Zobrazeno 1 - 10
of 133
pro vyhledávání: '"LE T. DUONG"'
Autor:
Isabel D. Colón-Bernal, Le T. Duong, Brenda Pennypacker, James Henderson, Kenneth M. Kozloff, Mark M. Banaszak Holl
Publikováno v:
Bone Reports, Vol 9, Iss , Pp 159-164 (2018)
Anti-resorptive drugs treat bone loss by blocking osteoclast activity through a variety of mechanisms of action. Once significant bone loss has occurred, the ability to restore biomechanical function may differ based on the drug chosen. To assess thi
Externí odkaz:
https://doaj.org/article/19b67fafdfc840fa834223fe7b3628d4
Autor:
Antonio Cabal, Donald S. Williams, Richa Y. Jayakar, Jingru Zhang, Swanand Sardesai, Le T. Duong
Publikováno v:
Bone Reports, Vol 6, Iss C, Pp 26-33 (2017)
The cathepsin K inhibitor odanacatib (ODN) is a potent and reversible inhibitor of osteoclastic resorption activity. This drug is currently under development for the treatment of postmenopausal osteoporosis. Previously, we described data on the treat
Externí odkaz:
https://doaj.org/article/f928a5ab9cbe4d71bb8d918e6d7b3bf4
Autor:
Meagan A. Cauble, Matthew J. Muckley, Ming Fang, Jeffrey A. Fessler, Kathleen Welch, Edward D. Rothman, Bradford G. Orr, Le T. Duong, Mark M. Banaszak Holl
Publikováno v:
Bone Reports, Vol 5, Iss , Pp 243-251 (2016)
The impact of estrogen depletion and drug treatment on type I collagen fibril nanomorphology and collagen fibril packing (microstructure) was evaluated by atomic force microscopy (AFM) using an ovariectomized (OVX) rabbit model of estrogen deficiency
Externí odkaz:
https://doaj.org/article/55178759ab6e4897b395d421f7282d87
Autor:
Barbara M. Misof, Paul Roschger, Charles Chen, Maureen Pickarski, Phaedra Messmer, Klaus Klaushofer, Le T. Duong
Publikováno v:
Bone Reports, Vol 5, Iss , Pp 62-69 (2016)
Odanacatib (ODN) is a selective and reversible inhibitor of cathepsin K which is an important enzyme for the degradation of collagen I. Aim of the present work was the head-to-head comparison between the effects of ODN and alendronate (ALN) on bone m
Externí odkaz:
https://doaj.org/article/00b5e204419c42a4b586d6915559e1d2
Autor:
Mary Wolf, Idriss Bennacef, Hyking Haley, Terence G. Hamill, G Wesolowski, Shawn J. Stachel, Le T. Duong, Mangay Williams, Diane J. Posavec, Mona Purcell, Eric D. Hostetler, Jeffrey L. Evelhoch, Marie A. Holahan, Daniel Rubins, Laura S. Lubbers, Kerry Riffel
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 64:159-167
The cathepsin K (CatK) enzyme is abundantly expressed in osteoclasts, and CatK inhibitors have been developed for the treatment of osteoporosis. In our effort to support discovery and clinical evaluations of a CatK inhibitor, we sought to discover a
Autor:
Robert R. Recker, Le T. Duong, Tobias J. de Villiers, Arthur C. Santora, Seth Clark, David W. Dempster, Hilde Giezek, Bente L. Langdahl, Ivo Valter, Cristiano A. F. Zerbini, D Cohn, Graham Ellis
Publikováno v:
Recker, R, Dempster, D, Langdahl, B, Giezek, H, Clark, S, Ellis, G, de Villiers, T, Valter, I, Zerbini, C A F, Cohn, D, Santora, A & Duong, L T 2020, ' Effects of Odanacatib on Bone Structure and Quality in Postmenopausal Women with Osteoporosis : 5-year Data from the Phase 3 Long-Term Odanacatib Fracture Trial (LOFT) and its Extension ', Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol. 35, no. 7, pp. 1289-1299 . https://doi.org/10.1002/jbmr.3994
Odanacatib (ODN), a selective oral inhibitor of cathepsin K, was an investigational agent previously in development for the treatment of osteoporosis. In this analysis, the effects of ODN on bone remodeling/modeling and structure were examined in the
Autor:
Idriss, Bennacef, Daniel, Rubins, Kerry, Riffel, Mangay, Williams, Diane J, Posavec, Marie A, Holahan, Mona L, Purcell, Hyking D, Haley, Mary, Wolf, Shawn J, Stachel, Laura S, Lubbers, Gregg A, Wesolowski, Le T, Duong, Terence G, Hamill, Jeffrey L, Evelhoch, Eric D, Hostetler
Publikováno v:
Journal of labelled compoundsradiopharmaceuticalsREFERENCES. 64(4)
The cathepsin K (CatK) enzyme is abundantly expressed in osteoclasts, and CatK inhibitors have been developed for the treatment of osteoporosis. In our effort to support discovery and clinical evaluations of a CatK inhibitor, we sought to discover a
Autor:
null Robert Recker, null David Dempster, null Bente Langdahl, null Hilde Giezek, null Seth Clark, null Graham Ellis, null Tobias Villiers, null Ivo Valter, null Cristiano A.F. Zerbini, null Dosinda Cohn, null Arthur Santora, null Le T. Duong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::040550212e92938c1d89b8005b96f4d6
https://doi.org/10.1002/jbmr.3994/v2/response1
https://doi.org/10.1002/jbmr.3994/v2/response1
Autor:
Kenneth M. Kozloff, James Henderson, Brenda L Pennypacker, Isabel D. Colón-Bernal, Le T. Duong, Mark M. Banaszak Holl
Publikováno v:
Bone Reports, Vol 9, Iss, Pp 159-164 (2018)
Bone Reports
Bone Reports
Anti-resorptive drugs treat bone loss by blocking osteoclast activity through a variety of mechanisms of action. Once significant bone loss has occurred, the ability to restore biomechanical function may differ based on the drug chosen. To assess thi
Publikováno v:
Journal of Cellular Physiology. 233:8666-8676
Osteoarthritis (OA) is a degenerative disease and a major cause of chronic disability in aging individuals. Cathepsin K (CatK), encoded by the Ctsk gene, has been implicated in the pathogenesis of pycnodysostosis and osteoporosis. The use of a select