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March 2012: View the entire issue
Cover story: Human mutations in MCM4
False-colored transmission electron microscopy image of a steroid-secreting adrenal cell. In this issue of the JCI, two independent groups of researchers have simultaneously identified the genetic cause of a human syndrome marked by growth retardation, adrenal insufficiency, and natural killer cell deficiency (pages 814 and 821). The mutation is in the MCM4 gene encoding minichromosome maintenance–complex component 4.
Image credit: Photo Researchers, Inc.
Also inside:
Maintaining protective antifungal immunity
Noncanonical TGF-β pathway to craniofacial defects
Enhancing the effectiveness of trastuzumab
FOSL2 promotes leptin gene expression
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Dermatology
Though it's the first thing we see when we look at each other, the skin may be occasionally forgotten as a site of clinically important disease. The reviews in this series highlight our current understanding of several common dermatological conditions, and describe how research in the field has played a major role in expanding our understanding of the basic biology of stem cells and cancer. Correspondingly, basic research findings have led to new insights into dermatological disease, often with impact on therapeutic strategies. Cover image credit: John Seykora
Sexually transmitted infections
View previous series
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β1 Integrin/FAK/cortactin signaling is essential for human head and neck cancer resistance to radiotherapy
Iris Eke, Yvonne Deuse, Stephanie Hehlgans, Kristin Gurtner, Mechthild Krause, Michael Baumann, Anna Shevchenko, Veit Sandfort, Nils Cordes
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c-Src and c-Abl kinases control hierarchic phosphorylation and function of the CagA effector protein in Western and East Asian Helicobacter pylori strains
Doreen Mueller, Nicole Tegtmeyer, Sabine Brandt, Yoshio Yamaoka, Eimear De Poire, Dionyssios Sgouras, Silja Wessler, Javier Torres, Adam Smolka, Steffen Backert
View article
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Copyright © 2012 American Society for Clinical Investigation.
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