Neurofibromatosis 2: loss of merlin's protective spell (Q41099831)

26 September 2017

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title

Neurofibromatosis 2: loss of merlin's protective spell (English)

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neurofibromatosis type II

26 September 2017

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1

Gusella JF

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26 September 2017

Ramesh V

2

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PubMed ID

8791482

26 September 2017

MacCollin M

series ordinal

3

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PubMed ID

8791482

26 September 2017

Jacoby LB

series ordinal

4

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26 September 2017

1 February 1996

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Current Opinion in Genetics & Development

26 September 2017

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26 September 2017

6

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26 September 2017

87-92

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26 September 2017

1

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Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

26 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Lens opacities in neurofibromatosis 2: further significant correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Alternative splicing of the NF2 gene and its mutation analysis of breast and colorectal cancers.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Exon scanning for mutation of the NF2 gene in schwannomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Expression of the neurofibromatosis 2 (NF2) gene isoforms during rat embryonic development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

The neurofibromatosis 2 (NF2) tumor suppressor gene encodes multiple alternatively spliced transcripts.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

An exon 8-spliced out transcript of neurofibromatosis 2 gene is constitutively expressed in various human tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

The murine NF2 homologue encodes a highly conserved merlin protein with alternative forms

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

The mouse neurofibromatosis type 2 gene maps to chromosome 11.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

The mouse homologue of the neurofibromatosis type 2 gene is highly conserved

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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Alternative transcripts in the mouse neurofibromatosis type 2 (NF2) gene are conserved and code for schwannomins with distinct C-terminal domains

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Characterization of the translocation breakpoint on chromosome 22q12.2 in a patient with neurofibromatosis type 2 (NF2).

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Germline mutations in the neurofibromatosis type 2 tumour suppressor gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

A 163-bp deletion in the neurofibromatosis 2 (NF2) gene associated with variant phenotypes [corrected]

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Screening for germ-line mutations in the NF2 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Analysis of mutations in theSCH gene in schwannomas

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

The neurofibromatosis type 2 gene is inactivated in schwannomas

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Evidence for subarachnoid spread in the development of multiple meningiomas

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Loss of heterozygosity on chromosome 22 in ovarian carcinoma is distal to and is not accompanied by mutations in NF2 at 22q12.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Analysis of theNF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

High frequency of inactivating mutations in the neurofibromatosis type 2 gene (NF2) in primary malignant mesotheliomas

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Membrane-actin microfilament connections: an increasing diversity of players related to band 4.1.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

cDNA cloning and sequencing of the protein-tyrosine kinase substrate, ezrin, reveals homology to band 4.1

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Radixin is a novel member of the band 4.1 family

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Perturbation of cell adhesion and microvilli formation by antisense oligonucleotides to ERM family members

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

ERM family members as molecular linkers between the cell surface glycoprotein CD44 and actin-based cytoskeletons

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

Pez: a novel human cDNA encoding protein tyrosine phosphatase- and ezrin-like domains

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990016-7

7 January 2021

10.1016/S0959-437X(96)90016-7

Identifiers

DOI

1 reference

26 September 2017

1 reference

PubMed ID

8791482