X. Yu

Interaction of the P-glycoprotein Multidrug Transporter with Peptides and Ionophores (*)

F. Sharom, G. DiDiodato, K. J. Ashbourne, 1995, The Journal of Biological Chemistry.

Sequence Characterization of matrix protein (M1) in influenza A viruses (H1, H3 and H5)

Yong Li, Jun Zhang, Lei Xu, 2011 .

Interaction of the P-glycoprotein multidrug transporter (MDR1) with high affinity peptide chemosensitizers in isolated membranes, reconstituted systems, and intact cells.

A. Monks, C. Hose, M. Müller, 1999, Biochemical pharmacology.

Synthetic hydrophobic peptides are substrates for P-glycoprotein and stimulate drug transport.

F. Sharom, X. Yu, G. Didiodato, 1996, The Biochemical journal.

Functional reconstitution of drug transport and ATPase activity in proteoliposomes containing partially purified P-glycoprotein.

F. Sharom, C. A. Doige, X. Yu, 1993, The Journal of biological chemistry.

Characterization of the ATPase activity of P-glycoprotein from multidrug-resistant Chinese hamster ovary cells.

F. Sharom, C. A. Doige, X. Yu, 1995, The Biochemical journal.