Home LiteratureArticle Details
PMID: 16818172 Published · ppublish English Journal Article Review

The genetic and molecular pathogenesis of NF1 and NF2.

Seminars in pediatric neurology ·Vol. 13 ·No. 1 ·2006-03-00 ·Pages 21-6

Yohay KH

Abstract

Neurofibromatosis types 1 and 2 (NF1 and NF2) are autosomal dominant phakomatoses. The NF1 and NF2 genes encode for neurofibromin and merlin, respectively. These 2 functionally unrelated proteins both act as tumor suppressor genes, possibly through modulation of the RAS/RAC oncogenic pathways. Improved understanding of the mechanisms by which these tumor suppressors act may allow for medical therapies for neurofibromatosis and may offer insights for cancer therapeutics.

MeSH Terms
Animals Genes, Tumor Suppressor/physiology Humans Neurofibromatosis 1/genetics Neurofibromatosis 2/genetics Neurofibromin 1/genetics Neurofibromin 2/genetics
Chemicals
Neurofibromin 1 Neurofibromin 2
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Yohay Kaleb H
Division of Child Neurology and Pediatrics, Johns Hopkins University, Baltimore, MD 21287, USA. kyohay@jhmi.edu
Article Info
Journal
Seminars in pediatric neurology
Abbr.
Semin Pediatr Neurol
ISSN
1071-9091
Published
2006-03-00
Pages
21-6
Language
English
Region
United States
NLM ID
9441351
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com