Lung infections associated with cystic fibrosis

JB Lyczak, CL Cannon, GB Pier - Clinical microbiology reviews, 2002 - Am Soc Microbiol
While originally characterized as a collection of related syndromes, cystic fibrosis (CF) is
now recognized as a single disease whose diverse symptoms stem from the wide tissue …

Electrolyte transport in the mammalian colon: mechanisms and implications for disease

K Kunzelmann, M Mall - Physiological reviews, 2002 - journals.physiology.org
The colonic epithelium has both absorptive and secretory functions. The transport is
characterized by a net absorption of NaCl, short-chain fatty acids (SCFA), and water …

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

JR Riordan, JM Rommens, B Kerem, NOA Alon… - Science, 1989 - science.org
Overlapping complementary DNA clones were isolated from epithelial cell libraries with a
genomic DNA segment containing a portion of the putative cystic fibrosis (CF) locus, which is …

Identification of the cystic fibrosis gene: chromosome walking and jumping

JM Rommens, MC Iannuzzi, B Kerem, ML Drumm… - Science, 1989 - science.org
An understanding of the basic defect in the inherited disorder cystic fibrosis requires cloning
of the cystic fibrosis gene and definition of its protein product. In the absence of direct …

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

SH Cheng, DP Rich, J Marshall, RJ Gregory, MJ Welsh… - Cell, 1991 - cell.com
CFTR, the protein associated with cystic fibrosis, is phosphorylated on serine residues in
response to CAMP agonists. Serines 660, 737, 795, and 613 were identified as in vivo …

In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium

MA Rosenfeld, K Yoshimura, BC Trapnell, K Yoneyama… - Cell, 1992 - cell.com
Direct transfer of the normal cystic fibrosis (CF) transmembrane conductance regulator
(CFTR) gene to airway epitheiium was evaluated using a replicationdeficient recombinant …

[HTML][HTML] Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoter.

TR Flotte, SA Afione, R Solow, ML Drumm… - Journal of Biological …, 1993 - Elsevier
Adeno-associated virus type 2 (AAV) vectors have been used for gene expression in
respiratory epithelial cells and may be useful in gene therapy for diseases like cystic fibrosis …

Neurotrophins promote motor neuron survival and are present in embryonic limb bud

CE Henderson, W Camu, C Mettling, A Gouin… - Nature, 1993 - nature.com
Embryonic spinal motor neurons are thought to depend for survival on unidentified factors
secreted both by their peripheral targets and by cells within the central nervous system1 …

Defective acidification of intracellular organelles in cystic fibrosis

J Barasch, B Kiss, A Prince, L Saiman, D Gruenert… - Nature, 1991 - nature.com
THE phenotype of cystic fibrosis (CF) includes abnormalities in transepithelial transport of Cl-
(refs 1–5), decreased sialylation and increased sulphation and fucosylation of …

ELAM-1 is an adhesion molecule for skin-homing T cells

LJ Picker, TK Kishimoto, CW Smith, RA Warnock… - Nature, 1991 - nature.com
ENDOTHELIAL cell leukocyte adhesion molecule-1 (ELAM-1) has been described as an
inducible endothelial cell-adhesion molecule for neutrophils, and is believed to have a key …