A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.
about
Sequencing and analysis of a South Asian-Indian personal genomeTargeted capture and massively parallel sequencing of 12 human exomesSIGLEC12, a human-specific segregating (pseudo)gene, encodes a signaling molecule expressed in prostate carcinomasEvolutionary dynamics of human Toll-like receptors and their different contributions to host defenseLoss of gene function and evolution of human phenotypesGenetic signatures of adaptation revealed from transcriptome sequencing of Arctic and red foxesGene inactivation and its implications for annotation in the era of personal genomicsA systematic survey of loss-of-function variants in human protein-coding genesEffect of duplicate genes on mouse genetic robustness: an update.Improved network performance via antagonism: From synthetic rescues to multi-drug combinations.Analysis of stop-gain and frameshift variants in human innate immunity genes.Loss-of-function variants in the genomes of healthy humansSelection on a variant associated with improved viral clearance drives local, adaptive pseudogenization of interferon lambda 4 (IFNL4)Personal receptor repertoires: olfaction as a model.Genome-wide discovery and information resource development of DNA polymorphisms in cassava.The impact of caspase-12 on susceptibility to candidemiaHigh-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes.Copy number variations in the genome of the Qatari populationMutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19pWidespread polymorphism in the positions of stop codons in Drosophila melanogasterRNA-Seq-Mediated Transcriptome Analysis of a Fiberless Mutant Cotton and Its Possible Origin Based on SNP Markers.Multiple loss-of-function variants of taste receptors in modern humans.Selection Against Maternal microRNA Target Sites in Maternal Transcripts.Effects of premature termination codon polymorphisms in the Drosophila pseudoobscura subclade.Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing.Premature termination codons in modern human genomesA catalog of hemizygous variation in 127 22q11 deletion patients.Are biological sensors modulated by their structural scaffolds? The role of the structural muscle proteins alpha-actinin-2 and alpha-actinin-3 as modulators of biological sensors.The role played by natural selection on Mendelian traits in humans.Associations of genetic polymorphisms of Siglecs with human diseases.Evaluation of MAGE-D4 expression in hepatocellular carcinoma in Japanese patients.Revisiting the morbid genome of Mendelian disorders.The distribution pattern of genetic variation in the transcript isoforms of the alternatively spliced protein-coding genes in the human genome.Characterizing the Extent of Human Genetic Variation for Performance-Related Traits
P2860
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P2860
A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.
description
article científic
@ca
article scientifique
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articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 05 February 2009
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
A genome-wide survey of the pr ...... acting on human nonsense SNPs.
@en
A genome-wide survey of the pr ...... acting on human nonsense SNPs.
@nl
type
label
A genome-wide survey of the pr ...... acting on human nonsense SNPs.
@en
A genome-wide survey of the pr ...... acting on human nonsense SNPs.
@nl
prefLabel
A genome-wide survey of the pr ...... acting on human nonsense SNPs.
@en
A genome-wide survey of the pr ...... acting on human nonsense SNPs.
@nl
P2093
P2860
P50
P1476
A genome-wide survey of the pr ...... acting on human nonsense SNPs.
@en
P2093
Bryndis Yngvadottir
Jonathan Morrison
Marcos Delgado
Steve Searle
P2860
P304
P356
10.1016/J.AJHG.2009.01.008
P407
P577
2009-02-05T00:00:00Z