戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 itor alone did not alter gestational length, treatment with 15-PGDH inhibitor + PGE2 or metabolism-re
2 leven (4%) of the 274 patients had PHD after treatment with (177)Lu-DOTATATE: 8 patients (2.9%) devel
3                                       In the treatment with 2% and 3% of chitosan in the solid solubl
4                                  Conversely, treatment with 4-methylumbelliferone, a small-molecule i
5 eek break, followed by a cycle of 3 weeks of treatment with a 1-week break, until disease progression
6                                              Treatment with a 50-mg once-daily dose of opicapone was
7                                Notably, sole treatment with a BDNF mimetic, 7,8-dihydroxyflavone hydr
8 the anti-CSF-1 receptor protected mice after treatment with a blocking antibody directed against PD-1
9 otein, and mycelial growth is impaired after treatment with a chitin-synthase inhibitor.
10 sing senescent cells in INK-ATTAC mice or by treatment with a combination of the senolytic drugs dasa
11                 Furthermore, pharmacological treatment with a Drd3 agonist, which increases Drd3(LS)
12                              INTERPRETATION: Treatment with a neurokinin 3 receptor antagonist (MLE49
13 somatic mutation associated with ECD enabled treatment with a new-targeted systemic agent.
14 ritic outgrowth and number of synapses after treatment with a PERK activator, tunicamycin.
15 starting the study, or had received previous treatment with a poly(ADP-ribose) polymerase inhibitor.
16                                   Sublingual treatment with a recombinant food allergen was safe and
17 -1 blocks nuclear localization of LysRS, but treatment with a reverse transcriptase inhibitor does no
18                         After a chemical pre-treatment with a silane derivative, bilirubin oxidase fr
19                     Here we demonstrate that treatment with a small-molecule Sigma1 inhibitor prevent
20                                              Treatment with a specific PI3Kdelta inhibitor Idelalisib
21                                              Treatment with a Syk inhibitor significantly reduced ren
22 between bacterial taxa in the protist-grazed treatments with a higher proportion of positive correlat
23 ease and conducting clinical trials of these treatments, with a focus on preventing congenital centra
24 ng damage and edema, which were absent after treatment with abatacept.
25                                          Pre-treatment with ABT-627 failed to decrease renal ER stres
26 ction (MI) of 12365 patients enrolled in the Treatment With Adenosine Diphosphate Receptor Inhibitors
27  serum BUN levels before and after the first treatment with ADVOS.
28 ings demonstrate that combining electrolytic treatment with aerobic biodegradation may be a promising
29 play high Akt activation and that a combined treatment with AKT inhibitors causes synergistic tumour
30 pitopes in brown algae are unmasked by a pre-treatment with alginate lyases to remove alginates.
31                                              Treatment with all-trans retinoic acid antagonizes stres
32 tive medications, or relapse while receiving treatment with alternative medications were included in
33 ith refractoriness, ineligibility to receive treatment with alternative medications, or relapse while
34 portacaval anastomosis rats were reversed by treatment with ammonia-lowering therapy.
35                                              Treatment with an Aha1 inhibitor, KU-177, dramatically r
36                                              Treatment with an antimalarial medication reduced parasi
37                                     Combined treatment with an EGFR tyrosine kinase inhibitor and Akt
38 ion phase, patients who had progressed after treatment with an EGFR tyrosine kinase inhibitor receive
39 l lineB double bond in 6 was achieved by the treatment with an isonitrile, which led to the formation
40                                              Treatment with anakinra did not affect peak Vo2 or VE/Vc
41                                We found that treatment with anle138b leads to massive melanoma cell d
42                                              Treatment with anti-Marco-neutralizing Abs and the class
43 itumor immune responses and are resistant to treatment with anti-PD-1.
44 associated with effective tumor control upon treatment with anti-PD-L1 therapy.
45                                              Treatment with anti-sclerostin antibody and zoledronic a
46 2 cells impaired epithelial integrity, while treatment with anti-TNF-alpha or anti-IL-4Ralpha monoclo
47 olated from liver biopsy led to the targeted treatment with anti-tumor necrosis factor-alpha, which w
48 th Nlrp12 deficency were reversed equally by treatment with antibodies targeting inflammatory cytokin
49 s with proximal deep-vein thrombosis despite treatment with anticoagulant therapy.
50 sfunction With Multimodality Imaging and Its Treatment with Anticoagulation) were included in this an
51 eneration (AMD) who are being considered for treatment with antioxidants and zinc.
52                            Immunosuppression treatment with antithymyocyte globulin, methylprednisolo
53                               Despite prompt treatment with appropriate antibiotics, there were varia
54  mTOR-induced cap-dependent translation, pre-treatment with AR antagonists including bicalutamide inc
55 cterized potential predictive biomarkers for treatment with AsiDNA, a novel first-in-class DNA repair
56 ts presented a good clinical response to the treatment, with at least stable disease, and only 1 had
57                             Furcation defect treatment with autologous PRF combined with 1% ALN gel r
58 formation was further supported by exogenous treatment with autophagy inducer tamoxifen, which rescue
59                                              Treatment with basimglurant was overall well-tolerated.
60 n's lymphoma and peripheral T-cell lymphoma, treatment with bendamustine alone only achieves modest i
61 se prion disease were completely restored by treatment with benzyl quinolone carboxylic acid (BQCA) a
62  removal of a terminal beta-GlcNAc moiety by treatment with beta-N-acetylglucosaminidase and selectiv
63                                  Maintenance treatment with bevacizumab monotherapy was continued unt
64 results from a study comparing initial HIV-1 treatment with bictegravir-a novel INSTI with a high in-
65                                              Treatment with bone morphogenetic protein or SHH pathway
66 ractory or relapsed myeloma who had received treatment with bortezomib, an immunomodulatory drug, or
67 ere insensitive to AtRALF1, and simultaneous treatment with both AtRALF1 and CML38 proteins restored
68                                              Treatment with both drugs was required to fully suppress
69 F are found in 50% of melanomas and although treatment with BRAF inhibitors (BRAFi) is effective, res
70 c and TfR gene expression was decreased upon treatment with BRD4 inhibitors and c-MYC small interferi
71 harmacological inhibition of cathepsin K, or treatment with calcineurin inhibitor rescued cells from
72                                              Treatment with camptothecin which transiently stabilized
73 urvived infection in the absence of or after treatment with candidate medical countermeasures.
74 and (3) T-cell ablation with rituximab after treatment with CD20-coexpressing CART123 (CART123-CD20).
75  reveals the potential for using combination treatment with CDK4/6 inhibitors and PD-1-PD-L1 immune c
76 served reduction in (18)F-FMISO uptake after treatment with cediranib may be mistakenly interpreted a
77                                    Long-term treatment with ceftriaxone attenuates the reinstatement
78 linked by isopeptide bonds, are dispersed by treatment with chemical denaturants or soluble competing
79  preterm birth and low birth weight included treatment with chemotherapy and a diagnosis of breast ca
80  cognitive difficulties up to 6 months after treatment with chemotherapy than do age-matched noncance
81 tients should have access to multiple cancer treatments with close monitoring while receiving regimen
82                                              Treatment with CN-105 was associated with a durable impr
83 e levels were measured using LC-MS following treatment with colistin (2 mg/L) or doripenem (25 mg/L)
84                                   Antibiotic treatment with combinations of clindamycin and rifampici
85 dverse reactions were minor and responded to treatment with corticosteroids and antihistamines.
86                                              Treatment with crenolanib attenuated the skin and heart
87                                              Treatment with CSF1R inhibitors disrupted this crosstalk
88 g propensity score-matched patients starting treatment with dabigatran or warfarin.
89 of a small number of genes, whereas combined treatment with DAC enhanced the effects of the latter fo
90                                              Treatment with DCA resulted in normalization of several
91  at baseline and at 1, 2, and 4 months after treatment with DEX implants.
92 upon inflammatory stimulation and subsequent treatment with dexamethasone, a powerful antiphlogistic
93                                     Combined treatment with DHA and Physcion activates AMP-activated
94 transcriptional regulation of SNCA following treatment with different drugs known to regulate alpha-S
95 -intact SOAT1-/SOAT2-CHO cells prepared by a treatment with digitonin (plasma membrane permeabilized)
96  to up-regulate IFN-beta and TNF-alpha after treatment with DMXAA or the natural STING ligand cyclic
97 3 subjecting to DNA-damaging stimuli such as treatment with doxorubicin, was also significantly inhib
98                                    Long-term treatment with doxycycline does not reduce fatigue sever
99 tion rates and reduces PHH symptoms, as does treatment with drugs that antagonize TLR4-NF-kappaB sign
100                                              Treatment with dual PI3K/mTOR inhibitor gedatolisib resu
101                        Conclusion Results of treatment with duloxetine for AIMSS were superior to tho
102                                 In contrast, treatment with dynasore failed to alter the surface memb
103 r growth but render tumor cells sensitive to treatment with EGFR tyrosine kinase inhibitors (TKI).
104                                              Treatment with either botulinum toxin ("chemodenervation
105                                 Importantly, treatment with either DAC or DAC+KDM5i induced a dramati
106                                   First-line treatment with either first-generation antipsychotics (a
107 x human fecal microbial communities, whereas treatment with either glycerol or L. reuteri alone was i
108                                     Although treatment with either IL-6 or soluble IL-6 receptor (sIL
109                        Furthermore, in utero treatment with either lithium chloride, an agonist of ca
110 es with NVAMD that were randomly assigned to treatment with either ranibizumab or bevacizumab.
111    In multivariable Cox regression analysis, treatment with either regimen (hazard ratio [HR], 0.43;
112  and a left ventricular EF of 40% or less to treatment with enalapril 10 mg twice daily or sacubitril
113 F, severe hyperkalemia is more likely during treatment with enalapril than with sacubitril/valsartan.
114                                         Oral treatment with enrofloxacin suppresses CS and production
115 ssigned with equal likelihood to 12 weeks of treatment with escitalopram (10-20 mg/day), duloxetine (
116 raction was observed with placebo treatment, treatment with estradiol attenuated the effects of ACE a
117                                              Treatment with ethosuximide significantly blocks seizure
118 cardiovascular effects of adding once-weekly treatment with exenatide to usual care in patients with
119 offer powerful tools for designing effective treatments with fewer side effects.
120                                              Treatments with fine sediment in the upper 20 cm of the
121 n-KO pups, the genetic deletion of Slc6a4 or treatment with Fluoxetine, a 5-HT reuptake inhibitor, re
122 eated with FK866 at 24, 12, and 0.5 h before treatment with GaIN/LPS and ConA.
123                                     Prior to treatment with GAs to promote germination, the seeds wer
124      In a model of endotoxemia in the mouse, treatment with glycerophosphoinositol reduced TNF-alpha
125                           Indeed, short-term treatment with growth hormone augmented senescent host l
126                                              Treatment with GSK2334470 or the CDK2 inhibitor dinacicl
127 T-risk (4Ts score >/=4 points), and received treatment with >/=1 dose of the aforementioned anticoagu
128                                              Treatment with HA35 normalized these changes and also pr
129 this sensitization was normalized by ex vivo treatment with HA35.
130  cells from ethanol- and pair-fed rats after treatment with HA35.
131 e combination of a propidium monoazide (PMA) treatment with haRPA, the so-called viability haRPA, is
132                                        After treatment with high-dose methylprednisolone (1 g/day, in
133 f PKM2 activity with TEPP-46 and shikonin or treatment with histone deacetylase inhibitors produced s
134 ondrial swelling, which was exacerbated upon treatment with hydrogen peroxide (H2O2).
135 ls maintained elevated BCR signaling despite treatment with ibrutinib, a Bruton's tyrosine kinase inh
136  pain reduction at 2 hours among single-dose treatment with ibuprofen and acetaminophen or with 3 dif
137 ple HPV types, including oncogenic types, by treatment with IFN-gamma, an antiviral cytokine that is
138 rs IRF1 and BATF were induced early on after treatment with IL-27 and were required for the different
139                                     Finally, treatment with IL233 increased the proportion of ST2-bea
140 ain regions implicated in depression and its treatment with imipramine or ketamine.
141 on induction of skin inflammation by topical treatment with imiquimod cream (Aldara).
142 une cell infiltration in claudin-low tumors, treatment with immune checkpoint inhibitory antibodies a
143 l terminal pathway activity under eculizumab treatment with important implications for anti-C5 therap
144 age efflux to draining lymph nodes following treatment with infliximab.
145 st 1 risk factor for hypoglycemia, 32 weeks' treatment with insulin degludec vs insulin glargine U100
146 ents developing depression in the context of treatment with interferon-alpha, a widely used model to
147               However, the ideal duration of treatment with interferon-free regimens, particularly in
148                                              Treatment with intravitreal aflibercept injection (2 mg)
149 (8.6) (VIVID) letters from the initiation of treatment with intravitreal aflibercept injection throug
150 n a subgroup of laser control eyes receiving treatment with intravitreal aflibercept injection.
151                                 We evaluated treatment with ipilimumab in asymptomatic or minimally s
152                                              Treatment with islet Ag-specific regulatory T cells led
153                                              Treatment with IVM increases the efficacy of ATP to acti
154 burden or survival distributions compared to treatment with (+)-JQ1.
155  blood of clinical responders after 12 wk of treatment with KD025.
156 D) during a depressive episode and following treatment with ketamine.
157 trollable movements known as dyskinesia upon treatment with L-DOPA.
158                        An 8-week duration of treatment with LDV/SOF is highly effective in properly s
159 ; (2) T-cell ablation with alemtuzumab after treatment with lentivirally transduced anti-CD123-4-1BB-
160                Compared with chlorthalidone, treatment with lisinopril is not associated with a meani
161                                              Treatment with locked nucleic acid anti-miR-29a signific
162 mab did not confer a survival advantage over treatment with lomustine alone in patients with progress
163 omewhat prolonged progression-free survival, treatment with lomustine plus bevacizumab did not confer
164 s whose asthma remained uncontrolled despite treatment with long-acting beta-agonists and medium-to-h
165 ts were randomly assigned (1:1:1) to receive treatment with long-acting pasireotide (60 mg intramuscu
166    However, high concentrations or prolonged treatment with low doses of HU can cause cell lethality.
167                         To determine whether treatment with mandibular advancement device, the main a
168                                 Endovascular treatment with mechanical thrombectomy (MT) is beneficia
169 ctancy greater than 4 weeks who consented to treatment with medication.
170     Assessments also gathered information on treatment with medications and confounding factors, such
171  carcinoma cells to apoptosis in response to treatment with microtubule-disrupting drugs, identifying
172   Transcriptional analysis showed that after treatment with miRYR2-U10, the ratio between wild-type a
173  were 129 patients with psoriasis undergoing treatment with MTX, while 107 patients (57 women and 50
174                These effects were blocked by treatment with Na2S or by overexpression of cystathionin
175 nced NSCLC, 27.7% (33/119) were suitable for treatment with National Comprehensive Cancer Network (NC
176                                    In vitro, treatment with NE attenuated TGF-beta-induced accumulati
177  1 decreased already after a short (3 hours) treatment with necrostatin-1 during renal ischemia-reper
178 oethite occurred in the zero and low PO4(3-) treatments, with negligible transformation in higher PO4
179                                              Treatment with netarsudil q.d. produced clinically and s
180 d histological damage are all ameliorated by treatment with NitroSynapsin, a new dual-action compound
181 red responses could be corrected in vitro by treatment with NKH-477, a compound discovered as protect
182 increased risk of virological failure during treatment with NNRTI-containing regimens.
183 inutes of exposure to CLCA1 or after a short treatment with nocodazole, consistent with the hypothesi
184  120min at 5 and 10mgL(-1), respectively, in treatments with O3 as gas and dissolved in water.
185           The cathepsin B knockdown and 24-h treatment with OA resulted in increased CD36 expression
186  with BSI due to ESBL-E who received empiric treatment with OADs or carbapenems was performed.
187           Patients were randomly assigned to treatment with octreotide LAR 20 mg every 21 days with e
188 ssed in normal mouse organs before and after treatment with olaparib (n = 14), a PARP inhibitor, or i
189       We evaluated whether response rates to treatment with omalizumab in patients with CSU are linke
190 cquiring mutations in response to vaccine or treatment with one or a cocktail of monoclonal antibodie
191           Participants received protocolized treatment with open-label venlafaxine, up to 300 mg/day
192 rcinoma tumors were allocated to RFA or sham treatment with or without a STAT3 inhibitor (S3I-201 or
193 nimals were allocated to hepatic RFA or sham treatment with or without STAT3 (signal transducer and a
194                                     Alginate treatments with or without vanillin were effective in pr
195                                              Treatment with oral corticosteroids may help to reduce t
196 ent and shorter length of hospital stay than treatment with oral morphine, with similar rates of adve
197 s on doxycycline is non-inferior to standard treatment with oral prednisolone for short-term blister
198 crease in the sensitivity of SHR movement to treatment with oryzalin.
199 e effects of which were overcome by combined treatment with osimertinib and SFK inhibitors.
200 S), and the association of immunosuppressive treatments with outcomes are unclear.
201                                              Treatment with (-)-P7C3-S243 blocked neurodegeneration i
202  was significantly affected (p < 0.05) after treatment with paclitaxel or nocodazole due to changes i
203                                              Treatment with PE (10(-5) m) or sodium nitroprusside (10
204 in patients develop anti-PEG antibody during treatment with PEGylated medicines, suggesting that gene
205 ast cancer were randomly assigned to receive treatment with perindopril, bisoprolol, or placebo (1:1:
206 thio phenolate species with a boronic ester, treatment with Ph3 BiF2 or Martin's sulfurane gave the c
207                                     A single treatment with Phen was sufficient to enhance the minera
208 were randomized to receive 12 weeks of blind treatment with placebo or MABp1, a true human antibody t
209 otic or occlusive lesions were randomized to treatment with plain balloon angioplasty (BA) followed b
210 ividuals with bacterial keratitis to topical treatment with povidone-iodine or antibiotics (neomycin-
211 onSG and 12 RD-SG patients were subjected to treatment with prednisone and/or glucocorticoid-sparing
212                                              Treatment with primaquine significantly reduced the memb
213  in patients with FH at 3 and 6 months after treatment with probucol, a cholesterol-lowering agent.
214 S were measured in healthy neutrophils after treatment with purified albumin from the study groups.
215                                    Long-term treatment with Py-Im polyamide demonstrated a global dec
216 notypes have been observed following chronic treatment with R-baclofen, a selective agonist of GABAB
217                                              Treatment with rAAV.Tbeta4 enhanced capillary density an
218  mice, which could be suppressed by combined treatment with rapamycin and an extracellular signal-reg
219 ompared to patients submitted to orthodontic treatment with rapid maxillary expansion and facemask th
220  25 (96%; 95% CI, 80-100) receiving the same treatment with RBV.
221           In this study, we demonstrate that treatment with recombinant human IL-37 reverses the decr
222                                              Treatment with recombinant S100A9 proteins increased AML
223 is inhibitory effect was fully reversible by treatment with reducing agents.
224 ot have a sustained virologic response after treatment with regimens containing direct-acting antivir
225                                              Treatment with replacement factor can lead to the develo
226                                              Treatment with RG-101, an N-acetylgalactosamine-conjugat
227                Combining D2 receptor agonist treatment with rM3Ds-dSPN stimulation reproduced all sym
228                                   Subsequent treatment with RNase H releases RNA-templated ligation p
229                                              Treatment with Ro 61-8048 decreased nicotine self-admini
230 this study, we assessed the effect of 2-year treatment with rosuvastatin on carotid IMT in children w
231                                              Treatment with sapropterin, a tetrahydrobiopterin analog
232 oximately 30% in cystic cholangiocytes after treatment with SBI-115 alone and by approximately 50% wh
233        Forty patients were randomized 1:1 to treatment with serelaxin intravenous (i.v.) infusion (fo
234                                              Treatment with serelaxin prevented cardiac and renal dys
235                                              Treatment with sitagliptin plus basal insulin is as effe
236       We assessed the efficacy of 8 weeks of treatment with sofosbuvir and velpatasvir plus the pange
237 stained virologic response after 12 weeks of treatment with sofosbuvir and velpatasvir.
238 ificant predictors of improved survival were treatment with sorafenib (hazard ratio [HR], 0.66; 95% c
239                                              Treatment with specific GSK3 inhibitor (L803-mts), start
240 tudy was to examine the associations between treatment with statins, renin-angiotensin system blocker
241                    Three years of continuous treatment with subcutaneous immunotherapy and sublingual
242 fants with the neonatal abstinence syndrome, treatment with sublingual buprenorphine resulted in a sh
243  (SC) expressing ENb-TRAIL, we show that the treatment with synthetic extracellular matrix (sECM) enc
244 s the rate of asthma exacerbations requiring treatment with systemic corticosteroids.
245 osphoproteome in the Jurkat T cell line upon treatment with T cell stimulating agents.
246 rm that both exemestane alone and sequential treatment with tamoxifen followed by exemestane are reas
247 dine and a platinum agent, followed by later treatment with taxanes and irinotecan, provides some ben
248                                     Finally, treatment with TC14012 also significantly increased PI3K
249 terone and age-associated memory impairment, treatment with testosterone for 1 year compared with pla
250 formed to combine direct comparisons between treatments with that of indirect simulated evidence.
251  levels of overexpressed FLIL33, reversed by treatment with the 20S proteasome inhibitor bortezomib.
252                                    Moreover, treatment with the alphaAnalogue was well tolerated with
253                                              Treatment with the anti-ERBB2 humanized monoclonal antib
254                            In mice with MAS, treatment with the anti-IFN-gamma antibody significantly
255                                              Treatment with the ATR-selective inhibitor AZ20 caused p
256 as it is rapidly phosphorylated in vivo upon treatment with the bacterial MAMP flg22.
257 l lines with acquired resistance to combined treatment with the BRAF inhibitor vemurafenib and the mi
258 pVHL), a negative regulator of HIF, and that treatment with the c-src inhibitor PP2 rescued this effe
259 ctivation of leukocytes with LPS followed by treatment with the calcium ionophore A23187 resulted in
260 n multiple cohorts of AML patients receiving treatment with the cytidine nucleoside analogue cytarabi
261                                              Treatment with the epithelial Na(+) channel blocker amil
262 he hydrogel, as well as cell viability after treatment with the hydrogel containing naringin, were ev
263                               Finally, daily treatment with the hypotonic 2-PMPA enema ameliorated ma
264 titutive activation was abrogated by ex vivo treatment with the janus kinase 1/2 inhibitor ruxolitini
265                                              Treatment with the Janus kinase 1/2 inhibitor ruxolitini
266 helix peptide, the present study showed that treatment with the Kalpha2 peptide fused with the TAT pe
267                           We have shown that treatment with the KATP channel agonist pinacidil increa
268 cation following infection with FHV, whereas treatment with the KATP channel antagonist tolbutamide d
269                                 In addition, treatment with the mitochondrial Ca(2+)-buffering protei
270                                              Treatment with the monoclonal antibody E06 or with apoli
271               These results were mimicked by treatment with the myosin II inhibitor blebbistatin.
272 timulated gene (ISG) transcription following treatment with the noncanonical cyclic dinucleotide 2',3
273                                   Low dosage treatment with the pBtk inhibitor Ibrutinib reversed the
274                                We found that treatment with the physiological NO donor S-nitrosogluta
275 WT vs. CD-WT mice, which was prevented by co-treatment with the reactive oxygen species scavenger Tem
276                           INTERPRETATION: Re-treatment with the same ACT shows similar efficacy as re
277 r epithelial cells in vitro and in vivo, and treatment with the small molecule TNFR inhibitor R-7050
278                                              Treatment with the small-molecule CD11b agonist LA1 led
279                             We compared this treatment with the standard of care, active surveillance
280 efficiently inhibited tumor growth following treatment with the therapeutic antibody rituximab.
281 d EG7-OVA tumor growth in mice, however only treatment with the thioether linked vaccine construct re
282 mplementary in vivo studies demonstrate that treatment with the TLR7 ligand imiquimod can inhibit Th1
283                                           On treatment with the toll-like receptor 7 agonist imquimod
284                          Systemic and ocular treatment with the TR antagonists NH-3 and 1-850 increas
285 ring the intracellular zinc concentration by treatment with the zinc chelator N,N,N'-tetrakis-(2'-pyr
286 psychotic medications were the pharmacologic treatments with the highest rates of prevention of relap
287                                              Treatment with this enzyme selectively causes cell cycle
288                                              Treatment with tocilizumab in 13 subjects resulted in ra
289 gely maintained after 16 weeks of successful treatment with topical triamcinolone.
290                                 Furthermore, treatment with tPA led to decompression of blood vessels
291     Macular oedema responded to intravitreal treatment with triamcinolone.
292                 Our results showed that upon treatment with triptolide, HIF-1alpha protein accumulate
293                                  Combination treatment with TSLDox and HT in vivo was significantly m
294 eases in VCAM-1 and leukocyte adhesion after treatment with tumour necrosis factor-alpha.
295 imes the upper limit of normal (ULN) despite treatment with ursodeoxycholic acid.
296       In a proof-of-concept setting systemic treatment with ustekinumab diminished imiquimod-induced
297                           We also found that treatment with VEGFA reduced expression of CX3CL1 in end
298 icant differences of the NOACs compared with treatment with warfarin across strata were evident.
299 re Brain Bank criteria, were on dopaminergic treatment with wearing-off effects, and were at Hoehn an
300 s and fracture resistance when compared with treatment with zoledronic acid alone.

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top