(Q28591993)

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

title

Targeted disruption of the mouse ferrochelatase gene producing an exon 10 deletion (English)

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

Ferrochelatase, mitochondrial

12 December 2019

main subject

1 reference

GOA release 2020-03-11

author

David A. Brenner

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

author name string

S T Magness

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

language of work or name

English

0 references

publication date

1 January 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

number of pages

14

1 reference

Biochimica et Biophysica Acta

inferred from page(s)

published in

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

volume

1453

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

issue

1

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

page(s)

161-174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

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

12 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Cloning of murine ferrochelatase

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Biphasic ordered induction of heme synthesis in differentiating murine erythroleukemia cells: role of erythroid 5-aminolevulinate synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

The "priming phenomenon" in the acute phototoxicity of erythropoietic protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Hepatic disease in erythropoietic protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

The liver in protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Liver transplantation in a patient with protoporphyria.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Deletion of the ferrochelatase gene in a patient with protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Four novel mutations in the ferrochelatase gene among erythropoietic protoporphyria patients

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

A novel mutation in the ferrochelatase gene associated with erythropoietic protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Molecular defect in human erythropoietic protoporphyria with fatal liver failure

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Screening for ferrochelatase mutations: molecular heterogeneity of erythropoietic protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Genetic aspects of erythropoietic protoporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Recessive inheritance of erythropoietic protoporphyria with liver failure

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Recessive inheritance of erythropoietic protoporphyria with liver failure

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Bovine protoporphyria: the first nonhuman model of this hereditary photosensitizing disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Ferrochelatase structural mutant (Fechm1Pas) in the house mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Molecular cloning and sequence analysis of cDNA encoding human ferrochelatase

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Function of the [2FE-2S] cluster in mammalian ferrochelatase: a possible role as a nitric oxide sensor

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Single-copy transgenic mice with chosen-site integration

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Ferrochelatase cDNA delivered by adenoviral vector corrects biochemical defect in protoporphyric cells

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

High-performance liquid chromatographic assays for protoporphyrinogen oxidase and ferrochelatase in human leucocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

An HPLC assay for rat liver ferrochelatase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Ferrochelatase activities in patients with erythropoietic protoporphyria and their families

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Inheritance in protoporphyria. Comparison of haem synthetase activity in skin fibroblasts with clinical features

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Erythropoietic protoporphyria.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Human protoporphyria: genetic heterogeneity at the ferrochelatase locus

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Methylation of the minimal promoter of an embryonic globin gene silences transcription in primary erythroid cells

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

CpG methylation within the 5' regulatory region of the BRCA1 gene is tumor specific and includes a putative CREB binding site

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Aberrant silencing of the CpG island-containing human O6-methylguanine DNA methyltransferase gene is associated with the loss of nucleosome-like positioning

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Tumour predisposition in mice heterozygous for a targeted mutation in Nf1

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

Metachromatic leukodystrophy: molecular genetics and an animal model

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2898%2900096-9

7 January 2021

10.1016/S0925-4439(98)00096-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9989256%20AND%20SRC:MED&resulttype=core&format=json