(Q30531015)

English

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis

scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis (English)

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

author name string

A G Menon

1

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

K M Anderson

2

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

V M Riccardi

3

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

R Y Chung

4

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

J M Whaley

5

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

D W Yandell

6

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

G E Farmer

7

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

R N Freiman

8

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

J K Lee

9

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

F P Li

10

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

language of work or name

0 references

publication date

1 July 1990

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

87

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

14

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

5435-5439

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

Von Recklinghausen neurofibromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Value of S-100 protein in the diagnosis of soft tissue tumors with particular reference to benign and malignant Schwann cell tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Human p53 cellular tumor antigen: cDNA sequence and expression in COS cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Characterization of the human p53 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Mutation is required to activate the p53 gene for cooperation with the ras oncogene and transformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

p53: a frequent target for genetic abnormalities in lung cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Mutations in the p53 gene occur in diverse human tumour types

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

The p53 proto-oncogene can act as a suppressor of transformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

20 June 2018

Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54339

26 November 2018

Physical mapping of a translocation breakpoint in neurofibromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2142531

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two NF1 translocations map within a 600-kilobase segment of 17q11.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2142531

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Implantation of human meningiomas into the subrenal capsule of the nude mouse. A model for studies of tumor growth

1 reference

https://pubmed.ncbi.nlm.nih.gov/2142531

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mechanism of activation of porcine pepsinogen

1 reference

https://pubmed.ncbi.nlm.nih.gov/2142531

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17

1 reference

https://pubmed.ncbi.nlm.nih.gov/2142531

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/2142531

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis. Conference statement. National Institutes of Health Consensus Development Conference

1 reference

https://pubmed.ncbi.nlm.nih.gov/2142531

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.87.14.5435

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

1990PNAS...87.5435M

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

ResearchGate publication ID

0 references

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