Genomic architecture of sickle cell disease in West African children. - Test2 - elhamkhani - TriplyDB

Genomic architecture of sickle cell disease in West African children.

Genomic architecture of sickle cell disease in West African children.

http://www.wikidata.org/entity/Q37584394

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Role of innate immunity-triggered pathways in the pathogenesis of Sickle Cell Disease: a meta-analysis of gene expression studies Association of circulating transcriptomic profiles with mortality in sickle cell disease.Sickle cell disease: tipping the balance of genomic research to catalyse discoveries in Africa.A common molecular signature of patients with sickle cell disease revealed by microarray meta-analysis and a genome-wide association study

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Genomic architecture of sickle cell disease in West African children.

http://www.wikidata.org/entity/Q37584394

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 14 February 2014

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Genomic architecture of sickle cell disease in West African children.

@en

Genomic architecture of sickle cell disease in West African children.

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type

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Genomic architecture of sickle cell disease in West African children.

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Genomic architecture of sickle cell disease in West African children.

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prefLabel

Genomic architecture of sickle cell disease in West African children.

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Genomic architecture of sickle cell disease in West African children.

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FGENE.2014.00026

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Frontiers in Genetics

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Genomic architecture of sickle cell disease in West African children.

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Ambaliou Sanni

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Elias Gbeha

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Jacklyn Quinlan

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Jean-Christophe Grenier

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Jean-Philippe Goulet

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Mohamed C Rahimy

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Philip Awadalla

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Selma Gomez

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Thibault de Malliard

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Vanessa Bruat

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P2860

Exploiting gene expression variation to capture gene-environment interactions for disease

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.

Inference of population structure using multilocus genotype data

PLINK: a tool set for whole-genome association and population-based linkage analyses

Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen

Principal components analysis corrects for stratification in genome-wide association studies

Purification and characterization of an alpha 1 beta 2 isoform of CapZ from human erythrocytes: cytosolic location and inability to bind to Mg2+ ghosts suggest that erythrocyte actin filaments are capped by adducin

Systematic identification of trans eQTLs as putative drivers of known disease associations

Genetics of gene expression and its effect on disease

An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis

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26

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scholarly article

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10.3389/FGENE.2014.00026

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2014-02-14T00:00:00Z

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sickle-cell disease

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