(Q22253401)

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Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

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Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation (English)

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DNA methylation

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ATRX chromatin remodeler

1 reference

GOA release 2020-03-11

author name string

R J Gibbons

1

author given names

Richard J.

author last names

Gibbons

1 reference

Dimensions Publication ID

7 February 2023

T L McDowell

2

author given names

Tarra L.

author last names

McDowell

1 reference

Dimensions Publication ID

7 February 2023

S Raman

3

author given names

Sundhya

author last names

Raman

1 reference

Dimensions Publication ID

7 February 2023

D M O'Rourke

4

author given names

Delia M.

author last names

O'Rourke

1 reference

Dimensions Publication ID

7 February 2023

D Garrick

5

author given names

David

author last names

Garrick

1 reference

Dimensions Publication ID

7 February 2023

H Ayyub

6

author given names

Helena

author last names

Ayyub

1 reference

Dimensions Publication ID

7 February 2023

D R Higgs

7

author given names

Douglas R.

author last names

Higgs

1 reference

Dimensions Publication ID

7 February 2023

language of work or name

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publication date

April 2000

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Nature Genetics

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24

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4

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368-71

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Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

1 reference

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Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain

1 reference

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Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

1 reference

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1 reference

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Characterisation of a human Y chromosome repeated sequence and related sequences in higher primates

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Human satellite I sequences include a male specific 2.47 kb tandemly repeated unit containing one Alu family member per repeat

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Structure and polymorphism of human telomere-associated DNA.

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Maintenance of genomic methylation requires a SWI2/SNF2-like protein

1 reference

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Arabidopsis thaliana DNA methylation mutants

1 reference

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Characterization of an Arabidopsis thaliana DNA hypomethylation mutant

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Gene silencing: Maintaining methylation patterns

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Cloning, expression and chromosome locations of the human DNMT3 gene family

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DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

1 reference

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Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

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Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation

1 reference

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Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation

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The relationship between chromosome structure and function at a human telomeric region

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Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres

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