Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types. (Q48181670)

9 February 2018

title

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

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9 February 2018

neurofibromatosis type II

main subject

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9

Gusella JF

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9 February 2018

Trofatter JA

8

object named as

Trofatter JA

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9 February 2018

author name string

Bianchi AB

1

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9 February 2018

Hara T

2

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9 February 2018

Ramesh V

3

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9 February 2018

Gao J

4

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9 February 2018

Klein-Szanto AJ

5

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9 February 2018

Morin F

6

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9 February 2018

Menon AG

7

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9 February 2018

Seizinger BR

10

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9 February 2018

language of work or name

English

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publication date

1 February 1994

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9 February 2018

published in

Nature Genetics

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9 February 2018

volume

6

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9 February 2018

issue

2

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9 February 2018

page(s)

185-192

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9 February 2018

https://scigraph.springernature.com/pub.10.1038/ng0294-185

exact match

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cites work

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

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Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred

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

21 January 2018

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

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A cytogenetic study of 53 human gliomas.

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Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coli.

21 January 2018

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Neurofibromatosis type 1 gene mutations in neuroblastoma

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Rate-limiting steps: The genetics of pediatric cancers

21 January 2018

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Alternative splicing in the control of gene expression

21 January 2018

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

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

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

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Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

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Molecular genetic approach to human meningioma: loss of genes on chromosome 22

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Parental origin of chromosome 22 loss in sporadic and NF2 neuromas

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Cytoskeleton--plasma membrane interactions

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A simple method for displaying the hydropathic character of a protein

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Mutation and cancer: statistical study of retinoblastoma

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Genomic alterations in human breast carcinomas

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7 January 2021

Heterogeneity for Allelic Loss in Human Breast Cancer

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7 January 2021

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma

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7 January 2021

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

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7 January 2021

Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines

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DNA sequencing with chain-terminating inhibitors

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7 January 2021

Identifiers

DOI

10.1038/NG0294-185

1 reference

9 February 2018

release_nlpfap357naerg7oya7gn7yaya

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/nlpfap357naerg7oya7gn7yaya

24 November 2022

mapped directly with Wikidata item

PubMed ID

8162073

1 reference

9 February 2018