Results 21 to 30 of about 6,707,659 (315)
Microbial Cell Factories, 2022 Background Macrolactins, a type of macrolide antibiotic, are toxic to the producer strains. As such, its level is usually maintained below the lethal concentration during the fermentation process.
Yuman Gan +7 more
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Acknowledgement to Reviewers of Marine Drugs in 2016
Marine Drugs, 2017 The editors of Marine Drugs would like to express their sincere gratitude to the following reviewers for assessing manuscripts in 2016. [...]
Marine Drugs Editorial Office
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Analysis of prescription and dispensation of psychotropic medications in two cities in the State of São Paulo, Brazil [PDF]
Brazilian Journal of Psychiatry, 2002 OBJECTIVES: To investigate the prescription and dispensation of psychotropic medications through the analysis of the prescriptions/notices kept at various institutions in two cities in the state of São Paulo. METHODS: The prescriptions kept at drugstores,
Ana Regina Noto +11 more
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Marine Drugs, 2023 Glycosaminoglycans (GAGs) with unique structures from marine animals show intriguing pharmacological activities and negligible biological risks, providing more options for us to explore safer agents.
Yue Yao +7 more
doaj +1 more source
Acknowledgement to Reviewers of Marine Drugs in 2018
Marine Drugs, 2019 Rigorous peer-review is the corner-stone of high-quality academic publishing [...]
Marine Drugs Editorial Office
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A research agenda for malaria eradication: drugs.
PLoS Medicine, 2011 Antimalarial drugs will be essential tools at all stages of malaria elimination along the path towards eradication, including the early control or "attack" phase to drive down transmission and the later stages of maintaining interruption of transmission,
malERA Consultative Group on Drugs
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The Integrated Model of Quality Management System of Laboratory Studies of Medicines (Review)
Разработка и регистрация лекарственных средств, 2021 Introduction. The publication is devoted to the role of laboratory research in ensuring the quality of domestic medicines and is a review and analysis of regulatory documents and current publications on this topic.Text.
A. I. Selezneva +6 more
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Cardiovascular Therapeutics, 2009 Understanding and documentation of drug–drug interactions (DDIs) are an important component of drug development, and of clinical therapeutics. Because clinical DDI studies are costly, time‐consuming, and involve some risk, not all clinical DDI questions can be realistically addressed through human DDI trials.In vitromodels have been used to identify ...
openaire +2 more sources
DARU Journal of Pharmaceutical Sciences, 2012 Editorial Active pharmaceutical ingredients (APIs) are most conveniently developed and delivered orally as solid dosage forms that contain a defined crystalline form of an API. Co-crystal is a crystalline entity formed by two different or more molecular entities where the intermolecular interactions are weak forces like hydrogen bonding and π-π ...
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Extensive impact of non-antibiotic drugs on human gut bacteria
Nature, 2018 A few commonly used non-antibiotic drugs have recently been associated with changes in gut microbiome composition, but the extent of this phenomenon is unknown.
Lisa Maier +12 more
semanticscholar +1 more source