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

Analysis of a Novel pncA Mutation for Susceptibility to Pyrazinamide Therapy.

American journal of respiratory and critical care medicine - 15 Aug 2018

Karmakar Malancha, Globan Maria, Fyfe Janet A M, Stinear Timothy P, Johnson Paul D R, Holmes Natasha E, Denholm Justin T, Ascher David B

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 Amidohydrolases
Share to Antitubercular Agents
Share to Mutation
Share to Pyrazinamide

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sequence Analysis, DNA

Share to Tuberculosis, Multidrug-Resistant

Source

Open in PubMed Open full text

Identifiers

PMID: 29694240
DOI: 10.1164/rccm.201712-2572LE
PMCID: PMC6118032

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Analysis of a Novel pncA Mutation for Susceptibility to Pyrazinamide Therapy.PMID 29694240Read ↗

Thiopurine S-methyltransferase deficiency associated with a novel mutation.Semantic proximity Read ↗

Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.Semantic proximity Read ↗

Characterization of a novel TPMT mutation associated with azathioprine-induced myelosuppression.Semantic proximity Read ↗

Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency.Semantic proximity Read ↗

Searching for mutations in the arylsulphatase A gene.Semantic proximity Read ↗

Urinary bladder cancer in a girl with a slow-acetylator genotype and treated with sulphasalazine.Semantic proximity Read ↗

Debrisoquine and N-acetylation polymorphism in Syria.Semantic proximity Read ↗

The molecular detection of the pseudodeficiency allele for arylsulphatase A in patients with neurological symptoms and low arylsulphatase A activity.Semantic proximity Read ↗

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