Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

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Epigenetic mechanisms in diabetic complications and metabolic memory.Set7 mediated interactions regulate transcriptional networks in embryonic stem cells.Current perspectives in Set7 mediated stem cell differentiation.

P2860

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Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

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http://www.wikidata.org/entity/Q58049788

description

article

@en

im Mai 2014 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована в травні 2014

@uk

name

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

@en

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

@nl

type

Item

label

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

@en

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

@nl

prefLabel

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

@en

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

@nl

P1476

Endothelial transcriptome in response to pharmacological methyltransferase inhibition

@en

P2093

Ana Z Fernandez

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

Jun Okabe

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

P2860

Identification of arginine- and lysine-methylation in the proteome of Saccharomyces cerevisiae and its functional implications

Ribosomal protein S2 is a substrate for mammalian PRMT3 (protein arginine methyltransferase 3)

Regulation of p53 activity through lysine methylation

Negative regulation of NF-kappaB action by Set9-mediated lysine methylation of the RelA subunit

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.

Fast and accurate short read alignment with Burrows-Wheeler transform

Set9, a novel histone H3 methyltransferase that facilitates transcription by precluding histone tail modifications required for heterochromatin formation.

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Potent inhibition of DOT1L as treatment of MLL-fusion leukemia

edgeR: a Bioconductor package for differential expression analysis of digital gene expression data

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1755-1762

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

P31

scholarly article

P356

10.1002/CMDC.201402091

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

P433

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

P478

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

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P577

2014-05-21T00:00:00Z

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

P698

24850797

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P921

Farmakologi

transcriptome

molecular medicine

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

about

P2860

P2860

Endothelial Transcriptome in Response to Pharmacological Methyltransferase Inhibition

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921