(Q50092603)

7 July 2018

title

Molecular genetic diagnosis of von Hippel-Lindau disease: analysis of five Japanese families (English)

1 reference

7 July 2018

von Hippel-Lindau disease

main subject

1 reference

H Kanno

1

1 reference

7 July 2018

T Shuin

2

1 reference

7 July 2018

K Kondo

3

1 reference

7 July 2018

S Ito

4

1 reference

7 July 2018

M Hosaka

5

1 reference

7 July 2018

S Torigoe

6

1 reference

7 July 2018

S Fujii

7

1 reference

7 July 2018

Y Tanaka

8

1 reference

7 July 2018

I Yamamoto

9

1 reference

7 July 2018

I Kim

10

1 reference

7 July 2018

M Yao

11

1 reference

7 July 2018

publication date

1 May 1996

1 reference

7 July 2018

Japanese Journal of Cancer Research

number of pages

6

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

7 July 2018

volume

87

1 reference

7 July 2018

issue

5

1 reference

7 July 2018

page(s)

423-428

1 reference

7 July 2018

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

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Expression of the Von Hippel-Lindau tumor suppressor gene, VHL, in human fetal kidney and during mouse embryogenesis

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Identification of the von Hippel-Lindau disease tumor suppressor gene

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas.

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas.

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

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

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Mutations of the VHL tumour suppressor gene in renal carcinoma

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Inhibition of Transcription Elongation by the VHL Tumor Suppressor Protein

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

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

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Cerebellar haemangioblastoma and von Hippel-Lindau disease

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

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

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

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

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Direct solid phase sequencing of genomic and plasmid DNA using magnetic beads as solid support.

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Von Hippel-Lindau disease: clinical and pathological manifestations in nine families with 50 affected members

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutations.

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921130

Mutation and cancer: statistical study of retinoblastoma

14 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1996.TB00240.X

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8641976

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1349-7006.1996.TB00240.X

1 reference

7 July 2018

PMC publication ID

5921130

1 reference

7 July 2018

PubMed publication ID

8641976

1 reference

7 July 2018