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1 f the head, neck, or uncinate process of the pancrease.
2 ISM was used to isolate islets from 10 human pancreases.
3 and IL18r on acinar cells in human and mouse pancreases.
4 eaky vessels were apparent in cd93-deficient pancreases.
5  clinical n=42) and 150 chronic pancreatitis pancreases.
6 ution in relation to islets in infused human pancreases.
7 labeling between perfused and syringe-loaded pancreases.
8 signal intensity between normal and diabetic pancreases.
9 31 (65%) of the 48 patients with functioning pancreases.
10 s to improve islet recovery from young donor pancreases.
11 s were not detectable in fetal and postnatal pancreases.
12 n), shorter cold ischemia time for recovered pancreases (355 vs. 630 min), and reduced mean cost per
13 onors and 31 organs (13 kidneys, 6 livers, 3 pancreases, 5 hearts, and 4 lungs) were ultimately trans
14                           Of 23 inaccessible pancreases, 9 (39%) underwent CB; pancreatic tissue was
15 der-drained pancreas transplants (25 SPK, 14 pancrease after kidney transplants [PAK], amd two pancre
16 c endothelial cells (ASECs) from three human pancreases and corroborate these findings with three pub
17 icensis; Jamaican fruit bat) bat kidneys and pancreases and identify key cell population, gene expres
18  donors underwent NRP from which 3 livers, 2 pancreases, and 14 kidneys were transplanted.
19  187 kidneys, 57 livers, 18 hearts, 5 kidney-pancreases, and 2 lungs.
20 y greater numbers of hearts, lungs, kidneys, pancreases, and intestines, but not livers.
21 eelike structures in lungs, kidneys, livers, pancreases, and mammary glands as well as digits and bon
22 ion after brain death (DBD) and low-risk DCD pancreases, as the number of DCD pancreas transplants in
23 tively) in human fetal, postnatal, and adult pancreases, as well as in isolated adult islets, and exa
24  yielded more than 200,000 IEQ from 19 of 21 pancreases (averaging 422,893 +/- 181,329 total IEQ and
25 for transplantation from 8 of 10 consecutive pancreases, averaging 6510 +/- 2150 islet equivalent num
26  patients in the comparator group lost their pancreases because of acute rejection (P<0.05).
27 d bihormonal endocrine cells in 7 of 9 human pancreases between CS16 and CS18, which were no longer d
28                             In the remaining pancreases, blood flow and pH were maintained throughout
29 romote regeneration and reduce damage in the pancreases, blood, guts, and nervous systems of mice, bu
30 a-cells were rarely found in human cadaveric pancreases but were in the range of 0.2-0.5% in human is
31   Insulin secretion was observed in all four pancreases, but was lowest in an older donation after ca
32 ication method (SM, standard method) and 132 pancreases by a refined University of Illinois at Chicag
33 isolated islets from 114 human cadaver donor pancreases by the automated Ricordi method, followed by
34                                     In older pancreases, collagen IV, V and VI were present throughou
35  cell types appear simultaneously, and early pancreases contain bihormonal cells.
36                                    Mice with pancreases containing an activated oncogenic allele of K
37 arge collection of human embryonic and fetal pancreases covering the first trimester of pregnancy to
38                                  Analysis of pancreases during ageing shows that in the presence of a
39 isparities between donors of used and unused pancreases, except age (median, 31 vs. 42 years).
40                             Jarid2-deficient pancreases exhibit impaired deposition of RNAPII-Ser5P,
41 pectively analyzed 376 islet isolations from pancreases flushed and transported with IGL-1 (n=95), UW
42                     Transplantation of fetal pancreases (FPs) may constitute an attractive alternativ
43                    Postmortem examination of pancreases from 68 Medalists showed that all had scatter
44                       Postmortem analysis of pancreases from 68 Medalists was performed.
45 ked for female islet beta cells in four male pancreases from autopsies, one from a T1D patient, emplo
46                                              Pancreases from both overweight (BMI > or = 26 but <30)
47 atory death (DCD) (Maastricht III & IV), and pancreases from brainstem deceased donors (DBD).
48 PTP1B and TCPTP expression was determined in pancreases from chow and high fat fed mice and the impac
49                          Livers, hearts, and pancreases from donors who die following ligature asphyx
50 brain stem death and DCD hearts, livers, and pancreases from donors who died following ligature asphy
51  in recipients of lungs, hearts, livers' and pancreases from donors who died following ligature asphy
52  a subset of these fatty acids was tested in pancreases from fed animals, the same rank order of effe
53                    Postmortem examination of pancreases from nine Medalists showed that all had insul
54 bserved in the kinetics of CVB4 clearance in pancreases from NOD, NOD IL-4-/-, and NOD IFN-gamma-/- m
55 ber of islet transplants, the suitability of pancreases from organ donors considered inappropriate fo
56 ence among transplant surgeons to transplant pancreases from small pediatric donors despite the optim
57  isolation of younger and fibrotic pediatric pancreases, gave increased islet yield with improved pat
58  graft function; all transplanted livers and pancreases had primary function.
59  vascular reconstruction of 65 kidneys and 5 pancreases, in 69 recipients.
60 tal system that is found in adult vertebrate pancreases, including the frog.
61 ing analyses in hereditary and idiopathic CP pancreases indicate differences in innate and adaptive i
62                               We divided the pancreases into two groups by donor body mass index (BMI
63 suring sufficient islet yield from preserved pancreases is a critical step in clinical islet transpla
64                 Enzymatic digestion of donor pancreases is a vital step in human and large mammalian
65 ucose metabolism in islets isolated from the pancreases of children with KATPHI who required pancreat
66 volved, as human amylin forms amyloid in the pancreases of diabetic patients, and oligomers have been
67 ntly larger beta-cell areas were observed in pancreases of fetuses and neonates from prepregnant HF-f
68                                              Pancreases of FTY720-treated diabetes-free mice showed p
69 mers form in the islets of Langerhans in the pancreases of many mammals.
70 h2 (or T cytolytic 2) cells are found in the pancreases of mice developing autoimmune diabetes.
71 increased, and TCPTP expression decreased in pancreases of mice fed a high fat diet, as well as in MI
72 l three virus doses, but day 3 titers in the pancreases of mice inoculated with 10(4) PFU were reduce
73 ormed on cDNAs from isolated islets or whole pancreases of NOD/Lt females 4 weeks after intrathymic i
74                                 Cells in the pancreases of nondiabetic mice treated with anti-IFN-gam
75 ncy of B:9-23-reactive CD4(+) T cells in the pancreases of prediabetic NOD mice.
76      Islet inflammation was 65% lower in the pancreases of rIFN-alpha mice.
77                        The islet area in the pancreases of the FTY720-treated db/db mice was more tha
78                   Islets were harvested from pancreases of those patients at our current good manufac
79                                          The pancreases of transduodenal sphincteroplasty/no prior su
80                        The results show that pancreases of transgenic mice expressing T1-127 and smal
81 l promoter with high-level penetrance in the pancreases of transgenic mice.
82                                     Exocrine pancreases of transgenic tadpoles expressing a dominant
83                              The majority of pancreases, offered in allocation, are discarded.
84 om pancreatitis (P<0.003) and deceased donor pancreases (P<0.001) than other standard ECs.
85 nt at cell membranes in homozygous p120(f/f) pancreases, potentially providing stability for maintena
86 ld improve islet yield and function from rat pancreases preserved for 6 and 24 hr.
87 port ex vivo normothermic perfusion of human pancreases procured but declined for transplantation, wi
88                      A significant number of pancreases procured for transplantation are deemed unsui
89 lying pathology in human as well as rat LADA pancreases provided identical results, allowing the conc
90 on of transplanted organs was less than 10%; pancreases refused due to "trauma", "age", or "resuscita
91                                        Among pancreases refused for "diabetes" or "malignancy" at lea
92 ment into the liver, with two to three donor pancreases required per recipient.
93 mmunofluorescent staining of fetal and adult pancreases revealed colocalization of GAD65 with alpha-
94                          The loss of several pancreases seems avoidable.
95                           Human and rat LADA pancreases showed differences in areas of the pancreas w
96  study, we examined 10 human cadaveric donor pancreases (tail and body regions) via integration of st
97 -dose RCEM was efficient in digesting entire pancreases to obtain higher yield (5535 +/- 830 and 2582
98 d by amylase, and exocrine function of human pancreases using EVNP and demonstrates the feasibility o
99 h purities of more than 50% (37.3% [19 of 51 pancreases] vs. 15.9% [10 of 63]; P=0.009).
100                      Islets in human and rat pancreases were analyzed by immunohistochemistry for imm
101                          Five declined human pancreases were assessed using this technique after a me
102                                              Pancreases were classified into five groups: fresh (grou
103                               Six additional pancreases were excised and transplanted separately.
104                      At 25 weeks of age, rat pancreases were harvested for histologic assessment.
105 hemia time, digestion time, or weight of the pancreases were observed between the two groups.
106 eases were transplanted; among these, 62% of pancreases were of potentially high quality (favorable d
107                                              Pancreases were placed in the two-layer method in 10 cas
108 ompared between two purification methods; 32 pancreases were processed by conventional Biocoll purifi
109                           Thirty-two porcine pancreases were procured in a controlled donation after
110 atic islets when sections from rat and mouse pancreases were reacted with a polyclonal antibody to re
111                              METHODS.: Human pancreases were retrieved from multiorgan donors with ap
112                                  Human adult pancreases were retrieved from older (mean age 55.7+/-3.
113 earts, 4 lungs, 21 livers, 28 kidneys, and 5 pancreases were successfully transplanted.
114              Thirty-seven percent of offered pancreases were transplanted; among these, 62% of pancre
115 ta-cells appeared histologically normal, the pancreases were unresponsive to perfusion with stimulato
116 ch as nitrite, are generated in precancerous pancreases, which induce massive DNA damage, including D
117 r islet yield from deceased and pancreatitis pancreases while retaining islet quality and function.
118       Human islet isolation from young donor pancreases (YDP) utilizing the current purified standard

 
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