(Q52006884)

19 April 2018

title

Nucleosome assembly on methylated CGG triplet repeats in the fragile X mental retardation gene 1 promoter. (English)

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19 April 2018

author name string

Godde JS

1

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19 April 2018

Kass SU

2

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19 April 2018

Hirst MC

3

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19 April 2018

Wolffe AP

4

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19 April 2018

language of work or name

English

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publication date

1 October 1996

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19 April 2018

Journal of Biological Chemistry

published in

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19 April 2018

volume

271

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19 April 2018

page(s)

24325-24328

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19 April 2018

issue

40

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19 April 2018

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

A YAC contig across the fragile X site defines the region of fragility

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Genotype prediction in the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Molecular heterogeneity of the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

DNA methylation represses FMR-1 transcription in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Molecular basis of genetic instability of triplet repeats

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Trinucleotide repeat expansions and human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

DNA methylation affects the formation of active chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

5-methylcytosine is localized in nucleosomes that contain histone H1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Binding of histone H1 to DNA is indifferent to methylation at CpG sequences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

A bacteriophage RNA polymerase transcribes through a Xenopus 5S RNA gene transcription complex without disrupting it.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Artificial nucleosome positioning sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Nucleosome arrays inhibit both initiation and elongation of transcripts by bacteriophage T7 RNA polymerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Two new cases of FMR1 deletion associated with mental impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

DNA and protein determinants of nucleosome positioning on sea urchin 5S rRNA gene sequences in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Nucleosome positioning is determined by the (H3-H4)2 tetramer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

In vitro DNA methylation inhibits FMR-1 promoter.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Trinucleotide repeats that expand in human disease form hairpin structures in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Transcription on nucleosomal templates by RNA polymerase II in vitro: inhibition of elongation with enhancement of sequence-specific pausing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

Structural details of an adenine tract that does not cause DNA to bend

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.40.24325

21 January 2018

Identifiers

DOI

10.1074/JBC.271.40.24325

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19 April 2018

PubMed ID

8798682

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19 April 2018