ライフサイエンスコーパス: cannulate

1 with induced chronic elevation of IOP) were cannulated.

2 (2%), intubated, and femoral artery and vein cannulated.

3 r was exposed and the intraosseous space was cannulated.

4 of adult porcine and canine ex vivo eyes was cannulated.

5 ley rats were anesthetized, and the duodenum cannulated.

6 nt' lymphatic vessels that can be surgically cannulated.

7 the draining prescapular lymph node had been cannulated.

8 The right femoral artery and vein were cannulated.

9 ein and the right external jugular vein were cannulated.

10 of explanted human hearts were isolated and cannulated.

11 After at least 6 wk, the duct is cannulated (40 min).

12 (1) It is possible to cannulate and to record electrical potentials from the V

13 The duodenum was also cannulated and a fasting saline-glucose solution was inf

14 artery and both internal jugular veins were cannulated and a flow probe was placed on the right caro

15 a mesenteric artery of male Wistar rats was cannulated and a short segment of the artery was mechani

16 The femoral artery and vein were cannulated and an extracorporeal circulation loop with 2

17 RESEARCH DESIGN AND METHODS-Rats were cannulated and bilateral guide cannulas inserted to the

18 ilis muscle of normotensive Wistar rats were cannulated and exposed to 140 mm Hg perfusion pressure f

19 Following recovery, the brachial artery was cannulated and flushed with 10 000 U of heparin.

20 Three to 6 weeks later, the eyes were cannulated and manometrically set to 10, 20, 30, 40, or

21 nd all feed arteries were counted, isolated, cannulated and maximally dilated for measurement of lumi

22 rom) isolated from gluteal fat biopsies were cannulated and perfused in chambers.

23 mflex branch of the left coronary artery was cannulated and perfused with blood from the left subclav

24 lated, and the left main coronary artery was cannulated and perfused.

25 ched control pigs (73 +/- 4 mg/dL), and then cannulated and pressurized for vasoreactivity study usin

26 10(-6) to 5 x 10(-5) mol/L) were studied in cannulated and pressurized gracilis muscle arterioles (

27 Arterioles were isolated, cannulated and pressurized in a microvessel bath with fi

28 n of the gastrocnemius muscle were isolated, cannulated and pressurized in a microvessel chamber with

29 micrometer) of male mice were isolated, then cannulated and pressurized in a vessel chamber.

30 iameters and indices of pumping in isolated, cannulated and pressurized segments of rat TD were measu

31 limb collateral arteries were then isolated, cannulated and pressurized via hydrostatic reservoirs to

32 c and ischemic regions of subepicardium were cannulated and pressurized without flow for in vitro stu

33 ents of the rat thoracic duct were isolated, cannulated and pressurized.

34 lymphatics and thoracic ducts were isolated, cannulated and pressurized.

35 The pulmonary vein ostia were cannulated and pulmonary venous pressure was measured be

36 eries (outside diameter, 50-150 microm) were cannulated and studied in vitro under physiologic condit

37 With fluoroscopic guidance, the cervix was cannulated and the endocervical canal was dilated with a

38 nternal jugular vein and carotid artery were cannulated and used for the AV-ECMO.

39 Bovine retinal central artery and vein were cannulated, and arterioles and venules were perfused wit

40 and five with early glaucoma, both eyes were cannulated, and IOP set to 10 mm Hg in one normal eye an

41 ely 75 mum internal diameter) were isolated, cannulated, and pressurized (55 cmH(2)O) without flow fo

42 57+/-3 microm; length, 4 mm) were isolated, cannulated, and pressurized (75 mm Hg; 37 degrees C).

43 Porcine coronary arterioles were isolated, cannulated, and pressurized for in vitro study.

44 , porcine coronary arterioles were isolated, cannulated, and pressurized for in vitro study.

45 cond-order retinal arterioles were isolated, cannulated, and pressurized to 55 cm H2O lumenal pressur

46 -70 mum in internal diameter) were isolated, cannulated, and pressurized to 55 cmH(2)O luminal pressu

47 50 to 100 microm in diameter) were isolated, cannulated, and pressurized to 60 cm H(2)O without flow

48 rterioles (40 to 110 microns) were isolated, cannulated, and pressurized to 60 cm H2O intraluminal pr

49 al vessels (50 to 100 microm) were isolated, cannulated, and pressurized to 60 cm H2O without flow fo

50 Porcine retinal arterioles were isolated, cannulated, and pressurized without flow for in vitro st

51 arterioles from porcine eyes were isolated, cannulated, and pressurized without flow.

52 In the present study, we cannulated animals bilaterally in both the VTA and the s

53 f either ATP or UTP at the downstream end of cannulated arteries evoked constriction, which only in t

54 er validated by demonstrating our ability to cannulate arterioles in two brain regions (cortex and su

55 We have recently demonstrated in isolated cannulated arterioles that adenosine and its metabolite,

56 om human right atrial appendages (n=78) were cannulated at a distending pressure of 60 mm Hg and zero

57 ppendages at the time of cardiac surgery and cannulated at a distending pressure of 60 mm Hg and zero

58 A vessel is cannulated at both ends with glass micropipettes and the

59 administered into the rumen of cattle dually cannulated at the rumen and duodenum.

60 enclozic acid which included a rat bile duct cannulated (BDC) study characterizing the biliary and ur

61 us bolus injection technique was used in the cannulated brachial vein and artery using leptin radioio

62 ere randomized into four groups: group I was cannulated but not bled (sham); group II received normal

63 Fifteen cannulated calves were studied to determine the efficien

64 Step increases in intraluminal pressure of cannulated cerebral arteries induced myogenic constricti

65 by measuring retrograde blood flow from the cannulated collateral-dependent artery.

66 ed both hypotheses directly by isolating and cannulating collecting lymphatic vessels from geneticall

67 g metabolic tracer techniques in chronically cannulated, conscious mice with one extra GK gene copy.

68 ollected in vitro mimics that collected from cannulated ducts of glands given low level stimulation i

69 ss pipettes with 2- to 3-microm tips used to cannulate episcleral veins.

70 eadings from 20 to 80 mm Hg (R(2) = 0.99) in cannulated eyes.

71 ) = 0.86, P < 0.0001) was similar to that in cannulated eyes.

72 In isolated, cannulated feed arteries ( approximately 70 microm in di

73 The carotid artery was cannulated for blood pressure monitoring and for assessi

74 njection, the main intestinal lymph duct was cannulated for collection of lymph.

75 The ileal vein was cannulated for drug injection.

76 A femoral artery was cannulated for measuring mean arterial blood pressure, m

77 A total of 69% of patients were cannulated for supraventricular tachycardia with a media

78 Arterioles from atria or ventricles were cannulated for videomicroscopy.

79 Experiment 1: Intravenously cannulated ICR mice received chow, PN, or PN + BBS injec

80 (30 mg/kg iv pentobarbital), intubated, and cannulated in one femoral artery and vein.

81 0 mg/kg pentobarbital, i.v.), intubated, and cannulated in one femoral artery, one femoral vein, and

82 The rats were then tracheostomized and cannulated in one femoral vein and artery.

83 Two HCAs were cannulated in series (a donor intact vessel upstream and

84 r exercise therapy, animals were chronically cannulated in the carotid artery (sampling) and jugular

85 Rats were chronically cannulated in the carotid artery (sampling), jugular vei

86 Male Wistar rats were chronically cannulated in the carotid artery (sampling), jugular vei

87 Male Wistar rats (n = 36), chronically cannulated in the carotid artery (sampling), jugular vei

88 sulinemic-euglycemic clamp, all animals were cannulated in the jugular vein (infusion) and carotid ar

89 Rats were then cannulated in the Nac core (NacC) or shell (NacS) and in

90 sively pretrained on DNMTP, then bilaterally cannulated into either the dorsal or ventral hippocampus

91 livary glands via retrograde infusion of the cannulated main excretory ducts of submandibular glands.

92 In the present study, cannulated male Sprague-Dawley rats were used to investi

93 s of influenza-specific IgA were measured in cannulated mice randomized to chow feeding or parenteral

94 TonoLab rebound tonometer was determined in cannulated mouse and rat eyes.

95 inst the manometric (true) IOP determined in cannulated mouse eyes ex vivo.

96 or IOPs in the range of 3.7 to 44.1 mm Hg in cannulated mouse eyes.

97 e counterregulatory responses in chronically cannulated nondiabetic and diabetic BB rats was explored

98 re was an increase in the number of patients cannulated per annum over the 10-year period studied.

99 The cannulated pieces of tissue were placed in culture mediu

100 Ileal cannulated pigs (50+/-1.9 kg) were fed a fibre-free diet

101 In cannulated pressurized MAs preconstricted 50% with norad

102 Application of KV1-C peptide to cannulated, pressurized cerebral arteries rapidly induce

103 Arterial segments were cannulated, pressurized to 80 mmHg and allowed to develo

104 and acetylcholine (NE+ACh) were measured in cannulated, pressurized vessels ex vivo.

105 re removed and the arterioles were isolated, cannulated, pressurized, and placed on an inverted micro

106 Of the 20 pairs of eyes that were cannulated, primary cells were obtained from 13.

107 Cannulated rabbit knee joints were infused with HA solut

108 studies investigating the use of previously cannulated RAs as grafts in coronary artery bypass surge

109 uss the impact this could have on previously cannulated RAs used as coronary artery bypass grafting c

110 cells, placed at multiple times into normal cannulated rat brain, produced focal sterile abscesses a

111 b and Tono-Pen tonometers were calibrated in cannulated rat eyes connected to a pressure transducer.

112 Isolated, cannulated rat femoral arterial branches were exposed in

113 urified kallistatin (0.07-1.42 nmol/kg) into cannulated rat jugular vein produced a 20-85 mmHg reduct

114 While the bile duct-cannulated rat model clearly demonstrates that the 3'-hy

115 In the non-iron-overloaded, bile-duct-cannulated rat, a single SC injection of HBED, 150 micro

116 ays, into the locus coeruleus of chronically cannulated rats and their hypnotic response to dexmedeto

117 In vivo experiments with cannulated rats bearing 9L gliosarcoma showed a preferen

118 essed in mesenteric lymph and carotid artery cannulated rats following intraduodenal infusion of lipi

119 Chronically cannulated rats underwent afferent ablation of the porta

120 series of studies in which free-feeding rLHa-cannulated rats were injected with opioid agonists (DAMG

121 VP-cannulated rats were subjected to 3 days of conditioning

122 lation, Taxotere, was conducted in bile duct cannulated rats.

123 Similarly, ex vivo studies of isolated, cannulated resistance arteries and large first-order art

124 ny (but not all) ex vivo studies of isolated cannulated resistance arteries and large, first-order ar

125 f the compounds are evaluated in a bile-duct-cannulated rodent model to determine iron clearance effi

126 of the compounds are assessed in a bile-duct-cannulated rodent model to determine iron clearance effi

127 po) and subcutaneously (sc) in the bile-duct-cannulated rodent model.

128 DFT conjugates was determined in a bile-duct-cannulated rodent model.

129 uivalent iron binding doses in the bile duct cannulated rodent, oral administration of the tricoordin

130 ffective at clearing iron from the bile duct-cannulated rodent; when given subcutaneously at a dose o

131 (ICE) in both non-iron-overloaded, bile duct-cannulated rodents and in iron-overloaded primates.

132 Two 4.0-mm cannulated screws were placed per level to fix facet joi

133 ontractions and fluid propulsion in isolated cannulated segments of sheep mesenteric lymphatics were

134 The mice were then cannulated such that the tip of the tubing was positione

135 Male Sprague Dawley rats were cannulated targeting central amygdala (CeA), medial amyg

136 Failure was due to inability to reach or cannulate the intact papilla or bilioenteric anastomosis

137 study hypothesis used ultrasound guidance to cannulate the internal jugular and subclavian of a human

138 We have directly cannulated the ovine lymphatic vessels to detail the in

139 ssing Ngb-Tg mice and wild type (WT) mice by cannulating the anterior chamber and transiently elevati

140 NRP was achieved by cannulating the aorta and vena cava after death.

141 d to the endoscopic technique (difficulty in cannulating the bile duct achievement of access to the b

142 recombinant tissue plasminogen activator, 3) cannulating the retinal vein transvitreally, or 4) trans

143 ant tissue plasminogen activator (rt-PA), 3) cannulating the retinal vein transvitreally, or 4) trans

144 ut before the operation, we spent 15 minutes cannulating their ducts, obtaining washings, and attempt

145 Intestinal lymph was collected by cannulating thoracic ducts of mesenteric lymphadenectomi

146 Bladders of urethane-anesthetized rats were cannulated through the dome for continuous-infusion cyst

147 d and contralateral control lymph nodes were cannulated throughout the experimental period.

148 the hippocampus, DKO mice were unilaterally cannulated to deliver forskolin.

149 The uterine arteries were cannulated to perfuse the organ with a buffer solution c

150 r tributary branch of the mesenteric vein is cannulated to provide endovascular access to the portal

151 usly monitored by a pressure sensor that was cannulated to the vitreous chamber.

152 60 mins of shock, the left renal artery was cannulated under fluoroscopy and perfused at pressures o

153 g eight patients, the cervix could be easily cannulated up to 7 months after dilation.

154 ultrasonic transit-time flowmeter and a non-cannulating V-shaped probe.

155 he prevalence of deep vein thrombosis in the cannulated vessel following extracorporeal membrane oxyg

156 ostdecannulation deep vein thrombosis in the cannulated vessel in adults who have received venovenous

157 retrieval, with another five centers (4.2%) cannulating vessels premortem.

158 In CSA group, the coronary sinus was cannulated via subclavian or femoral venous approaches,

159 Patients were cannulated via the ascending aorta or common femoral art

160 Porcine livers were cannulated via the hepatic artery, then perfused with PB

161 The ducts that had been cannulated were marked by instillation of dye or other m

162 To test this, rats were doubly cannulated with 1 cannula placed in the PVN and 1 cannul

163 The anterior chamber of adult rabbits was cannulated with a 25-gauge needle connected to an elevat

164 The brachial arterial was cannulated with a 27-gauge needle for drug infusion.

165 ia early were more likely to be successfully cannulated with a double-lumen venovenous catheter.

166 Arterioles were cannulated with a micropipette system and luminally pres

167 uced and the common bile duct was surgically cannulated with a pediatric feeding tube.

168 One femoral vein was cannulated with a pulmonary artery flotation catheter an

169 Eyes of anesthetized animals were cannulated with a very fine fluid-filled glass microneed

170 pproximately 210 microm o.d.) were isolated, cannulated with glass micropipettes, and pressurized to

171 MCAs (200-250 microm OD) were isolated, cannulated with glass micropipettes, and pressurized.

172 ng arterioles) were isolated from male rats, cannulated with glass micropipettes, and pressurized.

173 ppendages at the time of cardiac surgery and cannulated with glass micropipettes.

174 of 217 +/- 6 microm, n = 22) were isolated, cannulated with glass pipettes in an arteriograph and pr

175 pletion of the stress protocol, animals were cannulated with microdialysis guide cannulae over the nu

176 ned from patients during cardiac surgery and cannulated with micropipettes.

177 Male Sprague-Dawley rats were cannulated with one cannula placed in the PVN and two ca

178 To test this, rats were doubly cannulated with one cannula placed in the rNTS and one c

179 The eye was cannulated with two 23-gauge needles, one to manipulate