TABLE OF CONTENTS | ||||||||||||||||||||||||||||||||||||||||||||||
January 2015 Volume 15 Number 1 | ||||||||||||||||||||||||||||||||||||||||||||||
In this issue Research Highlights Reviews Perspectives
| ||||||||||||||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||
REVIEWS | Top | |||||||||||||||||||||||||||||||||||||||||||||
PI3K in cancer: divergent roles of isoforms, modes of activation and therapeutic targeting Lauren M. Thorpe, Haluk Yuzugullu & Jean J. Zhao p7 | doi:10.1038/nrc3860 Hyperactivation of phosphatidylinositol 3-kinase (PI3K) signalling cascades is one of the most common events in human cancers. This Review discusses recent advances in our knowledge of the roles of distinct PI3K isoforms in normal and oncogenic signalling, and the current state and future potential of targeting this pathway in the clinic. Abstract | Full Text | PDF | Supplementary information | ||||||||||||||||||||||||||||||||||||||||||||||
Molecular biology of bladder cancer: new insights into pathogenesis and clinical diversity Margaret A. Knowles & Carolyn D. Hurst p25 | doi:10.1038/nrc3817 This Review discusses recent advances in the molecular characterization of bladder cancer, which has provided insights into pathogenesis and subgroups of bladder cancers with different prognosis. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
Modelling bladder cancer in mice: opportunities and challenges Takashi Kobayashi, Tomasz B. Owczarek, James M. McKiernan & Cory Abate-Shen p42 | doi:10.1038/nrc3858 This Review surveys the available models of bladder cancer and discusses their advantages and limitations, making suggestions for their improvement. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
PERSPECTIVES | Top | |||||||||||||||||||||||||||||||||||||||||||||
TIMELINE VHL, the story of a tumour suppressor gene Lucy Gossage, Tim Eisen & Eamonn R. Maher p55 | doi:10.1038/nrc3844 The identification in 1993 of inherited mutations in the von Hippel-Lindau (VHL) gene in families with VHL disease was a seminal finding. This and subsequent discoveries have given the VHL tumour suppressor gene a central role in our understanding of the mechanisms of cellular oxygen sensing and in the pathobiology of clear-cell renal cell carcinoma. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
|
*2013 Journal Citation Report (Thomson Reuters, 2014) |
You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/myaccount For further technical assistance, please contact our registration department For print subscription enquiries, please contact our subscription department For other enquiries, please contact our feedback department Nature Publishing Group | 75 Varick Street, 9th Floor | New York | NY 10013-1917 | USA Nature Publishing Group's worldwide offices: Macmillan Publishers Limited is a company incorporated in England and Wales under company number 785998 and whose registered office is located at Brunel Road, Houndmills, Basingstoke, Hampshire RG21 6XS. © 2015 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. |
No comments:
Post a Comment