Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
about
Web-based, participant-driven studies yield novel genetic associations for common traitsAnaplerotic triheptanoin diet enhances mitochondrial substrate use to remodel the metabolome and improve lifespan, motor function, and sociability in MeCP2-null miceNovel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS dataCommon variants within MECP2 confer risk of systemic lupus erythematosusX-linked disorders with cerebellar dysgenesisComparative study of methyl-CpG-binding domain proteinsThe DNA sequence of the human X chromosomeAutistic phenotypes and genetic testing: state-of-the-art for the clinical geneticistGenetics of autism spectrum disorderAdvances in autism genetics: on the threshold of a new neurobiologyHistone deacetylase-independent transcriptional repression by methyl-CpG-binding protein 2.Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.X chromosome-wide analysis identifies DNA methylation sites influenced by cigarette smokingThe Ski protein family is required for MeCP2-mediated transcriptional repressionWSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci.Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardationCDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndromeTwo highly related p66 proteins comprise a new family of potent transcriptional repressors interacting with MBD2 and MBD3The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysisTranscriptional regulator PRDM12 is essential for human pain perceptionReduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndromeReelin promoter hypermethylation in schizophreniaMutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardationSpecific binding of the methyl binding domain protein 2 at the BRCA1-NBR2 locus.On the epigenetic regulation of the human reelin promoterMECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal originImprinting regulator DNMT3L is a transcriptional repressor associated with histone deacetylase activityCpG binding protein is crucial for early embryonic developmentThe chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesisX-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in miceThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Rett syndrome: revised diagnostic criteria and nomenclaturePathophysiology of locus ceruleus neurons in a mouse model of Rett syndromeRett syndrome and MeCP2: linking epigenetics and neuronal functionEmerging pharmacotherapies for neurodevelopmental disordersThe epigenetic landscape of addictionMethylation, memory and addictionMutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossEpigenetics in the mature mammalian brain: effects on behavior and synaptic transmission
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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
description
1999 nî lūn-bûn
@nan
1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@ast
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@en
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@en-gb
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@nl
type
label
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@ast
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@en
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@en-gb
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@nl
prefLabel
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@ast
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@en
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@en-gb
Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@nl
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Rett syndrome is caused by mut ...... g methyl-CpG-binding protein 2
@en
P2093
Charles Q. Tran
Ignatia B. Van den Veyver
Ruthie E. Amir
P2888
P304
P3181
P356
10.1038/13810
P407
P577
1999-10-01T00:00:00Z
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1002301472