Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Cytochrome p450A1 polymorphisms in a Caucasian population with porphyria cutanea tarda.

Experimental dermatology - 1 Dec 2003

Gardlo K, Selimovic D, Bolsen K, Ruzicka T, Abel J, Fritsch C

Abstract excerpt

Porphyria cutanea tarda (PCT) is the most frequent porphyria in humans. The familial type is in contrast to the sporadic type due to an inherited defect of the uroporphyrinogen-II-decarboxylase (URO-D) and both types need additional porphyrinogens to lead to the clinical manifestation of the dise...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cytochrome P-450 CYP1A1
Share to Cytochrome P-450 Enzyme System
Share to Odds Ratio

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Genetic

Share to Polymorphism, Restriction Fragment Length

Share to Porphyria Cutanea Tarda

Share to Porphyrins

Share to White People

Source

Identifiers

PMID: 14714565
DOI: 10.1111/j.0906-6705.2003.00095.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14714565-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cytochrome p450A1 polymorphisms in a Caucasian population with porphyria cutanea tarda.PMID 14714565Read ↗

Comprehensive cytochrome P450 CYP1A2 gene analysis in French caucasian patients with familial and sporadic porphyria cutanea tarda.Semantic proximity Read ↗

CYP1A2*1F and GSTM1 alleles are associated with susceptibility to porphyria cutanea tarda.Semantic proximity Read ↗

Association between CYP1A2 polymorphism and susceptibility to porphyria cutanea tarda.Semantic proximity Read ↗

The role of inherited and acquired factors in the development of porphyria cutanea tarda in the Argentinean population.Semantic proximity Read ↗

Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).Semantic proximity Read ↗

Porphyria Cutanea TardaSemantic proximity Read ↗

Precipitating/aggravating factors of porphyria cutanea tarda in Spanish patients.Semantic proximity Read ↗

Familial porphyria cutanea tarda in Spain: characterization of eight novel mutations in the UROD gene and haplotype analysis of the common p.G281E mutation.Semantic proximity Read ↗

Familial and sporadic porphyria cutanea tarda: clinical, biochemical and genetic features with emphasis on iron status.Semantic proximity Read ↗

Familial and sporadic porphyria cutanea tarda: characterization and diagnostic strategies.Semantic proximity Read ↗

Porphyria cutanea tarda in a Swedish population: risk factors and complications.Semantic proximity Read ↗

Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.