(Q55360778)

3 July 2018

title

Low incidence of a nucleotide sequence alteration of the neurofibromatosis 2 gene in human breast cancers. (English)

1 reference

3 July 2018

neurofibromatosis type II

main subject

1 reference

S Yaegashi

1

1 reference

3 July 2018

R Sachse

2

1 reference

3 July 2018

N Ohuchi

3

1 reference

3 July 2018

S Mori

4

1 reference

3 July 2018

T Sekiya

5

1 reference

3 July 2018

publication date

1 October 1995

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3 July 2018

number of pages

5

1 reference

Japanese Journal of Cancer Research

inferred from page(s)

published in

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3 July 2018

volume

86

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3 July 2018

page(s)

929-933

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3 July 2018

issue

10

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3 July 2018

Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

The mouse homologue of the neurofibromatosis type 2 gene is highly conserved

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Alternative splicing of the NF2 gene and its mutation analysis of breast and colorectal cancers.

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individuals

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Exon scanning for mutation of the NF2 gene in schwannomas.

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Mutational analysis of patients with neurofibromatosis 2

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Use of labeled primers in polymerase chain reaction (LP-PCR) for a rapid detection of the product

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Improved double-stranded DNA sequencing using the linear 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=5920597

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Heterogeneity for Allelic Loss in Human Breast Cancer

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

A general method for isolation of high molecular weight DNA from eukaryotes

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

The neurofibromatosis type 2 gene is inactivated in schwannomas

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

The neurofibromatosis 2 (NF2) tumor suppressor gene encodes multiple alternatively spliced transcripts.

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Analysis of the neurofibromatosis 2 gene in human breast and hepatocellular carcinomas.

12 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920597

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas

12 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1995.TB03003.X

Germline mutations in the neurofibromatosis type 2 tumour suppressor gene

21 January 2018

1 reference

12 December 2020

Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer

1 reference

12 December 2020

Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma

1 reference

12 December 2020

Allele-specific polymerase chain reaction: a method for amplification and sequence determination of a single component among a mixture of sequence variants

1 reference

12 December 2020

Deletion mapping of the long arm of chromosome 22 in human meningiomas

1 reference

12 December 2020

10.1111/J.1349-7006.1995.TB03003.X

Identifiers

DOI

1 reference

3 July 2018

PMCID

5920597

1 reference

3 July 2018

PubMed ID

7493911

1 reference

3 July 2018