Molecular and cellular mechanisms underlying the cognitive deficits associated with neurofibromatosis 1. (Q34156479)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12403561%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

review article

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title

Molecular and cellular mechanisms underlying the cognitive deficits associated with neurofibromatosis 1 (English)

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14 December 2019

2

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14 December 2019

author name string

Rui M Costa

series ordinal

1

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14 December 2019

publication date

1 August 2002

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Journal of Child Neurology

14 December 2019

published in

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14 December 2019

volume

17

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14 December 2019

issue

8

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14 December 2019

page(s)

622-6; discussion 627-9, 646-51

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NF1 tumor suppressor gene function: narrowing the GAP

14 December 2019

cites work

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Specific learning disability in children with neurofibromatosis type 1: significance of MRI abnormalities.

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Mouse neurofibromatosis type 1 cDNA sequence reveals high degree of conservation of both coding and non-coding mRNA segments.

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DNA sequences in the promoter region of the NF1 gene are highly conserved between human and mouse.

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Tumour predisposition in mice heterozygous for a targeted mutation in Nf1

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Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues

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Mouse tumor model for neurofibromatosis type 1

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Region-specific astrogliosis in brains of mice heterozygous for mutations in the neurofibromatosis type 1 (Nf1) tumor suppressor

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A mouse model for the learning and memory deficits associated with neurofibromatosis type I

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Relationship between T2-weighted hyperintensities (unidentified bright objects) and lower IQs in children with neurofibromatosis-1.

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The significance of MRI abnormalities in children with neurofibromatosis

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MRI in neurofibromatosis 1. The nature and evolution of increased intensity T2 weighted lesions and their relationship to intellectual impairment

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Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence

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Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1

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A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activity

21 January 2018

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Ablation of NF1 function in neurons induces abnormal development of cerebral cortex and reactive gliosis in the brain

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The catalytic domain of the neurofibromatosis type 1 gene product stimulates ras GTPase and complements ira mutants of S. cerevisiae

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The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins

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Requirement of Drosophila NF1 for activation of adenylyl cyclase by PACAP38-like neuropeptides

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A neurofibromatosis-1-regulated pathway is required for learning in Drosophila

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Mutations in the GAP-related domain impair the ability of neurofibromin to associate with microtubules.

21 January 2018

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Hyperactivation of p21(ras) and the hematopoietic-specific Rho GTPase, Rac2, cooperate to alter the proliferation of neurofibromin-deficient mast cells in vivo and in vitro

21 January 2018

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A circadian output in Drosophila mediated by neurofibromatosis-1 and Ras/MAPK.

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Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1.

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21 January 2018

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21 January 2018

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