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CFTR wt Allele

Known as: Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) wt Allele, dJ760C5.1, CF 
Human CFTR wild-type allele is located in the vicinity of 7q31.2 and is approximately 203 kb in length. This allele, which encodes cystic fibrosis… 
National Institutes of Health

Related topics

Related topics

5 relations
CFTR PathwayHomo sapiensIonophore activityLigand Binding

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
PD34-05 SPERM RETRIEVAL AND INTRACYTOPLASMIC SPERM INJECTION (ICSI) OUTCOMES IN MEN WITH CYSTIC FIBROSIS (CF) DISEASE VERSUS CONGENITAL BILATERAL ABSENCE OF THE VAS DEFERENS (CBAVD)
INTRODUCTION AND OBJECTIVES: Patients with obstructive azoospermia (OA) from CF and CBAVD share underlying genetic etiologies… 
2013
2013
Tandutinib (MLN518) reverses multidrug resistance by inhibiting the efflux activity of the multidrug resistance protein 7 (ABCC10)
It is well established that ATP-binding cassette (ABC) transporter-mediated multidrug resistance (MDR) is one of the major… 
2010
2010
Abstract 1519: Tyrosine kinase inhibitors are potent reversal agents for MRP7 (ABCC10)-mediated multidrug resistance
Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC ATP binding cassette (ABC) transporters play a… 
2006
2006
Faecal elastase‐1 concentration in cystic fibrosis patients with CFTR I1234V mutation
Aim: To assess the exocrine pancreatic function among cystic fibrosis patients with cystic fibrosis trans‐membrane conductance… 
2000
2000
A novel missense mutation (D110E) in exon 4 of CFTR (ABCC7) in a CF infant presenting with hypochloraemic metabolic alkalosis
2000
2000
Severe cystic fibrosis in a Japanese girl caused by two novel CFTR (ABCC7) gene mutations: M152R and 1540del10
2000
2000
Novel cystic fibrosis mutation L1093P: Functional analysis and possible Native American origin
A novel mutation was detected using single‐strand conformation polymorphism and heteroduplex analysis in a cystic fibrosis… 
Review
1993
Review
1993
Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene.
During our preliminary molecular survey of the cystic fibrosis (CF) AF508 mutation in 18 patients selected by positive sweat… 
1967
1967
The relation between Rorschach signs of aggression and behavioral aggression in emotionally disturbed boys.
Abstract Ratings of aggressive behavior were related to Rorschach signs of aggression for sixty-three boys at a residential… 
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