(Q33827866)

29 July 2017

1 reference

title

From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes (English)

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29 July 2017

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Gattermann N

1

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29 July 2017

1 February 2000

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29 July 2017

1 reference

29 July 2017

24

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29 July 2017

141-151

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29 July 2017

2

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Primary acquired sideroblastic anaemia

29 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Molecular defects of erythroid 5-aminolevulinate synthase in X-linked sideroblastic anemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Sideroblastic anaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Idiopathic refractory sideroblastic anemia: clinical and laboratory investigation of 17 patients and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Haem biosynthesis in refractory sideroblastic anaemia associated with the preleukaemic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Energy-dispersive X-ray analysis of the mitochondria of sideroblastic anaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Normal oxidative damage to mitochondrial and nuclear DNA is extensive

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Rapid evolution of animal mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Molecular clock of silent substitution: at least six-fold preponderance of silent changes in mitochondrial genes over those in nuclear genes

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Mitochondrial diseases in man and mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Refractory anaemia and mitochondrial cytopathy in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

11q-chromosome is associated with abnormal iron stores in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Erythroid and granulocyte/macrophage progenitor cells in primary acquired sideroblastic anemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Mitochondrial DNA sequence variation in human evolution and disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

No large deletions of mitochondrial DNA in acquired idiopathic sideroblastic anemia (AISA)

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Temperature-gradient gel electrophoresis of nucleic acids: analysis of conformational transitions, sequence variations, and protein-nucleic acid interactions.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

A heteroplasmic point mutation of mitochondrial tRNALeu(CUN) in non-lymphoid haemopoietic cell lineages from a patient with acquired idiopathic sideroblastic anaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

The MERRF mutation of mitochondrial DNA in the bone marrow of a patient with acquired idiopathic sideroblastic anemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

A role for mitochondrial DNA in the pathogenesis of radiation-induced myelodysplasia and secondary leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Prevalence and distribution of ringed sideroblasts in primary myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Oxidative damage and mitochondrial decay in aging

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Preferential amplification and phenotypic selection in a population of deleted and wild-type mitochondrial DNA in cultured cells

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

International Commission for Protection Against Environmental Mutagens and Carcinogens. Deoxyribonucleoside triphosphate levels: a critical factor in the maintenance of genetic stability

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Somatic mutations of the mitochondrial genome in human colorectal tumours

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Apoptosis and its role in the myelodysplastic syndromes: implications for disease natural history and treatment

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Mitochondrial control of apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Mitochondria and apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Cyclosporin A therapy in hypoplastic MDS patients and certain refractory anaemias without hypoplastic bone marrow

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

The mitochondrial permeability transition.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Maternally transmitted histocompatibility antigen of mice: a hydrophobic peptide of a mitochondrially encoded protein

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

Antithymocyte globulin for patients with myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2899%2900160-5

7 January 2021

10.1016/S0145-2126(99)00160-5

Identifiers

DOI

1 reference

29 July 2017

1 reference

PubMed ID

10654450