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资源简介：
Overview of CF mutations.
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创建时间：
2018-07-26
相关数据集
Supplementary Material for: A unique combination of heterozygous CFTR gene variants in a person with cystic fibrosis and M. abscessus infection
Introduction: Cystic fibrosis (CF) is a genetic disorder caused by mutations in the CFTR gene. A minority of people with CF carry two heterozygous CFTR mutations other than the common Phe508del, compl
DataCite Commons2025-03-28 更新70
Targeted Correction of CFTR Gene in Cystic Fibrosis iPS Exome Seq. Homo sapiens
Exome sequencing for determination of novel mutations in CF fibroblast, reprogrammed iPS, and 2 zinc finger corrected CFTR iPS clones.
NIAID Data Ecosystem60
Variant and genotype information following Next-generation sequencing (NGS) and Sanger sequencing of South African patients with cystic fibrosis
Supplementary 1 documents the variant information for a cohort of South African patients with cystic fibrosis, patients with suspected cystic fibrosis, and suspected carriers. The variants were discov
DataCite Commons2024-01-30 更新50
Homo sapiens Targeted Locus (Loci) - Amplicons from gene editing experiment
Cystic fibrosis (CF) bronchial epithelial cells were treated with nanoparticles containing peptide nucleic acid (PNA) and donor DNA designed to coordinate correction of the F508del CF mutation. PCR am
NIAID Data Ecosystem70
Chronically Infected Cystic Fibrosis Lungs Genome Sequencing
Regional Adaptations in Chronically Infected Cystic Fibrosis Lungs
NIAID Data Ecosystem50
