1 edition of Molecular approaches to drug abuse research found in the catalog.
Based on the papers and discussion from a technical review ... held on August 24-25, 1989--T.p. verso.G.P.O. sales statement incorrect in publication (v. 1)Shipping list no.: 91-779-P (v. 1)Includes bibliographical references.
|Statement||U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Drug Abuse|
|Publishers||U.S. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Drug Abuse|
|The Physical Object|
|Pagination||xvi, 132 p. :|
|Number of Pages||66|
|2||Research monograph (National Institute on Drug Abuse) -- 111.|
|3||Research monograph -- 111.|
|v. 1. Receptor cloning, neurotransmitter expression, and molecular genetics.|
nodata File Size: 5MB.
Gioffredi reported in 1897 that serum from addicted dogs could be injected into kittens, who were then protected against large doses of morphine Gioffredi, 1897. Although this model has given us a great deal of useful information, and continues to do so, I believe the best way to study drug abuse is to have a broader perspective that includes the full range of social and behavioral sciences. stress-regulatory neuronal circuitry in alcohol and substance abuse disorders• Such an approach is more likely to expand our knowledge and lead to a more complete understanding of the brain and behavior.
The goal of studying morphine was to find substitutes that were not habit forming. Cha-Molstad H, Yu JE, Feng Z, Lee SH, Kim JG, Yang P, Han B, Sung KW, Yoo YD, Hwang J, McGuire T, Shim SM, Song HD, Ganipisetti S, Wang N, Jang JM, Lee MJ, Kim SJ, Lee KH, Hong JT, Ciechanover A, Mook-Jung I, Kim KP, Xie, X.
Will the project benefit from unique features of the scientific environment, subject populations, or collaborative arrangements?
Over the years, however, NIDA's research budget has undergone unsettling perturbations as seen in changes of its extramural grant funding. NOTE: The content below does not comply with 508 standards. Published online 2013 Jan 5. The structure-activity analysis would indicate that the milbemycins having different functional groups at positions 13,14 and 5 generally retain biological activity. Reporting When multiple years are involved, awardees will be required to submit the annually and financial statements as required in the A final progress report, invention statement, and the expenditure data portion of the Federal Financial Report are required for closeout of an award, as described in the.
- Applicants must have an active DUNS number and SAM registration in order to complete the eRA Commons registration. Bishop, led to the claim that as long as the toxin or antibodies were balanced by a dose of morphine, the person would feel and function normally-a theory similar to that proposed for methadone treatment today Bishop, 1920. In particular, human genetic variation provides the basis for dissecting the genetic architecture of complex traits including drug response.
Activities: Common Fund Roadmap Epigenomics Program co-coordinatorInternational Human Epigenome Consortium representativeCF 4D-Nucleome Program project leadCF Extracellular RNA Communication Program project leadNIH Neuroscience Blueprint Coordinating Committee, Trans-NIH Transgenerational Workgroup, NIDA Genetics Workgroup, and NIDA Neuroscience Consortium.
Among the scientists and practitioners we are planning to invite to the workshop are a researcher who studies obsessive-compulsive behavior, an alcoholism researcher, a neurobiologist who conducts imaging studies of the brain during craving, drug abuse treatment practitioners who deal with craving in treatment settings, and basic behavioral scientists who view craving as a learned behavior.
1 coordinates and supplemental data from NETAFFX.