Allelic variation in gene expression is common in the human genome. - Wikidata - awgldk - TriplyDB

Allelic variation in gene expression is common in the human genome.

Allelic variation in gene expression is common in the human genome.

http://www.wikidata.org/entity/Q33682674

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Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapy Critical association of ncRNA with introns The application of single nucleotide polymorphism microarrays in cancer research Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism SNP-specific array-based allele-specific expression analysis DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency Detecting imbalanced expression of SNP alleles by minisequencing on microarrays Variations in genome-wide gene expression in identical twins - a study of primary osteoblast-like culture from female twins discordant for osteoporosis Simultaneous quantitative and allele-specific expression analysis with real competitive PCR Functional analysis of human and chimpanzee promoters.Local regulatory variation in Saccharomyces cerevisiae Heterozygous carriers of Nijmegen Breakage Syndrome have a distinct gene expression phenotype Early-onset Crohn's disease and autoimmunity associated with a variant in CTLA-4 Aberrant estrogen regulation of PEMT results in choline deficiency-associated liver dysfunction Inter-individual variation in DNA repair capacity: a need for multi-pathway functional assays to promote translational DNA repair research Zinc and zinc transporter regulation in pancreatic islets and the potential role of zinc in islet transplantation Allele-specific chromatin immunoprecipitation studies show genetic influence on chromatin state in human genome Down-regulation of ZnT8 expression in INS-1 rat pancreatic beta cells reduces insulin content and glucose-inducible insulin secretion Comparing methods for mapping cis acting polymorphisms using allelic expression ratios SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data.eQTL Mapping Using RNA-seq Data Polymorphisms of the IGF1R gene and their genetic effects on chicken early growth and carcass traits.A flexible Bayesian method for detecting allelic imbalance in RNA-seq data ASEQ: fast allele-specific studies from next-generation sequencing data.The impact of SNPs on the interpretation of SAGE and MPSS experimental data.High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.Allele-specific KRT1 expression is a complex trait.Identification of common genetic variation that modulates alternative splicing AffyMAPSDetector: a software tool to characterize Affymetrix GeneChip expression arrays with respect to SNPs.Cis sequence effects on gene expression High variability and non-neutral evolution of the mammalian avpr1a gene Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.Evolutionary signatures of common human cis-regulatory haplotypes.Allele-specific gene expression is widespread across the genome and biological processes Mutation detection by real-time PCR: a simple, robust and highly selective method.Allele-specific expression assays using Solexa Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes Transcript profiling of candidate genes in testis of pigs exhibiting large differences in androstenone levels SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr

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P2860

Allelic variation in gene expression is common in the human genome.

http://www.wikidata.org/entity/Q33682674

description

2003 nî lūn-bûn

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2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի օգոստոսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Allelic variation in gene expression is common in the human genome.

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Allelic variation in gene expression is common in the human genome.

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type

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Allelic variation in gene expression is common in the human genome.

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Allelic variation in gene expression is common in the human genome.

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Allelic variation in gene expression is common in the human genome.

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Allelic variation in gene expression is common in the human genome.

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Genome Research

P1476

Allelic variation in gene expression is common in the human genome.

@en

P2093

H Shuen Lo

http://www.w3.org/2001/XMLSchema#string

Howard H Yang

http://www.w3.org/2001/XMLSchema#string

Kenneth H Buetow

http://www.w3.org/2001/XMLSchema#string

Maxwell P Lee

http://www.w3.org/2001/XMLSchema#string

Sheryl Gere

http://www.w3.org/2001/XMLSchema#string

Ying Hu

http://www.w3.org/2001/XMLSchema#string

Zhining Wang

http://www.w3.org/2001/XMLSchema#string

P2860

Physiological functions of imprinted genes.

Biology of the X chromosome.

Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours.

Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M.

Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1.

Allelic Variation in Human Gene Expression

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1855-1862

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scholarly article

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10.1101/GR.1006603

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8

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13

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2003-08-01T00:00:00Z

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10627377

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12902379

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403776

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