Copy number variation of microRNA genes in the human genome
about
Micro spies from the brain to the periphery: new clues from studies on microRNAs in neuropsychiatric disordersInsights on the functional interactions between miRNAs and copy number variations in the aging brainMiRNAs and miRNA Polymorphisms Modify Drug ResponseCNVs-microRNAs interactions demonstrate unique characteristics in the human genome. An interspecies in silico analysisIncreased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sampleDeletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?Enhancer chip: detecting human copy number variations in regulatory elementsMicroevolution of nematode miRNAs reveals diverse modes of selection.miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disability.Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expressionAssessing the impact of copy number variants on miRNA genes in autism by Monte Carlo simulation.Copy number variations in high and low fertility breeding boars.MicroRNA-650 in a copy number-variable region regulates the production of interleukin 6 in human osteosarcoma cells.Copy Number Variants in Alzheimer's Disease.Tumor-suppressive microRNA silenced by tumor-specific DNA hypermethylation in cancer cells.An emerging role for microRNAs in NF1 tumorigenesis.Genomic alterations as mediators of miRNA dysregulation in ovarian cancer.MicroRNA expression and its clinical implications in Ewing's sarcoma.MicroRNA in intervertebral disc degeneration.MiR-23a in amplified 19p13.13 loci targets metallothionein 2A and promotes growth in gastric cancer cells.MicroRNAs as biomarkers for psychiatric disorders with a focus on autism spectrum disorder: Current progress in genetic association studies, expression profiling, and translational research.Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms.Challenges in using circulating miRNAs as cancer biomarkers.Insights into the regulation of human CNV-miRNAs from the view of their target genesAn MLPA-based strategy for discrete CNV genotyping: CNV-miRNAs as an example.Germline copy number variations are associated with breast cancer risk and prognosis.Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.Breast cancer associated germline structural variants harboring small noncoding RNAs impact post-transcriptional gene regulation.Association of Copy Number Variations in Autism Spectrum Disorders: A Systematic Review
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P2860
Copy number variation of microRNA genes in the human genome
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Copy number variation of microRNA genes in the human genome
@ast
Copy number variation of microRNA genes in the human genome
@en
type
label
Copy number variation of microRNA genes in the human genome
@ast
Copy number variation of microRNA genes in the human genome
@en
prefLabel
Copy number variation of microRNA genes in the human genome
@ast
Copy number variation of microRNA genes in the human genome
@en
P2860
P356
P1433
P1476
Copy number variation of microRNA genes in the human genome
@en
P2093
Maciej Szymanski
Wlodzimierz J Krzyzosiak
P2860
P2888
P356
10.1186/1471-2164-12-183
P407
P577
2011-04-12T00:00:00Z
P5875
P6179
1021108912