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It is a 3-in-1 reference ebook. It supplies an entire scientific dictionary protecting 1000s of phrases and expressions in terms of amphetamines. It additionally offers broad lists of bibliographic citations. eventually, it presents details to clients on how one can replace their wisdom utilizing a variety of net assets. The publication is designed for physicians, scientific scholars getting ready for Board examinations, clinical researchers, and sufferers who are looking to familiarize yourself with study devoted to amphetamines. in the event that your time is efficacious, this e-book is for you. First, you won't waste time looking out the web whereas lacking loads of correct info. moment, the booklet additionally saves you time indexing and defining entries. ultimately, you won't waste time and cash printing hundreds and hundreds of websites.
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Extra resources for Amphetamines - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References
Would like to use this model to establish more precisely the mechanisms underlying PCP- induced cell death. ; Professor; Pharmacology; Yale University 47 College Street, Suite 203 New Haven, Ct 065208047 Timing: Fiscal Year 2001; Project Start 01-MAY-1993; Project End 31-JAN-2004 Summary: (Applicant's Abstract): Biogenic amine transporters are responsible for terminating the synaptic action of serotonin (5-HT), dopamine (DA), and norepinephrine (NE). They are the molecular targets for antidepressants such as imipramine and Prozac as well as for psychostimulants such as cocaine and amphetamines.
Cmd=Retrieve&db=PubMed&list_ uids=9893403&dopt=Abstract · Automated determination of 'Ecstasy' and amphetamines in urine by SPME and capillary gas chromatography after propylchloroformate derivatisation. Author(s): Ugland HG, Krogh M, Rasmussen KE. Source: Journal of Pharmaceutical and Biomedical Analysis. 1999 March; 19(3-4): 463-75. cmd=Retrieve&db=PubMed&list_ uids=10704112&dopt=Abstract · Automated headspace solid-phase dynamic extraction for the determination of amphetamines and synthetic designer drugs in hair samples.
The primary objective of the present study is the design and synthesis of conformationally-restricted derivatives of fluoxetine, as potential pharmacologically active compounds. Both (R) and (S)-fluoxetine are flexible molecules. The (S)-isomer displays prolonged duration in man, which may contribute to side effects. Flexible molecules may have more than one site of action, with one preferred conformation at the receptor site. Side effects observed may be due to a low-energy conformation of fluoxetine at a second site.
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