Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? (Q29616332)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

30 April 2017

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? (English)

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1089071

neurodevelopmental disorder

27 March 2024

main subject

1 reference

based on heuristic

inferred from title

intracellular signaling peptides and proteins

1 reference

Europe PubMed Central

PubMed ID

14593168

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14593168

non-histone chromosomal proteins

27 March 2024

1 reference

Europe PubMed Central

PubMed ID

14593168

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14593168

27 March 2024

repressor proteins

1 reference

Europe PubMed Central

PubMed ID

14593168

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14593168

27 March 2024

1

Zoghbi HY

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

30 April 2017

language of work or name

1 reference

30 April 2017

publication date

31 October 2003

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

full work available at URL

30 April 2017

https://www.science.org/doi/pdf/10.1126/science.1089071

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1089071

27 March 2024

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

30 April 2017

volume

302

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

30 April 2017

issue

5646

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

30 April 2017

page(s)

826-30

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

Rett syndrome and MeCP2: linking epigenetics and neuronal function

30 April 2017

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A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

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Electroencephalographic findings in Rett syndrome

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Rett's syndrome. Correlation of electroencephalographic characteristics with clinical staging

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Neuroanatomy of Rett syndrome: a volumetric imaging study

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Immature pattern of brain activity in Rett syndrome.

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Microscopic Observations of the Brain in Rett Syndrome

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27 March 2024

News and comment

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Organ growth in Rett syndrome: a postmortem examination analysis.

27 March 2024

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

27 March 2024

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Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

27 March 2024

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Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

27 March 2024

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MECP2 mutations account for most cases of typical forms of Rett syndrome.

27 March 2024

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Two affected boys in a Rett syndrome family: clinical and molecular findings

27 March 2024

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MeCP2 mutations in children with and without the phenotype of Rett syndrome

27 March 2024

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Identification of MeCP2 mutations in a series of females with autistic disorder

27 March 2024

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MECP2 mutation in male patients with non-specific X-linked mental retardation.

27 March 2024

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A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

27 March 2024

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MECP2 is highly mutated in X-linked mental retardation.

27 March 2024

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A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

27 March 2024

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Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?

27 March 2024

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Levetiracetam for acute mania

27 March 2024

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The methyl-CpG binding domain and the evolving role of DNA methylation in animals

27 March 2024

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DNA methylation patterns and epigenetic memory

27 March 2024

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The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation

27 March 2024

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Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

27 March 2024

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Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

27 March 2024

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Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex.

27 March 2024

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Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

27 March 2024

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The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells

27 March 2024

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Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.

27 March 2024

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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

27 March 2024

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

27 March 2024

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Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

27 March 2024

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Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

27 March 2024

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27 March 2024

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27 March 2024

Brain volume in autism.

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Dissociations of cerebral cortex, subcortical and cerebral white matter volumes in autistic boys.

27 March 2024

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MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults.

27 March 2024

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Evidence of brain overgrowth in the first year of life in autism

27 March 2024

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Neocortical system abnormalities in autism: an fMRI study of spatial working memory.

27 March 2024

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Mind blindness and the brain in autism

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Neuropathology of infantile autism.

27 March 2024

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Is medical genetics neglecting epigenetics?

27 March 2024

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Infantile autism: a genetic study of 21 twin pairs

27 March 2024

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Autism as a strongly genetic disorder: evidence from a British twin study

27 March 2024

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A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

27 March 2024

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Genetics of austim: complex aetiology for a heterogeneous disorder

27 March 2024

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Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

27 March 2024

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A case of autism associated with partial tetrasomy 15.

27 March 2024

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Autism and maternally derived aberrations of chromosome 15q.

27 March 2024

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Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

27 March 2024

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Chromosomal abnormalities in a series of children with autistic disorder.

27 March 2024

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Three probands with autistic disorder and isodicentric chromosome 15.

27 March 2024

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The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

27 March 2024

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A family with a grand-maternally derived interstitial duplication of proximal 15q.

27 March 2024

66

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Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder.

27 March 2024

67

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Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb.

27 March 2024

69

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

27 March 2024

70

1 reference

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Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis

27 March 2024

72

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Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

27 March 2024

73

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Neurexin mediates the assembly of presynaptic terminals

27 March 2024

74

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Targeted disruption of the trkB neurotrophin receptor gene results in nervous system lesions and neonatal death

27 March 2024

75

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Structure and evolution of neurexin genes: insight into the mechanism of alternative splicing

27 March 2024

76

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Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

27 March 2024

77

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Autism in Angelman syndrome: a population-based study

27 March 2024

78

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A Rett patient with a typical Angelman EEG.

27 March 2024

79

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Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein

27 March 2024

80

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27 March 2024

Identifiers

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

30 April 2017

Consolidated OpenCitations Corpus – April 2017

1632186

1632186

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14593168

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017