Author: G. H. Coombs
Edition: 1
Binding: Paperback
ISBN: 0521626692
Feature:
Edition: 1
Binding: Paperback
ISBN: 0521626692
Feature:
Molecular Basis of Drug Design and Resistance (Parasitology)
This new collection of articles, edited by G. Search and download Molecular Basis of Drug Design and Resistance (Parasitology) for free H. Coombs and S. L. Croft include: The current status of antiparasite chemotherapy; A structure-based approach to drug discovery: crystallography and implications for the development of antiparasite drugs; Validating targets for antiparasite chemotherapy; Control of gene expression in viruses and protozoan parasites by antisense oligonucleotides; Parasite proteinases and amino acid metabolism: possibilities for chemotherapeutic exploitation; The mannitol cycle in Eimeria; New approaches to Leishmania chemotherapy: pteridine reductase 1 (PTR1) as a target and modulator of antifolate sensitivity; Target sites of anthelmintics; Quinoline resistance mechanisms in Plasmodium falciparum: the debate goes New Paperback.
Free Molecular Basis Of Drug Design And Resistance, 9780521626699
Molecular Basis Of Drug Design And Resistance, ISBN-13: 9780521626699, ISBN-10: 0521626692
One of the main problems concerning therapeutic tools for the treatment of parasitic diseases, including leishmaniasis, is that some field parasites are naturally resistant to the classical drugs; additionally, current therapies may select parasites prone to be resistant to the applied drugs. These features are (at least partially) responsible for the disappointing persistence of the disease and resultant deaths worldwide. This book provides a comprehensive view of the pathology of the disease itself, and of parasitic drug resistance, its molecular basis, consequences and possible treatments.
One of the main problems concerning therapeutic tools for the treatment of parasitic diseases, including leishmaniasis, is that some field parasites are naturally resistant to the classical drugs; additionally, current therapies may select parasites prone to be resistant to the applied drugs. These features are (at least partially) responsible for the disappointing persistence of the disease and resultant deaths worldwide. This book provides a comprehensive view of the pathology of the disease itself, and of parasitic drug resistance, its molecular basis, consequences and possible treatments.
One of the main problems concerning therapeutic tools for the treatment of parasitic diseases, including leishmaniasis, is that some field parasites are naturally resistant to the classical drugs; additionally, current therapies may select parasites prone to be resistant to the applied drugs. These features are (at least partially) responsible for the disappointing persistence of the disease and resultant deaths worldwide. This book provides a comprehensive view of the pathology of the disease itself, and of parasitic drug resistance, its molecular basis, consequences and possible treatments.
Molecular Basis of Drug Design and Resistance Free
Croft include: The current status of antiparasite chemotherapy; A structure-based approach to drug discovery: crystallography and implications for the development of antiparasite drugs; Validating targets for antiparasite chemotherapy; Control of gene expression in viruses and protozoan parasites by antisense oligonucleotides; Parasite proteinases and amino acid metabolism: possibilities for chemotherapeutic exploitation; The mannitol cycle in Eimeria; New approaches to Leishmania chemotherapy: pteridine reductase 1 (PTR1) as a target and modulator of antifolate sensitivity; Target sites of anthelmintics; Quinoline resistance mechanisms in Plasmodium falciparum: the debate goes Find and download medical book free in many categories here
