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1 tive than alendronate, which acts only as an antiresorptive.
2  in rats can be ameliorated by bone-targeted antiresorptives.
3 ng a window for prophylaxis with long-acting antiresorptives.
4 at intervals of 2 weeks, displays a powerful antiresorptive action in vivo.
5                                 Although the antiresorptive action of estrogen arises from the inhibi
6                                 However, the antiresorptive action of estrogen decreased the extent o
7                    This profound and lasting antiresorptive action of TSH is mimicked in cells that g
8  Representative inhibitors have demonstrated antiresorptive activity both in vitro and in vivo and th
9 e adsorption assay, and demonstrates in vivo antiresorptive activity in a parathyroid hormone-induced
10                                         This antiresorptive activity was abolished by phenylmethylsul
11 dronate (IG9402, a bisphosphonate that lacks antiresorptive activity) at 10(-9) to 10(-6) M prevented
12 r (AP22408) of Src that demonstrates in vivo antiresorptive activity.
13  impact of a locally or systemically applied antiresorptive agent (alendronate) on simvastatin-induce
14 thyroid hormone in the future, the choice of antiresorptive agent should be carefully considered.
15                      Alendronate (ALN) is an antiresorptive agent widely used for the treatment of os
16 e that combining parathyroid hormone with an antiresorptive agent will enhance its effect on bone min
17  is also possible that the combination of an antiresorptive agent with an anabolic agent could be mor
18 reatment (parathyroid hormone followed by an antiresorptive agent), which aims to maintain or build o
19 in the presence of zoledronic acid, a potent antiresorptive agent.
20 if parathyroid hormone is not followed by an antiresorptive agent.
21 y, whose appearance could be prevented by an antiresorptive agent.
22 ologists were less likely to be treated with antiresorptive agents (OR 0.49 [95% CI 0.28-0.86]).
23  use parathyroid hormone in combination with antiresorptive agents and sequentially are reviewed.
24                                        Novel antiresorptive agents are being developed.
25                                          The antiresorptive agents are clearly able to preserve bone
26                                              Antiresorptive agents are widely used to treat osteoporo
27                      Therapy with individual antiresorptive agents has been shown to be effective for
28    To reduce bone loss and improve strength, antiresorptive agents have been instituted.
29 e effects of these pharmacologically diverse antiresorptive agents on gene expression in bone has not
30                                              Antiresorptive agents such as bisphosphonates are used w
31 ciated bone disease are available, including antiresorptive agents such as denosumab and bisphosphona
32 rapy approaches with parathyroid hormone and antiresorptive agents to optimize efficacy outcomes.
33 fonamides like 55 form a new class of potent antiresorptive agents with possible therapeutic use in d
34                                              Antiresorptive agents, especially bisphosphonates, appea
35 se findings suggest that, among women taking antiresorptive agents, greater increases in BMD are asso
36 pounds for the development of a new class of antiresorptive agents.
37 rug therapy for osteoporosis including novel antiresorptive and anabolic agents that may become avail
38                 Bis-enoxacin, which has both antiresorptive and antibiotic activities, was more effec
39 mulation of this metabolite accounts for the antiresorptive and antimacrophage effects of clodronate.
40 moving beyond traditional monotherapies with antiresorptives and anabolic agents into new combination
41              Surprisingly, the bone-targeted antiresorptives bis-enoxacin and alendronate inhibited i
42            The exact mechanisms of action of antiresorptive bisphosphonate drugs remain unclear, alth
43  a new pyridinyl bisphosphonate, is a potent antiresorptive bone agent.
44        Botanicals and their relation to bone antiresorptive capacity, cognitive function, vascular ef
45  helper cells that can function as a pro- or antiresorptive cytokine, but the reason why IFN-gamma ha
46 s with additional drugs, especially the bone antiresorptive denosumab.
47 , calcium and vitamin D supplementation, and antiresorptive drug treatment.
48 gnificant association between overall use of antiresorptive drugs and the presence of knee pain and r
49                               Bisphosphonate antiresorptive drugs are the approved treatment for soli
50 ures are needed to determine whether and how antiresorptive drugs can be optimally used in conjunctio
51                                        While antiresorptive drugs have been the cornerstone of osteop
52 arily by stimulating bone formation, whereas antiresorptive drugs reduce bone resorption.
53                                              Antiresorptive drugs were prescribed in 26%, 12%, 7%, an
54  patients receiving long-term treatment with antiresorptive drugs.
55 mong these women, 214 (26.2%) were receiving antiresorptive drugs.
56       Overall these studies suggest that the antiresorptive effects of anti-TNF therapy are related t
57 group (p = 0.002), consistent with the known antiresorptive effects of bisphosphonates.
58 irect evidence that the antiinflammatory and antiresorptive effects of clodronate on macrophages and
59            These data demonstrate the potent antiresorptive effects of muRANK.Fc in vivo as well as h
60                                          The antiresorptive effects of TNF inhibitors are likely rela
61 e critical cytokine mediating the downstream antiresorptive effects of TSH on the skeleton.
62  R = 0.74, p < 0.0001) are closely linked to antiresorptive efficacy.
63                                Several novel antiresorptive mechanisms are currently under considerat
64  with 1995-1998, and the use of prescription antiresorptive medication increased approximately 2-fold
65 or measurement of bone mass, prescription of antiresorptive medication, and use of over-the-counter c
66 s (ONJ) is a rare but severe complication of antiresorptive medications, such as bisphosphonates, use
67 ss a conceptual framework of agents that are antiresorptive or anabolic, and review pathways that aff
68 ess fracture risk, and reduce that risk with antiresorptive or other available therapies.
69               The CoMFA predicted (rat) bone antiresorptive pLED values are in agreement with literat
70 the effectiveness of a regimen combining the antiresorptive properties of nasal calcitonin with the o
71                          In keeping with its antiresorptive properties, ritonavir impairs receptor ac
72  TIL may influence its anti-inflammatory and antiresorptive properties.
73   Transplant recipients were treated with an antiresorptive regimen that included a bisphosphonate st
74 ated, and no causal association between bone antiresorptive regimens and MRONJ has yet been establish
75  distinguishing features of the anabolic and antiresorptive therapies for the treatment of osteoporos
76 bitors of transforming growth factor-beta or antiresorptive therapies may be effective enhancers of a
77                                      Current antiresorptive therapies provide limited benefit, and no
78 seful to assess the response to anabolic and antiresorptive therapies, to assess compliance to therap
79 orosis has traditionally involved the use of antiresorptive therapies.
80 y result in the development of improved bone antiresorptive therapies.
81 to quantify bone turnover in women receiving antiresorptive therapy compared with that of untreated c
82  would provide a strong rationale for use of antiresorptive therapy for the prevention and treatment
83 continuation of this trial, we asked whether antiresorptive therapy is required to maintain gains in
84                                        While antiresorptive therapy is the mainstay of OI treatment,
85                           This suggests that antiresorptive therapy may be discontinued at the end of
86 o two years or less, the question of whether antiresorptive therapy should follow parathyroid hormone
87                                              Antiresorptive therapy with a bisphosphonate decreases t
88 pausal osteoporosis, but whether combination antiresorptive therapy with hormones and bisphosphonates
89 astogenesis and is a potential candidate for antiresorptive therapy.
90 agents might have greater potential than the antiresorptives to increase bone mass and to decrease fr
91  protection compared with either anabolic or antiresorptive treatment alone.
92 tomy and additionally changed by one or more antiresorptive treatment.
93 TCG) finds convincing evidence that adjuvant antiresorptive treatments provide persistent benefits to
94                                              Antiresorptive treatments such as bisphosphonates preven
95 nd systemic inflammation, and the success of antiresorptive treatments will rely on how effectively t

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