(Q24682982)

5

0 references

Pieter Wesseling

6

object named as

Pieter Wesseling

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author name string

Theo J M Hulsebos

1

0 references

Astrid S Plomp

2

0 references

Ruud A Wolterman

3

0 references

Els C Robanus-Maandag

American Journal of Human Genetics

4

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language of work or name

English

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publication date

April 2007

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published in

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volume

80

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page(s)

805-10

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issue

4

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cites work

Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Mutation and cancer: statistical study of retinoblastoma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Predisposition to atypical teratoid/rhabdoid tumor due to an inherited INI1 mutation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Diagnostic criteria for schwannomatosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

The mouse ortholog of the human SMARCB1 gene encodes two splice forms

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Schwannomatosis: a clinical and pathologic study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Molecular genetics of atypical teratoid/rhabdoid tumor

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

The SWI/SNF complex--chromatin and cancer.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Familial schwannomatosis: exclusion of the NF2 locus as the germline event

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Immunohistochemical analysis of hSNF5/INI1 in pediatric CNS neoplasms.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852715

Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17357086

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Somatic Instability of the NF2 Gene in Schwannomatosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17357086

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Loss of NF1 allele in Schwann cells but not in fibroblasts derived from an NF1-associated neurofibroma

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17357086