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1 f the head, neck, or uncinate process of the pancrease.
2 clinical n=42) and 150 chronic pancreatitis pancreases.
3 eaky vessels were apparent in cd93-deficient pancreases.
4 ution in relation to islets in infused human pancreases.
5 labeling between perfused and syringe-loaded pancreases.
6 signal intensity between normal and diabetic pancreases.
7 31 (65%) of the 48 patients with functioning pancreases.
8 s were not detectable in fetal and postnatal pancreases.
9 n), shorter cold ischemia time for recovered pancreases (355 vs. 630 min), and reduced mean cost per
11 der-drained pancreas transplants (25 SPK, 14 pancrease after kidney transplants [PAK], amd two pancre
14 ion after brain death (DBD) and low-risk DCD pancreases, as the number of DCD pancreas transplants in
15 tively) in human fetal, postnatal, and adult pancreases, as well as in isolated adult islets, and exa
16 yielded more than 200,000 IEQ from 19 of 21 pancreases (averaging 422,893 +/- 181,329 total IEQ and
17 for transplantation from 8 of 10 consecutive pancreases, averaging 6510 +/- 2150 islet equivalent num
20 a-cells were rarely found in human cadaveric pancreases but were in the range of 0.2-0.5% in human is
21 Insulin secretion was observed in all four pancreases, but was lowest in an older donation after ca
22 ication method (SM, standard method) and 132 pancreases by a refined University of Illinois at Chicag
23 isolated islets from 114 human cadaver donor pancreases by the automated Ricordi method, followed by
29 pectively analyzed 376 islet isolations from pancreases flushed and transported with IGL-1 (n=95), UW
31 ked for female islet beta cells in four male pancreases from autopsies, one from a T1D patient, emplo
34 PTP1B and TCPTP expression was determined in pancreases from chow and high fat fed mice and the impac
35 a subset of these fatty acids was tested in pancreases from fed animals, the same rank order of effe
37 bserved in the kinetics of CVB4 clearance in pancreases from NOD, NOD IL-4-/-, and NOD IFN-gamma-/- m
38 ber of islet transplants, the suitability of pancreases from organ donors considered inappropriate fo
42 suring sufficient islet yield from preserved pancreases is a critical step in clinical islet transpla
44 ucose metabolism in islets isolated from the pancreases of children with KATPHI who required pancreat
48 increased, and TCPTP expression decreased in pancreases of mice fed a high fat diet, as well as in MI
49 l three virus doses, but day 3 titers in the pancreases of mice inoculated with 10(4) PFU were reduce
50 ormed on cDNAs from isolated islets or whole pancreases of NOD/Lt females 4 weeks after intrathymic i
62 nt at cell membranes in homozygous p120(f/f) pancreases, potentially providing stability for maintena
64 port ex vivo normothermic perfusion of human pancreases procured but declined for transplantation, wi
66 on of transplanted organs was less than 10%; pancreases refused due to "trauma", "age", or "resuscita
68 mmunofluorescent staining of fetal and adult pancreases revealed colocalization of GAD65 with alpha-
70 -dose RCEM was efficient in digesting entire pancreases to obtain higher yield (5535 +/- 830 and 2582
71 d by amylase, and exocrine function of human pancreases using EVNP and demonstrates the feasibility o
78 eases were transplanted; among these, 62% of pancreases were of potentially high quality (favorable d
80 ompared between two purification methods; 32 pancreases were processed by conventional Biocoll purifi
81 atic islets when sections from rat and mouse pancreases were reacted with a polyclonal antibody to re
86 ta-cells appeared histologically normal, the pancreases were unresponsive to perfusion with stimulato
87 ch as nitrite, are generated in precancerous pancreases, which induce massive DNA damage, including D
88 r islet yield from deceased and pancreatitis pancreases while retaining islet quality and function.
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