نتایج جستجو برای: hts high throughput screening

تعداد نتایج: 2257310  

2015
Ya’nan Liu Qinggang Li Ping Zheng Zhidan Zhang Yongfei Liu Cunmin Sun Guoqiang Cao Wenjuan Zhou Xiaowei Wang Dawei Zhang Tongcun Zhang Jibin Sun Yanhe Ma

BACKGROUND L-Threonine is an important amino acid for animal feed. Though the industrial fermentation technology of threonine achieved a very high level, there is still significant room to further improve the industrial strains. The biosensor-based high-throughput screening (HTS) technology has demonstrated its powerful applications. Unfortunately, for most of valuable fine chemicals such as th...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
James Inglese Douglas S Auld Ajit Jadhav Ronald L Johnson Anton Simeonov Adam Yasgar Wei Zheng Christopher P Austin

High-throughput screening (HTS) of chemical compounds to identify modulators of molecular targets is a mainstay of pharmaceutical development. Increasingly, HTS is being used to identify chemical probes of gene, pathway, and cell functions, with the ultimate goal of comprehensively delineating relationships between chemical structures and biological activities. Achieving this goal will require ...

2012
Uma D. Vempati Magdalena J. Przydzial Caty Chung Saminda Abeyruwan Ahsan Mir Kunie Sakurai Ubbo Visser Vance P. Lemmon Stephan C. Schürer

Huge amounts of high-throughput screening (HTS) data for probe and drug development projects are being generated in the pharmaceutical industry and more recently in the public sector. The resulting experimental datasets are increasingly being disseminated via publically accessible repositories. However, existing repositories lack sufficient metadata to describe the experiments and are often dif...

2009
Qingliang Li Yanli Wang Stephen H. Bryant

MOTIVATION The comprehensive information of small molecules and their biological activities in PubChem brings great opportunities for academic researchers. However, mining high-throughput screening (HTS) assay data remains a great challenge given the very large data volume and the highly imbalanced nature with only small number of active compounds compared to inactive compounds. Therefore, ther...

Journal: :Chemical Reviews 2021

The complex interaction of cells with biomaterials (i.e., materiobiology) plays an increasingly pivotal role in the development novel implants, biomedical devices, and tissue engineering scaffolds to treat diseases, aid restoration bodily functions, construct healthy tissues, or regenerate diseased ones. However, conventional approaches are incapable screening huge amount potential material par...

Journal: :Genetics 2007
Norbert Perrimon Bernard Mathey-Prevot

RNA interference (RNAi) in tissue culture cells has emerged as an excellent methodology for identifying gene functions systematically and in an unbiased manner. Here, we describe how RNAi high-throughput screening (HTS) in Drosophila cells are currently being performed and emphasize the strengths and weaknesses of the approach. Further, to demonstrate the versatility of the technology, we provi...

Journal: :Drug discovery today 2001
D J. Christensen E B. Gottlin R E. Benson P T. Hamilton

Increasing bacterial drug resistance and hard-to-eradicate opportunistic infections have created a need for new antibiotics. Sequencing of microbial genomes has yielded many new potential targets for antibacterial drug discovery. However, little is known about the biochemical activities of many of these targets, making it difficult to develop HTS assays for them. Peptides isolated by phage disp...

Journal: :Current opinion in chemical biology 2008
Thomas Hesterkamp Mark Whittaker

Fragment-based drug discovery has the potential to supersede traditional high throughput screening based drug discovery for molecular targets amenable to structure determination. This is because the chemical diversity coverage is better accomplished by a fragment collection of reasonable size than by larger HTS collections. Furthermore, fragments have the potential to be efficient target binder...

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