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Biochemistry International|April 1, 1983
Use of non-physiological buffer systems in the analysis of methotrexate transport in L1210 cellsG B Henderson, E M ZevelyNucleic Acids Research|September 25, 1995
5'-Cholesteryl-phosphorothioate oligodeoxynucleotides: potent inhibition of methotrexate transport and antagonism of methotrexate toxicity in cells containing the reduced-folate carrierG B Henderson, C A SteinImmunopharmacology|October 1, 1996
Microbial/host interactions in health and disease: who controls the cytokine network?B Henderson, S Poole, M WilsonJournal of Periodontal Research|August 1, 1996
Cytokine-inducing components of periodontopathogenic bacteriaM Wilson, K Reddi, B HendersonArchives of Biochemistry and Biophysics|March 1, 1983
Structural requirements for anion substrates of the methotrexate transport system in L1210 cellsG B Henderson, E M ZevelyThe Journal of Biological Chemistry|October 5, 1987
Methotrexate efflux in L1210 cells. Kinetic and specificity properties of the efflux system sensitive to bromosulfophthalein and its possible identity with a system which mediates the efflux of 3',5'-cyclic AMPG B Henderson, J M TsujiBiochimica Et Biophysica Acta|January 22, 1981
Transport of methotrexate in L1210 cells. Mechanism for inhibition by p-chloromercuriphenylsulfonate and N-ethylmaleimideG B Henderson, E M ZevelyThe Journal of Membrane Biology|January 1, 1986
Properties of an anion/H+ cotransport system in L1210 cells that utilizes phthalate as a nonphysiological substrateG B Henderson, E M ZevelyProceedings of the National Academy of Sciences of the United States of America|December 1, 1971
Vitamin B 6 -responsive histidine deficiency in mutants of Salmonella typhimuriumG B Henderson, E E SnellPageof 63