The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts (Q33327379)

25 July 2017

The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts (English)

1 reference

Refractory anemia with ring sideroblasts

25 July 2017

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author

Eva Hellström-Lindberg

14

Eva Hellström-Lindberg

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Andrea Pellagatti

Andrea Pellagatti

2

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Jacqueline Boultwood

Jacqueline Boultwood

Aristoteles A N Giagounidis

1

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12

Aristoteles Giagounidis

1 reference

25 July 2017

8

Luca Malcovati

1 reference

25 July 2017

10

Martin Jädersten

1 reference

25 July 2017

11

Sally Killick

1 reference

25 July 2017

3

Maryam Nikpour

1 reference

25 July 2017

4

Beena Pushkaran

1 reference

25 July 2017

5

Carrie Fidler

1 reference

25 July 2017

6

Helen Cattan

1 reference

25 July 2017

16

James S Wainscoat

1 reference

25 July 2017

Tim J Littlewood

7

1 reference

25 July 2017

Matteo G Della Porta

9

1 reference

25 July 2017

David Bowen

13

1 reference

25 July 2017

Eva Hellström-Lindberg

14

1 reference

25 July 2017

Mario Cazzola

15

1 reference

25 July 2017

language of work or name

English

0 references

publication date

9 April 2008

1 reference

25 July 2017

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25 July 2017

3

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25 July 2017

e1970

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25 July 2017

4

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Creative Commons Attribution 4.0 International

25 July 2017

start time

9 April 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Lenalidomide inhibits the malignant clone and up-regulates the SPARC gene mapping to the commonly deleted region in 5q- syndrome patients

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21 June 2018

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Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis

21 June 2018

1 reference

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Transcriptional profiling of genes induced in the livers of patients treated with carbamazepine

21 June 2018

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Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia

21 June 2018

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Multiple mechanisms for hereditary sideroblastic anemia

21 June 2018

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

21 June 2018

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Human Elongator facilitates RNA polymerase II transcription through chromatin

21 June 2018

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Characterization of a six-subunit holo-elongator complex required for the regulated expression of a group of genes in Saccharomyces cerevisiae

21 June 2018

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Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation

21 June 2018

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21 June 2018

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Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)

21 June 2018

1 reference

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Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia

21 June 2018

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The ABC transporter Atm1p is required for mitochondrial iron homeostasis

21 June 2018

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X-linked sideroblastic anemia: identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley

21 June 2018

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Proposals for the classification of the myelodysplastic syndromes

21 June 2018

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The sideroblastic anemias

21 June 2018

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Usefulness and prognostic impact on survival of WHO reclassification in FAB low risk myelodyplastic syndromes

21 June 2018

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21 January 2018

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Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.

21 January 2018

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Candidate gene mutation analysis in idiopathic acquired sideroblastic anemia (refractory anemia with ringed sideroblasts).

21 January 2018

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Myelodysplastic syndromes

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12 December 2020

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

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Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation

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12 December 2020

RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload

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12 December 2020

10.1371/JOURNAL.PONE.0001970

Identifiers

DOI

1 reference

release_24hnn2paojhwfjmcz5tbwag3qi

25 July 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/24hnn2paojhwfjmcz5tbwag3qi

24 November 2022

mapped directly with Wikidata item

PMCID

2276313

1 reference

25 July 2017

1 reference