The ferrochelatase gene structure and molecular defects associated with erythropoietic protoporphyria (Q40433961)

20 September 2017

1 reference

title

The ferrochelatase gene structure and molecular defects associated with erythropoietic protoporphyria (English)

1 reference

20 September 2017

S. Taketani

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7592570

31 May 2024

H. Fujita

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7592570

31 May 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7592570

31 May 2024

publication date

1 April 1995

1 reference

full work available at URL

20 September 2017

http://link.springer.com/content/pdf/10.1007/BF02110038.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF02110038/fulltext.html

31 May 2024

1 reference

http://link.springer.com/content/pdf/10.1007/BF02110038

31 May 2024

1 reference

Journal of Bioenergetics and Biomembranes

31 May 2024

published in

1 reference

20 September 2017

volume

27

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20 September 2017

issue

2

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20 September 2017

page(s)

231-238

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Expression of ferrochelatase mRNA in erythroid and non-erythroid cells

20 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF02110038

Inhibition of ferrochelatase during differentiation of murine erythroleukaemia cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02110038

Sequential activation of genes for heme pathway enzymes during erythroid differentiation of mouse Friend virus-transformed erythroleukemia cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02110038

Nonsense mutations in the dihydrofolate reductase gene affect RNA processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02110038

A novel mutation in erythropoietic protoporphyria: an aberrant ferrochelatase mRNA caused by exon skipping during RNA splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02110038

Mammalian ferrochelatase. Expression and characterization of normal and two human protoporphyric ferrochelatases

21 January 2018

1 reference

12 December 2020

Characterization of ferrochelatase in kidney and erythroleukemia cells

1 reference

12 December 2020

Molecular defect in human erythropoietic protoporphyria with fatal liver failure

1 reference

12 December 2020

Bovine protoporphyria: documentation of autosomal recessive inheritance and comparison with the human disease through measurement of heme synthase activity

1 reference

12 December 2020

[Molecular biology of sideroblastic anemia and porphyria]

1 reference

12 December 2020

Study of factors causing excess protoporphyrin accumulation in cultured skin fibroblasts from patients with protoporphyria

1 reference

12 December 2020

Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease

1 reference

12 December 2020

Molecular defects in erythropoietic protoporphyria with terminal liver failure

1 reference

12 December 2020

The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria

1 reference

12 December 2020

Screening for ferrochelatase mutations: molecular heterogeneity of erythropoietic protoporphyria

1 reference

12 December 2020

Studies in porphyria: functional evidence for a partial deficiency of ferrochelatase activity in mitogen-stimulated lymphocytes from patients with erythropoietic protoporphyria

1 reference

12 December 2020

Dimethyl sulphoxide and haemin induce ferrochelatase mRNA by different mechanisms in murine erythroleukaemia cells

1 reference

12 December 2020

Regulating the fate of mRNA: the control of cellular iron metabolism

1 reference

12 December 2020

Mammalian ferrochelatase, a new addition to the metalloenzyme family.

1 reference

12 December 2020

Erythropoietic protoporphyria. A new porphyria syndrome with solar urticaria due to protoporphyrinaemia

1 reference

12 December 2020

Haem is necessary for a continued increase in ferrochelatase mRNA in murine erythroleukaemia cells during erythroid differentiation.

1 reference

12 December 2020

Two tissue-specific factors bind the erythroid promoter of the human porphobilinogen deaminase gene

1 reference

12 December 2020

The ferrochelatase from Saccharomyces cerevisiae. Sequence, disruption, and expression of its structural gene HEM15.

1 reference

12 December 2020

Molecular cloning and sequence analysis of cDNA encoding human ferrochelatase

1 reference

12 December 2020

Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene

1 reference

12 December 2020

Sequential induction of heme pathway enzymes during erythroid differentiation of mouse Friend leukemia virus-infected cells

1 reference

12 December 2020

Regulation of transcription by dimerization of erythroid factor NF-E2 p45 with small Maf proteins

1 reference

12 December 2020

Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2

1 reference

12 December 2020

Recessive inheritance of erythropoietic protoporphyria with liver failure

1 reference

12 December 2020

Molecular cloning, sequencing, and expression of mouse ferrochelatase.

1 reference

12 December 2020

The regulation of heme biosynthesis during erythropoietin-induced erythroid differentiation

1 reference

12 December 2020

Beta O-39 thalassemia gene: a premature termination codon causes beta-mRNA deficiency without affecting cytoplasmic beta-mRNA stability

1 reference

12 December 2020

A molecular defect in human protoporphyria

1 reference

12 December 2020

Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase gene

1 reference

12 December 2020

Heme biosynthesis in Friend erythroleukemia cells: control by ferrochelatase

1 reference

12 December 2020

Molecular analysis of functional and nonfunctional genes for human ferrochelatase: isolation and characterization of a FECH pseudogene and its sublocalization on chromosome 3.

1 reference

12 December 2020

The beta-globin dominant control region: hypersensitive site 2

1 reference

12 December 2020

Cis- and trans-acting elements involved in the regulation of the erythroid promoter of the human porphobilinogen deaminase gene

1 reference

12 December 2020

Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyria

1 reference

12 December 2020

A nonsense mutation causing decreased levels of insulin receptor mRNA: detection by a simplified technique for direct sequencing of genomic DNA amplified by the polymerase chain reaction

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the locus for human ferrochelatase (FECH).

1 reference

12 December 2020

Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression.

1 reference

12 December 2020

Coproporphyrinogen oxidase. Purification, molecular cloning, and induction of mRNA during erythroid differentiation

1 reference

12 December 2020

Ferrochelatase structural mutant (Fechm1Pas) in the house mouse

1 reference

12 December 2020

Molecular and genetic characterization of ferrochelatase

1 reference

12 December 2020

Molecular characterization of a ferrochelatase gene defect causing anomalous RNA splicing in erythropoietic protoporphyria

1 reference

12 December 2020

Uroporphyrinogen I synthase induction in normal human bone marrow cultures: an early and quantitative response of erythroid differentiation

1 reference

12 December 2020

Structure of the human ferrochelatase gene. Exon/intron gene organization and location of the gene to chromosome 18.

1 reference

12 December 2020

Globin gene regulation and switching: circa 1990.

1 reference

12 December 2020

Diminished erythroid ferrochelatase activity in protoporphyria

1 reference

12 December 2020

Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts

1 reference

12 December 2020

Recessive inheritance of erythropoietic protoporphyria with liver failure

series ordinal

46

1 reference

Journal of Biological Chemistry

31 May 2024

48

265

24637

S. Taketani

1990

1 reference

31 May 2024

Identifiers

DOI

10.1007/BF02110038

1 reference

20 September 2017

1 reference