(Q54656865)

2 June 2018

title

Molecular genetics alterations and tumor behavior of sporadic vestibular schwannoma from the People's Republic of China. (English)

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2 June 2018

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vestibular schwannoma

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Liu-Guan Bian

1

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2 June 2018

Wuttipong Tirakotai

2

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2 June 2018

Qing-Fang Sun

3

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2 June 2018

Wei-Guo Zhao

4

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2 June 2018

Jian-Kang Shen

5

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2 June 2018

Qi-Zhong Luo

6

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2 June 2018

publication date

1 July 2005

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2 June 2018

Journal of Neuro-Oncology

published in

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2 June 2018

volume

73

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2 June 2018

issue

3

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2 June 2018

page(s)

253-260

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2 June 2018

Loss of merlin expression in sporadic meningiomas, ependymomas and schwannomas

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11060-004-5176-3

Neurofibromatosis 2 (NF2) tumor suppressor schwannomin and its interacting protein HRS regulate STAT signaling

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Defects in neurofibromatosis 2 protein function can arise at multiple levels.

1 reference

12 December 2020

Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation

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12 December 2020

NF2: the wizardry of merlin

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12 December 2020

Immunohistochemical detection of schwannomin and neurofibromin in vestibular schwannomas, ependymomas and meningiomas.

1 reference

12 December 2020

Presymptomatic DNA and MRI diagnosis of neurofibromatosis 2 with mild clinical course in an extended pedigree

1 reference

12 December 2020

Expression of neurofibromatosis 2 protein in human brain tumors: an immunohistochemical study

1 reference

12 December 2020

Reduced expression of schwannomin/merlin in human sporadic meningiomas

1 reference

12 December 2020

Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas.

1 reference

12 December 2020

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

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the D22S264 locus

1 reference

12 December 2020

NF2 gene in neurofibromatosis type 2 patients.

1 reference

12 December 2020

Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis

1 reference

12 December 2020

Interdomain binding mediates tumor growth suppression by the NF2 gene product

1 reference

12 December 2020

Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease

1 reference

12 December 2020

High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of the NF2 gene and merlin occur by the tumorlet stage of schwannoma development in neurofibromatosis 2

1 reference

12 December 2020

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

1 reference

12 December 2020

Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.

1 reference

12 December 2020

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

1 reference

12 December 2020

Germline screening of the NF-2 gene in families with unilateral vestibular schwannoma

1 reference

12 December 2020

Somatic neurofibromatosis type 2 gene mutations and growth characteristics in vestibular schwannoma

1 reference

12 December 2020

Loss of alleles in vestibular schwannomas: use of microsatellite markers on chromosome 22

1 reference

12 December 2020

Genetic aberrations in sporadic and neurofibromatosis 2 (NF2)-associated schwannomas studied by comparative genomic hybridization (CGH).

1 reference

12 December 2020

A G-->A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2

1 reference

12 December 2020

Immunoblotting analysis of schwannomin/merlin in human schwannomas.

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the human CRYB2 gene locus (22q11.2)

1 reference

12 December 2020

The neurofibromatosis 2 tumor suppressor protein interacts with hepatocyte growth factor-regulated tyrosine kinase substrate

1 reference

12 December 2020

Management of 1000 vestibular schwannomas (acoustic neuromas): clinical presentation

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the D22S268 locus

1 reference

12 December 2020

Overexpression of the NF2 gene inhibits schwannoma cell proliferation through promoting PDGFR degradation

1 reference

12 December 2020

10.1007/S11060-004-5176-3

Identifiers

DOI

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2 June 2018

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2 June 2018