(Q34180570)

31 July 2017

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title

Molecular genetics of Rett syndrome (English)

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31 July 2017

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Shastry BS

1

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31 July 2017

publication date

1 May 2001

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Neurochemistry International

31 July 2017

published in

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31 July 2017

volume

38

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31 July 2017

issue

6

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31 July 2017

page(s)

503-508

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Rett syndrome, classical and atypical: genealogical support for common origin

31 July 2017

cites work

1 reference

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7 January 2021

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

Review of Rett syndrome.

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7 January 2021

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

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7 January 2021

Parental origin of the X chromosomes in Rett syndrome

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7 January 2021

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

1 reference

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7 January 2021

Another model for the inheritance of Rett syndrome

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7 January 2021

X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe

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7 January 2021

The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA

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7 January 2021

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7 January 2021

Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome

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7 January 2021

Towards gene therapy for the central nervous system

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7 January 2021

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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7 January 2021

Rett variants: a suggested model for inclusion criteria.

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7 January 2021

Clinical delineation of Rett syndrome variants

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7 January 2021

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

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7 January 2021

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

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7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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7 January 2021

Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X.

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7 January 2021

In vivo site-directed mutagenesis of the factor IX gene by chimeric RNA/DNA oligonucleotides

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7 January 2021

Methyl-CpG-binding protein MeCP2 represses Sp1-activated transcription of the human leukosialin gene when the promoter is methylated

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7 January 2021

High levels of cerebrospinal fluid glutamate in Rett syndrome

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7 January 2021

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 reference

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7 January 2021

Rett syndrome: biogenic amines and metabolites in postmortem brain

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7 January 2021

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

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7 January 2021

Tyrosine hydroxylase from cloning to neuropsychiatric disorders.

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7 January 2021

Gene transfer into hippocampal slice cultures with an adenovirus vector driven by cytomegalovirus promoter: stable co-expression of green fluorescent protein and lacZ genes

1 reference

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7 January 2021

The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.

1 reference

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7 January 2021

DNA methylation specifies chromosomal localization of MeCP2.

1 reference

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7 January 2021

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

1 reference

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7 January 2021

Mutation analysis of the M6b gene in patients with Rett syndrome.

1 reference

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7 January 2021

The genetic basis of Rett syndrome: candidate gene considerations.

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7 January 2021

The Rett syndrome: genetics and the future

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7 January 2021

Human gene targeting by viral vectors

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7 January 2021

Requirement of Rsk-2 for epidermal growth factor-activated phosphorylation of histone H3

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7 January 2021

A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.

1 reference

https://api.crossref.org/works/10.1016%2FS0197-0186%2800%2900118-2

7 January 2021

A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map.

1 reference

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7 January 2021

Overexpression of genes in health and sickness. A bird's eye view

1 reference

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7 January 2021

Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.

1 reference

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7 January 2021

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Neither uniparental disomy nor skewed X-inactivation explains Rett syndrome

1 reference

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7 January 2021

Neurochemical alterations in Rett syndrome

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7 January 2021

Breaking the silence in Rett syndrome

1 reference

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7 January 2021

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq

1 reference

https://api.crossref.org/works/10.1016%2FS0197-0186%2800%2900118-2

7 January 2021

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0197-0186%2800%2900118-2

7 January 2021

A de novo X;3 translocation in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0197-0186%2800%2900118-2

7 January 2021

10.1016/S0197-0186(00)00118-2

Identifiers

DOI

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31 July 2017

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