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The Journal of Biological Chemistry|June 16, 1995
Endothelial caveolae have the molecular transport machinery for vesicle budding, docking, and fusion including VAMP, NSF, SNAP, annexins, and GTPasesJ E Schnitzer, J Liu, P OhAdvanced Drug Delivery Reviews|September 12, 2001
Caveolae: from basic trafficking mechanisms to targeting transcytosis for tissue-specific drug and gene delivery in vivoJ E SchnitzerTrends in Cardiovascular Medicine|January 20, 2011
Update on the cellular and molecular basis of capillary permeabilityJ E SchnitzerBiophysical Journal|December 1, 1988
Analysis of steric partition behavior of molecules in membranes using statistical physics. Application to gel chromatography and electrophoresisJ E SchnitzerThe Yale Journal of Biology and Medicine|September 1, 1988
Glycocalyx electrostatic potential profile analysis: ion, pH, steric, and charge effectsJ E SchnitzerThe American Journal of Physiology|January 1, 1992
gp60 is an albumin-binding glycoprotein expressed by continuous endothelium involved in albumin transcytosisJ E SchnitzerThe Journal of Biological Chemistry|March 14, 1997
Organized endothelial cell surface signal transduction in caveolae distinct from glycosylphosphatidylinositol-anchored protein microdomainsJ Liu, P Oh, T Horner, et al.The Journal of Biological Chemistry|April 5, 1993
High affinity binding, endocytosis, and degradation of conformationally modified albumins. Potential role of gp30 and gp18 as novel scavenger receptorsJ E Schnitzer, J BravoThe American Journal of Physiology|July 1, 1992
Quantitation of specific binding of orosomucoid to cultured microvascular endothelium: role in capillary permeabilityJ E Schnitzer, E PinneyMolecular Biology of the Cell|March 17, 2001
Segregation of heterotrimeric G proteins in cell surface microdomains. G(q) binds caveolin to concentrate in caveolae, whereas G(i) and G(s) target lipid rafts by defaultP Oh, J E SchnitzerPageof 909