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 genomic CFTR DNA.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society - 1 Aug 2004

Férec Claude, Le Maréchal Cédric, Audrézet Marie-Pierre, Farinha Carlos M, Amaral Margarida D, Gallati Sabina, Sanz Javier, Steiner Bernhard, Mouchel Nathalie, Harris Ann, Schwarz Martin J

Abstract excerpt

There are numerous methodologies available for the analysis of genomic CFTR DNA. We present here the basic tools to allow a thorough investigation of the CFTR gene, beginning with the identification of potential regulatory regions using DNase I hypersensitive sites, and continuing with methods for the detection of mutations: denaturing High Performance Liquid Chromatography (dHPLC), Single Strand Conformation...

Read the complete abstract on PubMed

Topics

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

Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to CFTR gene

Share to Genetic Techniques

Share to Genome

Share to Mutation

Source

Identifiers

PMID: 15463917
DOI: 10.1016/j.jcf.2004.05.003

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Analysis of genomic CFTR DNA.PMID 15463917Read ↗

Mutation analysis of the CFTR gene in Slovak cystic fibrosis patients by DHPLC and subsequent sequencing: identification of four novel mutations.Semantic proximity Read ↗

CFTR mutations in the Algerian population.Semantic proximity Read ↗

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations.Semantic proximity Read ↗

Analysis of the complete coding region of the CFTR gene in ten Algerian cystic fibrosis families.Semantic proximity Read ↗

Quantification of CFTR transcripts.Semantic proximity Read ↗

[Functional characterization of naturally occurring CFTR mutants: interest for cystic fibrosis].Semantic proximity Read ↗

Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients.Semantic proximity Read ↗

Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy.Semantic proximity Read ↗

Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from north-eastern Italy: identification of 90% of the mutations.Semantic proximity Read ↗

DNA polymorphisms in potential regulatory elements of the CFTR gene alter transcription factor binding.Semantic proximity Read ↗

Detection of CFTR mutations using PCR/ARMS in a sample of Algerian population.Semantic proximity Read ↗

Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian population.Semantic proximity Read ↗

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