Results 241 to 250 of about 93,237 (289)
Targeting SLC7A5 in lung squamous cell carcinoma: implications for cancer metabolism shift and boron neutron capture therapy resistance. [PDF]
OncogenesisLin YJ +12 more
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Anticancer Potential of Myricetin against Huh7- and Hep3B-Derived Liver Cancer Stem Cells through the Regulation of Apoptosis, Autophagy, and Stemness. [PDF]
Biomol Ther (Seoul)Kwon M, Jung HJ.
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The effect of chloroquine on cervical cancer via the PI3K/AKT/MDM2 pathway. [PDF]
Discov OncolXu D +11 more
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Safeguarding artemisinin: integrating bioproduction innovation and resistance management for malaria eradication. [PDF]
Malar JFarmanpour Kalalagh K +7 more
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The specificity of chloroquine
Parasitology Today, 1992(Vol. 2) (Soulsby, E.J.L., ed.), pp 115-163, CRC Press I 5 Rosas, N., Sotelo, J. and Nieto, D. (1986) Arch. Neural 43, 353-356 16 Ito, A. et al. ( 1991 ) Mol. Biochern. Parasitol. 44, 43-52 17 Harrison, L.J.S., Delgado, J. and Parkhouse, R.M.E. (1990) Parasitology 100, 459-461 t 8 Zarlenga, D.S. et af. ( 1991 )Exp. Parasitol.
D J, Krogstad +2 more
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The American Journal of Tropical Medicine, 1948
Introduction. In the treatment of intestinal amebiasis two classes of drugs, viz., iodohydroxyquinolines and arsenicals, are generally satisfactory from the standpoint of curative action and lack of toxicity. These agents are, however, essentially ineffective against extra-intestinal amebiasis, the commonest lesion of which is found in the liver as ...
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Introduction. In the treatment of intestinal amebiasis two classes of drugs, viz., iodohydroxyquinolines and arsenicals, are generally satisfactory from the standpoint of curative action and lack of toxicity. These agents are, however, essentially ineffective against extra-intestinal amebiasis, the commonest lesion of which is found in the liver as ...
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Medicine, 2003
Abstract Quinine and chloroquine are the most common antimalarial drugs encountered in acute poisoning. Their severe toxicity in overdose results from cardiotoxicity secondary to membrane-stabilizing effects.
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Abstract Quinine and chloroquine are the most common antimalarial drugs encountered in acute poisoning. Their severe toxicity in overdose results from cardiotoxicity secondary to membrane-stabilizing effects.
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Archives of Otolaryngology - Head and Neck Surgery, 1968
CHLOROQUINE PHOSPHATE is a valuable drug used in the control of malaria and the treatment of amebiasis. The drug was developed in the United States during World War II for use as an antimalarial agent because of the shortage of quinine; the drug had been synthesized and studied as early as 1934 in Germany.
G J, Matz, R F, Naunton
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CHLOROQUINE PHOSPHATE is a valuable drug used in the control of malaria and the treatment of amebiasis. The drug was developed in the United States during World War II for use as an antimalarial agent because of the shortage of quinine; the drug had been synthesized and studied as early as 1934 in Germany.
G J, Matz, R F, Naunton
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Forensic Science, 1972
Abstract A narcotics addict, suspected of receiving an overdose of heroin, was found to have died from an overdose of chloroquine. Heroin and several tranquilizers were suspected materials but no drugs other than chloroquine were found in the blood or urine.
H M, Irvin, V L, Kyle, D T, Diosi
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Abstract A narcotics addict, suspected of receiving an overdose of heroin, was found to have died from an overdose of chloroquine. Heroin and several tranquilizers were suspected materials but no drugs other than chloroquine were found in the blood or urine.
H M, Irvin, V L, Kyle, D T, Diosi
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