✦ LIBER ✦

Exposure of an adriamycin-binding site on mast cell surface during exocytosis

✍ Scribed by Bartoli Klugmann, F.; Decorti, G.; Candussio, L.; Crivellato, E.; Mallardi, F.; Baldini, L.

Book ID: 122383236
Publisher: Elsevier Science
Year: 1990
Tongue: English
Weight: 132 KB
Volume: 22
Category: Article
ISSN: 1043-6618
DOI: 10.1016/S1043-6618(09)80045-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Exposure of an antigen of chromaffin gra

Exposure of an antigen of chromaffin granules on cell surface during exocytosis

✍ Lingg, G.; Fischer-Colbrie, R.; Schmidt, W.; Winkler, H. 📂 Article 📅 1983 🏛 Nature Publishing Group 🌐 English ⚖ 248 KB

Evidence of an adriamycin binding site i

Evidence of an adriamycin binding site in the secretory granules of the mast cell

✍ Giuliana Decorti; Fiora Bartoli Klugmann; Luigi Candussio; Luciano Baldini 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 680 KB

INFLUENCE OF BICARBONATE/CO2 ON THE EXPO

INFLUENCE OF BICARBONATE/CO2 ON THE EXPOSURE OF ZONA BINDING SITES ON THE SPERM SURFACE DURING INCUBATION IN VITRO

✍ W. Harkema; R.A.P. Harrison; N.G.A. Miller; H. Woelders 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB

Decrease of binding sites for phalloidin

Decrease of binding sites for phalloidin on the surface of liver cells during carbon tetrachloride intoxication

✍ R. Kroker; M. Frimmer 📂 Article 📅 1974 🏛 Springer-Verlag 🌐 English ⚖ 150 KB

Fragment-Based Identification of an Indu

Fragment-Based Identification of an Inducible Binding Site on Cell Surface Receptor CD44 for the Design of Protein–Carbohydrate Interaction Inhibitors

✍ Liu, Li-Kai; Finzel, Barry C. 📂 Article 📅 2014 🏛 American Chemical Society 🌐 English ⚖ 542 KB

Fragment-Based Identification of an Indu

Fragment-Based Identification of an Inducible Binding Site on Cell Surface Receptor CD44 for the Design of Protein–Carbohydrate Interaction Inhibitors

✍ Liu, Li-Kai; Finzel, Barry C. 📂 Article 📅 2014 🏛 American Chemical Society 🌐 English ⚖ 542 KB

Selective inhibitors of hyaluronan (HA) binding to the cell surface receptor CD44 will have value as probes of CD44-mediated signaling and have potential as therapeutic agents in chronic inflammation, cardiovascular disease, and cancer. Using biophysical binding assays, fragment screening, and cryst