Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma. (Q35889809)

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scientific article published in December 1994

Language	Label	Description	Also known as
English	Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma.	scientific article published in December 1994

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scholarly article

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29 October 2019

Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma (English)

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29 October 2019

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Whaley JM

1

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Naglich J

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Gelbert L

3

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Hsia YE

4

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Lamiell JM

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Green JS

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Collins D

7

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Neumann HP

8

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Laidlaw J

9

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Li FP

10

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1 December 1994

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29 October 2019

American Journal of Human Genetics

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29 October 2019

55

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29 October 2019

1092-1102

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29 October 2019

6

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29 October 2019

LINDAU'S DISEASE. REVIEW OF THE LITERATURE AND STUDY OF A LARGE KINDRED.

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Identification of the von Hippel-Lindau disease tumor suppressor gene

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Progression toward tumor cell phenotype is enhanced by overexpression of a mutant p53 tumor-suppressor gene isolated from nasopharyngeal carcinoma

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

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How sensitive is PCR-SSCP?

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Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease

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Mutations of the VHL tumour suppressor gene in renal carcinoma

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Segregation and linkage analyses of von Hippel Lindau disease among 220 descendants from one kindred

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Cytogenetic studies of tumor tissue from patients with nonfamilial renal cell carcinoma.

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Von Hippel-Lindau disease in a Newfoundland kindred

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Cerebellar haemangioblastoma and von Hippel-Lindau disease.

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Tissue-specific expression of a constitutional 3;6 translocation: development of multiple bilateral renal-cell carcinomas

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Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma

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Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma

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Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

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von Hippel-Lindau disease affecting 43 members of a single kindred

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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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Genetic changes in human adrenocortical carcinomas

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Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma

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Genetic mechanisms of tumor suppression by the human p53 gene

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Clinical features and natural history of von Hippel-Lindau disease

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Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus

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Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease

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Islet cell tumors in von Hippel-Lindau disease: increased prevalence and relationship to the multiple endocrine neoplasias

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Von Hippel-Lindau disease: a genetic study

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PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA

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Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus

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Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

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Allelotype of renal cell carcinoma

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7977367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific genetic change in tumors associated with von Hippel-Lindau disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/7977367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histopathological, cytogenetic, and molecular characterization of renal cortical tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/7977367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/7977367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7977367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TaqI and PstI RFLPs in the von Hippel-Lindau disease gene (VHL)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7977367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

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29 October 2019

1 reference

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29 October 2019

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