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Home » Newsletters » BioWorld Science

BioWorld Science

Oct. 25, 2019

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Anti-influenza drug candidate targeting the hemagglutinin stalk of influenza viruses

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Flavonoid baicalin upregulates miR-126-5p: a potential therapeutic strategy against atherosclerosis

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Hypertensive rats are more sensitive to TRPM8-mediated relaxation of the pudendal artery

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Heterozygous COL4A1 mutations are a potential autosomal dominant cause of CAKUT

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Circular RNA hsa_circ_0006848 identified as a potential diagnostic biomarker of early gastric cancer

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Phage-based nanoligands wrap up drugs for delivery across BBB

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Pliant enters collaboration and license agreement with Novartis for PLN-1474 in NASH

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Interim results from phase I trial of chimeric HA-based universal influenza virus vaccine candidates

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First patient dosed in phase IIb ReNeu study of mirdametinib in children and adults with NF1-PN

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FDA approves Botox for pediatric patients with lower limb spasticity

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Scynexis announces amendment to protocol for ongoing FURI study of ibrexafungerp

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EphB4 as a novel biomarker of imatinib resistance in CML

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Researchers identify 7B2CT as potential biomarker in chronic OA pain

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Serum chemerin shows potential as marker to diagnose and grade NAFLD

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SUVN-1702012 for psychiatric disorders balancing antipsychotic and motor side effects

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New glutamate receptor modulator DT-095435 shows impressive in vivo antiparkinsonian potential

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Aurigene Discovery Technologies divulges CDK12 and CDK13 inhibitors

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Janssen Pharmaceutica presents new ionotropic glutamate GluN2B receptor antagonists

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AbbVie and Galapagos identify mutant CFTR correctors for cystic fibrosis

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Merck KGaA synthesizes new IRAK inhibitors

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Japan Tobacco describes new SLC5A1 inhibitors

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Syros reports new data from phase II trial of SY-1425 in newly diagnosed unfit AML

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New phase I trial investigates MB-108 in recurrent glioblastoma multiforme

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NIAID awards contract to UAB to study Bexsero for gonorrhea prevention

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FDA approves Baxdela for community-acquired bacterial pneumonia

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European Commission approves Xospata for relapsed or refractory FLT3 mutation-positive AML

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FDA clears IND for phase I trial of SQZ-PBMC-HPV

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