Zobrazeno 1 - 10
of 585
pro vyhledávání: '"Webster S. S. Jee"'
Autor:
Simmons, David J.
Publikováno v:
Radiation Research, 1970 Jan 01. 41(1), 226-228.
Externí odkaz:
https://www.jstor.org/stable/3572909
Akademický článek
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Autor:
Kennedy, A. R.
Publikováno v:
Radiation Research, 1977 Mar 01. 69(3), 602-603.
Externí odkaz:
https://www.jstor.org/stable/3574671
Autor:
Liao Cui, Ting Li, Yuyu Liu, Le Zhou, Pinghua Li, Bilian Xu, Lianfang Huang, Yan Chen, Yanzhi Liu, Xiaoyan Tian, Webster S S Jee, Tie Wu
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e34647 (2012)
Glucocorticoid (GC) induced osteoporosis (GIO) is caused by the long-term use of GC for treatment of autoimmune and inflammatory diseases. The GC related disruption of bone marrow microcirculation and increased adipogenesis contribute to GIO developm
Externí odkaz:
https://doaj.org/article/2d56af49c6ad42a7b80a952a9dec5e26
Publikováno v:
Bone. 48:197-201
Sclerostin monoclonal antibody (Scl-Ab) has been shown to increase bone mass and bone strength by stimulating bone formation in an ovariectomy-induced bone loss rat model. The purpose of this study was to determine the effects of Scl-Ab in a rat immo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c437c3ef42b58e66bef5bb1499f854
https://doi.org/10.1016/j.bone.2010.09.009
https://doi.org/10.1016/j.bone.2010.09.009
Publikováno v:
Bone. 47:529-533
The current report describes the skeletal effects of a sclerostin monoclonal antibody (Scl-AbIII) treatment at a yellow (fatty) marrow skeletal site in adult female rats. Ten-month-old female Sprague–Dawley rats were treated with vehicle or Scl-AbI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354ccb297d5ddbef19588c9efda8d9ea
https://doi.org/10.1016/j.bone.2010.05.032
https://doi.org/10.1016/j.bone.2010.05.032
Autor:
Sol Epstein, Hua Zhu Ke, Timothy Jacobs, Xiao Guang Liang, Webster S. S. Jee, I.A. Katz, B. Stein, Mei Li, Ian I. Joffe
Publikováno v:
Journal of Bone and Mineral Research. 9:59-67
Cyclosporin A (CsA) administered to actively growing young rats produces a high-turnover osteopenia. We investigated and compared the effect of CsA on the bone mineral metabolism in young rats with that of older rats, which have a lower rate of bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e2395eac8239e93031c398b8c41355f
https://doi.org/10.1002/jbmr.5650090109
https://doi.org/10.1002/jbmr.5650090109
Publikováno v:
Journal of Bone and Mineral Research. 10:66-73
The objects of this study were to investigate whether prostaglandin E2 (PGE2) can prevent orchidectomy (ORX)-induced cancellous bone loss in growing male rats, and to determine the differential effects of PGE2 on sham-operated (sham) and ORX male rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::308cdbd545467980f7d28a5816094522
https://doi.org/10.1002/jbmr.5650100111
https://doi.org/10.1002/jbmr.5650100111
Autor:
C.M. Pirie, Yan Fei Ma, H.K. Chen, H.A. Simmons, David D. Thompson, Hua Zhu Ke, Webster S. S. Jee
Publikováno v:
Journal of Bone and Mineral Research. 10:1256-1262
Our previous studies indicated that droloxifene (DRO), a tissue-specific estrogen antagonist/agonist, prevented bone loss without causing uterine hypertrophy in growing ovariectomized (OVX) rats. Using dual-energy X-ray absorptiometry (DXA) and bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de3b0fd9e490e847bcee7578732c9fea
https://doi.org/10.1002/jbmr.5650100816
https://doi.org/10.1002/jbmr.5650100816
Publikováno v:
Journal of Bone and Mineral Research. 10:496-505
The purpose of this study was to determine if human parathyroid hormone-(1-38) (hPTH(1-38)) can restore cancellous bone mass to the established osteopenic, immobilized proximal tibial metaphyses of female rats. The right hindlimbs of 6-month-old fema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e3c9fc91c5bd575a62dd8c632301ea
https://doi.org/10.1002/jbmr.5650100322
https://doi.org/10.1002/jbmr.5650100322