics; Complex disease; Health inequalities;
Keywords: بیماری پیچیده; Inflammatory Bowel Disease; Pedigree; Complex Disease; Population IsolateAJ, Ashkenazi Jewish; AJex, Broad Institute AJ Crohn’s disease and control exome replication data set; CD, Crohn’s disease; FiDR, first-degree relative; GM-CSF, granulocyte-macrophag
Keywords: بیماری پیچیده; MS; Multiple Sclerosis; QTLs; quantitative trait loci; EAE; experimental autoimmune encephalomyelitis; IGN; imprinted gene networks; T1D; Type 1 Diabetes; RA; Rheumatoid Arthritis; SLE; Systemic Lupus Erythematosus; HLA; Human Leukocyte Antigen; GWAS; gen
Keywords: بیماری پیچیده; Periodontitis; Etiology; Complex disease; Multi-causality; Genetics; Candidate gene; GWAS;
Keywords: بیماری پیچیده; Genome; Genetic variation; Complex disease; Disease etiology; Functional analysis
Keywords: بیماری پیچیده; Complex disease; Pathway-based analysis; Algorithms; Software and databases
Keywords: بیماری پیچیده; ACE; angiotensin I converting enzyme; AGT; angiotensinogen; APOE; apolipoprotein E; APP; amyloid beta (A4) precursor protein; AR; androgen receptor; CADASIL; cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy; CST
Keywords: بیماری پیچیده; Biomarker discovery; Probabilistic modeling; Network analysis; Microarrays; RNA-Seq; Genomics; Breast cancer; Complex disease; Robust; Signaling and regulatory network
Genetic determinants of cholangiopathies: Molecular and systems genetics
Keywords: بیماری پیچیده; AP; alkaline phosphatase; ASBT; apical sodium bile acid transporter; BRIC; benign recurrent intrahepatic cholestasis; CC; collaborative cross; DILI; drug-induced liver injury; É£-GT; É£-glutamyl transpeptidase; GRP; genetic reference populations; GWAS; ge
Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis
Keywords: بیماری پیچیده; Vitamin D; Vitamin D binding protein; Juvenile idiopathic arthritis; Autoimmune disease; Epistasis; Complex disease
eQTL networks unveil enriched mRNA master integrators downstream of complex disease-associated SNPs
Keywords: بیماری پیچیده; Translational bioinformatics; Centrality; Complex diseases; eQTL; Single Nucleotide Polymorphism (SNP); Master integrator; Computational genomics; Genomics; Transcriptome; mRNA; Network biology; Big data; Computational biology; Computational medicine; Com
The variation game: Cracking complex genetic disorders with NGS and omics data
Keywords: بیماری پیچیده; Complex disease; NGS; Next generation sequencing; Omics; Interactome; Variation; SNV; SNP; CNV; Alternative splicing
Functional polymorphisms in Nrf2: implications for human disease
Keywords: بیماری پیچیده; AAO; age at onset; ALI; acute lung injury; AMD; age-related macular degeneration; ARE; antioxidant response element; BPD; bronchopulmonary dysplasia; β-TrCP; β-transducin repeats-containing proteins; CCA; cholangiocarcinoma; Cns; non-synonymous coding;
How next-generation sequencing is transforming complex disease genetics
Keywords: بیماری پیچیده; next-generation sequencing; complex disease; GWAS; functional genomics
Cochleovestibular Dysfunction in Patients With Diabetes Mellitus, Hypertension, and Dyslipidemia
Keywords: بیماری پیچیده; Prevention; Vertigo; Hearing loss; Complex disease; Multifactorial inheritancePrevención; Vértigo; Hipoacusia; Enfermedades crónicas de herencia compleja o poligénicas
Disfuncion cócleo-vestibular en pacientes con diabetes mellitus, hipertensión arterial sistémica y dislipidemia
Keywords: بیماری پیچیده; Prevención; Vértigo; Hipoacusia; Enfermedades crónicas de herencia compleja o poligénicasPrevention; Vertigo; Hearing loss; Complex disease; Multifactorial inheritance
Next-generation sequencing approaches for genetic mapping of complex diseases
Keywords: بیماری پیچیده; Next-generation sequencing; Complex disease; Genomics
Gene set analysis of genome-wide association studies: Methodological issues and perspectives
Keywords: بیماری پیچیده; Genome-wide association study; Gene set; Pathway; Gene-set enrichment analysis; Statistical significance; Complex disease
Differential expression pattern-based prioritization of candidate genes through integrating disease-specific expression data
Keywords: بیماری پیچیده; Prioritization; Differential expression pattern; Complex disease; Integration
Introduction to genetic epidemiology
Keywords: بیماری پیچیده; Genetics; Epidemiology; Mendelian disease; Complex disease; Linkage studies; Association studies; Age-related macular degeneration
Disease-driven detection of differential inherited SNP modules from SNP network
Keywords: بیماری پیچیده; SNPs; single-nucleotide polymorphisms; IBD; Identity by Descent; ER; excess retention; KEGG; Kyoto Encyclopedia of Genes and Genomes; KPD; Kofendrerd personality disorder; Complex disease; IBD profile; Risk SNP module; SNP adjacent network; Synergetic eff
Genetics of Restless Legs Syndrome: Mendelian, Complex, and Everything in Between
Keywords: بیماری پیچیده; Restless legs syndrome; Genetics; Complex disease; Linkage study; Genetic association study;
Update on the genetics and genomics of PBC
Keywords: بیماری پیچیده; Autoimmunity; Complex disease; Genomics; Genetics; PBC
Genome-Wide Association Studies in Nephrology Research
Keywords: بیماری پیچیده; Genome-wide association study; kidney; chronic kidney disease (CKD); glomerular filtration rate; complex disease; single-nucleotide polymorphism; diabetic nephropathy;
Genetic dissection of type 2 diabetes
Keywords: بیماری پیچیده; Genetics; Complex disease; Monogenic; Polygenic; Linkage study; Genome wide scan; Association study; Single nucleotide polymorphism; Epigenetic; Type 2 diabetes; Obesity
Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins
Keywords: بیماری پیچیده; Deafness; Mitochondrial; RNA modification; Ribosome; Phenotype; Systems biology; Complex disease
Spontaneous preterm birth in African Americans is associated with infection and inflammatory response gene variants
Keywords: بیماری پیچیده; complex disease; genetic epidemiology; infection/inflammation; reproductive genetics;
Mitochondrial DNA variant A4917G, smoking and spontaneous preterm birth
Keywords: بیماری پیچیده; Preterm birth; Smoking; Oxidative stress; mtDNA variation; Complex disease
Genome-wide SNP typing reveals signatures of population history
Keywords: بیماری پیچیده; Single-nucleotide polymorphism; Human populations; Complex disease
GABRB2 Association with Schizophrenia: Commonalities and Differences Between Ethnic Groups and Clinical Subtypes
Keywords: بیماری پیچیده; Complex disease; haplotype; population association; psychiatric disorder; SNP
Random allergen-specific IgE expression in atopic families: Evidence for inherited 'stochastic bias' in adverse immune response development to non-infectious antigens
Keywords: بیماری پیچیده; Allergen; Atopy; IgE; Complex disease; SPT;
An epidemiological study of familial neurocysticercosis in an endemic Mexican community
Keywords: بیماری پیچیده; Neurocysticercosis; Taenia solium; Complex disease; Genetic epidemiology; Mexico
Amyotrophic lateral sclerosis as a complex genetic disease
Keywords: بیماری پیچیده; Complex disease; Complex genetic; Amyotrophic lateral sclerosis; Sporadic; Association study; Gene; Genetic
An autosomal genomic screen for dementia in an extended Amish family
Keywords: بیماری پیچیده; Alzheimer disease; Genome screen; Linkage analysis; Complex disease; Isolated population;
Three autism candidate genes: a synthesis of human genetic analysis with other disciplines
Keywords: بیماری پیچیده; Autism; Genetics; Complex disease; Linkage Analysis; Linkage disequilibrium;