(Q63248767)

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Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12858175%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS) (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12858175%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Richard J Gibbons

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12858175%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Andrea Pellagatti

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12858175%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Jacqueline Boultwood

8

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12858175%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Cordelia Langford

7

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Cordelia Langford

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5 November 2019

James S. Wainscoat

9

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James S Wainscoat

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5 November 2019

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David Garrick

3

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5 November 2019

William G Wood

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12858175%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Nicola Malik

5

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Europe PubMed Central

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5 November 2019

Helena Ayyub

6

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5 November 2019

Douglas R Higgs

10

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5 November 2019

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1 August 2003

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5 November 2019

Nature Genetics

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5 November 2019

34

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5 November 2019

4

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5 November 2019

446-449

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Europe PubMed Central

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5 November 2019

https://scigraph.springernature.com/pub.10.1038/ng1213

0 references

Molecular-clinical spectrum of the ATR-X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical features and molecular analysis of acquired hemoglobin H disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

Global role for chromatin remodeling enzymes in mitotic gene expression

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplications

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

The McCune-Albright syndrome: a lethal gene surviving by mosaicism

1 reference

https://api.crossref.org/works/10.1038%2FNG1213

7 January 2021

based on heuristic

inferred from DOI database lookup

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