about
Systematic pharmacogenomics analysis of a Malay whole genome: proof of concept for personalized medicineProximity of H2A.Z containing nucleosome to the transcription start site influences gene expression levels in the mammalian liver and brainSystematic analysis and functional annotation of variations in the genome of an Indian individualmiR-34 is maternally inherited in Drosophila melanogaster and Danio rerioHigh resolution methylome map of rat indicates role of intragenic DNA methylation in identification of coding regionThe Zebrafish GenomeWiki: a crowdsourcing approach to connect the long tail for zebrafish gene annotationDynamic expression of long non-coding RNAs (lncRNAs) in adult zebrafishHuman 45,X fibroblast transcriptome reveals distinct differentially expressed genes including long noncoding RNAs potentially associated with the pathophysiology of Turner syndrome.Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism.De novo identification of viral pathogens from cell culture hologenomes.Reverse genetics screen in zebrafish identifies a role of miR-142a-3p in vascular development and integrityComparative whole-genome analysis of clinical isolates reveals characteristic architecture of Mycobacterium tuberculosis pangenome.In vivo protein trapping produces a functional expression codex of the vertebrate proteome.Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.A sequence-based variation map of zebrafish.Draft Genome Sequence of a Clinical Isolate of Multidrug-Resistant Mycobacterium tuberculosis East African Indian Strain OSDD271.FishMap: a community resource for zebrafish genomics.Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.Exome sequencing reveals a novel mutation, p.L325H, in the KRT5 gene associated with autosomal dominant Epidermolysis Bullosa Simplex Koebner type in a large family from western IndiaSilencing c-MYC expression by targeting quadruplex in P1 promoter using locked nucleic acid trap.Detection of altered global DNA methylation in coronary artery disease patients.FishMap Zv8 update--a genomic regulatory map of zebrafish.Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Ashok Patowary
@ast
Ashok Patowary
@en
Ashok Patowary
@es
Ashok Patowary
@fr
Ashok Patowary
@nl
Ashok Patowary
@sl
type
label
Ashok Patowary
@ast
Ashok Patowary
@en
Ashok Patowary
@es
Ashok Patowary
@fr
Ashok Patowary
@nl
Ashok Patowary
@sl
prefLabel
Ashok Patowary
@ast
Ashok Patowary
@en
Ashok Patowary
@es
Ashok Patowary
@fr
Ashok Patowary
@nl
Ashok Patowary
@sl
P106
P1153
24465559900
P21
P31
P496
0000-0001-7507-3907
P569
2000-01-01T00:00:00Z