Kemp:Reprints: Difference between revisions

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== [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=PureSearch&db=pubmed&details_term=Kemp%20ML%5Bau%5D%20OR%20Lambeth%20MJ%5Bau%5D%20AND%201996%5BPDAT%5D%20%3A%202007%5BPDAT%5D PubMed citations] ==
== [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=PureSearch&db=pubmed&details_term=Kemp%20ML%5Bau%5D%20OR%20Lambeth%20MJ%5Bau%5D%20AND%201996%5BPDAT%5D%20%3A%202007%5BPDAT%5D PubMed citations] ==

Revision as of 06:31, 26 July 2007

The Kemp Lab

Redox Systems Biology at Georgia Tech

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PubMed citations


Wille, L., Kemp, M.L., Sandy, P., Lewis, C.L., Lauffenburger, D.A. “Epi-allelic Erk1 and Erk2 knockdown series for quantitative analysis of T cell Erk regulation and IL-2 production”. Molecular Immunology, v.44(12):3085-91, 2007.

Kemp, M.L.,Wille, L., Lewis, C.L., Nicholson, L., Lauffenburger, D.A. “Quantitative network signal combinations downstream of TCR activation can predict IL-2 production response”. Journal of Immunology, v.178(8):4984-92, 2007.

Vinnakota, K., *Kemp, M.L., Kushmerick, M.J. “Dynamics of Muscle Glycogenolysis Modeled with pH Time-Course Computation and pH Dependent Reaction Equilibria and Enzyme Kinetics”. Biophysical Journal, v.91(4), p.1264-87, 2006.

Lambeth, M.J., Kushmerick, M.J., Marcinek, D.J., Conley, K.E. “Basal glycogenolysis in mouse skeletal muscle: in vitro model predicts in vivo fluxes”. Molecular Biology Reports, v.29 (1-2), p.135-139, 2002.

Lambeth, M.J., Kushmerick, M.J. “A computational model for glycogenolysis in skeletal muscle”. Annals of Biomedical Engineering, v.30 (6), p.808-827, 2002.