ライフサイエンスコーパス: MPA

1 MPA affected intracellular nucleotide levels, nucleotide

2 MPA exposure increased intracellular concentrations of f

3 MPA formation in patients with both acute and stable HF

4 MPA is able to modify E2-induced apoptosis in MCF-7:5C c

5 MPA significantly altered 35 proteins mainly related to

6 MPA treatment of Huh7 cells could suppress autophagy, ev

7 MPA treatment of infected mice resulted in 50% mortality

8 MPA was computed as 200 cGy/DTotal for each DTotal estim

9 MPA was significantly (p<.05) associated with BF%, diast

10 MPA, similar to dexamethasone, increases glucocorticoid

11 MPAs associated with Mon2 seem to be negatively predicti

12 MPAs associated with Mon2 were significantly lower in pa

13 MPAs often fail to reach their full potential as a conse

14 MPAs were analyzed by flow cytometry for the 3 monocyte

15 was linked to near infrared dye ICG-Der-02 (MPA) by the peptide for measurement in vivo.

16 Consequently, correlation with method 1 MPA was strongest for method 2 MPA (r = 0.99) and weakes

17 with method 1 MPA was strongest for method 2 MPA (r = 0.99) and weakest for method 4 (r = 0.

18 n the presence of rat digestive fluid, and 2-MPA-MG was subsequently re-esterified in the enterocyte

19 In contrast, 2-MPA-TG markedly increased lymphatic drug transport (80-f

20 lysed rapidly to 2-mycophenoloyl glycerol (2-MPA-MG) in the presence of rat digestive fluid, and 2-MP

21 (1,3-dipalmitoyl-2-mycophenoloyl glycerol, 2-MPA-TG) to facilitate metabolic integration into triglyc

22 Importantly, after administration of 2-MPA-TG, the concentrations of free MPA in the mesenteric

23 gement and fish population data (433 and 218 MPAs, respectively) to assess: MPA management processes;

24 Colloidal 3-mercaptopropionic acid (3-MPA) capped lead sulfide quantum dots were prepared in a

25 glycol)3-COOH (PEG), 3-MPA-LHDLHD-OH, and 3-MPA-HHHDD-OH.

26 aptoundecane(ethylene glycol)3-COOH (PEG), 3-MPA-LHDLHD-OH, and 3-MPA-HHHDD-OH.

27 we show that the conservation benefits of 87 MPAs investigated worldwide increase exponentially with

28 25 mg/day) plus medroxyprogesterone acetate (MPA) (<10 mg/day) or oral CEE alone and cardiovascular d

29 Medroxyprogesterone acetate (MPA) and dydrogesterone (DDG) are synthetic progestins w

30 l contraceptive medroxyprogesterone acetate (MPA) and progesterone and that uptake occurred primarily

31 one or CEE plus medroxyprogesterone acetate (MPA)) on global cognitive function in younger middle-age

32 ith TFV or TAF, Medroxyprogesterone acetate (MPA), but not Levonorgestrel, Norethisterone or progeste

33 Medroxyprogesterone acetate (MPA), designed to mimic the actions of the endogenous ho

34 estradiol (E2), medroxyprogesterone acetate (MPA), or E2+MPA.

35 etic progestin, medroxyprogesterone acetate (MPA).

36 .625 mg/d) plus medroxyprogesterone acetate (MPA, 2.5 mg/d) (n = 8506) vs placebo (n = 8102) for 5.6

37 .625 mg/d) plus medroxyprogesterone acetate (MPA; 2.5 mg/d) (n = 8506) or placebo (n = 8102).

38 ed for 6 wk with methylprednisolone acetate (MPA), a synthetic glucocorticoid.

39 to contaminated methylprednisolone acetate (MPA).

40 of contaminated methylprednisolone acetate (MPA).

41 us a progestin (medroxyprogesterone acetate, MPA) HRT increases this risk.

42 monolayer (SAM) of 3-mercaptopropionic acid (MPA) for immobilization of specific DNA probe via avidin

43 site covalently on 3-mercaptopropionic acid (MPA) on gold surface is demonstrated for the first time

44 s) and mercury ions, mercaptopropionic acid (MPA) was used as a highly unique acceptor for mercury io

45 rochloride (Cyst), 3-Mercaptopropionic acid (MPA), 11-Mercaptoundecanoic acid (MUDA) and 11-amino-1-u

46 by-layer assembly of mercaptopropionic acid (MPA), polyethylene glycol (PEG) functionalized gold nano

47 d with the help of 3-mercaptopropionic acid (MPA)-capped CdSe quantum dot (MPA-CdSe QD) and visible l

48 yclosporine A (CsA) or to mycophenolic acid (MPA) 1.44 g per day plus standard-exposure CsA.

49 mmunosuppressive drugs as mycophenolic acid (MPA) and anti-infectious agents, but some PTN remain une

50 d from day 5 according to mycophenolic acid (MPA) exposure (arm A) or a regimen with CS maintained up

51 s studies have shown that mycophenolic acid (MPA) has an anti-HCV activity.

52 olimus, prednisolone, and mycophenolic acid (MPA) in clinically relevant concentrations.

53 d, Nguyen et al show that mycophenolic acid (MPA) induces GTP depletion, which inhibits the function

54 Mycophenolic acid (MPA) is the active immunosuppressive substance in both m

55 Mycophenolic acid (MPA) is the active metabolite of mycophenolate mofetil,

56 g the negative effects of mycophenolic acid (MPA) on human intestinal cells.

57 The mycophenolic acid (MPA) preparations are one of the most commonly used immu

58 Control groups received mycophenolic acid (MPA) with standard-dose cyclosporine.

59 BEL, mycophenolic acid (MPA), and sirolimus, either alone or in combination, wer

60 a model immunomodulator, mycophenolic acid (MPA), to the lymphatic system after oral administration.

61 for the immunosuppressant mycophenolic acid (MPA).

62 r (S)-alpha-methoxy-alpha-phenylacetic acid (MPA) or (S)-phenylglycine methyl ester (PGME) linked thr

63 osphonate (DMMP) and methyl phosphonic acid (MPA) exhibit the reduced mobility values of 1.99 +/- 0.0

64 n thiol derivatives (mercaptopropionic acid, MPA) were chemically introduced on cyt c protein shell v

65 radiation, the maximum permissible activity (MPA) of (131)I to treat thyroid cancer is that which lim

66 ysical activity, moderate physical activity (MPA), vigorous physical activity (VPA), and moderate-to-

67 In addition, MPA Portable now supports state-of-the-art database sear

68 how ecological and physical contexts affect MPA performance.

69 The remaining agents (MPA, belatacept, and tofacitinib) had less apparent dose

70 e formation of monocyte-platelet aggregates (MPAs).

71 inferiority of maximum platelet aggregation (MPA) comparing the median for prasugrel 5 mg in VE versu

72 y index (PRI), maximal platelet aggregation (MPA) to adenosine phosphate, and VerifyNow P2Y12 platele

73 pecies has increased consistently inside all MPAs in the network, with an effect of geography on the

74 networks of MPAs operate if the space among MPAs is smaller than the dispersal capacity of the speci

75 tricular nucleus (PVN, 13%), SLEA (66%), and MPA (26%).

76 g/day), higher exposure EVR (3.0 mg/day) and MPA-treated patients had proteinuria >/= 300 mg/g Cr at

77 electrostatic interaction between DOTAP and MPA layer during the formation of DOPE-DOTAP-AuNP (DDA)

78 EVR and MPA were associated with similar efficacy among each of

79 lkyl chain prodrugs - MPA-C18AM (6-fold) and MPA-C18E (13-fold) still increased lymphatic drug transp

80 24 in the everolimus 3-8 and 6-12 ng/mL and MPA groups, respectively.

81 receiving everolimus 3-8 and 6-12 ng/mL and MPA, respectively.

82 These results suggest that both P4 and MPA may modulate inflammation in the ectocervix via this

83 This study shows that P4 and MPA significantly increase the expression of the IL-12p4

84 ays, we show that recruitment of the P4- and MPA-bound GR to the IL-12p40 promoter requires CCAAT enh

85 risingly and in contrast to prednisolone and MPA, neither tacrolimus nor everolimus could inhibit the

86 by tacrolimus, everolimus, prednisolone, and MPA (P<0.05).

87 ionships between the level of protection and MPA size, age, and enforcement.

88 nts, referred to determine (131)I uptake and MPA for initial treatment after thyroidectomy (n = 39),

89 Counts of total MPA and MPAs associated with Mon1 and Mon2 were significantly hi

90 inals (BNST, 59%), and medial preoptic area (MPA, 53%).

91 st entirely high seas marine protected area (MPA) in 2010.

92 In an old marine protected area (MPA), invasion of S. horneri was suppressed, likely due

93 relation to existing marine protected areas (MPAs) and the future alternative energy footprint identi

94 Marine protected areas (MPAs) are a cornerstone of marine conservation.

95 Marine protected areas (MPAs) are increasingly being used globally to conserve m

96 rsity, the number of marine protected areas (MPAs) is increasing rapidly, yet socio-economic benefits

97 Networks of marine protected areas (MPAs) often aim to maintain connectivity, but anticipati

98 the global system of marine-protected areas (MPAs) represents individual species and the breadth of e

99 oal for establishing marine protected areas (MPAs) to conserve the ocean's biodiversity was set in 20

100 such as networks of marine protected areas (MPAs).

101 s and its network of marine protected areas (MPAs).

102 ions associated with Marine Protected Areas (MPAs).

103 comprehensive human membrane protein array (MPA).

104 tion with the dilated main pulmonary artery (MPA).

105 (433 and 218 MPAs, respectively) to assess: MPA management processes; the effects of MPAs on fish po

106 In contrast to the original server-based MPA application, this newly developed tool no longer req

107 Because MPA based on blood measurements alone is comparable to M

108 because of the contribution of VPA, because MPA was unrelated to fatness (P >/= 0.077).

109 More emphasis is needed on better MPA design, durable management and compliance to ensure

110 ed on the 2,2-bismethylolpropionic acid (bis-MPA) monomer.

111 lyester dendritic architectures based on bis-MPA.

112 Both MPA and ETO reduce VSMC proliferation and migration (P <

113 Both MPA and mycophenolate mofetil are highly specific inhibi

114 ber and coverage of MPAs are increasing, but MPA implementation lags in many human-dominated regions.

115 and the anti-inflammatory cytokine IL-10, by MPA versus P4, in an in vitro cell culture model of the

116 ults reveal that suppression of autophagy by MPA plays a role in its anti-HCV activity.

117 pression of three autophagy-related genes by MPA involves in its antiviral mechanism.

118 expression, and T-cell activation induced by MPA, suggesting that the combination of the two agents a

119 and Atg7 were identified to be inhibited by MPA treatment.

120 partly recover HCV replication inhibited by MPA; however, silencing their expression by siRNAs could

121 ly, yet socio-economic benefits generated by MPAs remain difficult to predict and under debate.

122 , for myocardial infarction, results for CEE+MPA were in the direction of risk elevation in WHI and i

123 initiation, associations of CEE alone or CEE+MPA with most clinical outcomes were highly concordant b

124 In contrast, with genital CD4+ T cells, MPA suppressed TAF inhibition of HIV infection and lower

125 usion of lipid-based formulations containing MPA or MPA prodrugs.

126 included if they had received a contaminated MPA injection.

127 ngal meningitis associated with contaminated MPA injections.

128 es, in the context of managing and designing MPA networks, may ensure that conservation goals are ach

129 rements alone are sufficient for determining MPA.

130 ropionic acid (MPA)-capped CdSe quantum dot (MPA-CdSe QD) and visible light.

131 ion on Biological Diversity (CBD) has driven MPA establishment, with 193 parties committed to protect

132 2), medroxyprogesterone acetate (MPA), or E2+MPA.

133 Effective MPAs also had twice as many large (>250 mm total length)

134 ons of underwater survey data from effective MPAs with predictions based on survey data from fished c

135 Using effective MPAs with four or five key features as an unfished stand

136 r the designation and management of European MPAs.

137 ificant gap in our understanding of existing MPAs and future protection requirements.

138 0.065 ng/cm(2) for IMPA, 0.079 ng/cm(2) for MPA, 0.040 ng/cm(2) for EMPA, 0.078 ng/cm(2) for EHDMAP,

139 tion of 2-MPA-TG, the concentrations of free MPA in the mesenteric lymph nodes were significantly enh

140 We also estimate that the current global MPA system secures only 1.7% of the Tree of Life for cor

141 We assess the overlap of global MPAs with the ranges of 17,348 marine species (fishes, m

142 and at a 2-propanol flow rate of 160 muL/h, MPA demonstrated the greatest shift in mobility (1.58 cm

143 Upon reperfusion, a heterogeneous MPA recovery was observed, but not a de novo MPA decreas

144 g effectively and equitably managed, and how MPA management influences substantive outcomes remain un

145 However, MPA alone inhibited lymphoproliferation but significantl

146 on could induce cellular autophagy, however, MPA also exhibited its inhibitory effect on tunicamycin-

147 strongest predictors of conservation impact: MPAs with adequate staff capacity had ecological effects

148 gal genera were isolated from the implicated MPA vials.

149 of malformation (3.9% vs. 2.6%, P = 0.49) in MPA exposed versus unexposed cohorts of children.

150 12, significantly reduced the worm burden in MPA-treated mice undergoing hyperinfection with S. sterc

151 During ischaemia, a dramatic decrease in MPA, reaching the low/undetectable level comparable to t

152 yperinfection, were found in high numbers in MPA-treated, but not untreated, mice.

153 Indexed MPA diameter correlated with pulse wave velocity (P=0.04

154 ally relevant concentrations of 4.5-4.8 ng/L MPA, DDG and the mixture in eleuthero-embryos and at 43-

155 Self-seeding within higher-latitude MPAs tended to increase, and the role of low-latitude MP

156 ed to increase, and the role of low-latitude MPAs as a sink for urchins changed significantly in cont

157 ng of the (methyl) methylphosphonic acid ((M)MPA) product to the polyanions, which ultimately inhibit

158 Here we report that many MPAs failed to meet thresholds for effective and equitab

159 However, whether many MPAs are being effectively and equitably managed, and ho

160 1.42 +/- 0.3 g/day and the individual median MPA trough concentration in the time period of anticipat

161 fishes, and sea urchins in 24 Mediterranean MPAs.

162 we here introduce the MetaProteomeAnalyzer (MPA) Portable software.

163 For prasugrel 5 mg, MPA was significantly lower (57 +/- 14%) than clopidogre

164 e distribution of the MPAN reservoir (MPAN / MPA radical) reducing the fraction that can react with O

165 osphatidylcholine (p < 0.01 at 72 h; 100 muM MPA) which corresponded to the changes in lipid-metaboli

166 < 0.001 at 24 and 72 h; 5, 100, and 250 muM MPA) and upregulation of uridine and cytidine nucleotide

167 tidine nucleotides (p < 0.001 at 24 h; 5 muM MPA) occurred after exposure to MPA.

168 te, MPA-C18E; and octadecyl mycophenolamide, MPA-C18AM), to promote passive partitioning into lipids

169 nt among everolimus (EVR) and mycophenolate (MPA) treatment arms and used a time-dependent model to c

170 ) in KTR on sirolimus (SRL) + mycophenolate (MPA) or SRL + tacrolimus (Tac), relative to the control-

171 rial dilutions of tacrolimus, mycophenolate (MPA), sirolimus, tofacitinib, and belatacept.

172 phenolate, MPA-C8E; octadecyl mycophenolate, MPA-C18E; and octadecyl mycophenolamide, MPA-C18AM), to

173 lkyl chain derivatives (octyl mycophenolate, MPA-C8E; octadecyl mycophenolate, MPA-C18E; and octadecy

174 s resulted in nearly 10 million km(2) of new MPAs, a growth of ~360% in a decade.

175 Within newer MPAs with intermediate levels of interacting species, S.

176 MPA recovery was observed, but not a de novo MPA decrease.

177 r-mediated molecular mechanisms of action of MPA in the female genital tract.

178 To ensure that the benefits of MPA outweigh the risks, the Food and Drug Administration

179 Herein, a metal sensor consisting of MPA coated Mn doped ZnSe/ZnS colloidal nanoparticles was

180 h was strongly associated with the degree of MPA distension.

181 Equivalent and greater doses of MPA administered in buffer were not efficacious.

182 ing path nullifying the insulating effect of MPA and also act as a proper immobilization platform for

183 iRNAs could enhance the inhibitory effect of MPA on HCV.

184 Effects of MPA exposure and guanosine supplementation on nucleotide

185 Similarly, the endometria of MPA treated OVX-GPs displayed decreased alphaSMA stainin

186 We demonstrated that the incorporation of MPA functionalized gold nanoparticles (AuNPMPA) as an el

187 omass were only correlated with the level of MPA enforcement; fish density was higher in older, bette

188 The levels of MPA, which is known to interact with tacrolimus, were no

189 stration (FDA) required all manufacturers of MPA products to propose risk evaluation and mitigation s

190 However, the mechanism of MPA-mediated inhibition of HCV replication remains to be

191 7- cells generated in MLR in the presence of MPA and added as third component modulators in fresh MLR

192 n in T cells was observed in the presence of MPA, which also broadly upregulated chemokine production

193 transcytosis was observed in the presence of MPA.

194 animals administered equimolar quantities of MPA, suggesting the efficient conversion of the esterifi

195 The ratio of MPA to aortic size correlated with pulse wave velocity (

196 Cross-reference with previous studies of MPA-associated protein changes widely corroborated these

197 ween clinical isolates and injected vials of MPA, and described significant features of the fungal ag

198 openia more than 70 days after withdrawal of MPA did not support this hypothesis.

199 Although 71% of MPAs positively influenced fish populations, these conse

200 Globally, the number and coverage of MPAs are increasing, but MPA implementation lags in many

201 and resources, evaluation of the effects of MPAs is crucial to inform decisions.

202 ss: MPA management processes; the effects of MPAs on fish populations; and relationships between mana

203 Thus, continued global expansion of MPAs without adequate investment in human and financial

204 ade following implementation of a network of MPAs in the northern Channel Islands, California.

205 ly to change connectivity among a network of MPAs spanning over 1000 km of coastline off the coast of

206 Successful networks of MPAs operate if the space among MPAs is smaller than the

207 Whether the increase outside of MPAs is due to changes in fishing pressure, fisheries ma

208 for sea urchins, connectivity among pairs of MPAs generally decreased in both directions.

209 r kelp, poleward connectivity among pairs of MPAs tended to increase in the future, whereas equatorwa

210 s of connectivity between different pairs of MPAs were noteworthy.

211 nge in predicted connectivity among pairs of MPAs within the network did not change significantly ove

212 y patterns across populations in a series of MPAs in the common yellowhead Jawfish, Opistognathus aur

213 ansplanted men fathered 350 children (155 on MPA/195 not on MPA).

214 fathered 350 children (155 on MPA/195 not on MPA).

215 f lipid-based formulations containing MPA or MPA prodrugs.

216 targeted fish species also increased outside MPAs, although only 27% as rapidly as in the protected a

217 edentary [SED], light PA [LPA], moderate PA [MPA], moderate-to-vigorous PA, vigorous PA [VPA]) and he

218 ing and support the continuation of paternal MPA treatment before, during, and after conception.

219 The area under the peak (MPA) progressively decreased upon application of increas

220 produced 540QD-peptide-RB and 720QD-peptide-MPA probes, we successfully examined MMP-2 in live cells

221 ecovery efficiencies for methyl phosphonate (MPA), nerve agent degradate, and ethylhydrogen dimethylp

222 opausal women, hormone therapy with CEE plus MPA for a median of 5.6 years or with CEE alone for a me

223 During the CEE plus MPA intervention phase, the numbers of CHD cases were 19

224 x) per 10,000 women annually taking CEE plus MPA ranged from 12 excess cases for ages of 50-59 years

225 ion lasted a median of 5.6 years in CEE plus MPA trial and 7.2 years in CEE alone trial with 13 years

226 e numbers of CHD cases were 196 for CEE plus MPA vs 159 for placebo (hazard ratio [HR], 1.18; 95% CI,

227 cumulative follow-up (434 cases for CEE plus MPA vs 323 for placebo; HR, 1.28 [95% CI, 1.11-1.48]).

228 in the overall pooled cohort; with CEE plus MPA, the HR was 1.02 (95% CI, 0.96-1.08); and with CEE a

229 for other outcomes were similar to CEE plus MPA.

230 women taking HRT comprising an estrogen plus MPA may have an increased risk of breast cancer due to M

231 rmerly Wegener's), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis

232 32% to 64% of intersubject variation in PRI, MPA, and PRU.

233 ough two of the three alkyl chain prodrugs - MPA-C18AM (6-fold) and MPA-C18E (13-fold) still increase

234 We sought to determine whether reliable MPA values can be obtained by simplified procedures.

235 roarray analysis of VSMCs identified several MPA- and ETO-altered transcripts regulated by STAT1 sign

236 better enforced, and -interestingly- smaller MPAs.

237 patient death and graft loss, although SRL + MPA was associated with a lower risk for posttransplant

238 Compared with Tac + MPA, SRL + MPA, and SRL + Tac were associated with higher risks of

239 erostatus to any of the above viruses, SRL + MPA or SRL + Tac was not associated with a different mal

240 lected seabird habitat lies outside of state MPAs where threats from shipping, oil spills, and offsho

241 Strain MPA-C3 was isolated by incubating arsenic-bearing sedime

242 g of the 16S rRNA gene indicated that strain MPA-C3 is a member of the Deferribacteres family, with r

243 In addition to As(V), strain MPA-C3 utilizes NO3(-), Se(VI), Se(IV), fumarate and Fe(

244 itions by the metabolically versatile strain MPA-C3.

245 more data are needed to evaluate sufficient MPA sizes for protecting populations of species with var

246 Tac), relative to the control-regimen: Tac + MPA.

247 Compared with Tac + MPA, SRL + MPA, and SRL + Tac were associated with highe

248 Compared with Tac + MPA, SRL regimens were associated with higher risks for

249 In women, taking MPA is teratogenic and may also influence spermatogenesi

250 ad ecological effects 2.9 times greater than MPAs with inadequate capacity.

251 We conclude that MPA derived from confocal images provides a sensitive an

252 These findings demonstrate that MPA selectively compromises TFV and TAF protection in bl

253 Our data suggest that MPA and DDG and their mixtures induce multiple transcrip

254 These results suggest that MPA may play a significant role in regulating susceptibi

255 d and genital CD4+ T cells and suggests that MPA may decrease ARV protection in individuals who use A

256 ble management and compliance to ensure that MPAs achieve their desired conservation value.

257 We found that MPAs exchange migrants likely via intermediate unprotect

258 The MPA is, to our knowledge, the first of its kind and offe

259 The MPA network studied would be unable to maintain connecti

260 ristic behavior of linear diffusion, for the MPA-DOPE in presence of [Fe(CN)(6)](3-/4-) and [Ru(NH(3)

261 We speculate that distension of the MPA may play a major role in limiting full aortic expans

262 nic pressures, they also include much of the MPA network that may provide stepping-stone protection f

263 The elements of the MPA REMS include a medication guide and elements to assu

264 Although the impact of the MPA REMS on clinical practice is not clear, it is a step

265 e of the bilayer and semi circled DDA on the MPA and cysteamine layers were confirmed by the increase

266 nce of an array like semi circled DDA on the MPA and well separated DDA vesicles on the MUDA with var

267 Spherical nature of the DOPE on the MPA monolayer is confirmed by the appearance of sigmoida

268 PEG functionalized gold nanoparticles on the MPA surface provided good electron conducting path nulli

269 th candidate host receptors expressed on the MPA.

270 conventional methods, demonstrating that the MPA is an important tool for cellular receptor discovery

271 n in the everolimus groups compared with the MPA group.

272 Most (59%) of the MPAs studied had only one or two key features and were n

273 ETA) should be considered as alternatives to MPA.

274 on blood measurements alone is comparable to MPA obtained with combined body counting and blood sampl

275 rmation, and increased p62 level compared to MPA-untreated cells.

276 ed lymphatic drug transport when compared to MPA.

277 ve an increased risk of breast cancer due to MPA acting as a glucocorticoid and blunting E2-induced a

278 ant men per whether they had been exposed to MPA or not at time of conception.

279 me of pregnancies fathered by men exposed to MPA.

280 Paternal exposure to MPA did not increase the risk of adverse birth outcomes

281 24 h; 5 muM MPA) occurred after exposure to MPA.

282 the responses of zebrafish (Danio rerio) to MPA, DDG, and their binary mixtures at measured concentr

283 Counts of total MPA and MPAs associated with Mon1 and Mon2 were signific

284 utbreak and was also confirmed from unopened MPA vials.

285 ) unlike EVR 3.0 (HR 1.84; p < 0.001) versus MPA.

286 2000 renal transplant recipients, EVR versus MPA resulted in similar composite endpoint incidence eve

287 omparable efficacy and renal function versus MPA plus standard-exposure CsA over the 2-year period.

288 .5% (P = 0.03 vs. MPA), 30.6% (P = 0.007 vs. MPA), and 20.5% of patients receiving everolimus 3-8 and

289 nuation were reported in 28.5% (P = 0.03 vs. MPA), 30.6% (P = 0.007 vs. MPA), and 20.5% of patients r

290 (95% confidence interval for difference vs. MPA) were 32.9% (-2.2%, 13.0%), 26.9% (-7.9%, 6.8%), and

291 ur results offer strategic guidance on where MPAs should be placed to support the CBD's overall goal

292 V-specific Th1 cytokines versus Th2, whereas MPA preferentially inhibited Th2 cytokines.

293 This study investigated whether MPA has an effect on autophagy, a cellular machinery req

294 It is not known whether MPAs are affected in heart failure (HF), and we examined

295 hed MLRs either alone or in combination with MPA or sirolimus.

296 e bare gold electrode directly modified with MPA-cyt c to hydrogen peroxide (H(2)O(2)) was evaluated

297 easing the understanding of fetal risks with MPA products among patients and possibly practitioners.

298 ere performed on cultured VSMCs treated with MPA or etonogestrel (ETO).

299 Treatment with MPA-loaded nanogels increased the median survival time (

300 get of 10% of their geographic ranges within MPAs.