Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome
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Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysisIdentification and Treatment of Pathophysiological Comorbidities of Autism Spectrum Disorder to Achieve Optimal Outcomes.Neuropathological Mechanisms of Seizures in Autism Spectrum DisorderImpairment of TrkB-PSD-95 signaling in Angelman syndromeGastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.Mitochondria, bioenergetics, and the epigenome in eukaryotic and human evolutionTreatments for biomedical abnormalities associated with autism spectrum disorder.Loss of inherited genomic imprints in mice leads to severe disruption in placental lipid metabolismMitochondrial dysfunction can connect the diverse medical symptoms associated with autism spectrum disorders.Energetics, epigenetics, mitochondrial genetics.Neurodevelopmental Underpinnings of Angelman Syndrome.Mitochondrial and ion channel gene alterations in autism.A Novel Imprinted Gene NUWA Controls Mitochondrial Function in Early Seed Development in Arabidopsis.Mitochondrial Superoxide Contributes to Hippocampal Synaptic Dysfunction and Memory Deficits in Angelman Syndrome Model MiceA mitochondrial bioenergetic etiology of disease.Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure.Metabolic Dysfunction Underlying Autism Spectrum Disorder and Potential Treatment Approaches.HECT-type E3 ubiquitin ligases in nerve cell development and synapse physiology.Angelman syndrome: Current and emerging therapies in 2016.Autism spectrum disorder: neuropathology and animal models.Autistic Siblings with Novel Mutations in Two Different Genes: Insight for Genetic Workups of Autistic Siblings and Connection to Mitochondrial Dysfunction.Pharmacological therapies for Angelman syndrome.Subcellular organization of UBE3A in neurons.How Can a Ketogenic Diet Improve Motor Function?Ultrastructural synaptic changes associated with neurofibromatosis type 1: a quantitative analysis of hippocampal region CA1 in a Nf1(+/-) mouse model.Impaired Neurite Contact Guidance in Ubiquitin Ligase E3a (Ube3a)-Deficient Hippocampal Neurons on Nanostructured Substrates.Subcellular organization of UBE3A in human cerebral cortex
P2860
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P2860
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
Mitochondrial dysfunction in C ...... se model for Angelman syndrome
@ast
Mitochondrial dysfunction in C ...... se model for Angelman syndrome
@en
type
label
Mitochondrial dysfunction in C ...... se model for Angelman syndrome
@ast
Mitochondrial dysfunction in C ...... se model for Angelman syndrome
@en
prefLabel
Mitochondrial dysfunction in C ...... se model for Angelman syndrome
@ast
Mitochondrial dysfunction in C ...... se model for Angelman syndrome
@en
P2093
P2860
P1433
P1476
Mitochondrial dysfunction in C ...... se model for Angelman syndrome
@en
P2093
Allan Acab
Douglas C Wallace
Hailing Su
John H Weiss
Jouni Vesa
June-Anne Gold
Pinar E Coskun
Prasanth Potluri
Virginia E Kimonis
Weiwei Fan
P2860
P304
P356
10.1016/J.NEULET.2009.06.079
P407
P577
2009-06-27T00:00:00Z