Keywords: تنوع نسخه کپی (CNV); Copy number variation (CNV); Delayed radiation effects; DNA methylation (DNAm) age; Global DNA methylation; Loss of chromosome Y (LOY); Methylation array analysis; Radiation-induced genome instability (RIGI);
مقالات ISI تنوع نسخه کپی (CNV) (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: تنوع نسخه کپی (CNV); Copy number variation (CNV); Detection method; Personal identification; Physical feature;
Keywords: تنوع نسخه کپی (CNV); Bipolar disorder; Genetics; GWAS; Sequencing; Copy number variation (CNV); Family study; Personalized medicine; Pharmacogenetics;
Keywords: تنوع نسخه کپی (CNV); aneuploidy; chromosome disease; copy number variation (CNV); next generation sequencing (NGS); whole genome amplification (WGA);
Keywords: تنوع نسخه کپی (CNV); Copy number variation (CNV); Deafness; GJB2; Homozygosity mapping; Linkage analysis; Missing heritability; Next generation sequencing (NGS); Non-syndromic hearing loss (NSHL); Positional cloning;
Keywords: تنوع نسخه کپی (CNV); Copy number variation (CNV); Attention-deficit and hyperactivity disorder (ADHD); Autism; Schizophrenia;
Short communicationCopy-number variation of housekeeping gene rpl13a in rat strains selected for nervous system excitability
Keywords: تنوع نسخه کپی (CNV); Copy number variation (CNV); Quantitative real-time multicolor multiplex PCR (qmPCR); Nervous system excitability; Hippocampus; Bone marrow; Rat;
Cloning of the promoter of NDE1, a gene implicated in psychiatric and neurodevelopmental disorders through copy number variation
Keywords: تنوع نسخه کپی (CNV); CNV, copy number variation; NDE1, Nuclear Distribution Element 1; NDEL1, NDE-Like 1; UTR, untranslated regionalternate splicing; chromosome 16p13.11 duplication; copy number variation (CNV); Nuclear Distribution Element 1 (NDE1); promoter characterization
MGP-HMM: Detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts
Keywords: تنوع نسخه کپی (CNV); Tandem duplication; Mixture Gaussian density; Hidden Markov Model (HMM); Copy Number Variation (CNV); Next Generation Sequencing (NGS)
Identifying rhesus macaque gene orthologs using heterospecific human CNV probes
Keywords: تنوع نسخه کپی (CNV); Macaca mulatta; Copy number variation (CNV); Homo sapiens; Heterospecific sequence map
ReviewGenetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans
Keywords: تنوع نسخه کپی (CNV); Alzheimer's disease (AD); Mild cognitive impairment (MCI); Genome-wide association studies (GWAS); Next generation sequencing (NGS); Copy number variation (CNV); Biomarkers; Magnetic resonance imaging (MRI); Positron emission tomography (PET); Cerebrospin
Genome-wide copy number variation study reveals KCNIP1 as a modulator of insulin secretion
Keywords: تنوع نسخه کپی (CNV); Copy number variation (CNV); Association study; Type 2 diabetes; KCNIP1; Insulin secretion
Comprehensive survey of CNVs influencing gene expression in the human brain and its implications for pathophysiology
Keywords: تنوع نسخه کپی (CNV); 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
DYZ1 copy number variation, Y chromosome polymorphism and early recurrent spontaneous abortion/early embryo growth arrest
Keywords: تنوع نسخه کپی (CNV); Copy number variation (CNV); DYZ1 region; Y chromosome; Recurrent spontaneous abortion (RSA); Early embryo growth arrest;
Review ArticleAlzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans
Keywords: تنوع نسخه کپی (CNV); Alzheimer's Disease Neuroimaging Initiative (ADNI); Alzheimer's disease; Mild cognitive impairment (MCI); Genome-wide association studies (GWAS); Copy number variation (CNV); Magnetic resonance imaging (MRI); Cerebrospinal fluid (CSF);
Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population
Keywords: تنوع نسخه کپی (CNV); Copy number variation (CNV); Single-nucleotide polymorphism (SNP); Multi-allelic CNV genotype; Whole genome association study; Subarachnoid aneurismal hemorrhage (SAH);