(Q33373506)

26 July 2017

title

Congenital erythropoietic porphyria due to a mutation in GATA1: the first trans-acting mutation causative for a human porphyria (English)

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congenital erythropoietic porphyria

26 July 2017

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inferred from title

Erythropoietic porphyria

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2

David P Steensma

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26 July 2017

John D Phillips

1

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26 July 2017

Michael A Pulsipher

series ordinal

3

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26 July 2017

Gerald J Spangrude

series ordinal

4

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26 July 2017

James P Kushner

series ordinal

5

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26 July 2017

language of work or name

English

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publication date

5 December 2006

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26 July 2017

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26 July 2017

volume

109

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26 July 2017

issue

6

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26 July 2017

page(s)

2618-2621

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GATA transcription factors in hematologic disease

26 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

GATA1 in normal and malignant hematopoiesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Pseudohypoparathyroidism type Ib with disturbed imprinting in the GNAS1 cluster and Gsalpha deficiency in platelets.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

X-linked thrombocytopenia caused by a novel mutation of GATA-1

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Simultaneous determination of hydroxymethylbilane synthase and uroporphyrinogen III synthase in erythrocytes by high-performance liquid chromatography

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

DNA sequence variation associated with elevated fetal G gamma globin production

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

X-linked syndrome of platelet dysfunction, thrombocytopenia, and imbalanced globin chain synthesis with hemolysis.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Human uroporphyrinogen-III synthase: genomic organization, alternative promoters, and erythroid-specific expression

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Different sequence requirements for expression in erythroid and megakaryocytic cells within a regulatory element upstream of the GATA-1 gene.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852202

Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH condition

31 October 2018

1 reference

12 December 2020

Delta-aminolevulinic acid dehydratase assay

1 reference

12 December 2020

Analysis of porphyrin carboxylic acids in biological fluids by high-performance liquid chromatography

1 reference

12 December 2020

High performance liquid chromatographic separation of the globin chains of non-human hemoglobins

1 reference

12 December 2020

Analysis of hemoglobin F production in Saudi Arabian families with sickle cell anemia

1 reference

12 December 2020

Identification and quantification of hemoglobins A, F, S, and C by automated chromatography

1 reference

12 December 2020

Gene regulation in hematopoiesis: new lessons from thalassemia

1 reference

12 December 2020

10.1182/BLOOD-2006-06-022848

Identifiers

DOI

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26 July 2017

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26 July 2017

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