Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

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Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

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http://www.wikidata.org/entity/Q52629859

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

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Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

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label

Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

@en

Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

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Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

@en

Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

@nl

P1476

Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.

@en

P2093

Camilo Rojas

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Gavin Rumbaugh

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Jacob Ellegood

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Jason P Lerch

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Massimiliano Aceti

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Murat Kilinc

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Thomas Creson

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Thomas Vaissiere

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P2860

Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development

SynGAP regulates synaptic strength and mitogen-activated protein kinases in cultured neurons

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses.

De novo mutations in epileptic encephalopathies

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

Role of Unc51.1 and its binding partners in CNS axon outgrowth

Dysregulation and restoration of translational homeostasis in fragile X syndrome

Dysregulation of Mammalian Target of Rapamycin Signaling in Mouse Models of Autism

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.

P31

scholarly article

P356

10.1016/J.MCN.2018.03.008

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P577

2018-03-23T00:00:00Z

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P698

29580901

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P921

neurodevelopmental disorders

P932

6128754

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