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  • Book
    edited by Alan C. Swann, F. Gerard Moeller, Marijn Lijffijt.
    Contents:
    Beyond drugs : addictions in the context of recurrent/progressive psychiatric illness / Alan C. Swann
    Behavioral mechanisms in addiction / Margaret C. Wardle, Jin H. Yoon, Anka A. Vujanovic, Michael F. Weaver, Scott D. Lane, and Joy M. Schmitz
    The biology of nicotine addiction and factors that differentiate youth who smoke from those who do not / Felicia R. Carey and Anna V. Wilkinson
    Resilience and opiate misuse / Sameer Hassamal, Divya Ramesh, and F. Gerard Moeller
    Alcohol-related disorders : adaptations and progression to disordered drinking / Therese A. Kosten, Colin Haile, Marijn Lijffijt, and Alan C. Swann
    The neurobiology of behavioral sensitization / Jeffery D. Steketee
    Stress and addiction / Marijn Lijffijt
    The neurobiology of behavioral addictions : sexual addiction / Donald L. Hilton Jr., Stefanie Carnes, and Todd L. Love
    Norepinephrine as a therapeutic target for cocaine-use disorder / Colin N. Haile, Thomas F. Newton, and Thomas R. Kosten
    Cannnabis, endocannabinoids, and mechanisms of addiction / Christopher Rodgman and Christopher D. Verrico
    Cocaine addiction therapy pharmacogenetics / David A. Nielsen
    Increasing the information yield from clinical trials in addictions : Bayesian statistics, adaptive designs, and biomarker evaluation / Charles Green, Robert Suchting, Nuvan Rathnayaka, Margaret Wardle, and Joy M. Schmitz
    Mechanisms of sensitization to stress, affective episodes, and abused substances : implications for treatment and prevention / Robert M. Post.
    Digital Access Oxford 2016
  • Article
    Mattiasson B, Borrebaeck C, Sanfridson B, Mosbach K.
    Biochim Biophys Acta. 1977 Aug 11;483(2):221-7.
    A new method, thermometric enzyme linked immunosorbent assay (TELISA), for the assay of endogenous and exogenous compounds in biological fluids is described. It is based on the previously described enzyme linked immunosorbent assay technique, ELISA, but utilizes enzymic heat formation which is measured in an enzyme thermistor unit. In the model system studied determination of human serum albumin down to a concentration of 10(-10) M (5 ng/ml) was achieved, with both normal and catalase labelled human serum albumin competing for the binding sites on the immunosorbent, which was rabbit antihuman serum albumin immobilized onto Sepharose CL-4B.
    Digital Access Access Options