Guide: How to cite a E-book or PDF in Harvard PUCE style

Guide: How to cite a E-book or PDF in Harvard PUCE style

Cite A E-book or PDF in Harvard PUCE style

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Use the following template to cite a e-book or pdf using the Harvard PUCE citation style. For help with other source types, like books, PDFs, or websites, check out our other guides. To have your reference list or bibliography automatically made for you, try our free citation generator.

Key:

Pink text = information that you will need to find from the source.
Black text = text required by the Harvard PUCE style.

Reference list

Place this part in your bibliography or reference list at the end of your assignment.

Template:

Author Surname, Author Forename. (Year Published). Title (p. Pages Used). City: Publisher. Recuperado de: http://Website-Url

Example:

Moreno, E., Andradas, C., Medrano, M., Caffarel, M. M., Perez-Gomez, E., and Blasco-Benito, S. et al. (2014). Targeting CB2-GPR55 Receptor Heteromers Modulates Cancer Cell Signaling. Journal Of Biological Chemistry, 289(32), 21960-21972. doi:10.1074/jbc.m114.561761

In-text citation

Place this part right after the quote or reference to the source in your assignment.

Template

(Author Surname, Year Published)

Example

Significance: These heteromers may explain some of the biphasic effects of cannabinoids and constitute potential new targets in oncology.

Abstract

The G protein-coupled receptors CB2 (CB2R) and GPR55 are overexpressed in cancer cells and human tumors. As a modulation of GPR55 activity by cannabinoids has been suggested, we analyzed whether this receptor participates in cannabinoid effects on cancer cells. Here, we show that CB2R and GPR55 form heteromers in cancer cells, that these structures possess unique signaling properties, and that modulation of these heteromers can modify the antitumoral activity of cannabinoids in vivo. These findings unveil the existence of previously unknown signaling platforms that help explain the complex behavior of cannabinoids and may constitute new targets for therapeutic intervention in oncology. (Moreno et al., 2014)

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