(Q28269557)

English

Molecular defect in human erythropoietic protoporphyria with fatal liver failure

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scholarly article

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Molecular defect in human erythropoietic protoporphyria with fatal liver failure (English)

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erythropoietic protoporphyria

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based on heuristic

inferred from title

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author name string

Y Nakahashi

1

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H Miyazaki

2

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Y Kadota

3

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Y Naitoh

4

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K Inoue

5

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M Yamamoto

6

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N Hayashi

7

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S Taketani

8

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language of work or name

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publication date

May 1993

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91

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4

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303-6

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Hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Splicing of messenger RNA precursors

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ferrochelatase activity in human lymphocytes, as quantified by a new high-performance liquid-chromatographic method.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and sequence analysis of cDNA encoding human ferrochelatase

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal liver failure in protoporphyria. Synergism between ethanol excess and the genetic defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular defect in human protoporphyria

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA sequencing with chain-terminating inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exon definition may facilitate splice site selection in RNAs with multiple exons

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discrimination and quantitative analysis of wild type and point mutant early region 1B genes of adenovirus using oligodeoxyribonucleotide hybridization probes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8500787

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00217346

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