Publications by authors named "Martin Galvan"

A critical early step in drug discovery is the screening of a chemical library. Typically, promising compounds are identified in a primary screen and then more fully characterized in a dose-response analysis with 7-10 data points per compound. Here, we describe a robust microfluidic approach that increases the number of data points to approximately 10,000 per compound.

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New lead-identification methodologies such as high-throughput screening and combinatorial chemistry have been integrated into pharmaceutical research over the past 5-10 years. More rational use in the selection of potential preclinical candidates for some difficult targets has increased the chances of success.

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Objective: [corrected] The academic skills of medical students during their first year (class of 2004) were analyzed. Subjects included gross anatomy, cellular biology, developmental biology, biochemistry and molecular biology, public health I and medical psychology.

Results: Results showed that students attending morning classes achieved a higher score than those attending afternoon classes.

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