(Q47620432)

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Evaluation of NF2 and NF1 tumor suppressor genes in distinctive gastrointestinal nerve sheath tumors traditionally diagnosed as benign schwannomas: s study of 20 cases

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scholarly article

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Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

Evaluation of NF2 and NF1 tumor suppressor genes in distinctive gastrointestinal nerve sheath tumors traditionally diagnosed as benign schwannomas: s study of 20 cases (English)

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

8

object named as

Leslie H Sobin

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4 February 2018

http://europepmc.org/abstract/MED/13679444

Markku Miettinen

9

object named as

Markku Miettinen

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4 February 2018

http://europepmc.org/abstract/MED/13679444

1

object named as

Jerzy Lasota

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Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

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ORCID Public Data File 2021

Agnieszka Dansonka-Mieszkowska

3

object named as

Agnieszka Dansonka-Mieszkowska

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Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

6

object named as

Janusz Ryś

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Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

author name string

Bartek Wasag

2

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

Danuta Karcz

4

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

Carl L Millward

5

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

Jerzy Stachura

7

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4 February 2018

http://europepmc.org/abstract/MED/13679444

publication date

1 September 2003

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Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

Laboratory Investigation

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4 February 2018

http://europepmc.org/abstract/MED/13679444

83

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4 February 2018

http://europepmc.org/abstract/MED/13679444

9

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4 February 2018

http://europepmc.org/abstract/MED/13679444

1361-1371

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4 February 2018

http://europepmc.org/abstract/MED/13679444

https://scigraph.springernature.com/pub.10.1097/01.lab.0000087591.29639.e3

0 references

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

1 reference

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21 January 2018

NF1 tumor suppressor gene function: narrowing the GAP

1 reference

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21 January 2018

Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene

1 reference

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21 January 2018

Benign schwannoma of the gastrointestinal tract: a clinicopathologic and immunohistochemical study

1 reference

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Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1.

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Molecular insights into neurofibromatosis 2.

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Loss of merlin expression in sporadic meningiomas, ependymomas and schwannomas.

1 reference

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An RsaI polymorphism in the transcribed region of the neurofibromatosis (NF1)-gene.

1 reference

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The tumour suppressor protein NF2/merlin: the puzzle continues.

1 reference

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21 January 2018

A search for evidence of somatic mutations in the NF1 gene.

1 reference

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The involvement of calpain-dependent proteolysis of the tumor suppressor NF2 (merlin) in schwannomas and meningiomas

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Loss of NF1 alleles distinguish sporadic from NF1-associated pilocytic astrocytomas.

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Mutation and cancer: statistical study of retinoblastoma

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The neurofibromatosis type 2 gene is mutated in perineurial cell tumors: a molecular genetic study of eight cases.

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Characterisation of 16 polymorphic markers in the NF2 gene: application to hemizygosity detection.

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Genomic organization of the neurofibromatosis 1 gene (NF1).

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21 January 2018

Screening for germ-line mutations in the NF2 gene.

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Ras signaling and NF1.

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21 January 2018

Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 gene.

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Schwannomas in the colon and rectum: a clinicopathologic and immunohistochemical study of 20 cases

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21 January 2018

NF1 deletions in S-100 protein-positive and negative cells of sporadic and neurofibromatosis 1 (NF1)-associated plexiform neurofibromas and malignant peripheral nerve sheath tumors

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NF1 gene and neurofibromatosis 1

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

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Confirmation of a double-hit model for the NF1 gene in benign neurofibromas

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Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17.

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Analysis of the NF1 gene by temperature gradient gel electrophoresis reveals a high incidence of mutations in exon 4b.

1 reference

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

1 reference

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The neurofibromatosis type 2 gene is inactivated in schwannomas

1 reference

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Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

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The catalytic domain of the neurofibromatosis type 1 gene product stimulates ras GTPase and complements ira mutants of S. cerevisiae

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The neurofibromatosis type 1 gene encodes a protein related to GAP

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Crystalloid formation in gastrointestinal schwannoma.

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Neurofibromatosis type I tumor suppressor neurofibromin regulates neuronal differentiation via its GTPase-activating protein function toward Ras.

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Neurofibromas in NF1: Schwann cell origin and role of tumor environment

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NF2 gene in neurofibromatosis type 2 patients.

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Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 gene

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Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulations

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Analysis of mutations in theSCH gene in schwannomas

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A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene

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Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene

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Frequency and distribution of NF2 mutations in schwannomas

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Allelic loss of the NF1 gene in NF1-associated plexiform neurofibromas

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Frequent genomic imbalances in chromosomes 17, 19, and 22q in peripheral nerve sheath tumours detected by comparative genomic hybridization analysis

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Alterations at chromosome 17 loci in peripheral nerve sheath tumors

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10.1097/01.LAB.0000087591.29639.E3

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

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1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/13679444

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