The relationship of Rett syndrome and MECP2 disorders to autism.
about
Rett Syndrome: Crossing the Threshold to Clinical TranslationMECP2 disorders: from the clinic to mice and backSynaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.Molecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disordersAstrocytes: the missing link in neurologic disease?Mutation of the CH1 Domain in the Histone Acetyltransferase CREBBP Results in Autism-Relevant Behaviors in MiceVPA alleviates neurological deficits and restores gene expression in a mouse model of Rett syndromeRole of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy.Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout ratsHeterogeneity within Autism Spectrum Disorders: What have We Learned from Neuroimaging Studies?Overview of mouse models of autism spectrum disordersAstrocyte-specific regulation of hMeCP2 expression in Drosophila.Network models predict that reduced excitatory fluctuations can give rise to hippocampal network hyper-excitability in MeCP2-null micePhenotypic and molecular convergence of 2q23.1 deletion syndrome with other neurodevelopmental syndromes associated with autism spectrum disorder.Autism spectrum disorder and epilepsy: Disorders with a shared biology.Autism-Like Behavior and Epigenetic Changes Associated with Autism as Consequences of In Utero Exposure to Environmental Pollutants in a Mouse Model.Wild-type microglia do not reverse pathology in mouse models of Rett syndromeA Role for Diminished GABA Transporter Activity in the Cortical Discharge Phenotype of MeCP2-Deficient Mice.Breathing challenges in Rett syndrome: lessons learned from humans and animal models.Rett syndrome: a wide clinical and autonomic picture.Rescue of behavioral and EEG deficits in male and female Mecp2-deficient mice by delayed Mecp2 gene reactivation.Genes related to mitochondrial functions, protein degradation, and chromatin folding are differentially expressed in lymphomonocytes of Rett syndrome patientsBrief report: MECP2 mutations in people without Rett syndrome.The role of ionotropic glutamate receptors in childhood neurodevelopmental disorders: autism spectrum disorders and fragile x syndrome.The intervening domain from MeCP2 enhances the DNA affinity of the methyl binding domain and provides an independent DNA interaction site.Dysfunctional mTORC1 Signaling: A Convergent Mechanism between Syndromic and Nonsyndromic Forms of Autism Spectrum Disorder?Development of the Tailored Rett Intervention and Assessment Longitudinal (TRIAL) database and the Rett Evaluation of Symptoms and Treatments (REST) Questionnaire.Developmental profile of speech-language and communicative functions in an individual with the preserved speech variant of Rett syndrome.D-cycloserine improves synaptic transmission in an animal mode of Rett syndrome.Increased binding of MeCP2 to the GAD1 and RELN promoters may be mediated by an enrichment of 5-hmC in autism spectrum disorder (ASD) cerebellum.Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the diseaseThe feasibility of using actigraphy to characterize sleep in Rett syndrome.Common Defects of Spine Dynamics and Circuit Function in Neurodevelopmental Disorders: A Systematic Review of Findings From in Vivo Optical Imaging of Mouse Models.
P2860
Q26772909-F4F2AE18-85A1-42E9-939B-9390953E73C8Q26799760-DDE2F11D-602B-4D67-B317-02E52A719B73Q26829347-7D2D632A-65A7-47A6-BF1D-6C98FB1A0E6EQ26853035-1984D56A-56F3-4259-9C67-BB6DC9526C19Q26861132-F72773CD-AE5D-4B7A-BEC1-26DF71450D8FQ27332438-1D85B077-66B4-4DF6-BE26-8E06E951D4D4Q28540049-31A9E8DE-BA6E-4605-8937-BF2AD70A7712Q30235312-82065AB3-2DB9-4A99-88FC-EC429D971ECEQ30367333-A6EF3EC0-5DAE-4DDD-BDE0-96717E01DB9AQ30381238-DCB070EA-C3E1-4FFA-BA68-DCF31C319942Q30689991-24FC9926-6B8C-4C6C-BB3E-D3F2D80B7D7FQ34294538-D75BAAAE-356D-43CB-BAD5-7D744AFB65C7Q34515794-2D460200-531A-46A0-92A8-2222BCEF5F4FQ35123869-7CC2CEBD-36AE-4247-9783-D56764E6D8D7Q35585527-E9DFD8F3-B8AD-46DD-A2CD-BF2D18D5CAA0Q35762766-1884B626-5FE8-47FC-BA14-E76E457EE6B8Q36261010-F29CE557-4065-4147-B9C8-20E9DC0394D0Q36386922-68B20CF2-3174-4D8B-92E6-472E9902FCB3Q36799043-D8C184DB-B38E-4418-AE9B-74574DD77A30Q37265909-B5A9A076-F0B5-4CF8-BE9C-55FEE61B2878Q37294375-70BBF872-97B3-47CA-9E03-F466D24EB820Q37406408-706FD64E-F444-4981-9275-4E7D23A228A7Q37422466-FDE2D814-BEBA-4297-B787-9248250FAAF5Q37431830-54DA8116-9004-40B1-8C9C-51EF2702321AQ37559828-DF97AF16-9F83-4BB7-B46A-186D0BE9F9A4Q37615316-62D807BC-2DE5-4B2C-A750-71ECDDAED020Q37729341-CB9A0F57-FA81-4364-AD4A-2A787B91F2FEQ38715062-9EFCD93B-80DE-4B1E-8BDF-27E27A3EB8C9Q39381284-EA4952E1-459C-4086-997D-949462278797Q41433830-AB17252A-5002-4F1C-8361-967CC76551BCQ41897180-69B44636-B35A-4C3C-9B4E-8610F2AA6B4FQ42089130-A83443CA-B2E8-4DBC-8333-4877F0CF1245Q50324419-C461DF90-483A-4191-8244-24809CB2D6CCQ55474439-30295956-7496-4046-A011-D7BA2E266050
P2860
The relationship of Rett syndrome and MECP2 disorders to autism.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
The relationship of Rett syndrome and MECP2 disorders to autism.
@ast
The relationship of Rett syndrome and MECP2 disorders to autism.
@en
type
label
The relationship of Rett syndrome and MECP2 disorders to autism.
@ast
The relationship of Rett syndrome and MECP2 disorders to autism.
@en
prefLabel
The relationship of Rett syndrome and MECP2 disorders to autism.
@ast
The relationship of Rett syndrome and MECP2 disorders to autism.
@en
P2860
P921
P1476
The relationship of Rett syndrome and MECP2 disorders to autism
@en
P2093
Jeffrey Lorenz Neul
P2860
P304
P5008
P577
2012-09-01T00:00:00Z