about
Independent and population-specific association of risk variants at the IRGM locus with Crohn's diseaseCCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogsSteric antisense inhibition of AMPA receptor Q/R editing reveals tight coupling to intronic editing sites and splicingAllele-specific gene expression patterns in primary leukemic cells reveal regulation of gene expression by CpG site methylationImprinted and X-linked non-coding RNAs as potential regulators of human placental functionTargeted and genome-scale strategies reveal gene-body methylation signatures in human cellsCole-Carpenter syndrome is caused by a heterozygous missense mutation in P4HBAllele-specific chromatin immunoprecipitation studies show genetic influence on chromatin state in human genomeComparing computational methods for identification of allele-specific expression based on next generation sequencing data.Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.The repertoire and dynamics of evolutionary adaptations to controlled nutrient-limited environments in yeastRandom X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome.Patrocles: a database of polymorphic miRNA-mediated gene regulation in vertebratesIncreased NBCn1 expression, Na+/HCO3- co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension.High-resolution mapping of protein sequence-function relationships.Prohibitin expression deregulation in gastric cancer is associated with the 3' untranslated region 1630 C>T polymorphism and copy number variation.Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.Global analysis of the impact of environmental perturbation on cis-regulation of gene expressionAnalysis of allelic differential expression in the human genome using allele-specific serial analysis of gene expression tags.Reciprocal sign epistasis between frequently experimentally evolved adaptive mutations causes a rugged fitness landscape.Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discoverySuccessful computational prediction of novel imprinted genes from epigenomic features.Retrotransposon-induced heterochromatin spreading in the mouse revealed by insertional polymorphisms.Demonstrating polymorphic miRNA-mediated gene regulation in vivo: application to the g+6223G->A mutation of Texel sheep.Reduced expression of IFIH1 is protective for type 1 diabetes.A novel and rapid method of determining the effect of unclassified MLH1 genetic variants on differential allelic expressionIdentification of Kv11.1 isoform switch as a novel pathogenic mechanism of long-QT syndrome.Assessing the effect of the CLPG mutation on the microRNA catalog of skeletal muscle using high-throughput sequencing.A common BACE1 polymorphism is a risk factor for sporadic Creutzfeldt-Jakob diseaseThe cancer exome generated by alternative mRNA splicing dilutes predicted HLA class I epitope density.Gene-gene interaction and functional impact of polymorphisms on innate immune genes in controlling Plasmodium falciparum blood infection level.Low prevalence of connexin-40 gene variants in atrial tissues and blood from atrial fibrillation subjectsExome profiling of primary, metastatic and recurrent ovarian carcinomas in a BRCA1-positive patient.Variants in the 3' UTR of general Transcription factor IIF, polypeptide 2 affect female calving efficiency in Japanese Black cattleMeasuring the activity of protein variants on a large scale using deep mutational scanning.Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate geneGenetic variants in the upstream region of activin receptor IIA are associated with female fertility in Japanese Black cattle.A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattleRNA editing of protein sequences: a rare event in human transcriptomesRole of DNA methylation in expression control of the IKZF3-GSDMA region in human epithelial cells.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Survey of allelic expression using EST mining.
@en
Survey of allelic expression using EST mining.
@nl
type
label
Survey of allelic expression using EST mining.
@en
Survey of allelic expression using EST mining.
@nl
prefLabel
Survey of allelic expression using EST mining.
@en
Survey of allelic expression using EST mining.
@nl
P2093
P2860
P356
P1433
P1476
Survey of allelic expression using EST mining.
@en
P2093
Carole Dore
Eef Harmsen
Pierre Lepage
Scott Gurd
Thomas J Hudson
Tiffany Gaudin
Tomi Pastinen
P2860
P304
P356
10.1101/GR.4023805
P577
2005-11-01T00:00:00Z