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

White matter damage in neonatal enterovirus meningoencephalitis

24 Apr 2006

Abstract excerpt

Cytochrome P450 (P450) 2C9 is an important member of the P450 enzyme superfamily, with 58 CYP2C9 allelic variants previously reported. Genetic polymorphisms of CYP2C9 significantly influence the efficacy and safety of some drugs, which might cause adverse effects and therapeutic failure. The aim of this study was to assess the catalytic activities of 38 human CYP2C9 alleles, including 24 novel alleles (*36–*60)...

Read the complete abstract on PubMed

Topics

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

Share to Infectious Encephalopathies and Encephalitis
Share to RNA regulation and disease
Share to Viral Infections and Immunology Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 16636251
DOI: 10.1212/01.wnl.0000208429.69676.23

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

White matter damage in neonatal enterovirus meningoencephalitisPMID 16636251Read ↗

Biochemistry and molecular biology of the human CYP2C subfamily.Semantic proximity Read ↗

In vitro functional characterization of 37 CYP2C9 allelic isoforms found in Chinese Han population.Semantic proximity Read ↗

Substrate-dependent functional alterations of seven CYP2C9 variants found in Japanese subjects.Semantic proximity Read ↗

In vitro assessment of 36 CYP2C9 allelic isoforms found in the Chinese population on the metabolism of glimepiride.Semantic proximity Read ↗

Four novel defective alleles and comprehensive haplotype analysis of CYP2C9 in Japanese.Semantic proximity Read ↗

Identification and drug metabolic characterization of four new CYP2C9 variants CYP2C9*72-*75 in the Chinese Han populationSemantic proximity Read ↗

In vitro and in vivo characterization of 13 CYP2C9 allelic variants found in Chinese Han population.Semantic proximity Read ↗

Catalytic roles of CYP2C9 and its variants (CYP2C9*2 and CYP2C9*3) in lornoxicam 5'-hydroxylation.Semantic proximity Read ↗

Discovery of new potentially defective alleles of human CYP2C9.Semantic proximity Read ↗

Identification and functional characterization of a new CYP2C9 variant (CYP2C9*5) expressed among African Americans.Semantic proximity Read ↗

[Identification of a novel CYP2C9 gene mutation (1400T>C) and assessment of its enzymatic activity in vitro].Semantic proximity Read ↗

[Genetic polymorphism of the CYP2C subfamily].Semantic proximity Read ↗

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