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1 taxane C-10 hydroxyl acetyl transferase from Taxus.
2 sels were randomly assigned 3:2 to CoStar or Taxus.
3 1,675 (98.5%) were evaluable (CoStar = 989; Taxus = 686), including 1,330 (79%) single-vessel and 34
4 10-O-acetyltransferase along with five other Taxus acyltransferases on the paclitaxel (Taxol) biosynt
6 low to intermediate Synergy Between PCI With Taxus and Cardiac Surgery (SYNTAX) score (random-effects
7 ween Percutaneous Coronary Intervention With Taxus and Cardiac Surgery (SYNTAX) Score is an objective
8 ween Percutaneous Coronary Intervention with Taxus and Cardiac Surgery (SYNTAX) score of 32 or lower
10 ween Percutaneous Coronary Intervention With TAXUS and Cardiac Surgery (SYNTAX) trial demonstrated th
11 ween Percutaneous Coronary Intervention With TAXUS and Cardiac Surgery (SYNTAX) trial is a multicente
12 ween percutaneous coronary intervention with TAXus and cardiac surgery (SYNTAX) trial is the most imp
13 LM patients in the Synergy Between PCI With Taxus and Cardiac Surgery (SYNTAX) trial, the largest tr
16 ercutaneous coronary intervention (PCI) with TAXUS and Cardiac Surgery trial, 1800 patients with 3-ve
17 tion of the SYNTAX (Synergy Between PCI With Taxus and Cardiac Surgery) score has prompted a renewed
18 P<0.0001), SYNTAX (Synergy Between PCI With Taxus and Cardiac Surgery) score of >/=11 (the sample me
19 ween Percutaneous Coronary Intervention With Taxus and Cardiac Surgery) score quantifies the extent o
21 d diabetes, SYNTAX (Synergy between PCI with Taxus and Cardiac Surgery) score, treatment of saphenous
22 ween Percutaneous Coronary Intervention With Taxus and Cardiac Surgery) scores and lesion characteris
23 ween percutaneous coronary intervention with TAXus and cardiac surgery) study randomly assigned 1,800
24 ween Percutaneous Coronary Intervention With Taxus and Cardiac Surgery) trial, patients with 3-vessel
27 similar in the 2 groups, 16.4% and 22.5% in TAXUS and control, respectively (P=0.12), including comp
28 ercutaneous coronary intervention (PCI) With Taxus and coronary artery bypass surgery (CABG)] score i
31 her (Cordis Corp., Miami Lakes, Florida) and Taxus (Boston Scientific Corp., Natick, Massachusetts) D
32 r the Cypher (Cordis, Miami, Florida) or the Taxus (Boston Scientific, Maple Grove, Minnesota) stent
34 akes, Florida) and paclitaxel-eluting stent (TAXUS, Boston Scientific Corp., Natick, Massachusetts) w
35 SES, n = 69), and paclitaxel-eluting stents (Taxus, Boston Scientific, Natick, Massachusetts) (PES, n
37 ted with recombinant taxadiene synthase from Taxus brevifolia to elucidate the stereochemistry of the
38 ep of Taxol biosynthesis in the Pacific yew (Taxus brevifolia) is the cyclization of the linear isopr
39 urified taxadiene synthase from Pacific yew (Taxus brevifolia) stems to examine the possibility of a
41 lex diterpene obtained from the Pacific yew, Taxus brevifolia, is arguably the most important new dru
43 grandis and taxadiene synthase (C(20)) from Taxus brevifolia], all of which are involved in natural
44 nt geranylgeranyl diphosphate synthases from Taxus canadensis and Abies grandis yielded a functional
47 cytochrome P450 oxygenases led to the use of Taxus cell cultures induced for Taxol production and the
48 mRNA isolated from methyl jasmonate-induced Taxus cells, from which several full-length acyltransfer
49 mRNA isolated from methyl jasmonate-induced Taxus cells, from which the full-length 10-deacetylbacca
50 cal to the recombinant enzyme and clone from Taxus chinensis, acquired recently by a reverse genetics
52 ariety of taxane in extracts of a variety of Taxus cultivars were converted to a 10-deacetylbaccatin
53 ammonia lyase-like sequence acquired from a Taxus cuspidata cDNA library was expressed functionally
54 om sequencing of a cDNA library derived from Taxus cuspidata cells (induced for taxoid biosynthesis w
55 library constructed from mRNA isolated from Taxus cuspidata cells induced for Taxol production with
56 library (constructed from mRNA isolated from Taxus cuspidata cells induced with methyl jasmonate for
57 III:10beta-O-acetyltransferase isolated from Taxus cuspidata regiospecifically transfers short-chain
60 xol) biosynthetic pathway and one additional Taxus-derived acyltransferases of unknown function were
61 s, Menlo Park, California) with those of the Taxus DES (Boston Scientific, Maple Grove, Minnesota) in
62 The CoStar DES is not noninferior to the Taxus DES based on per-patient clinical and per-vessel a
65 Late stent thrombosis (LST) after Cypher and Taxus drug-eluting stent placement has emerged as a majo
67 diabetes, 3-vessel disease, or high SYNTAX (TAXUS Drug-Eluting Stent Versus Coronary Artery Bypass S
68 Comparison Between DES Limus Carbostent and Taxus Drug-Eluting Stents in the Treatment of De Novo Co
69 e arterial reaction to overlapping Cypher or Taxus drug-eluting stents was examined in rabbits with b
70 (3:1), controlled, multicenter study of the TAXUS Element (vs. TAXUS Express) PES for the treatment
73 of the Safety and Efficacy of the Use of the TAXUS Element Paclitaxel-Eluting Coronary Stent System f
74 of the Safety and Efficacy of the Use of the TAXUS Element Paclitaxel-Eluting Coronary Stent System)
75 and efficacy of the novel platinum chromium TAXUS Element paclitaxel-eluting stent (PES) compared wi
76 A prespecified analysis was conducted of the Taxus Element vs Xience Prime in a Diabetic Population (
79 y artery bypass graft surgery [CABG]) versus TAXUS Express (Boston Scientific, Natick, Massachusetts)
80 nia) everolimus-eluting stent (EES) with the TAXUS Express (Boston Scientific, Natick, Massachusetts)
81 t is non-inferiority of TAXUS Liberte versus TAXUS Express for 9-month target vessel revascularizatio
83 ours of symptom onset were randomized 3:1 to TAXUS EXPRESS paclitaxel-eluting stents (PES) or EXPRESS
85 p is an entry-criteria-matched population of TAXUS Express patients from the TAXUS IV and V trials.
86 itaxel-eluting stent (PES) compared with the TAXUS Express PES (Boston Scientific, Natick, Massachuse
90 multicenter study of the TAXUS Element (vs. TAXUS Express) PES for the treatment of de novo coronary
94 were randomized (1:1) between a drug-eluting TAXUS Express2 and an uncoated Express2 control stent.
96 onfirmed increased risk following use of the Taxus Express2 stent but not the Angio-Seal STS device.
97 ow-up, IVUS lumen volumes were larger in the TAXUS group (123 +/- 43 mm(3) vs. 104 +/- 44 mm(3), p =
98 ears there were more stent thromboses in the Taxus group (hazard ratio 0.19 [95% confidence interval
99 hrombosis occurred in 1.28% +/- 0.31% in the Taxus group and 0.76% +/- 0.23% in the bare-metal stent
100 get-vessel revascularization was 9.1% in the TAXUS group and 19.4% in the control group (P=0.0027; re
103 ase using a single pAclitaXel elUting Stent [TAXUS]-I, -II, -IV, and -VI) (RR = 1.01, 95% CI 0.40 to
106 al restenosis rates from both the Pacitaxil (TAXUS IV) and Sirolimus (SIRIUS) drug eluting stents sug
110 2.53, p = 0.99), trials with longer lesions (TAXUS-IV and -VI) (RR = 0.62, 95% CI 0.2 to 1.91, p = 0.
111 follow-up on revascularization rates in the TAXUS-IV trial and to determine whether the relative ben
123 nt in Patients with Coronary Artery Disease (TAXUS-IV) trial because of the high incidence of silent
124 th De Novo Coronary Artery Lesions (SIRIUS), TAXUS-IV, and the First and Second First Use to Undersco
126 y (TL-PAS) contributed patients treated with TAXUS Liberte paclitaxel-eluting stent and prasugrel to
127 or 30 months reduced ischemic events for the TAXUS Liberte paclitaxel-eluting stent patient subset fr
128 al antiplatelet therapy with prasugrel after TAXUS Liberte paclitaxel-eluting stent remains unknown,
131 ssess non-inferiority of the next-generation TAXUS Liberte stent (Boston Scientific Corp., Natick, Ma
132 ntly lower in-stent LLL at 6 months than the Taxus Liberte stent did, with a trend toward better 12-m
136 The primary end point is non-inferiority of TAXUS Liberte versus TAXUS Express for 9-month target ve
138 permanent-polymer paclitaxel-eluting stents (Taxus Liberte, Boston Scientific, Natick, Massachusetts)
139 e the treatment of more complex lesions with TAXUS Liberte, the primary end point was met, demonstrat
140 ng clinical and angiographic outcomes of the TAXUS Moderate Release paclitaxel-eluting stent in the t
143 months was 11.0% for CoStar versus 6.9% for Taxus (p < 0.005), including adjudicated death (0.5% vs.
146 were available in 170 patients, including 88 TAXUS patients and 82 controls, at implantation and at n
150 aclitaxel:N-benzoyltransferase (NDTBT), from Taxus plants, transfers a benzoyl group from the corresp
152 nt-based meta-analysis using the 4 principal TAXUS randomized trials (3,445 patients) with a follow-u
157 re similar in men and women treated with the TAXUS stent (8.6% vs. 7.6%, respectively, p = 0.80), as
158 restenosis in women was randomization to the TAXUS stent (OR = 0.28 [95% CI 0.11 to 0.74], p = 0.01).
159 sel revascularization rate was 7.9% with the TAXUS stent and 18.6% with the bare-metal stent (p = 0.0
161 w-release, polymer-based, paclitaxel-eluting TAXUS stent compared to bare-metal stents in patients un
163 hs for the polymer-based, paclitaxel-eluting TAXUS stent compared with the EXPRESS stent is preserved
164 ients per 6 months) were similar between the Taxus stent group (0.59 [95% confidence interval 0.22 to
166 mpared to control stents, treatment with the TAXUS stent in women resulted in a significant reduction
167 w-release, polymer-based, paclitaxel-eluting TAXUS stent or a bare-metal EXPRESS stent (Boston Scient
168 w-release, polymer-based, paclitaxel-eluting TAXUS stent or a bare-metal EXPRESS stent (Boston Scient
169 w-release, polymer-based, paclitaxel-eluting TAXUS stent or an identical bare-metal stent; 536 (41%)
170 w-release, polymer-based, paclitaxel-eluting TAXUS stent or an identical-appearing bare-metal EXPRESS
171 ate-release polymer-based paclitaxel-eluting TAXUS stent or the bare-metal EXPRESS stent (Boston Scie
172 randomized to either the paclitaxel-eluting TAXUS stent or to its bare-metal equivalent, we defined
174 n 2.5- to 3.75-mm vessels were randomized to TAXUS stent versus bare-metal EXPRESS stents (Boston Sci
176 s (including 187 women) were assigned to the TAXUS stent, and 652 (180 women) received the control st
182 r, a modest increase in risk is present with Taxus stents beyond 6 months, possibly because of inadeq
186 stablished polymer-based, paclitaxel-elution TAXUS technology with the more advanced Liberte stent pl
187 e cardiac events (MACE) occurred in 13.5% of TAXUS-treated patients versus 21.2% treated with the con
191 differential display-cloning approach, using Taxus (yew) cells induced for Taxol production, yielded
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