Read e-book online A Brief History of Disease, Science and Medicine PDF

By Michael Kennedy

ISBN-10: 0974946656

ISBN-13: 9780974946658

This creation to the background of drugs starts with the evolution of infectious illnesses on the finish of the final ice age. It describes the foundation of technological know-how and medication in historic civilizations, together with China and India. the 1st 3rd of the publication covers the early interval that's thought of the "classical" background of drugs. the rest describes the evolution of contemporary medication and surgical procedure as much as the current. the ultimate bankruptcy is a heritage of scientific economics and explains the beginning of medical health insurance, HMOs and scientific malpractice court cases, matters defined nowhere else within the clinical institution curriculum.

There is a forty web page index and over 550 footnotes, such a lot of them references to the unique articles defined within the textual content. A bibliography of crucial resources is additionally incorporated.

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Extra info for A Brief History of Disease, Science and Medicine

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Even a genomic library covering the whole pathogen can eventually be built up from such fragments. However, in most cases only a few specific probes need to be selected as diagnostics. This selection process can be simplified by subtractive hybridization or genomic subtraction. The non-specific DNA that is common between the pathogen and another organism, such as its host, is depleted while that specific to the pathogen only is enriched. This is done by hybridizing labelled DNA from the target organism - the pathogen - with an excess (100-200 times the amount) of DNA from the driver, which can be a related organism or the host.

Generally, probes consist of a few kilobases (kb) of DNA but may be as short as 15-20 bp or as large as 30 kb. Most often, the probes for a specific purpose are screened from randomly cloned fragments of DNA. Even a genomic library covering the whole pathogen can eventually be built up from such fragments. However, in most cases only a few specific probes need to be selected as diagnostics. This selection process can be simplified by subtractive hybridization or genomic subtraction. The non-specific DNA that is common between the pathogen and another organism, such as its host, is depleted while that specific to the pathogen only is enriched.

For this reason, polyclonal antibodies are often preferred. These are purified from crude immune serum or antiserum humanely collected from the blood of living animals that have been injected with doses of antigenic material from the pathogen; usually this must be done only in registered premises. g. g. , 1988). The sources of these immunogens have included purified material, electrophoresis bands, crude mycelial culture extracts (Ouellette and Benhamou, 1987) and freeze dried mycelium (Fox and Hahne, 1988).

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A Brief History of Disease, Science and Medicine by Michael Kennedy


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