(Q35747010)

English

Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas

scientific article published on August 2001

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Europe PubMed Central

PubMed publication ID

10 August 2017

Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

author name string

Boström J

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Meyer-Puttlitz B

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Wolter M

3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Blaschke B

4

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Weber RG

5

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Lichter P

6

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Ichimura K

7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Collins VP

8

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Reifenberger G

9

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

language of work or name

0 references

publication date

1 August 2001

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

The American Journal of Pathology

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Europe PubMed Central

PubMed publication ID

10 August 2017

159

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

661-669

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Two arginine rich domains in the p14ARF tumour suppressor mediate nucleolar localization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Amplification and expression of cyclin D genes (CCND1, CCND2 and CCND3) in human malignant gliomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Mutations in human ARF exon 2 disrupt its nucleolar localization and impair its ability to block nuclear export of MDM2 and p53

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

The p53 pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Identification of functional elements of p18INK4C essential for binding and inhibition of cyclin-dependent kinase (CDK) 4 and CDK6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Tumor suppressor p16INK4A: determination of solution structure and analyses of its interaction with cyclin-dependent kinase 4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Review of alterations of the cyclin-dependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia-lymphoma cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Structure of the gene encoding the human cyclin-dependent kinase inhibitor p18 and mutational analysis in breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Characterization of the cyclin-dependent kinase inhibitory domain of the INK4 family as a model for a synthetic tumour suppressor molecule

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Crystal structure of the CDK4/6 inhibitory protein p18INK4c provides insights into ankyrin-like repeat structure/function and tumor-derived p16INK4 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Analysis of genomic alterations in benign, atypical, and anaplastic meningiomas: toward a genetic model of meningioma progression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Deletion mapping of the short arm of chromosome 1 identifies a common region of deletion distal to D1S496 in human meningiomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Alterations in DNA methylation: a fundamental aspect of neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Analysis of p53 mutation and epidermal growth factor receptor amplification in recurrent gliomas with malignant progression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Genomic instability in 1p and human malignancies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Growth suppression by p18, a p16INK4/MTS1- and p14INK4B/MTS2-related CDK6 inhibitor, correlates with wild-type pRb function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 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=1850553

12 July 2018

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

12 July 2018

Infrequent alterations of the p15, p16, CDK4 and cyclin D1 genes in non-astrocytic human brain tumors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

27 July 2018

Chordoid glioma of the third ventricle: immunohistochemical and molecular genetic characterization of a novel tumor entity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

Identification of two distinct deleted regions on the short arm of chromosome 1 and rare mutation of the CDKN2C gene from 1p32 in oligodendroglial tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

"Malignancy" in meningiomas: a clinicopathologic study of 116 patients, with grading implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

The p16INK4a/CDKN2A tumor suppressor and its relatives.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

Human glioblastomas with no alterations of the CDKN2A (p16INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

Mutations of the p53 tumor suppressor gene in neoplasms of the human nervous system.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

Cytogenetic changes in 67 cranial and spinal meningiomas: relation to histopathological and clinical pattern

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

Chromosomal deletions in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

Allelic loss at 1p is associated with tumor progression of meningiomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850553

25 September 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Cytogenetic, molecular genetic and pathological analyses in 126 meningiomas

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Analysis of the p16INK4A, p15INK4B and p18INK4C genes in multiple myeloma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Molecular analysis of alterations of the p18INK4c gene in human meningiomas

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Homozygous deletions of the CDKN2/p16 gene in dural hemangiopericytomas

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Analysis of cell cycle regulators: p16INK4A, pRb, and CDK4 in low- and high-grade meningiomas

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Alterations in DNA Methylation: A Fundamental Aspect of Neoplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Detection of gains and losses in 18 meningiomas by comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Accumulation of wild‐type p53 in meningiomas

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Detection of TP53 gene mutation in human meningiomas: a study using immunohistochemistry, polymerase chain reaction/single-strand conformation polymorphism and DNA sequencing techniques on paraffin-embedded samples

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961737-3

7 January 2021

Deletion of chromosome 1p and loss of expression of alkaline phosphatase indicate progression of meningiomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/11485924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic losses on chromosomes 14, 10, and 1 in atypical and malignant meningiomas: a genetic model of meningioma progression

1 reference

https://pubmed.ncbi.nlm.nih.gov/11485924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous deletions of cyclin-dependent kinase inhibitor genes, p16(INK4A) and p18, in childhood T cell lineage acute lymphoblastic leukemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/11485924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity

1 reference

https://pubmed.ncbi.nlm.nih.gov/11485924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tight association of loss of merlin expression with loss of heterozygosity at chromosome 22q in sporadic meningiomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/11485924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S0002-9440(10)61737-3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

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