Keywords: کپی تغییرات شماره; Supernumerary marker chromosomes derived from chromosome 19; Chromosome 19 duplications; Copy number variations; Array-CGH;
مقالات ISI کپی تغییرات شماره (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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: کپی تغییرات شماره; ADHD; attention deficit hyperactivity disorder; ASD; autism spectrum disorders; CGH; comparative genomic hybridization; CHO; carbohydrate attachment; CNV; copy number variations; DGAP; developmental genome anatomy project; FISH; fluorescent in situ hybrid
Keywords: کپی تغییرات شماره; CNVs; copy number variations; ASD; autism spectrum disorder; aCGH; array comparative genomic hybridization; SCQ; social and communication questionnaire; IQ; intelligence quotient; EEG; electroencephalograph; MRI; magnetic resonance imaging; PEP; prolyl en
Keywords: کپی تغییرات شماره; Copy number variations; Gene expression analysis; Multiplex polymerase chain reaction; Gel electrophoresis coupled to inductively coupled plasma mass spectrometry; Reverse transcription-quantitative polymerase chain reaction;
Keywords: کپی تغییرات شماره; AD; Alzheimer's disease; CNVs; Copy number variations; DEGs; Differentially expressed genes; PPPM; Predictive preventive and personalised medicine; PPIs; Protein-protein interactions; SNPs; Single nucleotide polymorphisms; Network science; Alzheimer's d
Keywords: کپی تغییرات شماره; SLE; systemic lupus erythematosus; GWAS; genome-wide association studies; FPRP; false positive report probability; BFDP; Bayesian false discovery probability; OR; odds ratio; CI; confidence interval; SNP; single nucleotide polymorphism; ID; identification
Keywords: کپی تغییرات شماره; NSCLC; non-small cell lung cancer; AD; adenocarcinoma; SCC; squamous cell carcinoma; FLC; familial lung cancer; WGS; whole genome sequencing; PBMCs; peripheral blood mononuclear cells; PCR; polymerase chain reaction; min; minute; sec; second; InDels; smal
Keywords: کپی تغییرات شماره; ADHD; Attention Deficit and Hyperactivity Disorder; ACMG; American College of Medical Genetics; AR; Autosomal Recessive; ASD; Autism Spectrum Disorders; aCGH; array Comparative Genomic Hybridization; BP; BreakPoints; CK1; Casein- Kinase 1; CdLS; Cornelia
Keywords: کپی تغییرات شماره; Comparative genomic hybridisation; copy number variations; melanoma; melanocytic naevi; virtual karyotyping;
Keywords: کپی تغییرات شماره; Epilepsy; Intellectual disability; Copy number variations; SNP-array; Lennox-Gastaut syndrome;
Keywords: کپی تغییرات شماره; corpus callosum; agenesis of corpus callosum; dysgenesis of corpus callosum; CNV; SNP array; chromosomal microarray; CNVs; Copy number variations; DGV; Database of genomic variants; NF1; Neurofibromatosis type 1; SHH; Sonic hedgehog; VOUS; Variants of unk
Keywords: کپی تغییرات شماره; RSA; recurrent spontaneous abortion; CGH; comparative genomic hybridization; CNVs; copy number variations; IL; interleukin; SNP; single nucleotide polymorphism; bp; base pair; GO; gene ontology; HLA; human leukocyte antigen; Th1; T-helper1; Th2; T-helper2
Keywords: کپی تغییرات شماره; chromosome aberrations; comparative genomic hybridization; genome-wide association study; high-throughput nucleotide sequencing; molecular diagnosis; patient care; AVSD; atrioventricular septal defect; CHD; congenital heart disease; CMA; chromosomal micro
Keywords: کپی تغییرات شماره; ATM; ataxia-telangiectasia mutated; BCL2L1; BCL2 like 1; CGH; comparative genomic hybridization; CHK; checkpoint kinase 1; CIN; chromosomal instability; CNVs; copy number variations; DNMT3B; DNA methyltransferase 3B; DPPA3; developmental pluripotency asso
Keywords: کپی تغییرات شماره; CSCC; cervical squamous cell carcinoma; hrHPV; high-risk human papilloma virus; CNVs; copy number variations; CGH-SNP; comparative genomic hybridization-single nucleotide polymorphism; TCGA; The Cancer Genome Atlas; PPI; protein-protein interaction; PARP1
Keywords: کپی تغییرات شماره; copy number variations; human β-defensin; polymorphisms; psoriasis
Keywords: کپی تغییرات شماره; Type 2 diabetes mellitus; Copy number variations; Enrichment; Molecular interaction and network;
Keywords: کپی تغییرات شماره; ACC; agenesis of the corpus callosum; aCGH; array comparative genomic hybridization; ADHD; Attention deficit hyperactivity disorder; ASD; autism spectrum disorders; BCAA; branched-chain amino acids; BCKD; branched-chain α-ketoacid dehydrogenase complex;
Keywords: کپی تغییرات شماره; Radiogenomic modeling; Copy number variations; Normal tissue toxicity; Radiotherapy; Prostate cancer;
Keywords: کپی تغییرات شماره; ALL; acute lymphoblastic leukemia; AML; acute myeloid leukemia; BWA; Burrows Wheeler Alignment tool; CGH; comparative genomic hybridization; CNV; copy number variations; DGV; database of genomic variants; EGA; European Genome-phenome Archive; FISH; fluore
Keywords: کپی تغییرات شماره; Molecular Classification; Genomic Profiling; Outcome; Targeted Therapies; CI; confidence interval; CNV; copy number variations; EGFR; epidermal growth factor receptor; EpCAM; epithelial cellular adhesion molecule; FDR; false discovery rate; FF; fresh-froz
Keywords: کپی تغییرات شماره; Chromosomal aberrations; Cerebral visual impairment; Aneuploidy; Copy number variations; Genetic;
Keywords: کپی تغییرات شماره; Penetrance; Expressivity; Copy number variations; Modifier genes; Epigenetics; Environmental factors; Oligogenic inheritance; Digenic inheritance
Keywords: کپی تغییرات شماره; TRE; transcription factor response element; CNV; copy number variations; GEO; gene expression omnibus; ER stress; endoplasmic reticulum stress; Signaling pathway; Transcription factor; In vitro profiling; Integrative functional genomics; Gastric cancer;
Keywords: کپی تغییرات شماره; Cognition; copy number variations; intelligence; mutations; schizophrenia; ventricles;
Associations of GBP2 gene copy number variations with growth traits and transcriptional expression in Chinese cattle
Keywords: کپی تغییرات شماره; CNVs; Copy number variations; AJ; Angusâ¯Ãâ¯Jiaxian cattle; CDM; Chaidamu cattle; CJ; Charlotteâ¯Ãâ¯Jiaxian; FoSTeS; Fork Stalling and Template Switching; GBP2; guanylate binding protein 2; GWAS; genome-wide association study; JA; Jian cattle; JJ; J
Copy number variation in VEGF gene as a biomarker of susceptibility to age-related macular degeneration
Keywords: کپی تغییرات شماره; Age-related macular degeneration; Copy number variations; VEGF; HTRA1; VLDR genes and Malaysia;
A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome
Keywords: کپی تغییرات شماره; 22q11DS; Copy number variations; Intellectual disabilities;
Genome-wide structural mutations among the lines resulting from genetic instability in peanut (Arachis hypogaea L.)
Keywords: کپی تغییرات شماره; Peanut; Mutants with genome instability; AhMITE1 transpositions; Single nucleotide polymorphisms; Copy number variations;
Copy number variation analysis and methylome profiling of a GNAQ-mutant primary meningeal melanocytic tumor and its liver metastasis
Keywords: کپی تغییرات شماره; Meningeal melanocytic tumor; Meningeal melanoma; Liver metastasis; GNAQ; Copy number variations; Methylation; Ipilimumab;
Clinical characterization of an APP mutation (V717I) in five Han Chinese families with early-onset Alzheimer's disease
Keywords: کپی تغییرات شماره; Early-onset familial Alzheimer's disease; APPV717I mutation; Apolipoprotein E genotype; Phenotype heterogeneity; Copy number variations;
Chromosome instability in tumor resection margins of primary OSCC is a predictor of local recurrence
Keywords: کپی تغییرات شماره; OSCC; oral cavity squamous cell carcinoma; FISH; fluorescence in situ hybridization; CI; chromosomal instable neoplasia; CIS; carcinoma in situ; LOH; loss of heterozygosity; MPTC; Maastricht Pathology Tissue Collection Department; CNV; copy number variati
Chromosomal uniparental disomy 16 and fetal intrauterine growth restriction
Keywords: کپی تغییرات شماره; AC; abdominal circumference; BPD; biparietal diameter; CNVs; copy number variations; CDT1; chromatin licensing and DNA replication factor 1; CMA; chromosome microarray analysis; CMV; cytomegalovirus; DMRs; differentially methylated regions; ET; embryo tra
Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome
Keywords: کپی تغییرات شماره; Marfan syndrome; MLPA; FBN1; Gross deletion; Phenotype; cbEGF; Calcium-binding EGF-like domains; TB; TGFβ binding domains; CNVs; copy number variations; FBN1; fibrillin-1; MFS; Marfan syndrome; MLPA; multiplex ligation-dependent probe amplification; PGM;
Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes
Keywords: کپی تغییرات شماره; CNV; copy number variations; QMPSF; quantitative multiplex PCR assay of short fluorescent fragments; IPSS; International Prognostic Scoring System; Copy number variations; EPO; SEC-61; Cytogenetics and myelodysplastic syndromes;
MLPA-based approach for initial and simultaneous detection of GBA deletions and recombinant alleles in patients affected by Gaucher Disease
Keywords: کپی تغییرات شماره; Gaucher Disease; Multiplex Ligation-dependent Probe Amplification (MLPA); Copy number variations; Gene-pseudogene complex rearrangements; Deletions; GBA gene;
High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families
Keywords: کپی تغییرات شماره; ACRD; autism chromosome rearrangement database; AutDB; autism database; CNVs; copy number variants; DGVs; database of genomic variants; GABA; gamma-aminobutyric acid; qPCR; quantitative real-time PCR; SNPs; single nucleotide polymorphisms; autism; copy nu
CPAS: A trans-omics pathway analysis tool for jointly analyzing DNA copy number variations and mRNA expression profiles data
Keywords: کپی تغییرات شماره; Copy number variations; Gene expression; Pathway analysis; CPAS;
Concurrent copy number variations on chromosome 8 and 22 combined with mutation at FGA locus revealed in a parentage testing case
Keywords: کپی تغییرات شماره; Copy number variations; Paternity testing; Short tandem repeats; Mutation; Tri-allele;
Analysis of copy number variations by SNP50 BeadChip array in Chinese sheep
Keywords: کپی تغییرات شماره; Ovis aries; Sheep; Copy number variations; SNP50 BeadChip array
Contactin-5 expression during development and wiring of the thalamocortical system
Keywords: کپی تغییرات شماره; AD; anterodorsal; ASD; autism spectrum disorder; AV; anteroventral; CNTN; contactin; CNTNAP; contactin-associated protein-like; CNVs; copy number variations; CPu; caudate putamen; LD; laterodorsal; LP; lateral posterior; PBS; phosphate-buffered saline; PF
Enhancing ergosterol production in Pichia pastoris GS115 by overexpressing squalene synthase gene from Glycyrrhiza uralensis
Keywords: کپی تغییرات شماره; Glycyrrhiza uralensis; GuSQS1; Over-expression; Pichia pastoris; Copy number variations
RNA-Seq SSRs and small RNA-Seq SSRs: New approaches in cancer biomarker discovery
Keywords: کپی تغییرات شماره; 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;
Associations of MYH3 gene copy number variations with transcriptional expression and growth traits in Chinese cattle
Keywords: کپی تغییرات شماره; CNVs; copy number variations; SNPs; single nucleotide polymorphisms; MYH3; myosin heavy chain 3; CGH; comparative genomic hybridization; NY; Nanyang cattle; QC; Qinchuan cattle; LX; Luxi cattle; CY; Chinese Caoyuan cattle; MYH1; myosin heavy chain 1; qPCR
Tri-allelic pattern at the TPOX locus: A familial study
Keywords: کپی تغییرات شماره; CNVs; copy number variations; STR; short tandem repeat; TPOX; thyroid peroxidase; FBI; Federal Bureau Investigation; CODIS; Combined DNA Index System; DNA; deoxyribonucleic acid; GTG; G-banded chromosome; pb; base pair; PCR; polymerase chain reaction; X-S
Comprehensive survey of CNVs influencing gene expression in the human brain and its implications for pathophysiology
Keywords: کپی تغییرات شماره; CNVs; copy number variations; LCLs; lymphoblastoid cell lines; CNVRs; copy number variable regions; eCNVRs; expression influencing copy number variable regions; kb; kilo base pairs; Mb; mega base pairs; fdr; false discovery rate; Copy number variation (CN
The expression and roles of Nde1 and Ndel1 in the adult mammalian central nervous system
Keywords: کپی تغییرات شماره; BSA; bovine serum albumin; CNV; copy number variations; Disc1; disrupted in schizophrenia 1; FBS; fetal bovine serum; Nde1; nuclear distribution factor E; Ndel1; nuclear distribution protein nudE-like 1; PBS; phosphate-buffered saline; RT-PCR; reverse-tra
Absence of nasal bone and brachydactyly: A probable new familial syndrome
Keywords: کپی تغییرات شماره; OMIM; Online Mendelian Inheritance in Man; CT; Computed Tomography; CGH; Comparative Genomic Hybridization; HOXD13; Homeobox D13; CNVs; Copy Number Variations; FND1; Frontonasal Dysplasia-1; GCM syndrome; Gorlin-Chaudhry-Moss syndrome; Brachydactyly; Nasa
3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination
Keywords: کپی تغییرات شماره; FOXP1; forkhead box P1; FOXP2; forkhead box P2; CNTNAP2; contactin associated protein-like 2; SNP-array; single-nucleotide polymorphism array; CNVs; copy number variations; SNP-arrays; 3p14.1; FOXP1 deletion;
Single nucleotide polymorphism array analysis in men with idiopathic azoospermia or oligoasthenozoospermia syndrome
Keywords: کپی تغییرات شماره; Male factor infertility; copy number variations; SNP array; calcium-activated chloride channels;