A particular GAP in mind

Y. Zhu, L. R. Parada

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Type 1 neurofibromatosis is a syndrome caused by mutation of the gene NF1, which encodes neurofibromin - a tumor suppressor related to the Ras GAP signaling proteins. A new study of mice that lack a splice variant of neurofibromin discloses learning impairments similar to those of people with neurofibromatosis, and raises questions about the signaling pathways implicating neurofibromin isoforms during synaptic plasticity.

Original languageEnglish (US)
Pages (from-to)354-355
Number of pages2
JournalNature Genetics
Volume27
Issue number4
DOIs
StatePublished - 2001

Fingerprint

Neurofibromin 1
ras GTPase-Activating Proteins
GTPase-Activating Proteins
ras Proteins
Neurofibromatoses
Neuronal Plasticity
Neurofibromatosis 1
Protein Isoforms
Learning
Mutation
Genes
Neoplasms

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Zhu, Y., & Parada, L. R. (2001). A particular GAP in mind. Nature Genetics, 27(4), 354-355. https://doi.org/10.1038/86835

A particular GAP in mind. / Zhu, Y.; Parada, L. R.

In: Nature Genetics, Vol. 27, No. 4, 2001, p. 354-355.

Research output: Contribution to journalArticle

Zhu, Y & Parada, LR 2001, 'A particular GAP in mind', Nature Genetics, vol. 27, no. 4, pp. 354-355. https://doi.org/10.1038/86835
Zhu, Y. ; Parada, L. R. / A particular GAP in mind. In: Nature Genetics. 2001 ; Vol. 27, No. 4. pp. 354-355.
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