(Q39069727)

8 September 2017

title

Identification of two novel Shank3 transcripts in the developing mouse neocortex (English)

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8 September 2017

Chikako Waga

1

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8 September 2017

Hirotsugu Asano

2

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8 September 2017

Tomomi Sanagi

3

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8 September 2017

Eri Suzuki

4

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8 September 2017

Yasuko Nakamura

5

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8 September 2017

Akiko Tsuchiya

6

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8 September 2017

Masayuki Itoh

7

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8 September 2017

Yu-ichi Goto

8

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8 September 2017

Shinichi Kohsaka

9

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8 September 2017

Shigeo Uchino

10

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8 September 2017

language of work or name

English

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publication date

14 November 2013

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Journal of Neurochemistry

8 September 2017

number of pages

14

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based on heuristic

inferred from page(s)

published in

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8 September 2017

volume

128

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8 September 2017

issue

2

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8 September 2017

page(s)

280-293

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

8 September 2017

cites work

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DNA methylation regulates tissue-specific expression of Shank3.

21 January 2018

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Differential expression and dendritic transcript localization of Shank family members: identification of a dendritic targeting element in the 3' untranslated region of Shank1 mRNA.

21 January 2018

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C-terminal synaptic targeting elements for postsynaptic density proteins ProSAP1/Shank2 and ProSAP2/Shank3.

21 January 2018

1 reference

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

21 January 2018

1 reference

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

21 January 2018

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MeCP2, a key contributor to neurological disease, activates and represses transcription

21 January 2018

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Epigenome analyses using BAC microarrays identify evolutionary conservation of tissue-specific methylation of SHANK3.

21 January 2018

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

21 January 2018

1 reference

Differential changes in mGlu2 and mGlu3 gene expression following pilocarpine-induced status epilepticus: a comparative real-time PCR analysis

21 January 2018

1 reference

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

21 January 2018

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Novel de novo SHANK3 mutation in autistic patients

21 January 2018

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 January 2018

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Inhibition of NMDA receptors induces delayed neuronal maturation and sustained proliferation of progenitor cells during neocortical development

21 January 2018

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Recent advances in MeCP2 structure and function

21 January 2018

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Modeling autism by SHANK gene mutations in mice

21 January 2018

1 reference

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

21 January 2018

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Characterization of the Shank family of synaptic proteins. Multiple genes, alternative splicing, and differential expression in brain and development

21 January 2018

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Conserved role of intragenic DNA methylation in regulating alternative promoters

21 January 2018

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Contribution of SHANK3 mutations to autism spectrum disorder

21 January 2018

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Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin

21 January 2018

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Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

21 January 2018

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Direct interaction of post-synaptic density-95/Dlg/ZO-1 domain-containing synaptic molecule Shank3 with GluR1 alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor

21 January 2018

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Novel variants of the SHANK3 gene in Japanese autistic patients with severe delayed speech development

21 January 2018

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Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

21 January 2018

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A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q

21 January 2018

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Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/JNC.12505

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8 September 2017

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