SYNGAP1 mutations: Clinical, genetic, and pathophysiological features-Reference-Cited by-同舟云学术

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SYNGAP1 mutations: Clinical, genetic, and pathophysiological features

Published:2019-08-24 Issue:1 Volume:78 Page:65-76
ISSN:0736-5748
Container-title:International Journal of Developmental Neuroscience
language:en
Short-container-title:Int. j. dev. neurosci.

Author:

Agarwal Mudit¹,Johnston Michael V.²,Stafstrom Carl E.³

Affiliation:

1. All India Institute of Medical SciencesNew DelhiIndia

2. Department of Neurology and Developmental MedicineThe Kennedy Krieger InstituteBaltimoreMDUnited States

3. Division of Pediatric NeurologyThe Johns Hopkins University School of MedicineBaltimoreMDUnited States

Publisher

Wiley

Subject

Developmental Biology,Developmental Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1016/j.ijdevneu.2019.08.003

Reference133 articles.

1. Syngap1 Haploinsufficiency Damages a Postnatal Critical Period of Pyramidal Cell Structural Maturation Linked to Cortical Circuit Assembly

2. Rapid Dispersion of SynGAP from Synaptic Spines Triggers AMPA Receptor Insertion and Spine Enlargement during LTP

3. Convergence of Hippocampal Pathophysiology in Syngap+/- and Fmr1-/y Mice

4. Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function

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1. A 10-Year Review on Advancements in Identifying and Treating Intellectual Disability Caused by Genetic Variations;Genes;2024-08-24

2. Accelerating therapeutic development and clinical trial readiness for STXBP1 and SYNGAP1 disorders;Current Problems in Pediatric and Adolescent Health Care;2024-08

3. Behavioural phenotype of SYNGAP1‐related intellectual disability;Journal of Intellectual Disability Research;2024-05-23

4. Visual social attention in SYNGAP1‐related intellectual disability;Autism Research;2024-05-03

5. Overexpression of SYNGAP1 suppresses the proliferation of rectal adenocarcinoma via Wnt/β-Catenin signaling pathway;Discover Oncology;2024-04-29

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