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1 All metastases were intramyocardial.
8 infarction model of type 1 diabetic rats by intramyocardial administration of an adenoviral vector e
9 of this study was to investigate the role of intramyocardial administration of chimeric ephrinA1-Fc i
11 e of Radiology, Saeed et al (1) describe the intramyocardial administration of VM202, a newly constru
13 rformed with immunocompromised mice by using intramyocardial adoptive transfer injection after infarc
14 myocardial thickness, a diffuse increase in intramyocardial and epicardial fat, little inflammation,
16 -20+/-2% versus -17+/-3%; P<0.01) and showed intramyocardial and pericardial late gadolinium enhancem
17 impairs the survival of endothelial cells in intramyocardial arteries and capillaries in the early po
19 re-related mortality with tissue disruption, intramyocardial bleeding, and increased cardiac dysfunct
20 dge, we demonstrate NOX5 expression in human intramyocardial blood vessels and cardiomyocytes, with s
21 ed to the endothelium of a limited number of intramyocardial blood vessels and to a limited number of
24 h manifested as an increase in NOX5-positive intramyocardial blood vessels, as well as in endothelium
26 supply/demand mismatch or remodeling of the intramyocardial blood vessels; they represent a dynamic
27 ator-dilution methods provide an estimate of intramyocardial blood volume (BV) and perfusion (F), whi
34 eta t)), where A, beta, and A x beta reflect intramyocardial blood volume, red cell velocity, and flo
36 This study evaluates the effect of repeated intramyocardial bone marrow cell injection in patients w
38 t ventricular hypertrophy and compression of intramyocardial branches of the epicardial coronary arte
39 2 weeks after cell transplantation indicated intramyocardial calcification in 4 of 14 surviving rats
43 senchymal stromal cells ex vivo, followed by intramyocardial cell administration in normal and infarc
45 The study evaluated a nonsurgical means of intramyocardial cell introduction using the coronary ven
47 self-assembling nanofibers can now establish intramyocardial cellular microenvironments by injection.
52 th single-vessel disease demonstrate reduced intramyocardial circumferential shortening throughout th
54 cy reordering was applied to distinguish new intramyocardial collateral vessels from normal circulati
56 involved in promoting adverse remodeling of intramyocardial coronary arteries and arterioles by fibr
57 ed with control hearts but normalized in the intramyocardial coronary arteries and smaller vessels in
58 onuclear cell infiltration and vasculitis of intramyocardial coronary arteries were significantly red
59 linear branching structures consistent with intramyocardial coronary arteries, which were not clearl
61 ated adventitial/interstitial fibroblasts of intramyocardial coronary arterioles but decreased prolif
62 ings indicate that noninvasive assessment of intramyocardial coronary vasculature and measurement of
65 ary artery ligation followed by peri-infarct intramyocardial delivery of adenoviral vector expressing
69 Pim1 overexpression enhanced the effect of intramyocardial delivery of CSCs to infarcted porcine he
71 Early phase clinical trials suggest that intramyocardial delivery of ixmyelocel-T might improve c
73 rat hearts demonstrated that pretreatment by intramyocardial delivery of PDGF-AB promotes angiogenesi
76 s into cardiac progenitor cells, followed by intramyocardial delivery of the progenitor cells into ne
77 n of Ca2+ oscillations in hCPCs before their intramyocardial delivery to infarcted hearts was associa
84 ess data transmission system that analyzes 9 intramyocardial electrogram parameters recorded from 4 o
87 ECGI can noninvasively estimate the depth of intramyocardial electrophysiological events and provides
88 cells in the mediastinal lymph nodes and the intramyocardial endothelium were both activated in respo
91 cardial fat thickness, percent fibrosis, and intramyocardial fat infiltration were measured in 16 sec
93 6%) patients on the RV and LV, respectively, intramyocardial fat on multidetector computed tomography
97 sulin and plasma FFA levels can regulate the intramyocardial fate of fatty acids in humans with type
98 ine the relation between regional changes in intramyocardial function and global left ventricular (LV
103 uction ( MVO microvascular obstruction ) and intramyocardial hemorrhage ( IMH intramyocardial hemorrh
106 S0, no MVO microvascular obstruction or IMH intramyocardial hemorrhage (n = 68); S1, MVO microvascul
107 ; S1, MVO microvascular obstruction , no IMH intramyocardial hemorrhage (n = 84); and S2, MVO microva
108 ces in microvascular obstruction (p = 0.19), intramyocardial hemorrhage (p = 0.19), or ejection fract
109 ction ) and intramyocardial hemorrhage ( IMH intramyocardial hemorrhage ) helped define three infarct
110 asured myocardial salvage, and the extent of intramyocardial hemorrhage and microvascular obstruction
112 dium at risk, microvascular obstruction, and intramyocardial hemorrhage in both acute setting and lat
113 overy is impaired in infarcted segments with intramyocardial hemorrhage or microvascular obstruction.
114 cardioprotective strategy and the degree of intramyocardial hemorrhage or microvascular obstruction.
116 ion, late gadolinium enhancement, edema, and intramyocardial hemorrhage) and hard events (all-cause m
117 , myocardium at risk, infarct size, salvage, intramyocardial hemorrhage, and microvascular obstructio
118 , myocardium at risk, infarct size, salvage, intramyocardial hemorrhage, and microvascular obstructio
119 nhancement (SEE), microvascular obstruction, intramyocardial hemorrhage, and salvage index (MSI) were
123 ia-reperfusion injuries, indicated by severe intramyocardial hemorrhage; however, monocyte recruitmen
125 o evaluate the associated salutary effect of intramyocardial hydrogel injection on the remodeling res
127 heral blood mononuclear cells (PBMNCs) after intramyocardial (IM), intracoronary (IC), and interstiti
129 he process of cardiac remodeling by reducing intramyocardial inflammation, collagen deposition and ca
131 domized into three groups, each receiving an intramyocardial injection (IMI) of a single dose at thre
132 idence interval, 3.7 to 14.5), as did direct intramyocardial injection and intravenous infusion, wher
134 ice with acute myocardial infarction (MI) by intramyocardial injection exhibited significantly higher
137 trial, 30 patients were randomized (2:1) to intramyocardial injection of 25 million MPCs or medium d
138 underwent myocardial infarction followed by intramyocardial injection of 5x10(5) ASC, MSC, fibroblas
140 ta-Gal (control) genes was induced by either intramyocardial injection of AAV serotype 2 (AAV2) or sy
141 thermore, cardiac overexpression of Nur77 by intramyocardial injection of Ad-Nur77 substantially inhi
146 d angiogenesis is being studied after direct intramyocardial injection of angiogenic peptides or plas
148 7.2+/-13.3 years) received transendocardial, intramyocardial injection of autologous bone marrow prog
150 l and early-phase clinical data suggest that intramyocardial injection of autologous CD34+ cells can
160 modynamic indexes in the mini-pig model, but intramyocardial injection of CDCs or cardiospheres has n
163 d by repeat thoracotomy for randomization to intramyocardial injection of CSCs (n=13) or vehicle alon
164 zed into 3 groups of 16 rats, each receiving intramyocardial injection of either 7x10(5) DiI-labeled
165 oupled device imaging, rats (n=20) underwent intramyocardial injection of embryonic rat H9c2 cardiomy
166 descending coronary artery and peri-infarct intramyocardial injection of ESA, SDF-1alpha, or saline.
168 erior descending coronary artery followed by intramyocardial injection of FLT3 ligand (FL) or vehicle
171 rly, using a coronary artery ligation model, intramyocardial injection of IL-18BP MSCs improved LV ej
172 left ventricular function was observed after intramyocardial injection of myoendothelial cells when c
173 t anterior descending artery, catheter-based intramyocardial injection of NIS(pos)-hiPSCs guided by 3
174 ays; intracoronary injection of BM cells and intramyocardial injection of phosphate-buffered saline r
175 sion using naked DNA gene therapy via direct intramyocardial injection of plasmid DNA encoding VEGF (
176 erior descending coronary artery with direct intramyocardial injection of replication-deficient adeno
177 erior descending coronary artery with direct intramyocardial injection of replication-deficient recom
179 tation as well as in situ activation through intramyocardial injection of specific growth factors has
183 =8) and control (n=6) athymic rats underwent intramyocardial injection of up to 2x10(9) pfu of Ad-CMV
184 to examine the effect of late autologous CSC intramyocardial injection on long-term cardiac structure
186 ort, we have tested the feasibility of using intramyocardial injection or intracoronary infusions of
187 = 9), or placebo (n = 10) were delivered by intramyocardial injection to immunosuppressed Yorkshire
189 expanded from sheep bone marrow, and direct intramyocardial injection was performed within the borde
192 nce interval, -15.9 to -3.0), whereas direct intramyocardial injection, intravenous infusion, and int
199 animals were grouped (n=20/group) to receive intramyocardial injections of 70 microL of basal medium
201 Patients with refractory angina who received intramyocardial injections of autologous CD34+ cells (10
203 nt study demonstrates the relative safety of intramyocardial injections of bone marrow-derived stem c
205 week after the MI, the pigs received direct intramyocardial injections of either a recombinant adeno
207 owing week, swine were randomized to receive intramyocardial injections of PBS control (n=10), circul
208 t left coronary artery ligation and received intramyocardial injections of Sca-1(+)CD31(-) cells gene
220 magnetic resonance imaging (MRI) to measure intramyocardial lipid levels and fibrosis as possible co
230 logy allows minimally invasive evaluation of intramyocardial microcirculatory function and permits as
233 was used to explore the distribution of the intramyocardial microvessels (group 2, n = 4; three-dime
235 MR fluoroscopy has the potential to guide intramyocardial MSC injection to desirable targets, such
238 hanced MAO-A activity coupled with increased intramyocardial norepinephrine availability results in a
239 transgenic male rats through either a direct intramyocardial or a retrograde intracoronary route.
241 demonstrate an impaired ability to increase intramyocardial oxygenation during vasodilatory stress,
242 atory stress to index the ability to augment intramyocardial oxygenation in hypertensive hypertrophy,
243 ligation of the coronary artery followed by intramyocardial PBS injections (control group), and LAD
245 Connexin 40 immunostaining demonstrated intramyocardial Purkinje fibers at sites of reentry in t
248 second, it may lead to the establishment of intramyocardial reentry, at which time the Purkinje syst
250 hat MR tagging could be used to quantify the intramyocardial response to low-dose dobutamine and rela
254 MB) is the term for the muscle overlying the intramyocardial segment of the epicardial coronary arter
256 stem cells) were identified by MRI as large intramyocardial signal voids that persisted at 3 weeks (
257 rdial structure, cardiomyocyte function, and intramyocardial signaling were shown to be specifically
260 e resistant to diabetes-induced increases in intramyocardial TAG levels, lipotoxicity, and cardiac dy
268 ge future clinical trials of catheter-based, intramyocardial transplantation of autologous CD34+ MNCs
269 We investigated whether catheter-based, intramyocardial transplantation of autologous endothelia
272 (MI) to investigate the functional impact of intramyocardial transplantation of hiPSC-derived cardiom
275 ght atrial re-entry, which entailed a longer intramyocardial traversal but did not cross the tricuspi
276 c cardiomyopathy is associated with enhanced intramyocardial triacylglycerol (TAG) levels, the role o
278 ion, induced microinfarctions, and increased intramyocardial triglyceride deposition, features sugges
279 ere metabolic dysregulation characterized by intramyocardial triglyceride overload and changes in gen
280 ned to 1 of 4 treatment groups: Combo group, intramyocardial vascular endothelial growth factor (VEGF
281 rt disease had a variable response to single intramyocardial vector administration, ranging from mini
282 arts had a significantly lower percentage of intramyocardial vessel volume and a significantly higher
283 ng study reports the reduction in normalized intramyocardial vessel volume within the aged heart, in
284 ass, which increased with age, the total and intramyocardial vessel volumes were lower, whereas the e
286 easurement of phasic changes in aBV in large intramyocardial vessels using either Definity (group 1;
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