CFTR expression and activity from the human CFTR locus in BAC vectors, with regulatory regions, isolated by a single-step procedure (Q45859592)

17 December 2017

title

CFTR expression and activity from the human CFTR locus in BAC vectors, with regulatory regions, isolated by a single-step procedure (English)

1 reference

17 December 2017

author

Enea Gino Di Domenico

2

1 reference

17 December 2017

Massimo Conese

6

1 reference

17 December 2017

author name string

C Auriche

1

1 reference

17 December 2017

S Pierandrei

3

1 reference

17 December 2017

M Lucarelli

4

1 reference

17 December 2017

S Castellani

5

1 reference

17 December 2017

R Melani

7

1 reference

17 December 2017

O Zegarra-Moran

8

1 reference

17 December 2017

F Ascenzioni

9

1 reference

17 December 2017

language of work or name

1 reference

10 June 2010

1 reference

17 December 2017

published in

Gene Therapy

1 reference

17 December 2017

volume

17

1 reference

17 December 2017

issue

11

1 reference

17 December 2017

page(s)

1341-1354

1 reference

17 December 2017

https://scigraph.springernature.com/pub.10.1038/gt.2010.89

exact match

0 references

cites work

CFTR as a cAMP-dependent regulator of sodium channels

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Cystic fibrosis mortality and survival in the UK: 1947-2003

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Recent advances in cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Gene transfer to the lung: lessons learned from more than 2 decades of CF gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Gene transfer of CFTR to airway epithelia: low levels of expression are sufficient to correct Cl- transport and overexpression can generate basolateral CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Genomic context vectors and artificial chromosomes for cystic fibrosis gene therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Immunocytochemical localization of the cystic fibrosis gene product CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Cystic Fibrosis: Lessons from the Sweat Gland

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

A yeast artificial chromosome contig encompassing the cystic fibrosis locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Complementation of null CF mice with a human CFTR YAC transgene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Characterization of DNASE I hypersensitive sites in the 120kb 5' to the CFTR gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

A regulatory element in intron 1 of the cystic fibrosis transmembrane conductance regulator gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

An insulator element 3' to the CFTR gene binds CTCF and reveals an active chromatin hub in primary cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Airway epithelial control of Pseudomonas aeruginosa infection in cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Recovery and potential utility of YACs as circular YACs/BACs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Pulsed field separation of large supercoiled and open-circular DNAs and its application to bacterial artificial chromosome cloning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Evidence for direct CFTR inhibition by CFTR(inh)-172 based on Arg347 mutagenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Retrofitting BACs with G418 resistance, luciferase, and oriP and EBNA-1 - new vectors for in vitro and in vivo delivery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

CFTR expression from a BAC carrying the complete human gene and associated regulatory elements.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Efficient combination of large DNA in vitro: in gel site specific recombination (IGSSR) of PAC fragments containing alpha satellite DNA and the human HPRT gene locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Bacterial transfer of large functional genomic DNA into human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Cl transport in complemented CF bronchial epithelial cells correlates with CFTR mRNA expression levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Unimpaired lysosomal acidification in respiratory epithelial cells in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

CFTR is a pattern recognition molecule that extracts Pseudomonas aeruginosa LPS from the outer membrane into epithelial cells and activates NF-kappa B translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Infectious delivery of a 135-kb LDLR genomic locus leads to regulated complementation of low-density lipoprotein receptor deficiency in human cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

A new logic for DNA engineering using recombination in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

A second set of loxP marker cassettes for Cre-mediated multiple gene knockouts in budding yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Restoration of bacterial killing activity of human respiratory cystic fibrosis cells through cationic vector-mediated cystic fibrosis transmembrane conductance regulator gene transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Domain interdependence in the biosynthetic assembly of CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Molecular and cytological analysis of a 5.5 Mb minichromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Functional human CFTR produced by a stable minichromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Biochemical methods to assess CFTR expression and membrane localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

7 January 2021

Submucosal glands are the predominant site of CFTR expression in the human bronchus

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

7 January 2021

Multiple potential intragenic regulatory elements in the CFTR gene

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

7 January 2021

Functional analysis of mutations in the putative binding site for cystic fibrosis transmembrane conductance regulator potentiators. Interaction between activation and inhibition

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

7 January 2021

IL-4 is a potent modulator of ion transport in the human bronchial epithelium in vitro

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

7 January 2021

A 96-well formatted method for exon and exon/intron boundary full sequencing of the CFTR gene

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

7 January 2021

Simultaneous cycle sequencing assessment of (TG)m and Tn tract length in CFTR gene.

1 reference

https://api.crossref.org/works/10.1038%2FGT.2010.89

7 January 2021

Identifiers

DOI

10.1038/GT.2010.89

1 reference

17 December 2017

Dimensions Publication ID

0 references

1 reference

17 December 2017