(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

page(s)

826-30

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

Rett syndrome and MeCP2: linking epigenetics and neuronal function

30 April 2017

cites work

1

1 reference

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

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

27 March 2024

4

1 reference

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

Electroencephalographic findings in Rett syndrome

27 March 2024

5

1 reference

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

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

27 March 2024

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1 reference

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Neuroanatomy of Rett syndrome: a volumetric imaging study

27 March 2024

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1 reference

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Immature pattern of brain activity in Rett syndrome.

27 March 2024

8

1 reference

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

Microscopic Observations of the Brain in Rett Syndrome

27 March 2024

9

1 reference

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

27 March 2024

News and comment

10

1 reference

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

Organ growth in Rett syndrome: a postmortem examination analysis.

27 March 2024

13

1 reference

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

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

27 March 2024

14

1 reference

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

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

27 March 2024

15

1 reference

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

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

27 March 2024

16

1 reference

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

27 March 2024

17

1 reference

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

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

27 March 2024

18

1 reference

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

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

27 March 2024

19

1 reference

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

27 March 2024

20

1 reference

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

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

27 March 2024

21

1 reference

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

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

27 March 2024

22

1 reference

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

MECP2 is highly mutated in X-linked mental retardation.

27 March 2024

23

1 reference

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

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

27 March 2024

24

1 reference

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

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

25

1 reference

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

Levetiracetam for acute mania

27 March 2024

26

1 reference

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

27 March 2024

27

1 reference

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DNA methylation patterns and epigenetic memory

27 March 2024

28

1 reference

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

27 March 2024

29

1 reference

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

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

30

1 reference

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

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

27 March 2024

31

1 reference

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

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

27 March 2024

32

1 reference

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

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

27 March 2024

33

1 reference

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

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

27 March 2024

34

1 reference

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

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

27 March 2024

35

1 reference

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

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

27 March 2024

36

1 reference

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

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

27 March 2024

37

1 reference

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

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

27 March 2024

38

1 reference

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

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

27 March 2024

39

1 reference

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

27 March 2024

40

2

425

2003

1 reference

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

27 March 2024

Brain volume in autism.

43

1 reference

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

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

27 March 2024

44

1 reference

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

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

27 March 2024

45

1 reference

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

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

27 March 2024

46

1 reference

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

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

27 March 2024

47

1 reference

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

Mind blindness and the brain in autism

27 March 2024

48

1 reference

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

Neuropathology of infantile autism.

27 March 2024

49

1 reference

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

Is medical genetics neglecting epigenetics?

27 March 2024

51

1 reference

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

Infantile autism: a genetic study of 21 twin pairs

27 March 2024

52

1 reference

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

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

27 March 2024

53

1 reference

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

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

27 March 2024

54

1 reference

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

Genetics of austim: complex aetiology for a heterogeneous disorder

27 March 2024

55

1 reference

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

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

27 March 2024

57

1 reference

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

A case of autism associated with partial tetrasomy 15.

27 March 2024

59

1 reference

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

Autism and maternally derived aberrations of chromosome 15q.

27 March 2024

61

1 reference

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

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

27 March 2024

62

1 reference

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

Chromosomal abnormalities in a series of children with autistic disorder.

27 March 2024

63

1 reference

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

Three probands with autistic disorder and isodicentric chromosome 15.

27 March 2024

64

1 reference

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

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

27 March 2024

65

1 reference

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

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

27 March 2024

66

1 reference

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

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

27 March 2024

67

1 reference

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

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

27 March 2024

69

1 reference

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

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

27 March 2024

70

1 reference

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

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

27 March 2024

72

1 reference

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

Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

27 March 2024

73

1 reference

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

Neurexin mediates the assembly of presynaptic terminals

27 March 2024

74

1 reference

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

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

27 March 2024

75

1 reference

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

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

27 March 2024

76

1 reference

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

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

27 March 2024

77

1 reference

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

Autism in Angelman syndrome: a population-based study

27 March 2024

78

1 reference

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

A Rett patient with a typical Angelman EEG.

27 March 2024

79

1 reference

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

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

27 March 2024

80

1 reference

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

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