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1 BTT also reacts with sulfur to form an oligomer/polymer
2 BTT patients incurred an increased risk of 1-year mortal
3 BTT reacts with lithium metal to form lithium 1,3,5-benz
4 BTT was more cost-effective at $205 to $272/disability-a
5 BTT(NDI)(3) self-assembles in apolar solvents into highl
6 BTT-1023 is a fully human monoclonal anti-VAP-1 antibody
7 BTT-VAD therapy is associated with improved survival and
8 y, in under flow conditions (90 dynes/cm(2)) BTT-3033, but not BTT-3034, inhibited collagen binding b
9 ased metal-organic framework Cr3 [(Cr4 Cl)3 (BTT)8 ]2 (Cr-BTT; BTT(3-) =1,3,5-benzenetristetrazolate)
10 hange of the guest Mn2+ ions in Mn3[(Mn4Cl)3(BTT)8(CH3OH)10]2 (1-Mn2+; BTT=1,3,5-benzenetristetrazola
11 -) enables formation of [Mn(DMF)6]3[(Mn4Cl)3(BTT)8(H2O)12]2.42DMF.11H2O.20CH3OH, featuring a porous m
12 and 1,3,5-tris(2H-tetrazol-5-yl)benzene (H(3)BTT), promoted by a urea derivative, leads to a highly p
13 t ambient temperatures, the M(3)[(M(4)Cl)(3)(BTT)(8)](2) (M-BTT; BTT(3-) = 1,3,5-benzenetristetrazola
14 nthesis and properties of Zn(3)[(Zn(4)Cl)(3)(BTT)(8)](2) (ZnZnBTT, BTT(3-) = 1,3,5-benzenetristetrazo
15 the general formula M(II)(3)[(M(II)(4)Cl)(3)(BTT)(8)](2), which adopts an anionic, sodalite-like stru
21 Thus, the binding sites for BTT-3033 and BTT-3034 are differentially available in distinct integr
22 imilar sulfonamide derivatives, BTT-3033 and BTT-3034, and show that, under static conditions, they h
25 olyte additive, i.e., 1,3,5-benzenetrithiol (BTT), which is used to construct solid-electrolyte inter
27 sustained improvements from baseline in both BTT and DT patients in median MLWHF scores (by 40 and 42
28 ntricular assist devices (LVAD) as a bridge (BTT) to heart transplantation (HTX) may be limited by th
30 framework Cr3 [(Cr4 Cl)3 (BTT)8 ]2 (Cr-BTT; BTT(3-) =1,3,5-benzenetristetrazolate), featuring coordi
31 es, the M(3)[(M(4)Cl)(3)(BTT)(8)](2) (M-BTT; BTT(3-) = 1,3,5-benzenetristetrazolate) series of framew
33 gned C(3)-symmetric disc-shaped chromophore, BTT(NDI)(3), features electron accepting naphthalene dii
35 ganic framework Cr3 [(Cr4 Cl)3 (BTT)8 ]2 (Cr-BTT; BTT(3-) =1,3,5-benzenetristetrazolate), featuring c
36 red spectroscopy studies of Mn-, Fe-, and Cu-BTT, allowing the thermodynamics of H(2) adsorption to b
37 tructurally similar sulfonamide derivatives, BTT-3033 and BTT-3034, and show that, under static condi
39 -dicarboxylic acid bis-(2-butyloctyl) ester (BTT) and 4,8-bis(2-butyloctyl)benzo[1,2-b:4,5-b']dithiop
40 to evaluate survival benefits and costs for BTT-VAD versus nonbridged heart transplant recipients.
41 rovides poor discrimination of mortality for BTT patients and only modest discrimination for DT patie
44 roups was 8%, 7%, and 16%, respectively, for BTT patients; 9%, 12%, and 19%, respectively, for DT pat
46 gers a unidirectional electron transfer from BTT to NDI and results in (BTT(*+)-NDI(*-)) lifetimes th
50 estimated human effective dose due to (124)I-BTT-1023 was 0.55 mSv/MBq, if blockage of thyroid uptake
53 ron transfer from BTT to NDI and results in (BTT(*+)-NDI(*-)) lifetimes that are by up to 3 orders of
54 proach that employs a DNA-conjugated ligand (BTT-DNA) to localize and concentrate copper ions at the
56 ratures, the M(3)[(M(4)Cl)(3)(BTT)(8)](2) (M-BTT; BTT(3-) = 1,3,5-benzenetristetrazolate) series of f
58 ns in Mn3[(Mn4Cl)3(BTT)8(CH3OH)10]2 (1-Mn2+; BTT=1,3,5-benzenetristetrazolate) with selected cations
60 onditions (90 dynes/cm(2)) BTT-3033, but not BTT-3034, inhibited collagen binding by an alpha2 varian
61 al, we elucidate how CO(2) binds to a novel "BTT-type" metal-organic framework (MOF) featuring open m
63 ysis estimated a 59%, 54%, and 43% chance of BTT-VAD therapy being cost-effective for high-, medium-,
66 present study were to evaluate the impact of BTT with LVAD on posttransplantation survival, to descri
67 center was associated with increased odds of BTT intent at implant and subsequent transplant receipt
68 ciated with a 79% increased adjusted odds of BTT LVAD designation (odds ratio, 1.79; 95% CI, 1.35-2.3
71 ng CHO cell adhesion to collagen I, but only BTT-3033 blocks platelet attachment under flow (90 dynes
72 odds ratio of 1-year mortality for patients BTT with LVAD compared with those with medical managemen
78 patients, with 1-year mortality in high-risk BTT patients at 17.6% compared with 10.4% in high-risk m
80 market approval, actual patient care setting BTT population support the original findings from the pi
83 to variations in the age range analyzed, the BTT treatment threshold, or rates of treatment access, a
88 ot change the comparative superiority of the BTT strategy, nor did titrating treatment using fasting
91 However, if insulin were unavailable, the BTT strategy would no longer be superior for preventing
92 only accepted willingness-to-pay thresholds, BTT-VAD therapy is likely to be cost-effective relative
94 n VAs and mortality in bridge to transplant (BTT) and destination therapy (DT) LVAD patients, separat
96 Device in the ADVANCE bridge to transplant (BTT) trial and continued access protocol were reviewed.
97 California) LVAD as a bridge to transplant (BTT, n = 486) and DT (n = 638) and 114 DT patients with
99 nton, California) bridge to transplantation (BTT) (n = 281) and destination therapy (DT) (n = 374) tr
101 ALF patients as a bridge to transplantation (BTT), and as definitive therapy for toxic ingestion or i
103 ffectiveness of a bridge-to-transplantation (BTT)-VAD approach relative to direct heart transplantati
104 target, a benefit-based tailored treatment (BTT) strategy emphasizing lowering CVD risk, or a hybrid
105 ]), with a benefit-based tailored treatment (BTT) strategy, aiming to lower estimated risk for compli
110 of Zn(3)[(Zn(4)Cl)(3)(BTT)(8)](2) (ZnZnBTT, BTT(3-) = 1,3,5-benzenetristetrazolate), a heretofore un