(Q34388261)

1 August 2017

Temporal lobe pleomorphic xanthoastrocytoma and acquired BRAF mutation in an adolescent with the constitutional 22q11.2 deletion syndrome (English)

1 reference

Pleomorphic xanthoastrocytoma

1 August 2017

1 reference

1 reference

Jeffrey C Murray

1

1 reference

1 August 2017

David J Donahue

2

1 reference

1 August 2017

Saleem I Malik

3

1 reference

1 August 2017

Yvette B Dzurik

4

1 reference

1 August 2017

Emily Z Braly

5

1 reference

1 August 2017

Margaret J Dougherty

6

1 reference

1 August 2017

Katherine W Eaton

7

1 reference

1 August 2017

Jaclyn A Biegel

8

1 reference

1 August 2017

21 August 2010

1 reference

Journal of Neuro-Oncology

1 August 2017

1 reference

1 August 2017

102

1 reference

1 August 2017

3

1 reference

1 August 2017

509-514

1 reference

https://scigraph.springernature.com/pub.10.1007/s11060-010-0350-2

1 August 2017

0 references

cites work

Activating mutations in BRAF characterize a spectrum of pediatric low-grade gliomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Tandem duplication producing a novel oncogenic BRAF fusion gene defines the majority of pilocytic astrocytomas

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Detailed analysis of 22q11.2 with a high density MLPA probe set

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

BRAF(E600) in benign and malignant human tumours

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Mutations of the BRAF gene in human cancer

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Genetic imbalances in pleomorphic xanthoastrocytoma detected by comparative genomic hybridization and literature review

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

The 22q11.2 deletion syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Pleomorphic xanthoastrocytoma: favorable outcome after complete surgical resection

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Cytogenetic findings in a pleomorphic xanthoastrocytoma

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Histopathological features of recurrent pleomorphic xanthoastrocytomas: further corroboration of the glial nature of this neoplasm. A study of 3 cases.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2998545

Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas.

28 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11060-010-0350-2

Activation of the ERK/MAPK pathway: a signature genetic defect in posterior fossa pilocytic astrocytomas.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11060-010-0350-2

Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20730472

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Neoplastic disease and deletion 22q11.2: a multicentric study and report of two cases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20730472

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S11060-010-0350-2

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference

1 August 2017

1 reference