Mitochondrial dysfunction in Pten haplo-insufficient mice with social deficits and repetitive behavior: interplay between Pten and p53
about
A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.Identification and Treatment of Pathophysiological Comorbidities of Autism Spectrum Disorder to Achieve Optimal Outcomes.Roles of PTEN with DNA Repair in Parkinson's DiseaseOn metabolic reprogramming and tumor biology: A comprehensive survey of metabolism in breast cancerA common molecular signature in ASD gene expression: following Root 66 to autismPrimary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and TreatmentPremutation in the Fragile X Mental Retardation 1 (FMR1) Gene Affects Maternal Zn-milk and Perinatal Brain Bioenergetics and Scaffolding.Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.Superimposing Status Epilepticus on Neuron Subset-Specific PTEN Haploinsufficient and Wild Type Mice Results in Long-term Changes in Behavior.Advanced pharmacotherapy evidenced by pathogenesis of autism spectrum disorder.Treatments for biomedical abnormalities associated with autism spectrum disorder.Autism-Like Behaviours and Memory Deficits Result from a Western Diet in Mice.Associated features in females with an FMR1 premutationGenomic studies in fragile X premutation carriers.Overview of mouse models of autism spectrum disordersNeuronal SUMOylation: mechanisms, physiology, and roles in neuronal dysfunction.Potential therapeutic use of the ketogenic diet in autism spectrum disordersSchizophrenia interactome with 504 novel protein-protein interactionsSustained activation of Akt elicits mitochondrial dysfunction to block Plasmodium falciparum infection in the mosquito hostPKD1 mediates negative feedback of PI3K/Akt activation in response to G protein-coupled receptors.Modulation of the genome and epigenome of individuals susceptible to autism by environmental risk factorsImpact of a novel homozygous mutation in nicotinamide nucleotide transhydrogenase on mitochondrial DNA integrity in a case of familial glucocorticoid deficiency.Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion SyndromeMonogenic mouse models of autism spectrum disorders: Common mechanisms and missing links.Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.Toxicity of the flame-retardant BDE-49 on brain mitochondria and neuronal progenitor striatal cells enhanced by a PTEN-deficient backgroundGestational exposure to a viral mimetic poly(i:C) results in long-lasting changes in mitochondrial function by leucocytes in the adult offspring.mTOR, a Potential Target to Treat Autism Spectrum Disorder.Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure.Advancing the discovery of medications for autism spectrum disorder using new technologies to reveal social brain circuitry in rodents.Host-pathogen interactions in malaria: cross-kingdom signaling and mitochondrial regulation.The Antisense Transcriptome and the Human Brain.Epigenetic Treatment of Neuropsychiatric Disorders: Autism and Schizophrenia.Identification of likely associations between cerebral folate deficiency and complex genetic- and metabolic pathogenesis of autism spectrum disorders by utilization of a pilot interaction modeling approach.Implications of the FMR1 Premutation for Children, Adolescents, Adults, and Their Families.Regulatory Role of Redox Balance in Determination of Neural Precursor Cell Fate.Altered Bioenergetics in Primary Dermal Fibroblasts from Adult Carriers of the FMR1 Premutation Before the Onset of the Neurodegenerative Disease Fragile X-Associated Tremor/Ataxia Syndrome.Autism spectrum disorder and Li-Fraumeni syndrome: purely coincidental or mechanistically associated?Autistic Siblings with Novel Mutations in Two Different Genes: Insight for Genetic Workups of Autistic Siblings and Connection to Mitochondrial Dysfunction.Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism.
P2860
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P2860
Mitochondrial dysfunction in Pten haplo-insufficient mice with social deficits and repetitive behavior: interplay between Pten and p53
description
2012 nî lūn-bûn
@nan
2012 թուականին հրատարակուած գիտական յօդուած
@hyw
2012 թվականին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@ast
Mitochondrial dysfunction in P ...... interplay between Pten and p53
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Mitochondrial dysfunction in P ...... interplay between Pten and p53
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Mitochondrial dysfunction in P ...... interplay between Pten and p53
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type
label
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@ast
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@en
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@en-gb
Mitochondrial dysfunction in P ...... interplay between Pten and p53
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altLabel
Mitochondrial Dysfunction in P ...... Interplay between Pten and p53
@en
prefLabel
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@ast
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@en
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@en-gb
Mitochondrial dysfunction in P ...... interplay between Pten and p53
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P2093
P2860
P3181
P1433
P1476
Mitochondrial dysfunction in P ...... interplay between Pten and p53
@en
P2093
Alicja Omanska-Klusek
Catherine Ross-Inta
Connie Hung
Danielle Sakaguchi
Eleonora Napoli
James Angelastro
Robert Schoenfeld
Sarah Wong
Yasuko Fujisawa
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0042504
P407
P577
2012-01-01T00:00:00Z