MAP'ing CNS development and cognition: an ERKsome process (Q24621710)

The spread of Ras activity triggered by activation of a single dendritic spine

Europe PubMed Central

title

MAP'ing CNS development and cognition: an ERKsome process (English)

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author name string

Ivy S Samuels

series ordinal

1

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Sulagna C Saitta

series ordinal

2

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Gary E Landreth

series ordinal

3

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language of work or name

English

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publication date

29 January 2009

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published in

Neuron

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volume

61

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issue

2

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page(s)

160-7

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cites work

1 reference

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Mouse and human phenotypes indicate a critical conserved role for ERK2 signaling in neural crest development

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Loss of glutamatergic pyramidal neurons in frontal and temporal cortex resulting from attenuation of FGFR1 signaling is associated with spontaneous hyperactivity in mice

7 April 2017

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Spatial and temporal patterns of ERK signaling during mouse embryogenesis

7 April 2017

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Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis

7 April 2017

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MAPK cascade signalling and synaptic plasticity

7 April 2017

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An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination

7 April 2017

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Circadian oscillation of hippocampal MAPK activity and cAmp: implications for memory persistence.

7 April 2017

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Neurofibromin regulation of ERK signaling modulates GABA release and learning

27 September 2017

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Deletion of ERK2 mitogen-activated protein kinase identifies its key roles in cortical neurogenesis and cognitive function.

27 September 2017

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Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome.

27 September 2017

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27 September 2017

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27 September 2017

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Essential role of B-Raf in oligodendrocyte maturation and myelination during postnatal central nervous system development

27 September 2017

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The extracellular signal-regulated kinase pathway contributes to the control of behavioral excitement

27 September 2017

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22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome

27 September 2017

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Recurrent 16p11.2 microdeletions in autism

27 September 2017

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Role of intermediate progenitor cells in cerebral cortex development

27 September 2017

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Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment

27 September 2017

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Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype

27 September 2017

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27 September 2017

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Control of CNS cell-fate decisions by SHP-2 and its dysregulation in Noonan syndrome

27 September 2017

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Raf kinase signaling functions in sensory neuron differentiation and axon growth in vivo

27 September 2017

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27 September 2017

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HRAS and the Costello syndrome

27 September 2017

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Signal transduction mechanisms in memory disorders

27 September 2017

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DiGeorge syndrome and pharyngeal apparatus development

27 September 2017

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Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction

27 September 2017

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Role of MAPKs in development and differentiation: lessons from knockout mice.

27 September 2017

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Mitogen-activated protein kinase/extracellular regulated kinase signalling and memory stabilization: a review

27 September 2017

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Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.

27 September 2017

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CCAAT/enhancer-binding protein phosphorylation biases cortical precursors to generate neurons rather than astrocytes in vivo.

27 September 2017

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The ERK cascade: a prototype of MAPK signaling

27 September 2017

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22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords

27 September 2017

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Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome.

27 September 2017

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An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome

27 September 2017

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27 September 2017

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Mice lacking the ERK1 isoform of MAP kinase are unimpaired in emotional learning

27 September 2017

1 reference

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27 September 2017

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27 September 2017

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Activation of p42 mitogen-activated protein kinase in hippocampal long term potentiation.

30 May 2018

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Erk kinases link pre-B cell receptor signaling to transcriptional events required for early B cell expansion.

30 May 2018

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Extracellular signal-regulated kinase 2 (ERK2) knockdown mice show deficits in long-term memory; ERK2 has a specific function in learning and memory.

28 November 2018

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Fibroblast growth factor receptor 3 kinase domain mutation increases cortical progenitor proliferation via mitogen-activated protein kinase activation.

28 November 2018

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28 November 2018

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28 November 2018

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Extracellular-signal regulated kinase 1-dependent metabotropic glutamate receptor 5-induced long-term depression in the bed nucleus of the stria terminalis is disrupted by cocaine administration.

28 November 2018

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Knockout of ERK1 enhances cocaine-evoked immediate early gene expression and behavioral plasticity

28 November 2018

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Fibroblast growth factor 2 is required for maintaining the neural stem cell pool in the mouse brain subventricular zone.

28 November 2018

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28 November 2018

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Costello syndrome and neurological abnormalities

28 November 2018

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The isthmic organizer signal FGF8 is required for cell survival in the prospective midbrain and cerebellum.

28 November 2018

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An essential role for a MEK-C/EBP pathway during growth factor-regulated cortical neurogenesis.

28 November 2018

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Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory

28 November 2018

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Fgf signalling through MAPK cascade is required for development of the subpallial telencephalon in zebrafish embryos.

28 November 2018

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Changes in cerebral cortex size are governed by fibroblast growth factor during embryogenesis

28 November 2018

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A novel 22q11.2 microdeletion in DiGeorge syndrome

28 November 2018

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Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study

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Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

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A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation

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10.1016/J.NEURON.2009.01.001

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DOI

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release_jeyex3lt6jcr3g2copjsqero3y

1440807

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24 November 2022

mapped directly with Wikidata item

1440807

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