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March 2012 Volume 13 Number 3 | |||||||||||||||||||||||||||||||||||||
In this issue Research Highlights Reviews Perspectives
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REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
Understanding transgenerational epigenetic inheritance via the gametes in mammals Lucia Daxinger & Emma Whitelaw p153 | doi:10.1038/nrg3188 Some epigenetic information can be passed from parents to offspring, but it is difficult to identify the molecular basis of information transferred through the gametes. This Review evaluates the extent of our understanding in mammals. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Sex and the singular DM domain: insights into sexual regulation, evolution and plasticity Clinton K. Matson & David Zarkower p163 | doi:10.1038/nrg3161 This article reviews our growing understanding of the varied roles of DM domain genes in metazoan sexual development: in the evolution of sexually dimorphic traits and new sex-determining mechanisms and, more recently, in maintaining cell fate in the gonad. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Article series: Genome-wide association studies Human genetic susceptibility to infectious disease Stephen J. Chapman & Adrian V. S. Hill p175 | doi:10.1038/nrg3114 The discovery of common and rare genetic variants underlying infectious disease susceptibility in humans highlights the involvement of shared host signalling pathways in diverse infectious diseases, and provides insights into the genetic control of immune signalling. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Causes and consequences of aneuploidy in cancer David J. Gordon, Benjamin Resio & David Pellman p189 | doi:10.1038/nrg3123 Aneuploidy — an abnormal number of chromosomes — typically has a detrimental effect on viability. Somewhat paradoxically, it is a remarkably common feature of cancer. This Review discusses how aneuploidy occurs, the cellular responses to aneuploidy and how aneuploidy can provide particular selective advantages during tumorigenesis. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Transcription as a source of genome instability Nayun Kim & Sue Jinks-Robertson p204 | doi:10.1038/nrg3152 Transcription poses a risk to the genome through transcription-associated mutagenesis and recombination. This Review discusses recent findings about influences on this genomic instability, such as the rate and direction of transcription or nucleic acid structures, and how these phenomena may be considered across species. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
PERSPECTIVES | Top | ||||||||||||||||||||||||||||||||||||
OPINION Article series: Modelling Cellular genomics for complex traits Emmanouil T. Dermitzakis p215 | doi:10.1038/nrg3115 The author discusses the advantages and challenges of 'cellular phenotyping' and the way in which this integrated analysis of cellular phenotypes is likely to advance our understanding of the genetic and long-term environmental influences on complex traits. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Erratum: Protein–RNA interactions: new genomic technologies and perspectives Julian König, Kathi Zarnack, Nicholas M. Luscombe & Jernej Ule p220 | doi:10.1038/nrg3183 Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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*2010 Journal Citation Report (Thomson Reuters, 2011) |
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