Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Michael S. Donoviel"'
Autor:
Peter Vogel, Michael S Donoviel, Robert Read, Gwenn M Hansen, Jill Hazlewood, Stephen J Anderson, Weimei Sun, Jonathan Swaffield, Tamas Oravecz
Publikováno v:
PLoS ONE, Vol 4, Iss 1, p e4112 (2009)
BACKGROUND: S1PL is an aldehyde-lyase that irreversibly cleaves sphingosine 1-phosphate (S1P) in the terminal step of sphingolipid catabolism. Because S1P modulates a wide range of physiological processes, its concentration must be tightly regulated
Externí odkaz:
https://doaj.org/article/7172458c7cd84783a0429e05ecd639e9
Autor:
Alan Wilson, Iris B. Owusu, Boteju Lakmal W, Saadat Aleem, Philip Manton Brown, Jack Yan, Theodore C. Jessop, David J. Augeri, Suman Layek, Zhong Lai, S. David Kimball, Jill Hazelwood, William Heydorn, Kenneth G. Carson, Tamas Oravecz, Liam Moran, Suma Gopinathan, Haiming Zhang, Michael S. Donoviel, Amr Nouraldeen, William K. Sonnenburg, Jeffrey T. Bagdanoff, Jeffrey A. Kramer, Alan Main, Barbara Brooks, Li Dong, James E. Tarver, Padmaja Yalamanchili, Kenny Frazier, Marianne Carlsen, Mark S. Bednarz
Publikováno v:
Journal of Medicinal Chemistry. 53:8650-8662
Sphingosine 1-phosphate lyase (S1PL) has been characterized as a novel target for the treatment of autoimmune disorders using genetic and pharmacological methods. Medicinal chemistry efforts targeting S1PL by direct in vivo evaluation of synthetic an
Autor:
Qingyun Liu, Weimei Sun, Amr Nouraldeen, Lawrence F. Courtney, Alan Wilson, Suman Layek, Marianne Carlsen, Sean Yu, Mark S. Bednarz, Zhong Lai, Ann Marie Digeorge-Foushee, Tamas Oravecz, Jerry A. Taylor, Traci Smith, Haiming Zhang, Liam Moran, Jonathan C. Swaffield, Debra Bruce, Jill Hazelwood, Simon D.P. Baugh, David J. Augeri, Emily O’Neill, Joseph Barbosa, Kristen M. Terranova, Suma Gopinathan, Gardyan Michael Walter, Huy Van Nguyen, S. David Kimball, Jeffrey T. Bagdanoff, Jack Yan, Theodore C. Jessop, Michael S. Donoviel, Qinghong Fu, Jeffrey A. Kramer, Alan Main, James E. Tarver, Kenneth G. Carson
Publikováno v:
Journal of Medicinal Chemistry. 52:3941-3953
During nearly a decade of research dedicated to the study of sphingosine signaling pathways, we identified sphingosine-1-phosphate lyase (S1PL) as a drug target for the treatment of autoimmune disorders. S1PL catalyzes the irreversible decomposition
Autor:
Michael Maceyka, Sarah Spiegel, Tamas Oravecz, Nitai C. Hait, Subramaniam Ramachandran, Sheldon Milstien, Kazuaki Takabe, Michael S. Donoviel
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 29(12)
Sphingosine 1-phosphate (S1P) is a pleiotropic bioactive sphingolipid metabolite that regulates numerous processes important for immune responses. S1P is made within cells and must be transported out of cells to exert its effects through activation o
Autor:
Jeffrey T, Bagdanoff, Michael S, Donoviel, Amr, Nouraldeen, Marianne, Carlsen, Theodore C, Jessop, James, Tarver, Saadat, Aleem, Li, Dong, Haiming, Zhang, Lakmal, Boteju, Jill, Hazelwood, Jack, Yan, Mark, Bednarz, Suman, Layek, Iris B, Owusu, Suma, Gopinathan, Liam, Moran, Zhong, Lai, Jeff, Kramer, S David, Kimball, Padmaja, Yalamanchili, William E, Heydorn, Kenny S, Frazier, Barbara, Brooks, Philip, Brown, Alan, Wilson, William K, Sonnenburg, Alan, Main, Kenneth G, Carson, Tamas, Oravecz, David J, Augeri
Publikováno v:
Journal of medicinal chemistry. 53(24)
Sphingosine 1-phosphate lyase (S1PL) has been characterized as a novel target for the treatment of autoimmune disorders using genetic and pharmacological methods. Medicinal chemistry efforts targeting S1PL by direct in vivo evaluation of synthetic an
Autor:
Weimei Sun, Gwenn M. Hansen, Tamas Oravecz, Peter Vogel, Michael S. Donoviel, R. Read, Stephen J. Anderson, Jonathan C. Swaffield, Jill Hazlewood
Publikováno v:
PLoS ONE, Vol 4, Iss 1, p e4112 (2009)
PLoS ONE
PLoS ONE
BACKGROUND: S1PL is an aldehyde-lyase that irreversibly cleaves sphingosine 1-phosphate (S1P) in the terminal step of sphingolipid catabolism. Because S1P modulates a wide range of physiological processes, its concentration must be tightly regulated
Autor:
Kathleen H. Holt, Anne V. Philips, Robert Brommage, Brian Zambrowicz, William J. Paradee, Gwenn M. Hansen, Arthur T. Sands, Christopher M. DaCosta, Adisak Suwanichkul, Deon D. Smith, Derek E. Eberhart, Urvi Desai, David R. Powell, Jean Pierre Revelli, Laura L. Kirkpatrick, Kenneth A. Platt, Kenneth J Coker, Gregory K. Fontenot, Michael R. Kelly, Michael S. Donoviel, Dorit B. Donoviel
Publikováno v:
Obesity (Silver Spring, Md.). 16(10)
We developed a high-throughput approach to knockout (KO) and phenotype mouse orthologs of the 5,000 potential drug targets in the human genome. As part of the phenotypic screen, dual-energy X-ray absorptiometry (DXA) technology estimates body-fat sto
Autor:
Michael S. Donoviel, Elton T. Young
Publikováno v:
Genetics. 143(3)
Two cis-acting elements have been identified that act synergistically to regulate expression of the glucose-repressed alcohol dehydrogenase 2 (ADH2) gene. UAS1 is bound by the trans-activator Adrlp. UAS2 is thought to be the binding site for an unide
Autor:
Michael S. Donoviel, Weimei Sun, Jonathan C. Swaffield, Kenneth G. Carson, Alan Main, Brian Zambrowicz, James Piggott, Qingyun Liu, Arthur T. Sands, S. David Kimball, C. Alexander Turner, David J. Augeri, Stephen J. Anderson, Tamas Oravecz
Publikováno v:
Blood. 110:2292-2292
The ceramide metabolite sphingosine 1-phosphate (S1P) is an important modulator of a wide variety of physiologic functions via its action as a second messenger in intracellular signaling pathways and its extracellular interaction with specific G prot
Autor:
Michael S. Donoviel, Brenda J. Andrews
Publikováno v:
Science. 270:251-251
The crystal structure of a heterodimeric transcriptional repressor from yeast, a 1/alpha-2, reported in the same issue of Science , reveals a mechanism for ensuring DNA-binding specificity that may be used by many other DNA-binding heterodimers. B. J