Zobrazeno 1 - 5
of 5
pro vyhledávání: '"D R, Magnin"'
Autor:
J. K. Rinehart, Shih-Jung Lan, Kern G. Jolibois, Richard E. Gregg, Lori Kunselman, John K. Dickson, D. C. Hsieh, Edward W. Petrillo, J. W. Hillyer, Stephen S. Kalinowski, T. W. Harrity, Kasim A. Mookhtiar, D. R. Magnin, Carl P. Ciosek, Scott A. Biller
Publikováno v:
Journal of Medicinal Chemistry. 39:661-664
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5b70c081e9fadb62956e1df3d4864d8
https://doi.org/10.1021/jm950735s
https://doi.org/10.1021/jm950735s
Autor:
R. M. Lawrence, Janette V. H. Logan, Eric M. Gordon, Carl P. Ciosek, Lori Kunselman, John K. Dickson, Kern G. Jolibois, K A Hamilton, Thomas Harrity, D. R. Magnin
Publikováno v:
Journal of Biological Chemistry. 268:24832-24837
Squalene synthase catalyzes the reductive dimerization of two molecules of farnesyl diphosphate to form squalene at the final branchpoint of the cholesterol biosynthetic pathway. We report herein that isoprenyl 1,1-bisphosphonates and related analogs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab2367d707a8e07c23ac7372d729d301
https://doi.org/10.1016/s0021-9258(19)74540-2
https://doi.org/10.1016/s0021-9258(19)74540-2
Autor:
D. C. Hsieh, T. W. Harrity, Janette V. H. Logan, Shih-Jung Lan, R. B. Sulsky, Carl P. Ciosek, Lori Kunselman, Ying Chen, Dorothy Slusarchyk, J. K. Rinehart, Olga M. Fryszman, D. R. Magnin, Lois C. Rich, John K. Dickson, Scott A. Biller, Ellen Sieber-McMaster, R. M. Lawrence, Kern G. Jolibois, Sarah C. Traeger
Publikováno v:
Journal of medicinal chemistry. 39(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e277f5e9be8e9a9a2dc470041f18bd8
https://pubmed.ncbi.nlm.nih.gov/8576905
https://pubmed.ncbi.nlm.nih.gov/8576905
Autor:
C P, Ciosek, D R, Magnin, T W, Harrity, J V, Logan, J K, Dickson, E M, Gordon, K A, Hamilton, K G, Jolibois, L K, Kunselman, R M, Lawrence
Publikováno v:
The Journal of biological chemistry. 268(33)
Squalene synthase catalyzes the reductive dimerization of two molecules of farnesyl diphosphate to form squalene at the final branchpoint of the cholesterol biosynthetic pathway. We report herein that isoprenyl 1,1-bisphosphonates and related analogs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf62b86422cb852b8dae7ad70355ac74
https://pubmed.ncbi.nlm.nih.gov/8227045
https://pubmed.ncbi.nlm.nih.gov/8227045
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc6310a024e56f0a89c3345061703b27
https://doi.org/10.1002/chin.198417347
https://doi.org/10.1002/chin.198417347