Discover Community Create You

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

The association between genetic polymorphisms of coproporphyrinogen oxidase and an atypical porphyrinogenic response to mercury exposure in humans

7 Apr 2005

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Heme Oxygenase-1 and Carbon Monoxide
Share to Neonatal Health and Biochemistry
Share to Porphyrin Metabolism and Disorders

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 15967199
DOI: 10.1016/j.taap.2004.12.016

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The association between genetic polymorphisms of coproporphyrinogen oxidase and an atypical porphyrinogenic response to mercury exposure in humansPMID 15967199Read ↗

Cloning, expression, and biochemical properties of CPOX4, a genetic variant of coproporphyrinogen oxidase that affects susceptibility to mercury toxicity in humans.Semantic proximity Read ↗

The association between a genetic polymorphism of coproporphyrinogen oxidase, dental mercury exposure and neurobehavioral response in humans.Semantic proximity Read ↗

Three novel mutations in the coproporphyrinogen oxidase gene.Semantic proximity Read ↗

Modification of neurobehavioral effects of mercury by a genetic polymorphism of coproporphyrinogen oxidase in children.Semantic proximity Read ↗

Three novel mutations in the protoporphyrinogen oxidase gene in Japanese patients with variegate porphyria.Semantic proximity Read ↗

Biochemical and genetic characterization of four cases of hereditary coproporphyria in Spain.Semantic proximity Read ↗

Glutathione-related genetic polymorphisms are associated with mercury retention and nephrotoxicity in gold-mining settings of a Colombian population.Semantic proximity Read ↗

A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.Semantic proximity Read ↗

CYP3A Polymorphism and Chronic Mercury Intoxication.Semantic proximity Read ↗

Genetic polymorphisms are associated with hair, blood, and urine mercury levels in the American Dental Association (ADA) study participants.Semantic proximity Read ↗

Porphyrin accumulation in humans with common dysfunctional variants of ABCG2, a porphyrin transporter: potential association with acquired photosensitivity.Semantic proximity Read ↗

Genetic Aspects of Susceptibility to Mercury Toxicity: An Overview.Semantic proximity Read ↗

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