✦ LIBER ✦

Glycosyl acceptors in intact and permeabilized normal and cystic fibrosis fibroblasts

✍ Scribed by Victoria L. Rudick; Michael J. Rudick; Patricia M. Jones

Publisher: John Wiley and Sons
Year: 1983
Tongue: English
Weight: 811 KB
Volume: 115
Category: Article
ISSN: 0021-9541
DOI: 10.1002/jcp.1041150207

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Membrane function in cystic fibrosis. I.

Membrane function in cystic fibrosis. I. Putrescine transport in normal and cystic fibrosis fibroblasts

✍ JoAnn C. Kelly; A. Gib DeBusk 📂 Article 📅 1977 🏛 Springer 🌐 English ⚖ 517 KB

Putrescine transport was examined in normal and cystic fibrosis fibroblasts. No differences were observed in accumulation pattern, kinetics of uptake, or efflux between CF and normal cells. In both growing and growth-arrested CF and normal fibroblasts, exogenously supplied putrescine remained unchan

Membrane function in cystic fibrosis. II

Membrane function in cystic fibrosis. II. Methionine transport in normal and cystic fibrosis fibroblasts

✍ Jerome L. Sullivan; JoAnn C. Kelly; William B. Roess; A. Gib DeBusk 📂 Article 📅 1977 🏛 Springer 🌐 English ⚖ 393 KB

Initial rate kinetics of methionine transport, time course of accumulation of methionine, and efflux of accumulated methionine were studied in three normal and four CF human diploid fibroblast strains. The range of apparent Km's was 12.7-32.1 micrometer for the CF strains and 18.3-39.2 micrometer fo

Glycosylation of VSV glycoprotein is sim

Glycosylation of VSV glycoprotein is similar in cystic fibrosis, heterozygous carrier, and normal human fibroblasts

✍ Hunt, Lawrence A. ;Summers, Donald F. 📂 Article 📅 1977 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 494 KB

## Abstract The single envelope glycoprotein of vesicular stomatitis virus was used as a specific probe of glycosyltransferase activities in fibroblasts from two cystic fibrosis patients, an obligate heterozygous carrier and a normal individual. Gel filtration of pronasedigested glycopeptides from

Differences in the incorporation of thym

Differences in the incorporation of thymidine into DNA of normal and cystic fibrosis fibroblasts in vitro

✍ S. C. Barranco; W. E. Bolton; B. R. Haenelt; C. W. Abell 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 English ⚖ 709 KB

## Abstract Although similar fractions of cells were in the S phase of the cell cycle, normal human skin fibroblasts were shown to incorporate more than twice the ^3^HTdR into their DNA in vitro than did cells obtained from individuals with cystic fibrosis (CF). Obligate heterozygotes incorporated

Kinetic studies of normal and variant hy

Kinetic studies of normal and variant hypoxanthine phosphoribosyltransferases in intact fibroblasts

✍ Theodore Page; Bohdan Bakay; William L. Nyhan 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 311 KB

The instability of many mutant enzymes prevents their study by classical in vitro techniques.

Regulation of electrogenic anion secreti

Regulation of electrogenic anion secretion in normal and cystic fibrosis gallbladder mucosa

✍ Thierry Chinet; Laura Fouassier; Nathalie Dray-Charier; Mama Imam-Ghali; Hugues 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB

Fluid and ion transport across biliary epithelium contributes to bile flow. Alterations of this function may explain hepatobiliary complications in cystic fibrosis (CF). We investigated electrogenic anion transport across intact non-CF and CF human gallbladder mucosa in Ussing-type chambers. In non-