(Q40341032)

19 September 2017

Mutations in the transcriptional repressor REST predispose to Wilms tumor (English)

1 reference

Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumor.

19 September 2017

corrigendum / erratum

0 references

author

Neil J. Sebire

23

1 reference

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6 June 2020

Nazneen Rahman

25

1 reference

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6 June 2020

Anna Zachariou

4

1 reference

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6 June 2020

Elise Ruark

6

1 reference

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6 June 2020

Shawn Yost

10

1 reference

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6 June 2020

Anna Elliott

11

1 reference

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6 June 2020

Juliet C Gray

14

1 reference

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6 June 2020

20

Anthony Renwick

1 reference

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6 June 2020

22

Charles Stiller

1 reference

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6 June 2020

author name string

Shazia S Mahamdallie

1

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6 June 2020

Sandra Hanks

2

1 reference

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6 June 2020

Kristen L Karlin

3

1 reference

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6 June 2020

Elizabeth R Perdeaux

5

1 reference

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6 June 2020

Chad A Shaw

7

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6 June 2020

Alexander Renwick

8

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6 June 2020

Emma Ramsay

9

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6 June 2020

Jillian Birch

12

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6 June 2020

Michael Capra

13

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6 June 2020

Juliet Hale

15

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6 June 2020

Judith Kingston

16

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6 June 2020

Gill Levitt

17

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6 June 2020

Thomas McLean

18

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6 June 2020

Eamonn Sheridan

19

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6 June 2020

Sheila Seal

21

1 reference

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6 June 2020

Thomas F Westbrook

24

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6 June 2020

language of work or name

English

0 references

publication date

9 November 2015

1 reference

19 September 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26551668%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

volume

47

1 reference

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6 June 2020

page(s)

1471-1474

1 reference

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6 June 2020

issue

12

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng.3440

6 June 2020

exact match

0 references

cites work

The yin and yang of kidney development and Wilms' tumors

1 reference

REST: transcriptional and epigenetic regulator.

21 January 2018

1 reference

Chromatin crosstalk in development and disease: lessons from REST

21 January 2018

1 reference

Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour

21 January 2018

1 reference

Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour.

21 January 2018

1 reference

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

21 January 2018

1 reference

Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2

21 January 2018

1 reference

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

21 January 2018

1 reference

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

21 January 2018

1 reference

REST and stress resistance in ageing and Alzheimer's disease

21 January 2018

1 reference

The role of REST in transcriptional and epigenetic dysregulation in Huntington's disease

21 January 2018

1 reference

DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome

21 January 2018

1 reference

Reduced expression of the neuron restrictive silencer factor permits transcription of glycine receptor alpha1 subunit in small-cell lung cancer cells

21 January 2018

1 reference

Regulation of the NRSF/REST gene by methylation and CREB affects the cellular phenotype of small-cell lung cancer

21 January 2018

1 reference

IB1/JIP-1 controls JNK activation and increased during prostatic LNCaP cells neuroendocrine differentiation

21 January 2018

1 reference

REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis.

21 January 2018

1 reference

Frequency and Heritability ofWT1Mutations in Nonsyndromic Wilms' Tumor Patients: A UK Children’s Cancer Study Group Study

21 January 2018

1 reference

Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice

21 January 2018

1 reference

Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads

21 January 2018

1 reference

Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications

21 January 2018

1 reference

The ICR1000 UK exome series: a resource of gene variation in an outbred population

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26551668

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26551668

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The oncogenic STP axis promotes triple-negative breast cancer via degradation of the REST tumor suppressor

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26551668