(Q36048466)

11 August 2017

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title

The genetic basis of cancer of kidney cancer: implications for gene-specific clinical management (English)

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11 August 2017

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W Marston Linehan

1

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11 August 2017

Robert L Grubb

2

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11 August 2017

Jonathan A Coleman

3

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11 August 2017

Berton Zbar

4

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11 August 2017

McClellan M Walther

5

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11 August 2017

publication date

1 March 2005

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11 August 2017

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11 August 2017

volume

95 Suppl 2

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11 August 2017

page(s)

2-7

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Rising incidence of renal cell cancer in the United States

11 August 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

von Hippel-Lindau disease

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Mutations of the VHL tumour suppressor gene in renal carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Regulation of hypoxia-inducible mRNAs by the von Hippel-Lindau tumor suppressor protein requires binding to complexes containing elongins B/C and Cul2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Rbx1, a component of the VHL tumor suppressor complex and SCF ubiquitin ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

The von Hippel-Lindau tumor-suppressor gene product forms a stable complex with human CUL-2, a member of the Cdc53 family of proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Hereditary Multiple Fibrofolliculomas With Trichodiscomas and Acrochordons

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Birt-Hogg-Dubé syndrome: a novel marker of kidney neoplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Birt-Hogg-Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Inherited susceptibility to uterine leiomyomas and renal cell cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Renal Tumors in the Birt-Hogg-Dubé Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2005.05189.X

10.1111/J.1464-410X.2005.05189.X

21 January 2018

Identifiers

DOI

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11 August 2017

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