(Q33327379)

25 July 2017

title

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

1 reference

Refractory anemia with ring sideroblasts

25 July 2017

main subject

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author

Eva Hellström-Lindberg

14

Eva Hellström-Lindberg

0 references

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

volume

3

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25 July 2017

issue

4

1 reference

25 July 2017

page(s)

e1970

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Creative Commons Attribution 4.0 International

25 July 2017

copyright license

start time

9 April 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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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Rtf1 is a multifunctional component of the Paf1 complex that regulates gene expression by directing cotranscriptional histone modification

21 June 2018

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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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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

1 reference

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21 June 2018

1 reference

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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

1 reference

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The ABC transporter Atm1p is required for mitochondrial iron homeostasis

21 June 2018

1 reference

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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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Granulocyte colony-stimulating factor inhibits spontaneous cytochrome c release and mitochondria-dependent apoptosis of myelodysplastic syndrome hematopoietic progenitors

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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21 January 2018

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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

1 reference

12 December 2020

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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

PMC publication ID

2276313

1 reference

25 July 2017

1 reference