Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Volume 13 Issue 9, September 2014

'Administering biopharmaceuticals' by Susanne Harris, inspired by the Review on p655.

Comment

  • How can real-world data from electronic health records be harnessed to improve the effectiveness and efficiency of clinical trials?

    • John Parkinson
    Comment

    Advertisement

Top of page ⤴

News and Analysis

  • The European Investment Bank has invested €75 million in a risk-sharing drug development deal with the pharmaceutical company UCB, potentially opening up a new source of research and development (R&D) funding.

    • Asher Mullard
    News and Analysis
Top of page ⤴

News in Brief

Top of page ⤴

Biobusiness Briefs

Top of page ⤴

Patent Watch

Top of page ⤴

An Audience With

  • Bob More, venture capitalist with the Bill and Melinda Gates Foundation, discusses the challenges of aligning financial and philanthropic interests.

    An Audience With
Top of page ⤴

From the Analyst's Couch

  • The developmental pipeline of HIV antiretroviral therapies is large and diverse, spanning a number of different drug classes. This article provides an overview of the agents in development, including combination therapies, and an analysis of the market for current and future HIV treatments.

    • Angel Wong
    From the Analyst's Couch
Top of page ⤴

Research Highlight

Top of page ⤴

In Brief

Top of page ⤴

Review Article

  • Histone deacetylases (HDACs) are a class of epigenetic enzymes that remove acetyl groups from lysine residues on histones and other proteins. In this Review, the authors highlight the role of HDACs in cancer, neurological diseases and immune disorders, and discuss the development of small-molecule inhibitors.

    • Katrina J. Falkenberg
    • Ricky W. Johnstone
    Review Article
  • G protein-coupled receptors (GPCRs) are highly successful drug targets, particularly for central nervous system (CNS) disorders. Compared to traditional drugs that target the orthosteric ligand-binding site of GPCRs, allosteric modulators have the potential to achieve greater subtype selectivity and allow the normal function of endogenous ligands to be preserved. Conn and colleagues reflect on the key principles for successful optimization of GPCR allosteric modulators.

    • P. Jeffrey Conn
    • Craig W. Lindsley
    • Colleen M. Niswender
    Review Article
Top of page ⤴

Erratum

Top of page ⤴

Search

Quick links