Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data (Q30690943)

19 August 2017

Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data (English)

1 reference

19 August 2017

Viatcheslav Mordvinov

object named as

Viatcheslav A Mordvinov

6

0 references

author name string

Leonid O Bryzgalov

1

1 reference

19 August 2017

Elena V Antontseva

2

1 reference

19 August 2017

Marina Yu Matveeva

3

1 reference

19 August 2017

Alexander G Shilov

4

1 reference

19 August 2017

Elena V Kashina

5

1 reference

19 August 2017

Tatyana I Merkulova

7

1 reference

19 August 2017

language of work or name

English

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publication date

29 October 2013

1 reference

19 August 2017

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19 August 2017

8

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19 August 2017

10

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19 August 2017

e78833

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Creative Commons Attribution 4.0 International

19 August 2017

start time

29 October 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Regulation of CCL2 Expression by an Upstream TALE Homeodomain Protein-Binding Site That Synergizes with the Site Created by the A-2578G SNP

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9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response

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14 July 2018

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14 July 2018

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Variation in transcription factor binding among humans

14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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Insights from genomic profiling of transcription factors

14 July 2018

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Cis-regulatory mutations in human disease

14 July 2018

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14 July 2018

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Identification of candidate regulatory SNPs by combination of transcription-factor-binding site prediction, SNP genotyping and haploChIP

14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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A survey of genomic properties for the detection of regulatory polymorphisms

14 July 2018

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14 July 2018

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A single-nucleotide polymorphism in a half-binding site creates p53 and estrogen receptor control of vascular endothelial growth factor receptor 1.

14 July 2018

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14 July 2018

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A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter

14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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Identification of functional SNPs in the 5-prime flanking sequences of human genes

14 July 2018

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Functional analysis of polymorphisms in the promoter regions of genes on 22q11.

14 July 2018

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14 July 2018

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14 July 2018

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Functional analysis of human promoter polymorphisms.

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Hereditary persistence of alpha-fetoprotein is due to both proximal and distal hepatocyte nuclear factor-1 site mutations

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PubMed

https://pubmed.ncbi.nlm.nih.gov/24205329

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0078833

1 reference

19 August 2017

0 references

1 reference

19 August 2017

PubMed publication ID

24205329

1 reference