Citation: Rh. Liu et Fj. Sharom, PROXIMITY OF THE NUCLEOTIDE-BINDING DOMAINS OF THE P-GLYCOPROTEIN MULTIDRUG TRANSPORTER TO THE MEMBRANE-SURFACE - A RESONANCE ENERGY-TRANSFER STUDY, Biochemistry, 37(18), 1998, pp. 6503-6512
Citation: Fj. Sharom et al., LINEAR AND CYCLIC-PEPTIDES AS SUBSTRATES AND MODULATORS OF P-GLYCOPROTEIN - PEPTIDE BINDING AND EFFECTS ON DRUG TRANSPORT AND ACCUMULATION, Biochemical journal, 333, 1998, pp. 621-630
Citation: Mt. Letho et Fj. Sharom, RELEASE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED ENZYME ECTO-5'-NUCLEOTIDASE BY PHOSPHOLIPASE-C - CATALYTIC ACTIVATION AND MODULATION BY THE LIPID BILAYER, Biochemical journal, 332, 1998, pp. 101-109
Citation: Y. Romsicki et Fj. Sharom, THE ATPASE AND ATP-BINDING FUNCTIONS OF P-GLYCOPROTEIN - MODULATION BY INTERACTION WITH DEFINED PHOSPHOLIPIDS, European journal of biochemistry, 256(1), 1998, pp. 170-178
Citation: Jwk. Chu et al., BIOCHEMICAL-CHANGES IN THE EQUINE CAPSULE FOLLOWING PROSTAGLANDIN-INDUCED PREGNANCY FAILURE, Molecular reproduction and development, 46(3), 1997, pp. 286-295
Citation: Fj. Sharom, THE P-GLYCOPROTEIN MULTIDRUG TRANSPORTER - INTERACTIONS WITH MEMBRANE-LIPIDS, AND THEIR MODULATION OF ACTIVITY, Biochemical Society transactions, 25(3), 1997, pp. 1088-1096
Citation: Y. Romsicki et Fj. Sharom, INTERACTION OF P-GLYCOPROTEIN WITH DEFINED PHOSPHOLIPID-BILAYERS - A DIFFERENTIAL SCANNING CALORIMETRIC STUDY, Biochemistry, 36(32), 1997, pp. 9807-9815
Citation: Rh. Liu et Fj. Sharom, FLUORESCENCE STUDIES ON THE NUCLEOTIDE-BINDING DOMAINS OF THE P-GLYCOPROTEIN MULTIDRUG TRANSPORTER, Biochemistry, 36(10), 1997, pp. 2836-2843
Citation: G. Didiodato et Fj. Sharom, INTERACTION OF COMBINATIONS OF DRUGS, CHEMOSENSITIZERS, AND PEPTIDES WITH THE P-GLYCOPROTEIN MULTIDRUG TRANSPORTER, Biochemical pharmacology, 53(12), 1997, pp. 1789-1797
Citation: Fj. Sharom et al., MODULATION OF THE CLEAVAGE OF GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED PROTEINS BY SPECIFIC BACTERIAL PHOSPHOLIPASES, Biochemistry and cell biology, 74(5), 1996, pp. 701-713
Citation: Fj. Sharom et al., SYNTHETIC HYDROPHOBIC PEPTIDES ARE SUBSTRATES FOR P-GLYCOPROTEIN AND STIMULATE DRUG TRANSPORT, Biochemical journal, 320, 1996, pp. 421-428
Citation: Rh. Liu et Fj. Sharom, SITE-DIRECTED FLUORESCENCE LABELING OF P-GLYCOPROTEIN ON CYSTEINE RESIDUES IN THE NUCLEOTIDE-BINDING DOMAINS, Biochemistry, 35(36), 1996, pp. 11865-11873
Citation: Fj. Sharom et al., CHARACTERIZATION OF THE ATPASE ACTIVITY OF P-GLYCOPROTEIN FROM MULTIDRUG-RESISTANT CHINESE-HAMSTER OVARY CELLS, Biochemical journal, 308, 1995, pp. 381-390
Citation: Fj. Sharom, CHARACTERIZATION AND FUNCTIONAL RECONSTITUTION OF THE MULTIDRUG TRANSPORTER, Journal of bioenergetics and biomembranes, 27(1), 1995, pp. 15-22
Authors:
SHAROM FJ
DIDIODATO G
YU XH
ASHBOURNE KJD
Citation: Fj. Sharom et al., INTERACTION OF THE P-GLYCOPROTEIN MULTIDRUG TRANSPORTER WITH PEPTIDESAND IONOPHORES, The Journal of biological chemistry, 270(17), 1995, pp. 10334-10341
Citation: P. Lu et Fj. Sharom, GANGLIOSIDES ARE POTENT IMMUNOSUPPRESSORS OF IL-2-MEDIATED T-CELL PROLIFERATION IN A LOW-PROTEIN ENVIRONMENT, Immunology, 86(3), 1995, pp. 356-363
Citation: Dw. Loe et Fj. Sharom, INTERACTION OF MULTIDRUG-RESISTANT CHINESE-HAMSTER OVARY CELLS WITH THE PEPTIDE IONOPHORE GRAMICIDIN-D, Biochimica et biophysica acta. Biomembranes, 1190(1), 1994, pp. 72-84