Table of contents


From the editors

p239 | doi:10.1038/nrg1487

Top

Research Highlights

Evolution: The advantages of sex | PDF (89 KB)

p240 | doi:10.1038/nrg1851

Chromosome biology: Even chromosomes have their weaknesses | PDF (136 KB)

p241 | doi:10.1038/nrg1846

Genetic variation: When more is more | PDF (115 KB)

p242 | doi:10.1038/nrg1842

Synthetic biology: Building up a picture of gene regulation | PDF (115 KB)

p242 | doi:10.1038/nrg1844

RNA world: Behind the scenes | PDF (60 KB)

p242 | doi:10.1038/nrg1852

In brief

Evolution | Evo–Devo | Human Disease | Epigenetics | PDF (65 KB)

p243 | doi:10.1038/nrg1848

In the news

Keeping up with the Grewcocks | PDF (105 KB)

p244 | doi:10.1038/nrg1841

Neurogenetics: A male gene for a male brain | PDF (105 KB)

p244 | doi:10.1038/nrg1843

Cancer genetics: From expression signatures to their regulators | PDF (105 KB)

p244 | doi:10.1038/nrg1845

In brief

Technology | Network Biology | Lifespan | PDF (67 KB)

p245 | doi:10.1038/nrg1849

Human evolution: Following the signposts of selection | PDF (114 KB)

p246 | doi:10.1038/nrg1850

Evolution: A small leap for adaptation | PDF (60 KB)

p246 | doi:10.1038/nrg1853

Top

Focus on: Monogenic disorders

Reviews

Human monogenic disorders — a source of novel drug targets

Ryan R. Brinkman, Marie-Pierre Dubé, Guy A. Rouleau, Andrew C. Orr & Mark E. Samuels

p249 | doi:10.1038/nrg1828

Pharmaceutical industry and medical professionals have been concerned by the lack of novel drugs and drug candidates in the pipeline. These authors discuss evidence to indicate that human monogenic disorders are a valuable, but so far largely neglected, source of novel drug targets.

Genetic medicines: treatment strategies for hereditary disorders

Timothy P. O'Connor & Ronald G. Crystal

p261 | doi:10.1038/nrg1829

More than 1,800 genes are known to cause hereditary disorders in humans. This review discusses the use of genetic medicines to treat monogenic hereditary disorders, and the technical, regulatory and economic challenges that genetic medicine must confront to become a reality.

Perspective

Opinion
Mendelian disorders deserve more attention

Stylianos E. Antonarakis & Jacques S. Beckmann

p277 | doi:10.1038/nrg1826

Multifactorial disorders have grabbed the limelight in recent years, at the expense of research on monogenic traits. This shift in emphasis might not be fully justified, given the insight that seemingly 'simple' disorders can bring to genome function and complex disease aetiology.

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Reviews

Left–right asymmetry in the vertebrate embryo: from early information to higher-level integration

Ángel Raya & Juan Carlos Izpisúa Belmonte

p283 | doi:10.1038/nrg1830

How left–right asymmetries are established in vertebrate embryos has fascinated developmental biologists for decades. Recent evidence from a range of species provides insights into the genetic and epigenetic mechanisms that are involved, particularly in the early stages of generating left–right asymmetry.

Genetic susceptibility to infectious disease: lessons from mouse models of leishmaniasis

Marie Lipoldová & Peter Demant

p294 | doi:10.1038/nrg1832

Studies of susceptibility to leishmaniasis illustrate the power of mouse genetics to increase our understanding of host responses to infection. Mouse models have begun to reveal a network of genetically regulated responses, some of which overlap with those triggered by other infections.

Genetics of Parkinson disease: paradigm shifts and future prospects

Matthew James Farrer

p306 | doi:10.1038/nrg1831

Genetic studies of Parkinson disease have stimulated progress in understanding many aspects of this debilitating neurodegenerative disorder. A combination of mapping disease genes in humans and studying their functions in model organisms provides new hope for treatment and prevention.

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Perspective

Timeline

From teratocarcinomas to embryonic stem cells and beyond: a history of embryonic stem cell research

Davor Solter

p319 | doi:10.1038/nrg1827

The recent eruption of interest in embryonic stem cell research is fuelled by the promise and potential of this work. But current work is firmly grounded in several decades of fascinating research that are engagingly summarized here by the author.

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