(Q38450295)

English

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with α thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations

scientific article published on October 30, 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with α thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations (English)

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

alpha thalassemia

1 reference

based on heuristic

inferred from title

myelodysplastic syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

David P. Steensma

1

object named as

David P. Steensma

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14592816

27 March 2024

author name string

Douglas R. Higgs

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14592816

27 March 2024

Chris A. Fisher

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1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14592816

27 March 2024

Richard J. Gibbons

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14592816

27 March 2024

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publication date

30 October 2003

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Europe PubMed Central

PubMed publication ID

3 September 2017

full work available at URL

https://ashpublications.org/blood/article-pdf/103/6/2019/1696001/zh800604002019.pdf

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online access status

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14592816

27 March 2024

http://ashpublications.org/blood/article-pdf/103/6/2019/1696001/zh800604002019.pdf

Portable Document Format

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

103

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Europe PubMed Central

PubMed publication ID

3 September 2017

6

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Europe PubMed Central

PubMed publication ID

3 September 2017

2019-2026

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Europe PubMed Central

PubMed publication ID

3 September 2017

Alpha-thalassaemia

2

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10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

The beta-thalassemias

3

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10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

7 Increased HbF in adult life

5

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10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Fetal hemoglobin levels in adults

6

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Decrease in the Concentration of Haemoglobin A2 during Erythroleukaemia

7

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis

8

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Clinical features and molecular analysis of acquired hemoglobin H disease

9

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Acquired beta thalassaemia trait in MDS

10

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Erythroleukemia Manifesting δβ-Thalassemia

11

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Hemoglobin H disease: not necessarily a benign disorder.

12

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia

14

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

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

15

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

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

16

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Nomenclature for the description of human sequence variations

17

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Globin Synthesis in Thalassaemia: An in vitro Study

18

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Haemoglobin Synthesis in β-Thalassaemia

19

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

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

20

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

The PHD finger: implications for chromatin-mediated transcriptional regulation

21

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains

22

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

23

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

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

24

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

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

25

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

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

26

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies

27

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

The promyelocytic leukemia nuclear body: sites of activity?

28

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).

29

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Clonality in the myelodysplastic syndromes

35

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Mutational analysis of the ATRX gene by DGGE: a powerful diagnostic approach for the ATRX syndrome

37

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations

38

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Characterizing mutations in samples with low-level mosaicism by collection and analysis of DHPLC fractionated heteroduplexes.

39

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Low level mosaicism detectable by DHPLC but not by direct sequencing

40

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography

41

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Acute myeloid leukemia

42

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Chromosome and molecular abnormalities in myelodysplastic syndromes

43

1 reference

10.1182/BLOOD-2003-09-3360

https://api.crossref.org/works/10.1182/BLOOD-2003-09-3360

27 March 2024

Identifiers

10.1182/BLOOD-2003-09-3360

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

ResearchGate publication ID

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