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1 ts using CMRL 1066 medium (used for clinical islet transplantation).
2 undergoing total pancreatectomy (autologous islet transplantation).
3 tained normoglycemia for up to 60 days after islet transplantation.
4 tion of therapeutic interventions, including islet transplantation.
5 ft function still remains inconsistent after islet transplantation.
6 as a new approach to improve the outcomes of islet transplantation.
7 rix components present in pancreas, prior to islet transplantation.
8 rapies, as adjuncts for immunosuppression in islet transplantation.
9 for insulin independence after single-donor islet transplantation.
10 for patients with type 1 diabetes undergoing islet transplantation.
11 DSCs as a novel adjunctive immunotherapy for islet transplantation.
12 three patients immediately after intraportal islet transplantation.
13 ight, and fasting blood glucose levels after islet transplantation.
14 tolerance induction for clinical xenogeneic islet transplantation.
15 hat GABA might find applications in clinical islet transplantation.
16 (de novo expression or titer increase) after islet transplantation.
17 Rs may be a useful adjunct therapy for human islet transplantation.
18 t rejection is one of the main obstacles for islet transplantation.
19 ulin-dependent) diabetes mellitus, including islet transplantation.
20 justify early clinical trials of IDN6556 in islet transplantation.
21 rategy is likely to improve outcome in human islet transplantation.
22 n of a macrochamber specially engineered for islet transplantation.
23 their depletion can thus be advantageous for islet transplantation.
24 nd protein expression levels increased after islet transplantation.
25 fect of B-cell depletion in murine models of islet transplantation.
26 beneficial as an alternative to intrahepatic islet transplantation.
27 i-islet immune response in various models of islet transplantation.
28 ly aid in increasing the success of clinical islet transplantation.
29 in early islet graft loss after intraportal islet transplantation.
30 n vivo in allogenic and autoimmune models of islet transplantation.
31 ytotoxicity, but not splenic NK cells, after islet transplantation.
32 pendence in type 1 diabetic recipients after islet transplantation.
33 RL) has beneficial effects on beta cells for islet transplantation.
34 ation and beta-cell death by apoptosis after islet transplantation.
35 status affect the choice between pancreas or islet transplantation.
36 tation with islet grafts in a mouse model of islet transplantation.
37 ts instead of culturing for current clinical islet transplantation.
38 its potential use in the context of clinical islet transplantation.
39 ow use this purification method for clinical islet transplantation.
40 te (GFR) have been observed after successful islet transplantation.
41 might be an alternative site for pancreatic islet transplantation.
42 unction with low dose tacrolimus, in current islet transplantation.
43 ur way to clinical use of in vivo imaging of islet transplantation.
44 ing of LMW-DS for the prevention of IBMIR in islet transplantation.
45 the outcome of diabetic patients undergoing islet transplantation.
46 contribution by the European Consortium for Islet Transplantation.
47 lity, negatively affecting outcomes of human islet transplantation.
48 ch to successfully establishing subcutaneous islet transplantation.
49 ntly used immune suppression (IS) regimen in islet transplantation.
50 erred with severe hypoglycemia, suitable for islet transplantation.
51 its importance in clinical settings such as islet transplantation.
52 viable islet mass after clinical intraportal islet transplantation.
53 is currently incompatible with intrahepatic islet transplantation.
54 lear cell co-cultured exosomes for improving islet transplantation.
55 tuate disease and are rapidly reactivated by islet transplantation.
56 beta cell dysfunction in type 2 diabetes and islet transplantation.
57 unction, both of which hinder the success of islet transplantation.
60 s revealed US $57,525 of additional cost for islet transplantation 5 years after transplantation.
61 1 diabetes receiving an intra-BM allogeneic islet transplantation: a feasibility study in patients w
62 ise for overcoming two major issues in human islet transplantation: (a) poor yield of islets from don
65 istry reports have suggested that results of islet transplantation alone in this indication may be ab
67 in our program where nine patients underwent islet transplantation alone treated with Edmonton immuno
69 centrations were monitored for 30 days after islet transplantation and animals were then subjected to
70 with type 1 diabetes who received pancreatic islet transplantation and anti-CD25 mAb as induction the
71 use of rapamycin as an immunosuppressant in islet transplantation and as a second-line agent in othe
73 improving beta-cell survival following human islet transplantation and increasing beta-cells in patie
75 mulates specifically in the beta-cells after islet transplantation and is a promising tracer for noni
76 e results and could be performed both before islet transplantation and on preserved cell blocks at an
77 potential to improve graft survival in human islet transplantation and other cellular therapies on th
78 sulin production in both type 2 diabetes and islet transplantation and point to the potential for the
79 ed macaques underwent intraportal allogeneic islet transplantation and received basiliximab and sirol
80 at the adrenal may be an attractive site for islet transplantation and that GHRH analogs might allow
81 mycin could negatively impact the success of islet transplantation and the adaptation of beta-cells t
82 ediated attack is a substantial challenge in islet transplantation and this will extend to applicatio
84 Ig)-like transcript (ILT) 3-Fc in pancreatic islet transplantation and to determine its mechanism of
85 study aimed to evaluate long-term effects of islet transplantation and to outline possible influentia
88 ost active region in the field of pancreatic islet transplantation, and many of the leading groups ar
89 moglycemia in diabetic mice after pancreatic islet transplantation, and results in reduced tumor volu
91 eversal of liver ischemia due to intraportal islet transplantation are detectable using T2-weighted M
96 aft survival limits the long-term success of islet transplantation as a potential curative therapy fo
99 from patients with autologous and allogeneic islet transplantation as well as total pancreatectomy al
103 biomarker to detect graft damage in clinical islet transplantation because serum C-peptide and proins
106 roves islet graft survival after intraportal islet transplantation by mitigation of coagulation in IB
107 e results provide evidence that intrahepatic islet transplantation can restore glucose counterregulat
110 onal Institutes of Health-sponsored Clinical Islet Transplantation (CIT) Consortium jointly developed
115 bjects with severe hypoglycemia suitable for islet transplantation, CSII decreased hypoglycemia frequ
117 Subcutaneous tissue is a promising site for islet transplantation, due to its large area and accessi
118 is the current site of choice for pancreatic islet transplantation, even though it is far from being
121 enchymal stem cells for tissue regeneration, islet transplantation for diabetes treatment, and T cell
124 ucted in 35 subjects submitted to pancreatic islet transplantation for treatment of unstable type 1 d
127 cells within islets results in diabetes, and islet transplantation from cadaveric donors can cure the
129 e of the recipient of an intra-BM allogeneic islet transplantation had a primary nonfunction, as show
133 his article, we address the question whether islet transplantation has indeed bridged the gap with wh
142 omposite measure of beta cell function after islet transplantation, has limited sensitivity because o
146 study was to determine whether intrahepatic islet transplantation improves endogenous glucose produc
148 e report that the efficiency of subcutaneous islet transplantation in a Lewis rat model is significan
149 nvestigate tolerance induction protocols for islet transplantation in a setting of autoimmunity.
150 ent of glycemic control following pancreatic islet transplantation in animal models is discussed.
155 nd monitors comprehensive data on allogeneic islet transplantation in North America, Europe, and Aust
156 the metabolic outcomes and graft survival of islet transplantation in our program where nine patients
160 have concentrated their efforts on improving islet transplantation, in particular by fabricating bioa
161 autoimmune setting, such as with pancreas or islet transplantation into a type 1 diabetic individual,
165 -producing beta cells in type 1 diabetes and islet transplantation involves a variety of immune pathw
177 pancreatic beta-cells through deceased donor islet transplantation is a proven therapy for preventing
180 ulin delivery are inadequate, and allogeneic islet transplantation is a safe alternative for those pa
182 reatment of patients with type 1 diabetes by islet transplantation is affected by a multitude of fact
193 rease of MMP-9 expression and activity after islet transplantation is directly related to enhanced le
200 nsulin resistance, and their avoidance after islet transplantation is preferred from a metabolic stan
205 l state of type-1 diabetes as well as during islet transplantation.Islet transplantation is considere
206 h the liver is the primary site for clinical islet transplantation, it poses several restrictions, es
207 onal status and behavior are associated with islet transplantation (ITx) and to assess their possible
208 , synergistically enhance angiogenesis after islet transplantation leading to stable engraftment.
209 oidance of steroids; however, the outcome of islet transplantation may differ in kidney transplant re
210 with insulin independence after single-donor islet transplantation may help to select recipient-donor
212 tched, nonlymphopenic, immunocompetent mouse islet transplantation model, alloTregs but not nTregs pr
213 ransplantation has already been proven in an islet transplantation model, skin graft survival could n
220 slets at 4 degrees C improves the outcome of islet transplantation more efficiently than preservation
222 Because of the lack of tissue available for islet transplantation, new sources of beta-cells have be
227 ry confirm the inarguably positive impact of islet transplantation on metabolic control in T1 diabete
229 ted with type 1 diabetes mellitus (allogenic islet transplantation), or the prevention of surgical di
230 ing SI_INS mRNA and SI_16h insulin predicted islet transplantation outcome in nonobese diabetic (NOD)
231 nors (H-2(d)) to assess alloimmunization and islet transplantation outcomes in Akita recipients.
243 type 1 diabetic recipients after intraportal islet transplantation raises a question about the suitab
245 primary efficacy and the safety outcomes of islet transplantation reported to the NIDDK and JDRF fun
247 ycemic variability compared with MDI whereas islet transplantation resolved hypoglycemia and further
248 intained for many years following successful islet transplantation, restoration of normal functional
251 adverse events in Trials of Adult Pancreatic Islet Transplantation." RESULTS: There were no deaths or
252 cemia alone, coadministration of leptin with islet transplantation robustly improved control of gluco
255 ortal system may not be the optimal site for islet transplantation, several extrahepatic sites have b
256 tabolic outcomes of autologous and allogenic islet transplantation, shedding close light on our own l
257 ng during radiologic or surgical intraportal islet transplantation significantly impair primary graft
258 s a suitable polymer to create an artificial islet transplantation site under the skin and supports i
263 Muscle is a promising alternative site for islet transplantation that facilitates rapid restoration
264 is preclinical in vivo large animal model of islet transplantation, the effect of triple-drug immunos
265 ro and in vivo in syngeneic murine models of islet transplantation, the function of conformally coate
269 reated 4 weeks before diabetes induction and islet transplantation through the transient placement of
270 s are lost in the early phase after clinical islet transplantation, through apoptosis, necrosis, or i
271 r immunosuppression limit the indication for islet transplantation to a small group of patients.
272 sirolimus+tacrolimus regimen 6 months before islet transplantation to exclude negative effects on kid
273 ous subcutaneous insulin infusion (CSII) and islet transplantation to reduce hypoglycemia and glycemi
275 Here, we employ a sensitized murine model of islet transplantation to test strategies that promote lo
277 immunity were performed antemortem after her islet transplantations to test in vitro for evidence of
279 bolic effects of diabetes were eliminated by islet transplantation (transplanted knockout (TKO)).
280 tion may lead to an alternative approach for islet transplantation treatment for diabetic patients.
281 active model for insulin supplementation and islet transplantation trials, and for studying developme
286 ation before and 6 months after intrahepatic islet transplantation using stepped hyperinsulinemic-hyp
290 Using polymer scaffolds as a platform for islet transplantation, we investigated the hypothesis th
291 h T1D and end-stage renal failure undergoing islet transplantation were compared to 70 patients match
293 ents reached normoglycemia after intraportal islet transplantation when they were treated with AAT co
294 unstable type 1 diabetes mellitus underwent islet transplantation with alemtuzumab induction and sir
297 study, using a murine model of subcutaneous islet transplantation with matrigel basement membrane ma
299 le investigational agent for use in clinical islet transplantation without relying upon CD154 blockad
300 lopment of a novel strategy for pig-to-human islet transplantation without side effects of systemic i