Distinct expression profiles of Mecp2 transcripts with different lengths of 3'UTR in the brain and visceral organs during mouse development. (Q48959692)

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scientific article published in April 2005

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English	Distinct expression profiles of Mecp2 transcripts with different lengths of 3'UTR in the brain and visceral organs during mouse development.	scientific article published in April 2005

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scholarly article

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

Distinct expression profiles of Mecp2 transcripts with different lengths of 3'UTR in the brain and visceral organs during mouse development. (English)

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

John Christodoulou

3

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

author name string

Gregory J Pelka

1

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

Catherine M Watson

2

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Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

Patrick P L Tam

4

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Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

publication date

1 April 2005

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Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

85

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17 February 2018

http://europepmc.org/abstract/MED/15780747

4

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17 February 2018

http://europepmc.org/abstract/MED/15780747

441-452

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17 February 2018

http://europepmc.org/abstract/MED/15780747

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

1 reference

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

1 reference

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7 January 2021

The major form of MeCP2 has a novel N-terminus generated by alternative splicing

1 reference

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7 January 2021

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

1 reference

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7 January 2021

Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

1 reference

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7 January 2021

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression

1 reference

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7 January 2021

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions

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

1 reference

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

1 reference

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

1 reference

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

1 reference

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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

1 reference

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Methyl-CpG-binding proteins. Targeting specific gene repression.

1 reference

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Identification and characterization of a family of mammalian methyl-CpG binding proteins

1 reference

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Methyl CpG-binding proteins and transcriptional repression

1 reference

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Mammalian polyadenylation sites: implications for differential display.

1 reference

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Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome

1 reference

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Expression patterns of two human genes coding for different rab GDP-dissociation inhibitors (GDIs), extremely conserved proteins involved in cellular transport

1 reference

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7 January 2021

Neurobiology of Rett syndrome: a genetic disorder of synapse development

1 reference

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Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: an immunochemical study of subcellular fractions.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.12.002

7 January 2021

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

1 reference

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7 January 2021

Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.12.002

7 January 2021

Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain

1 reference

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7 January 2021

X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.12.002

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Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Gene silencing using micro-RNA designed hairpins

1 reference

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MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism

1 reference

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7 January 2021

Prediction of mammalian microRNA targets

1 reference

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7 January 2021

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.12.002

7 January 2021

The spectrum of phenotypes in females with Rett Syndrome

1 reference

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A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos

1 reference

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Impact of node ablation on the morphogenesis of the body axis and the lateral asymmetry of the mouse embryo during early organogenesis.

1 reference

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7 January 2021

Identifiers

10.1016/J.YGENO.2004.12.002

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/15780747

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