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| TABLE OF CONTENTS | ||||||||||||||||||||||||||||||||||||||||
| September 2017 Volume 18 Number 9 | ||||||||||||||||||||||||||||||||||||||||
| | In this issue
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| REVIEWS | Top | |||||||||||||||||||||||||||||||||||||||
| Genes and molecular pathways underpinning ciliopathies Jeremy F. Reiter & Michel R. Leroux p533 | doi:10.1038/nrm.2017.60 Motile and non-motile primary cilia are nearly ubiquitous cellular organelles. Dysfunction of cilia is being found to cause increasing numbers of diseases that are known as ciliopathies. The characterization of ciliopathy-associated proteins and phenotypes is increasing our understanding of how cilia are formed and compartmentalized and how they function to maintain human health. Abstract | Full Text | PDF | Supplementary information | ||||||||||||||||||||||||||||||||||||||||
| Understanding nucleosome dynamics and their links to gene expression and DNA replication William K. M. Lai & B. Franklin Pugh p548 | doi:10.1038/nrm.2017.47 The presence of nucleosomes and their substructures affects local chromatin structure and function. Thus, nucleosome occupancy, their exact positioning and composition need to be dynamically regulated. Advances in genomic technologies have improved our understanding of nucleosome dynamics in various cellular processes, most notably DNA replication and transcription. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||
Mechanisms of DNA-protein crosslink repair Julian Stingele, Roberto Bellelli & Simon J. Boulton p563 | doi:10.1038/nrm.2017.56 Covalent DNA-protein crosslinks (DPCs) are induced by various compounds, which include widely used anticancer drugs, and are highly cytotoxic. Recent studies have revealed the mechanisms and the regulation of DPC repair pathways and suggest that components of these pathways can serve as targets for anticancer therapies. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||
| ANALYSIS | Top | |||||||||||||||||||||||||||||||||||||||
| Classification and function of small open reading frames Juan-Pablo Couso & Pedro Patraquim p575 | doi:10.1038/nrm.2017.58 A comprehensive analysis of small open reading frames (smORFs) in flies, mice and humans supports their classification into different functional groups, from inert DNA sequences to transcribed and translated smORFs that have various activities. The different smORF classes could represent steps in gene, peptide and protein evolution. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||
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