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TABLE OF CONTENTS | |||||||||||||||||||||||||||||||||||||||||||||||
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December 2013 Volume 11 Number 12 | |||||||||||||||||||||||||||||||||||||||||||||||
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EDITORIAL | Top | ||||||||||||||||||||||||||||||||||||||||||||||
A broad rejuvenation p815 | doi:10.1038/nrmicro3174 As World AIDS Day approaches, and the 30th anniversary year of the isolation of HIV-1 draws to a close, it is timely to reflect on the past, present and future of HIV/AIDS research. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||||||||
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NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||||||||||||
GENOME WATCH Playing fast and loose with mutation Alison E. Mather & Simon R. Harris p822 | doi:10.1038/nrmicro3164 This month's Genome Watch investigates the role of hypermutation in chronic bacterial infection and its implications for phylogenomic analyses. | |||||||||||||||||||||||||||||||||||||||||||||||
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REVIEWS | Top | ||||||||||||||||||||||||||||||||||||||||||||||
Targeting lipid biosynthesis and salvage in apicomplexan parasites for improved chemotherapies Isabelle Coppens p823 | doi:10.1038/nrmicro3139 Apicomplexan parasites have unique lipid-scavenging and -synthesis pathways that are not found in their mammalian hosts. Coppens gives an overview of these pathways in Plasmodium spp., Toxoplasma gondii and Cryptosporidium spp. and highlights promising drug targets to interfere with the parasites' high demand for isoprenoids, sphingolipids and cholesterol. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||||||||
A decade after SARS: strategies for controlling emerging coronaviruses Rachel L. Graham, Eric F. Donaldson & Ralph S. Baric p836 | doi:10.1038/nrmicro3143 The emergence of severe acute respiratory syndrome (SARS) coronavirus and, more recently, Middle East respiratory syndrome (MERS) coronavirus has highlighted the pathogenic and epidemic potential of this virus family. Here, Graham, Donaldson and Baric review key biological properties of coronaviruses and how to target them with potential therapeutics. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||||||||
![]() Antimalarial drug discovery — approaches and progress towards new medicines Erika L. Flannery, Arnab K. Chatterjee & Elizabeth A. Winzeler p849 | doi:10.1038/nrmicro3138 Current antimalarial therapy heavily relies on artemisinins, a drug class that only targets the blood stages of the parasite and which is increasingly feared to elicit drug resistance. Flannery, Chatterjee and Winzeler discuss the approaches used to develop novel drugs that are active against different life cycle stages with the ultimate aim of eliminating malaria. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||||||||
Keeping it quiet: chromatin control of gammaherpesvirus latency Paul M. Lieberman p863 | doi:10.1038/nrmicro3135 Epstein–Barr virus (EBV) and Kaposi's sarcoma-associated herpesvirus (KSHV) establish latent infections, during which the viral genomes are maintained in the host cell as viral episomes. As discussed by Lieberman, latency depends on numerous factors, including viral genome chromatinization and epigenetic modification, as well as tight control of the latency transcription programme. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||||||||
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PERSPECTIVES | Top | ||||||||||||||||||||||||||||||||||||||||||||||
TIMELINE Past, present and future: 30 years of HIV research Françoise Barré-Sinoussi, Anna Laura Ross & Jean-François Delfraissy p877 | doi:10.1038/nrmicro3132 The isolation of HIV-1 was a fundamental step for understanding HIV and the disease it causes. Here, Françoise Barré-Sinoussi, Anna Laura Ross and Jean-François Delfraissy look back on three decades of research that have changed the lives of people infected with HIV and have inspired hope for a cure. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||||||||
OPINION Development of vaccines for Candida albicans: fighting a skilled transformer Antonio Cassone p884 | doi:10.1038/nrmicro3156 Antonio Cassone outlines why he thinks univalent subunit vaccines targeting Candida albicans are unlikely to succeed and argues that the development of a multivalent vaccine could be a better approach. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||||||||
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*2012 Journal Citation Report (Thomson Reuters, 2013) |
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