(Q35247152)

7 August 2017

Recurrent chromosomal gains and heterogeneous driver mutations characterise papillary renal cancer evolution (English)

1 reference

7 August 2017

Chiara Bardella

5

0 references

Francesc Castro-giner

Francesc Castro-Giner

8

0 references

Stuart Horswell

Stuart Horswell

3

0 references

Ignacio Varela

Ignacio Varela

30

0 references

Charles Swanton

Charles Swanton

44

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Peter J. Ratcliffe

Peter Ratcliffe

42

0 references

Sharmin Begum

28

Sharmin Begum

1 reference

7 August 2017

45

Ian Tomlinson

1 reference

ORCID Public Data File 2021

7 August 2017

1 reference

Benjamin Phillimore

27

Benjamin Phillimore

1 reference

7 August 2017

6

Andrew Rowan

1 reference

7 August 2017

4

Max Salm

1 reference

7 August 2017

19

Lisa Pickering

1 reference

7 August 2017

21

David L Nicol

1 reference

7 August 2017

7

Mark Stares

1 reference

7 August 2017

31

Ashish Chandra

1 reference

7 August 2017

23

Gordon Stamp

1 reference

7 August 2017

9

Rosalie Fisher

1 reference

7 August 2017

2

Carolina Navas

1 reference

7 August 2017

33

Alexander Polson

1 reference

7 August 2017

32

Catherine Horsfield

1 reference

7 August 2017

10

Elza C de Bruin

1 reference

7 August 2017

22

Steven Hazell

1 reference

7 August 2017

39

Eamonn Maher

1 reference

7 August 2017

Michal Kovac

1

1 reference

7 August 2017

Monika Kovacova

11

1 reference

7 August 2017

Maggie Gorman

12

1 reference

7 August 2017

Seiko Makino

13

1 reference

7 August 2017

Jennet Williams

14

1 reference

7 August 2017

Emma Jaeger

15

1 reference

7 August 2017

Angela Jones

16

1 reference

7 August 2017

Kimberley Howarth

17

1 reference

7 August 2017

James Larkin

18

1 reference

7 August 2017

Martin Gore

20

1 reference

7 August 2017

Tim O'Brien

24

1 reference

7 August 2017

Ben Challacombe

25

1 reference

7 August 2017

Nik Matthews

26

1 reference

7 August 2017

Adam Rabinowitz

29

1 reference

7 August 2017

Maxine Tran

34

1 reference

7 August 2017

Rupesh Bhatt

35

1 reference

7 August 2017

Luigi Terracciano

36

1 reference

7 August 2017

Serenella Eppenberger-Castori

37

1 reference

7 August 2017

Andrew Protheroe

38

1 reference

7 August 2017

Mona El Bahrawy

40

1 reference

7 August 2017

Stewart Fleming

41

1 reference

7 August 2017

Karl Heinimann

43

1 reference

7 August 2017

language of work or name

English

0 references

publication date

19 March 2015

1 reference

7 August 2017

Nature Communications

1 reference

7 August 2017

6

1 reference

7 August 2017

6336

1 reference

Creative Commons Attribution 4.0 International

7 August 2017

start time

19 March 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/ncomms7336

0 references

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MET is a potential target across all papillary renal cell carcinomas: result from a large molecular study of pRCC with CGH array and matching gene expression array

12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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Chromoplexy: a new category of complex rearrangements in the cancer genome

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Genomic copy number alterations in clear cell renal carcinoma: associations with case characteristics and mechanisms of VHL gene inactivation

12 July 2018

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Fumarate hydratase inactivation in renal tumors: HIF1α, NRF2, and "cryptic targets" of transcription factors

12 July 2018

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Absolute quantification of somatic DNA alterations in human cancer

12 July 2018

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Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

12 July 2018

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VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

12 July 2018

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Renal cyst formation in Fh1-deficient mice is independent of the Hif/Phd pathway: roles for fumarate in KEAP1 succination and Nrf2 signaling

12 July 2018

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Succination of Keap1 and activation of Nrf2-dependent antioxidant pathways in FH-deficient papillary renal cell carcinoma type 2.

12 July 2018

1 reference

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Inactivating mutations of the chromatin remodeling gene ARID2 in hepatocellular carcinoma

12 July 2018

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Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

12 July 2018

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Massive genomic rearrangement acquired in a single catastrophic event during cancer development

12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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Detection of DNA copy number changes and oncogenic signaling abnormalities from gene expression data reveals MYC activation in high-grade papillary renal cell carcinoma

12 July 2018

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12 July 2018

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Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome

12 July 2018

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Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

12 July 2018

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Mapping of the 7q31 subregion common to the small chromosome 7 derivatives from two sporadic papillary renal cell carcinomas: increased copy number and overexpression of the MET proto-oncogene

12 July 2018

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Chromosomal imbalances in papillary renal cell carcinoma: genetic differences between histological subtypes

12 July 2018

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Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas

12 July 2018

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Chromosome imbalances in papillary renal cell carcinoma and first cytogenetic data of familial cases analyzed by comparative genomic hybridization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383019

The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383019

Identification of the von Hippel-Lindau disease tumor suppressor gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383019

Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383019

Evidence for polyclonal origin of multifocal clear cell renal cell carcinoma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4383019

CUL3 and NRF2 mutations confer an NRF2 activation phenotype in a sporadic form of papillary renal cell carcinoma

26 September 2018

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12 December 2020

Genetic subtyping of renal cell carcinoma by comparative genomic hybridization

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12 December 2020

Clear-cell and papillary carcinoma of the kidney: an analysis of chromosome 3, 7, and 17 abnormalities by microsatellite amplification, cytogenetics, and fluorescence in situ hybridization

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12 December 2020

Cytogenetic and molecular findings in 75 clear cell renal cell carcinomas

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12 December 2020

Clonal origin of multifocal renal cell carcinoma as determined by microsatellite analysis

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12 December 2020

Identifiers

DOI

10.1038/NCOMMS7336

1 reference

7 August 2017

0 references

1 reference

7 August 2017

1 reference