(Q47981361)

English

Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis.

scientific article published in July 1998

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scholarly article

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis. (English)

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

renal cell carcinoma

1 reference

based on heuristic

inferred from title

author name string

S C Clifford

1

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

A H Prowse

2

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

N A Affara

3

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

C H Buys

4

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

E R Maher

5

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

publication date

1 July 1998

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

22

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

200-209

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

3

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

1 reference

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21 January 2018

Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

1 reference

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21 January 2018

Parental-origin-specific epigenetic modification of the mouse H19 gene

1 reference

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21 January 2018

Somatic mutations of the von Hippel-Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

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

1 reference

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21 January 2018

Mutations of the VHL tumour suppressor gene in renal carcinoma

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

Tumour suppression by the human von Hippel-Lindau gene product

1 reference

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21 January 2018

A cell cycle regulator potentially involved in genesis of many tumor types

1 reference

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21 January 2018

Definition of a tumor suppressor locus within human chromosome 3p21-p22

1 reference

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21 January 2018

Identification of the von Hippel-Lindau disease tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

5' CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

1 reference

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21 January 2018

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

1 reference

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21 January 2018

A tumor suppressor locus within 3p14-p12 mediates rapid cell death of renal cell carcinoma in vivo

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Comprehensive allelotyping of human renal cell carcinomas using microsatellite DNA probes

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

A second-generation linkage map of the human genome

1 reference

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21 January 2018

Dinucleotide repeats flanking the renal carcinoma breakpoint at 3p14.2

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199807%2922%3A3%3C200%3A%3AAID-GCC5%3E3.0.CO%3B2-%23

21 January 2018

Identifiers

10.1002/(SICI)1098-2264(199807)22:3<200::AID-GCC5>3.0.CO;2-#

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

release_evg4ciyrdfeuhprqheyiw3rzya

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https://api.fatcat.wiki/v0/release/evg4ciyrdfeuhprqheyiw3rzya

24 November 2022

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mapped directly with Wikidata item

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/9624531

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