Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sangeeta B, English"'
Autor:
Rebekah Jackson, Matthew C. Wolfgang, Jeffrey K. Ichikawa, Atul J. Butte, Stephen Lory, Sangeeta B. English
Publikováno v:
Cellular Microbiology. 7:1635-1646
The type III secretion system (TTSS) is a dedicated bacterial pathogen protein targeting system that directly affects host cell signalling and response pathways. Our goal was to identify host responses to the Pseudomonas aeruginosa effectors, introdu
Autor:
Frank G. Rothman, John M. Sedivy, Atul J. Butte, David G. Ginzinger, Antonei B. Csoka, Gerald Schatten, Carl P. Simkevich, Sangeeta B. English
Publikováno v:
Aging Cell. 3:235-243
Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disease with widespread phenotypic features resembling premature aging. HGPS was recently shown to be caused by dominant mutations in the LMNA gene, resulting in the in-frame deletion of 5
Autor:
Atul J. Butte, Sangeeta B. English
Publikováno v:
Bioinformatics (Oxford, England). 23(21)
Motivation: Genome-wide experiments only rarely show resounding success in yielding genes associated with complex polygenic disorders. We evaluate 49 obesity-related genome-wide experiments with publicly available findings including microarray, genet
Autor:
Jeffrey K, Ichikawa, Sangeeta B, English, Matthew C, Wolfgang, Rebekah, Jackson, Atul J, Butte, Stephen, Lory
Publikováno v:
Cellular microbiology. 7(11)
The type III secretion system (TTSS) is a dedicated bacterial pathogen protein targeting system that directly affects host cell signalling and response pathways. Our goal was to identify host responses to the Pseudomonas aeruginosa effectors, introdu
Autor:
Antonei B, Csoka, Sangeeta B, English, Carl P, Simkevich, David G, Ginzinger, Atul J, Butte, Gerald P, Schatten, Frank G, Rothman, John M, Sedivy
Publikováno v:
Aging cell. 3(4)
Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disease with widespread phenotypic features resembling premature aging. HGPS was recently shown to be caused by dominant mutations in the LMNA gene, resulting in the in-frame deletion of 5
Autor:
Sangeeta B. English, Atul J. Butte
Publikováno v:
Bioinformatics; Nov2007, Vol. 23 Issue 21, p2910-2910, 1p