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1 Advanced Accelerator Applications (Novartis).
2 al Research, which is the research engine of Novartis.
3 ugh Spark Therapeutics and worldwide through Novartis.
4 ncer Research UK, Target Ovarian Cancer, and Novartis.
5 mistry programmes pursued at AstraZeneca and Novartis.
6 spitals, French Society of Rheumatology, and Novartis.
7 titute, Korea Health Technology R&D Project, Novartis.
8 been optimized to clinical candidates by GNF/Novartis.
9 g Foundation, Roche Diagnostics, Pfizer, and Novartis.
10 art Foundation, UK Medical Research Council, Novartis.
11 fficacy >70%) in a large siRNA data set from Novartis.
12 alition), Breast Cancer Research Foundation, Novartis.
13 1 R132H by Ivosidenib and another inhibitor, Novartis 224, is readily resolved as a two-stage process
14 17 ((177)Lu-vipivotide tetraxetan, Pluvicto, Novartis/AAA) was approved on March 23, 2022, based on t
15 mithKline) and 5-HT type 4 agonist (Zelnorm, Novartis, AB) drugs on the dynamics of bolus progression
19 t health facilities were allowed to purchase Novartis Access medicines from the Mission for Essential
23 s received the H1N1 vaccine (15-microg dose; Novartis), and antibody titers at baseline and after imm
25 ions from AstraZeneca, Boehringer Ingelheim, Novartis, and Sepracor; GlaxoSmithKline; Centers for Med
27 ly known as LCZ696 and currently marketed by Novartis as Entresto) combines the angiotensin receptor
28 Although imatinib mesylate (STI571, Gleevec, Novartis, Basal, Switzerland) produces high rates of com
29 in-1-yl]phenyl} propanenitrile (NVP-BEZ235) (Novartis, Basel Switzerland), a dual phosphatidylinosito
31 antibodies (IL-2RAs): basiliximab (Simulect; Novartis, Basel, Switzerland) and daclizumab (Zenapax; R
32 oup C received cyclosporine A (CsA) (Neoral, Novartis, Basel, Switzerland) and sirolimus with target
33 nhibitor imatinib mesylate (Gleevec, STI571; Novartis, Basel, Switzerland) has shown remarkable effic
37 with higher selectivity as recently shown by Novartis but that there is little compelling reason to e
38 complex, LCZ696, developed by scientists at Novartis, combines an angiotensin receptor blocker with
39 Cancer Foundation of Australia, Endocyte (a Novartis company), Australian Nuclear Science and Techno
42 high-throughput phenotypic screen using the Novartis compound library and identified candidate chemi
48 e to pollen from a Bt corn hybrid containing Novartis event 176 on two species of Lepidoptera, black
49 paring the observed RPE gene profiles to the Novartis expression database (SymAtlas) of 78 tissues.
51 not inferior to deferoxamine (DFO; Desferal, Novartis) for the removal of cardiac iron in beta-thalas
54 ith the HDAC inhibitor LBH589 (Panobinostat, Novartis, Germany); levels of proliferation, apoptosis,
56 and U01NS077352; NIH grant P50HD103526; and Novartis IIT grant AFQ056X2201T for provision of AFQ056.
60 Jose M. Carballido, Executive Director at Novartis Institutes for BioMedical Research, and Pere Sa
61 versity and Inclusion (D&I) globally for the Novartis Institutes for BioMedical Research, which is th
64 leagues shows that deferasirox (DFX; Exjade, Novartis) is not inferior to deferoxamine (DFO; Desferal
65 rmany and Canada), Servier, GlaxoSmithKline, Novartis, King Pharma, and national or local organisatio
67 el, Accommodations, Expenses; Advisory Board Novartis: Membership on an entity's Board of Directors o
68 studies in the treated patients was Impact (Novartis/Nestle), which contains omega-3 fatty acids, ar
69 randomized to receive either the IMN Impact (Novartis Nutrition), an enteral feed supplemented with a
70 ependent CE analyses not sponsored by either Novartis or Amgen, the makers of ZA and denosumab, respe
75 Safety Review Committee (SRC), supported by Novartis Pharma AG, analyzed investigator-reported cases
76 , Switzerland) versus ranibizumab (Lucentis; Novartis Pharma AG, Basel, Switzerland) for neovascular
77 We tested the effect of everolimus (RAD, Novartis Pharma AG, Basel, Switzerland) on human PTLD-de
79 of AML were treated with PSC 833 (Valspodar; Novartis Pharmaceutical Corporation, East Hanover, NJ),
83 Institute, National Clinical Trials Network, Novartis Pharmaceuticals Corporation, and The Hope Found
85 inhibitor STI571 (formerly called CGP57148B, Novartis Pharmaceuticals) inhibits BCR/ABL, TEL/ABL, and
86 le-center trial ( NCT02491281 ; sponsored by Novartis Pharmaceuticals), 28 patients with knee OA were
87 ; CT1418 (Celltech Therapeutics); CGS27023A (Novartis Pharmaceuticals); and RO31-9790 (Roche), with I
91 tis Pharmaceuticals, Hanover, NJ) (Zortress; Novartis Pharmaceuticals, Basel, Switzerland) is intende
92 r, the advent of imatinib mesylate (Gleevec, Novartis Pharmaceuticals, Basel, Switzerland), formerly
93 herapy, such as the use of STI-571 (Gleevec; Novartis Pharmaceuticals, East Hanover, NJ) for treatmen
94 xample, vorinostat and panobinostat (LBH589; Novartis Pharmaceuticals, East Hanover, NJ), have shown
95 of rapamycin inhibitor everolimus (Certican; Novartis Pharmaceuticals, Hanover, NJ) (Zortress; Novart
98 newer formulations of cyclosporine, Neoral (Novartis Pharmaceuticals; Basle, Switzerland), and other
106 evidence generated by this study will inform Novartis's efforts to improve their programme going forw
108 ancer Research UK, Medical Research Council, Novartis, Sanofi-Aventis, Pfizer, Janssen, Astellas, NIH
111 ), with unrestricted educational grants from Novartis, Schering Health Care, Chugai, Pharmion, Celgen
112 ite in EED discovered by in-house screening, Novartis scientists have now produced a compound that sh
115 for these domains as well as integrated the Novartis SymAtlas2 dataset for both human and mouse whic
116 g Center, Weiss Family Kidney Research Fund, Novartis, The Sidney Kimmel Center for Prostate and Urol
117 ciety of Great Britain and Northern Ireland, Novartis, UK National Institute for Health Research (NIH
118 kinase inhibitor imatinib mesylate (Gleevec, Novartis) ultimately led to the discovery of the FIP1L1-
122 m and the oil-in-water-based emulsions MF59 (Novartis Vaccines and Diagnostics), AS03 and AS04 (Glaxo
123 MF59-adjuvanted trivalent influenza vaccine (Novartis Vaccines and Diagnostics, Siena, Italy) has bee
124 ine (serotypes Ia, Ib, and III, with CRM197 [Novartis Vaccines, Siena, Italy]) intramuscularly at 24-
125 a novel synthetic Smo inhibitor, NVP-LDE225 (Novartis), which decreased MM cell viability by inducing
126 ia drug STI571 [imatinib mesylate (Gleevec); Novartis], which potently and selectively blocks Abl kin