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Channelopathies in fragile X syndrome
Pan Yue Deng
,
Vitaly A. Klyachko
Department of Cell Biology & Physiology
Center for the Investigation of Membrane Excitability Diseases
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
DBBS - Neurosciences
Intellectual and Developmental Disabilities Research Center (IDDRC)
Hope Center for Neurological Disorders
Research output
:
Contribution to journal
›
Review article
›
peer-review
82
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Scopus citations
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Keyphrases
Fragile X Syndrome
100%
Channelopathy
100%
Ion Channels
40%
Fragile X Mental Retardation Protein
40%
Dysregulated
20%
Therapeutic Implications
20%
Protein-protein Interaction
20%
Intellectual Disability
20%
Autism
20%
Neuronal Excitability
20%
Synaptic Function
20%
Ion Channel Function
20%
Behavioral Phenotype
20%
Genetic Interventions
20%
Translational Control
20%
Second Messenger Pathways
20%
Ion Range
20%
Pharmacological Interventions
20%
Promising Therapeutics
20%
Monogenic Cause
20%
Knowledge State
20%
Ion Channel Dysfunction
20%
Neuroscience
Fragile X Syndrome
100%
Channelopathy
100%
Ion Channel
60%
Fragile X Mental Retardation Protein
40%
Neuronal Excitability
20%
Second Messenger System
20%
Intellectual Disability
20%
Autism
20%
Genetics
20%
Biochemistry, Genetics and Molecular Biology
Channelopathy
100%
Ion Channel
75%
Genetics
25%
Second Messenger System
25%
Excitability
25%
Animal Model
25%
Intellectual Disability
25%