(Q48181670)

9 February 2018

title

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

1 reference

9 February 2018

neurofibromatosis type II

main subject

1 reference

9

Gusella JF

1 reference

9 February 2018

Trofatter JA

8

object named as

Trofatter JA

1 reference

9 February 2018

author name string

Bianchi AB

1

1 reference

9 February 2018

Hara T

2

1 reference

9 February 2018

Ramesh V

3

1 reference

9 February 2018

Gao J

4

1 reference

9 February 2018

Klein-Szanto AJ

5

1 reference

9 February 2018

Morin F

6

1 reference

9 February 2018

Menon AG

7

1 reference

9 February 2018

Seizinger BR

10

1 reference

9 February 2018

language of work or name

English

0 references

publication date

1 February 1994

1 reference

9 February 2018

published in

Nature Genetics

1 reference

9 February 2018

volume

6

1 reference

9 February 2018

issue

2

1 reference

9 February 2018

page(s)

185-192

1 reference

9 February 2018

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

A cytogenetic study of 53 human gliomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

Neurofibromatosis type 1 gene mutations in neuroblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

Rate-limiting steps: The genetics of pediatric cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

Alternative splicing in the control of gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

Parental origin of chromosome 22 loss in sporadic and NF2 neuromas

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

Cytoskeleton--plasma membrane interactions

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

A simple method for displaying the hydropathic character of a protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

Genomic alterations in human breast carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

Heterogeneity for Allelic Loss in Human Breast Cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-185

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

1 reference

9 February 2018