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Bringing patient data into the open Joanne Kotz doi:10.1038/scibx.2012.644 Two groups have come to the conclusion that breakthroughs in translational medicine require collecting large-scale data on patients, including outcomes, and making those data available to translational researchers. Sage Bionetworks launched a portal through which users can contribute their own health and genomic data for research, and a report from the U.S. National Academy of Sciences is calling for the creation of a national infrastructure for accessing and analyzing open-source patient data. Full Text | PDF
GSK completes its Canadian tripod Michael J. Haas doi:10.1038/scibx.2012.645 GlaxoSmithKline has announced its third major academic collaboration in Canada in the past two years—a deal with the Centre for Drug Research and Development to identify and fund academic research in the country. Full Text | PDF
Reining in pain Lev Osherovich doi:10.1038/scibx.2012.646 UCSF researchers have shown that neuronal precursor cells from fetal mouse brains can be transplanted into the spinal cord of adult mice to treat neuropathic pain. The embryonic brain cells are being developed by Neurona. Full Text | PDF
ADORAble implants Kai-Jye Lou doi:10.1038/scibx.2012.647 NYU researchers have shown that adenosine A2A receptor agonists can block the inflammation and bone destruction that stems from debris flaking off joint implants, a leading cause of implant failure. The group now needs to translate the findings into a product that companies can test in the clinic. Full Text | PDF
CC chemokine receptor 5 (CCR5; CD195) doi:10.1038/scibx.2012.648 In vitro and mouse studies suggest CCR5 antagonists could help prevent breast cancer metastasis. Full Text | PDF
Ataxia telangiectasia mutated (ATM); c-Met proto-oncogene (MET; HGFR); p53 doi:10.1038/scibx.2012.649 Computational pathway analysis and a cell-based genomewide small hairpin RNA screen suggest inhibition of ATM or MET could improve the efficacy of the small molecule p53 pathway activator Nutlin-3 in cancer. Full Text | PDF
BCL2-associated X protein (BAX) doi:10.1038/scibx.2012.650 An in vitro and cell culture study identified a small molecule activator of the proapoptotic B cell lymphoma 2 (BCL-2; BCL2) family member BAX that could help treat cancer. Full Text | PDF
Guanine nucleotide binding protein β-polypeptide 2-like 1 (GNB2L1; RACK1) doi:10.1038/scibx.2012.651 Patient sample and mouse studies suggest inhibiting RACK1 could help treat hepatocellular carcinoma (HCC). Full Text | PDF
Forkhead box O1 (FOXO1); epidermal growth factor receptor (EGFR) doi:10.1038/scibx.2012.652 Studies in cell culture and in mice suggest trifluoperazine hydrochloride (TFP) could help restore the sensitivity of lung cancer to EGFR-targeting therapies. Full Text | PDF
MAP kinase kinase kinase 7 (MAP3K7; TAK1) doi:10.1038/scibx.2012.653 In vitro studies suggest TAK1 inhibitors could help treat lymphoma. Full Text | PDF
G protein–coupled receptor 21 (GPR21) doi:10.1038/scibx.2012.654 Mouse studies suggest inhibiting GPR21 could help treat or prevent type 2 diabetes. Full Text | PDF
Agouti related protein (AGRP); forkhead box O1 (FOXO1); G protein–coupled receptor 17 (GPR17) doi:10.1038/scibx.2012.655 Mouse and in vitro studies suggest inhibiting FOXO1-GPR17 signaling could help treat obesity. Full Text | PDF
Ebola glycoprotein GP1; Ebola glycoprotein GP2 doi:10.1038/scibx.2012.656 Nonhuman primate studies suggest a mAb-based treatment could help improve survival after an Ebola infection. Full Text | PDF
Platelet factor 4 (PF4; CXCL4) doi:10.1038/scibx.2012.657 Cell culture studies suggest CXCL4 could help prevent HIV replication. Full Text | PDF
Periostin (POSTN) doi:10.1038/scibx.2012.658 In vitro and mouse studies suggest blocking POSTN could help treat atopic dermatitis. Full Text | PDF
Toll-interleukin 1 receptor domain containing adaptor protein (TIRAP); toll-like receptor 4 (TLR4); TLR2; tumor necrosis factor-α (TNF-α); IL-6 doi:10.1038/scibx.2012.659 In vitro and mouse studies suggest Tirap-derived peptides could help treat inflammatory disease. Full Text | PDF
β-Amyloid (Aβ) doi:10.1038/scibx.2012.660 In vitro assays suggest conjugates of benzothiazole-based molecules and Cu2+ chelators could help treat AD. Full Text | PDF
Sterile α and TIR motif containing 1 (SARM1) doi:10.1038/scibx.2012.661 In vitro, fly and mouse studies suggest inhibiting SARM1 could help prevent axon loss after injury. Full Text | PDF
Thrombin (Factor IIa; F2) doi:10.1038/scibx.2012.662 Rat studies suggest detecting thrombin activity in the brain could help diagnose stroke and inhibiting thrombin during stroke could help reduce neurovascular damage. Full Text | PDF
Combinatorial chemistry method for identifying boronic acid–based inhibitors of oxygenase enzymes doi:10.1038/scibx.2012.663 A combinatorial chemistry method for identifying boronic acid–based inhibitors of oxygenase enzymes could help identify new therapeutic leads. Full Text | PDF
A mouse model of Gleevec-resistant gastrointestinal stromal tumors (GISTs) could aid the identification of new therapies doi:10.1038/scibx.2012.664 A mouse model of Gleevec-resistant GIST could help identify new GIST therapies. Full Text | PDF
In vitro microvasculature network model doi:10.1038/scibx.2012.665 An in vitro model of organ microvasculature could be useful for identifying compounds that target the vasculature to treat cardiovascular diseases. Full Text | PDF
Mouse model of human mucosa associated lymphoma tissue (MALT) lymphoma doi:10.1038/scibx.2012.666 A MALT lymphoma model could be used to test therapeutics for the disease. Full Text | PDF
Vaginal delivery of antiviral-loaded mucus-penetrating particles (MPPs) doi:10.1038/scibx.2012.667 Vaginal delivery of antiviral-loaded MPPs could be used to prevent viral infections. Full Text | PDF
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