Identification of common genetic variants that account for transcript isoform variation between human populations. - Test2 - elhamkhani - TriplyDB

Identification of common genetic variants that account for transcript isoform variation between human populations.

Identification of common genetic variants that account for transcript isoform variation between human populations.

http://www.wikidata.org/entity/Q37149649

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Genetic variation of pre-mRNA alternative splicing in human populations In vitro human cell line models to predict clinical response to anticancer drugs Pharmacogenomic discovery using cell-based models Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset Exprtarget: an integrative approach to predicting human microRNA targets Exploring the genetic basis of variation in gene predictions with a synthetic association study Emerging concepts in biomarker discovery; the US-Japan Workshop on Immunological Molecular Markers in Oncology Gene-environment interactions and health inequalities: views of underserved communities Statistical Modeling of RNA-Seq Data.Differential splicing using whole-transcript microarrays.Alternative splicing of TCF7L2 gene in omental and subcutaneous adipose tissue and risk of type 2 diabetes.Fine-scale variation and genetic determinants of alternative splicing across individuals.Normal colon epithelium: a dataset for the analysis of gene expression and alternative splicing events in colon disease Cytokines interleukin-1beta and tumor necrosis factor-alpha regulate different transcriptional and alternative splicing networks in primary beta-cells Impact of the 1000 genomes project on the next wave of pharmacogenomic discovery Exon array analysis using re-defined probe sets results in reliable identification of alternatively spliced genes in non-small cell lung cancer.Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats.Gene expression and genetic variation data implicate PCLO in bipolar disorder.A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.Evolution of alternative splicing in primate brain transcriptomes.Transcriptome sequencing from diverse human populations reveals differentiated regulatory architecture GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease Regional differences in awareness and attitudes regarding genetic testing for disease risk and ancestry.Integrating heterogeneous high-throughput data for meta-dimensional pharmacogenomics and disease-related studies miRNA-mediated relationships between Cis-SNP genotypes and transcript intensities in lymphocyte cell lines Detection of parent-of-origin specific expression quantitative trait loci by cis-association analysis of gene expression in trios Calling sample mix-ups in cancer population studies.Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts.Variants affecting exon skipping contribute to complex traits.Context-dependent robustness to 5' splice site polymorphisms in human populations.Constant splice-isoform ratios in human lymphoblastoid cells support the concept of a splico-stat Global properties and functional complexity of human gene regulatory variation The use of genomic information to optimize cancer chemotherapy The contribution of the functional IL6R polymorphism rs2228145, eQTLs and other genome-wide SNPs to the heritability of plasma sIL-6R levels.EPS8 inhibition increases cisplatin sensitivity in lung cancer cells.Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing Estimation of alternative splicing variability in human populations.Bioinformatic Resources of microRNA Sequences, Gene Targets, and Genetic Variation.Genome-wide analysis links NFATC2 with asparaginase hypersensitivity.Characterization of Visceral and Subcutaneous Adipose Tissue Transcriptome and Biological Pathways in Pregnant and Non-Pregnant Women: Evidence for Pregnancy-Related Regional-Specific Differences in Adipose Tissue.

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P2860

Identification of common genetic variants that account for transcript isoform variation between human populations.

http://www.wikidata.org/entity/Q37149649

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 04 December 2008

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

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name

Identification of common genet ...... ion between human populations.

@en

Identification of common genet ...... ion between human populations.

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type

label

Identification of common genet ...... ion between human populations.

@en

Identification of common genet ...... ion between human populations.

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prefLabel

Identification of common genet ...... ion between human populations.

@en

Identification of common genet ...... ion between human populations.

@nl

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Identification of common genet ...... tion between human populations

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Anthony C Schweitzer

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John E Blume

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Lijun He

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M Eileen Dolan

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Nancy J Cox

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Shiwei Duan

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Steven A Wisel

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Tina X Chen

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Wasim K Bleibel

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Wei Zhang

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P2860

Initial sequencing and analysis of the human genome

Genome-wide associations of gene expression variation in humans

The Sequence of the Human Genome

Gene ontology: tool for the unification of biology

Common genetic variants account for differences in gene expression among ethnic groups

The DAVID Gene Functional Classification Tool: a novel biological module-centric algorithm to functionally analyze large gene lists

Cluster analysis and display of genome-wide expression patterns

A second generation human haplotype map of over 3.1 million SNPs

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

A haplotype map of the human genome

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10.1007/S00439-008-0601-X

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1

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