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Survey of variation in human transcription factors reveals prevalent DNA binding changes.

Survey of variation in human transcription factors reveals prevalent DNA binding changes.

http://www.wikidata.org/entity/Q36781032

about

Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability Taming Human Genetic Variability: Transcriptomic Meta-Analysis Guides the Experimental Design and Interpretation of iPSC-Based Disease Modeling.An efficient algorithm for improving structure-based prediction of transcription factor binding sites iRegNet3D: three-dimensional integrated regulatory network for the genomic analysis of coding and non-coding disease mutations.Proteomic analysis of hair shafts from monozygotic twins: Expression profiles and genetically variant peptides.Proteome-Scale Human Interactomics.Epigenomic and transcriptional control of insulin resistance.Functional variomics and network perturbation: connecting genotype to phenotype in cancer.Transcription factor-DNA binding: beyond binding site motifs.Isoelectric point-based fractionation by HiRIEF coupled to LC-MS allows for in-depth quantitative analysis of the phosphoproteome.Sparse conserved under-methylated CpGs are associated with high-order chromatin structure Tartrate-resistant acid phosphatase (TRAP/ACP5) promotes metastasis-related properties via TGFβ2/TβR and CD44 in MDA-MB-231 breast cancer cells.Systematic identification of regulatory variants associated with cancer risk.Identification of Human Lineage-Specific Transcriptional Coregulators Enabled by a Glossary of Binding Modules and Tunable Genomic Backgrounds.Sequence2Vec: A novel embedding approach for modeling transcription factor binding affinity landscape.Variant Interpretation: Functional Assays to the Rescue.Organizing combinatorial transcription factor recruitment at cis-regulatory modules.Base-resolution stratification of cancer mutations using functional variomics.Somatic Superenhancer Duplications and Hotspot Mutations Lead to Oncogenic Activation of the KLF5 Transcription Factor.Exploring Variation in Known Pharmacogenetic Variants and its Association with Drug Response in Different Mexican Populations.A unified approach for quantifying and interpreting DNA shape readout by transcription factors.New considerations for hiPSC-based models of neuropsychiatric disorders.Conservation of DNA and ligand binding properties of retinoid X receptor from the placozoan Trichoplax adhaerens to human.Network-based approaches that exploit inferred transcription factor activity to analyze the impact of genetic variation on gene expression.Direct measurement of pervasive weak repression by microRNAs and their role at the network level.Cellular network perturbations by disease-associated variants.DNA Motif Recognition Modeling from Protein Sequences

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P2860

Survey of variation in human transcription factors reveals prevalent DNA binding changes.

http://www.wikidata.org/entity/Q36781032

description

2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Survey of variation in human transcription factors reveals prevalent DNA binding changes.

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Survey of variation in human transcription factors reveals prevalent DNA binding changes.

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type

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Survey of variation in human transcription factors reveals prevalent DNA binding changes.

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Survey of variation in human transcription factors reveals prevalent DNA binding changes.

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prefLabel

Survey of variation in human transcription factors reveals prevalent DNA binding changes.

@ast

Survey of variation in human transcription factors reveals prevalent DNA binding changes.

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Survey of variation in human transcription factors reveals prevalent DNA binding changes.

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Anastasia Vedenko

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David E Hill

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Elizabeth J Rossin

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Jaie Woodard

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Jesse V Kurland

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Kian Hong Kock

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Leila Shokri

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Luca Mariani

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Luis A Barrera

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Manolis Kellis

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P2860

Structure of the forkhead domain of FOXP2 bound to DNA

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor

Crystal structure of the human FOXK1a-DNA complex and its implications on the diverse binding specificity of winged helix/forkhead proteins

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

A map of human genome variation from population-scale sequencing

Crystal structure of the human FOXO3a-DBD/DNA complex suggests the effects of post-translational modification

Structural Basis for DNA Recognition by FoxO1 and Its Regulation by Posttranslational Modification

Structure of the FoxM1 DNA-recognition domain bound to a promoter sequence

Structure of the human FOXO4-DBD-DNA complex at 1.9 Å resolution reveals new details of FOXO binding to the DNA

Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

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Stephen S. Gisselbrecht

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2016-03-24T00:00:00Z

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