Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Janet F. FORSTNER"'
Publikováno v:
Attachment of Organisms to the Gut Mucosa ISBN: 9781351069977
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56ca9364446adb8e5aa5e782e19eec60
https://doi.org/10.1201/9781351069977-3
https://doi.org/10.1201/9781351069977-3
Publikováno v:
Infection and Immunity. 72:4188-4199
Well-differentiated cultures established from airway epithelia of patients with cystic fibrosis (CF cultures) exhibited goblet cell hyperplasia, increased secretion of mucus, and higher basal levels of interleukin-8 than similarly cultured cells from
Autor:
Jim Hu, Yu Hua Chow, Geraldine Kent, Umadevi S. Sajjan, Bernard Martin, David R. Koehler, A. Keith Tanswell, Colin McKerlie, Janet F. Forstner
Publikováno v:
Proceedings of the National Academy of Sciences. 100:15364-15369
We developed a helper-dependent adenoviral vector for cystic fibrosis lung gene therapy. The vector expresses cystic fibrosis transmembrane conductance regulator ( Cftr ) using control elements from cytokeratin 18 . The vector expressed properly loca
Autor:
Sameera Rahman, Rongquan Wang, Sherilyn L. Bell, Ismat A Khatri, Gongqiao Xu, Janet F. Forstner
Publikováno v:
Biochemical Journal. 373:893-900
Within the C-terminal domain of many secretory mucins is a ‘cystine knot’ (CK), which is needed for dimer formation in the endoplasmic reticulum. Previous studies indicate that in addition to an unpaired cysteine, the three intramolecular cystine
Publikováno v:
Biochemical Journal. 372:263-270
In a previous study we showed, by transient expression studies in COS-1 cells, that the C-terminal domain of rat intestinal membrane mucin Muc3 was cleaved between glycine and serine within a GSIVV (one-letter) amino acid sequence during its residenc
Autor:
J. Thomas Lamont, K. Ramakrishnan Bhaskar, S Umadevi Sajjan, Janet F. Forstner, Ismat A Khatri, Catherine K Y Ho
Publikováno v:
Pediatric Research. 53:619-627
Cystic fibrosis (CF) patients develop chronic lung infections associated with airway obstruction by viscous and insoluble mucus secretions. Although mucus glycoproteins (mucins) are thought to be responsible for mucus plugs, other glycoconjugate comp
Publikováno v:
Microbiology. 149:961-971
Burkholderia cepacia is an opportunistic respiratory pathogen in cystic fibrosis patients. One highly transmissible and virulent clone belonging to genomovar IIIa expresses pili with unique cable morphology, which enable the bacterium to bind cytoker
Publikováno v:
Microbiology. 148:3477-3484
The Burkholderia cepacia complex consists of several closely related bacterial species (or genomovars) which although generally not pathogenic for healthy individuals, contribute significantly to morbidity and mortality among persons with cystic fibr
Publikováno v:
Cellular Microbiology. 4:73-86
A highly transmissible strain of Burkholderia cepacia from genomovar III carries the cable pilin gene, expresses the 22 kDa adhesin (cblA +ve/Adh +ve), binds to cytokeratin 13 (CK13) and is invasive. CK13 is expressed abundantly in the airway epithel
Autor:
Carola Sjolin, Brent Steer, Annie Lu, Geraldine Kent, Gregory P. Downey, Yi Jun Wu, Janet F. Forstner, Vera Cherapanov, George Thanassoulis, Colin McKerlie, Uma Sajjan, Ori D. Rotstein
Publikováno v:
Infection and Immunity. 69:5138-5150
Progressive pulmonary infection is the dominant clinical feature of cystic fibrosis (CF), but the molecular basis for this susceptibility remains incompletely understood. To study this problem, we developed a model of chronic pneumonia by repeated in