Advertisement |
|
iCell® & MyCell® Human Cells Reinvent Discovery Research
- Ready-made iPSC-derived cells: Cardiomyocytes, neurons, hepatocytes, endothelial cells, and more
- Made-to-order cells
from your donor samples or CDI disease cell lines including
cardiomyopathies / arrhythmias, neurological disorders, muscular
dystrophies, and more
- Enabling disease modeling, cell therapy, tissue engineering, and more
| |
|
|
|
|
TABLE OF CONTENTS
|
1 July 2013
|
| | |
| News Analysis Research Highlights Research & Reviews Careers |
|
Nature Reviews Drug Discovery is on Twitter
| |
|
|
Advertisement |
|
|
|
|
News
| Top |
|
|
|
Silver makes antibiotics thousands of times more effective doi:10.1038/nature.2013.13232 Ancient antimicrobial treatment could help to solve modern bacterial resistance. Full Text |
|
|
|
Blocking boozy memories reduces risk of relapse doi:10.1038/nature.2013.13252 Molecule associated with learning and memory could be key to treating alcoholism. Full Text |
|
|
|
Simple molecule prevents mole rats from getting cancer doi:10.1038/nature.2013.13236 Sugar matrix surrounding cells traps would-be tumours in long-lived mammal. Full Text |
|
|
|
Inducing translation doi:10.1038/nbt.2602 The
field of induced pluripotent stem cells is barely seven years old, but
already three groups are close to launching clinical trials. Ken Garber
looks into the prospects and perils. Full Text |
|
Analysis
| Top |
|
|
|
Interfacing with Ras doi:10.1038/scibx.2013.588 A
German team has identified a compound that disrupts a protein-protein
interaction that localizes K-Ras to the cell membrane, thus selectively
inhibiting tumor growth. The interface provides a new small molecule
binding site for the handful of companies and academics working on ways
to tackle the previously undruggable Ras family. Full Text |
|
|
|
RON's new role doi:10.1038/scibx.2013.507 A
team has shown that inhibiting the kinase RON could fight cancer
metastasis by stimulating an antitumour immune response, building a case
for focusing drug discovery efforts specifically against RON, which has
long been neglected in favour of its relative, MET. Full Text |
|
Research Highlights
| Top |
|
|
|
Inflammatory disorders: Targeting TRAFs tames inflammation doi:10.1038/nrd4029 Inhibition
of tumour necrosis factor receptor-associated factors (TRAFs) through
FBX03 could represent a novel potential anti-inflammatory therapeutic
strategy. Full Text |
|
|
|
G protein-coupled receptors: Pioneering Frizzled family receptor structure solved doi:10.1038/nrd4030 A
crystal structure of the human Smoothened (SMO) receptor — an essential
component of the Hedgehog signalling pathway — bound to an antitumour
compound has been solved. Full Text |
|
|
|
Analgesia: A new player in neuropathic pain pathogenesis doi:10.1038/nrd4031 The
WNT family of proteins, which are involved in the regulation of
cellular processes during nervous system development, have a key role in
the pathogenesis of neuropathic pain. Full Text |
|
Research & Reviews
| Top |
|
|
|
Advances in the development of nucleoside and nucleotide analogues for cancer and viral diseases doi:10.1038/nrd4010 Although
nucleoside analogues have been used clinically for decades, efforts
continue to improve response rates and reduce side effects. This article
highlights recent progress in the development of new nucleoside and
nucleotide analogues for cancer and viral diseases. Full Text |
|
|
|
The emerging mutational landscape of G proteins and G-protein-coupled receptors in cancer doi:10.1038/nrc3521 This
article discusses deep sequencing studies indicating that nearly 20% of
human tumours harbour mutations in G-protein-coupled receptors (GPCRs)
and the implications for GPCRs as therapeutic targets in oncology. Full Text |
|
|
|
The good, the bad and the ugly — TFH cells in human health and disease doi:10.1038/nri3447 An increasing number of studies have highlighted new aspects of the differentiation and function of T follicular helper (TFH) cells in disease, which might represent targets for novel therapeutics. Full Text |
|
|
|
Small molecule inhibition of the KRAS–PDEδ interaction impairs oncogenic KRAS signalling doi:10.1038/nature12205 Interfering
with binding of PDEδ to KRAS with small molecules provides a novel
opportunity to suppress oncogenic RAS signalling by altering its
localization to endomembranes. Full Text |
|
| |
|
|
|
No comments:
Post a Comment