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1 1000 cDNA libraries, each from an individual pancreatic islet cell.
2 owed that this protein is expressed in human pancreatic islet cells.
3  apparatus which directs STF-1 expression to pancreatic islet cells.
4 ly different experiments and five studies of pancreatic islet cells.
5 regulated by enhancers that operate in human pancreatic islet cells.
6 ar contexts, including hormone production in pancreatic islet cells.
7 hondrial interaction leading to apoptosis in pancreatic islet cells.
8  platform for RNA sequencing of single mouse pancreatic islet cells.
9 rly endoderm stage cells (CXCR4+ cells), and pancreatic islet cells.
10 Here we explored whether Hes3 also regulates pancreatic islet cells.
11 of adenovirus as a gene delivery vehicle for pancreatic islet cells.
12 regulatory models for the differentiation of pancreatic islet cells.
13  CD40L-induced upregulation of CD40 in human pancreatic islet cells.
14 tocin injection were transplanted with human pancreatic islet cells.
15 d mechanisms that stimulate proliferation of pancreatic islet cells.
16 which is required for the differentiation of pancreatic islet cells.
17 ed insulin action and abnormalities in their pancreatic islet cells.
18 ic acid (GABA) is stored in microvesicles in pancreatic islet cells.
19  by mammalian promoters into human and mouse pancreatic islet cells.
20 , no aP2 expression was detected in isolated pancreatic islet cells.
21 y was predominantly detected in pancreas and pancreatic islet cells.
22  demonstrates the presence of Kv1.7 in mouse pancreatic islet cells.
23 driver gene mutations, including significant pancreatic islet cell adaptation in obesity-associated t
24        This postulate was tested in a murine pancreatic islet cell allograft model in which a novel m
25 ed in significantly longer survival of DBA/2 pancreatic islet cell allografts in the B6AFl recipient
26 ue sites throughout the rat genome in normal pancreatic islet cells, allowing us to identify the chan
27 re expressed selectively in beta cell lines, pancreatic islet cells and brain.
28                                              Pancreatic islet cells and neurons share common function
29 tion of whole organs or free tissues such as pancreatic islet cells and should facilitate studies of
30 man HIP cells into endocrinologically active pancreatic islet cells and showed that they survived in
31 endent protein kinase (PKR) are expressed by pancreatic islet cells and that IFNs (IFN-alpha and IFN-
32    There is a reciprocal interaction between pancreatic islet cells and vascular endothelial cells (E
33 ncer subtyping, (ii) single-cell genomics of pancreatic islet cells, and (iii) metaanalysis of lung a
34 eavours that focus on the differentiation of pancreatic islet cells, and their applications in regene
35 matopoietic and parenchymal cells, including pancreatic islet cells; and PD-L2, which is restricted t
36 isease mediated by T lymphocytes recognizing pancreatic islet cell antigens.
37  receptors, expressed on enteroendocrine and pancreatic islet cells, augments glucagon counterregulat
38 tly directing differentiation toward desired pancreatic islet cells, but cellular phenotypes in termi
39 n-coupled receptors (GPCRs) are expressed in pancreatic islet cells, but the majority have unknown fu
40 of insulin receptor mRNA was examined in rat pancreatic islet cells by single-cell reverse transcript
41 inium chelates (GG) were coencapsulated with pancreatic islet cells by using protamine sulfate as a c
42 tively, these data indicate that adult human pancreatic islet cells can be expanded by three serial p
43               In a transgenic mouse model of pancreatic islet cell carcinogenesis (RIP1-Tag2), an ang
44 hepsins are up-regulated in a mouse model of pancreatic islet cell carcinogenesis (RIP1-Tag2), and tu
45  By using a mouse model of multistage murine pancreatic islet cell carcinogenesis in which cysteine c
46 with ovarian cancer (5.0 mg/kg) and one with pancreatic islet cell carcinoma (15.0 mg/kg), achieved a
47              These mice reproducibly develop pancreatic islet cell carcinoma and squamous cell carcin
48 g transgenic model of angiogenesis-dependent pancreatic islet cell carcinoma and the 4T1 model of met
49 ns in genetically engineered mouse models of pancreatic islet cell carcinoma, in which oncogenic tran
50 pression and glycogenolysis that result from pancreatic islet cell defects.
51                                              Pancreatic islet cells derived from human pluripotent st
52                 It is currently thought that pancreatic islet cells develop from undifferentiated pro
53  probed the role of activin signaling during pancreatic islet cell development and regeneration.
54                                              Pancreatic islet cell development is regulated by transc
55 n factors in the gene network that regulates pancreatic islet cell development.
56 sional islet cell-like clusters that express pancreatic islet cell differentiation-related transcript
57                              Thus, mammalian pancreatic islet cells display cell-type-specific epigen
58  As early as 7 days following Men1 excision, pancreatic islet cells display increased proliferation,
59 2 diabetes (T2D) exert their effects through pancreatic islet-cell dysfunction, we performed a genome
60 that Nkx2.2 and NeuroD1 interact to regulate pancreatic islet cell fates, and this epistatic relation
61 ular regulatory program to correctly specify pancreatic islet cell fates.
62 proach may provide a potential new source of pancreatic islet cells for transplantation.
63 s using streptozotocin (STZ)-treated primary pancreatic islet cells from ICR mice to unravel the prot
64                                   Allogeneic pancreatic islet cells from unrelated donors were subseq
65 glucagon secretion resulting from changes in pancreatic islet cell function and/or mass.
66                       TSPAN-7 is enriched in pancreatic islet cells; however, the function of islet T
67                       We found a decrease in pancreatic islet cell hyperplasia, fat accumulation in t
68 expressing the PEPCK-TAg transgene developed pancreatic islet cell hyperplasias and carcinomas, with
69  Immunocytochemistry revealed that, although pancreatic islet cells in the STZ-treated rats were spar
70 (-/-) background into mice expressing OVA in pancreatic islet cells induces acute insulitis and diabe
71 ed EPCs could play a role in the response to pancreatic islet cell injury.
72                                          The pancreatic islet cells invariably stained for growth hor
73 f human islet amyloid polypeptide (hIAPP) in pancreatic islet cells is implicated in the pathogenesis
74 ose levels, insulin sensitivity and restored pancreatic islet cell mass, neuronal innervation and mic
75  cytoprotective, or antiapoptotic genes into pancreatic islet cells may allow enhanced posttransplant
76 -phosphatase almost exclusively expressed in pancreatic islet cells, may underlie variation in fastin
77 PGE2 We tested the hypothesis that enriching pancreatic islet cell membranes with EPA, thereby reduci
78 associated with loss of tolerance to several pancreatic islet cell molecules, including insulin, glut
79    In the exercising MC4R knockout mice, the pancreatic islet cell morphology and other physiological
80 ge experimental differences, five studies of pancreatic islet cells, mouse embryogenesis datasets and
81 Rabbits were treated with alloxan to destroy pancreatic islet cells, or mock-treated with vehicle, an
82  1 x 10(-4)), 67 SNPs for type 2 diabetes in pancreatic islet cells (P = 0.003) and the liver (P = 0.
83                             Organ growth and pancreatic islet cell proliferation and mass were examin
84 med at evaluating the effect of rapamycin on pancreatic islet cell proliferation in vivo.
85 nd whether mutation of Men1 acutely promotes pancreatic islet cell proliferation in vivo.
86 s to the full spectrum of fractionated human pancreatic islet cell proteins to determine whether nume
87                                              Pancreatic islet cells provide the major source of count
88 pite their origins in different germ layers, pancreatic islet cells share many common developmental f
89 rotein Nkx2.2 (Nkx2-2) is a key regulator of pancreatic islet cell specification in mice; Nkx2.2 is e
90 ontaining transcription factor essential for pancreatic islet cell specification.
91                 Applying the method to mouse pancreatic islet-cell subsets, we detected both expected
92 osely related cell types (for example, other pancreatic islet cells such as alpha-cells, or other cel
93 icates that the plasticity of differentiated pancreatic islet cells, suggested by earlier static and
94 tion and characterization of a cDNA from rat pancreatic islet cells that encodes a new related kinase
95         This is particularly problematic for pancreatic islet cells that have high O(2) requirements.
96 d applicability to sophisticated analyses of pancreatic islet cells that reveal new biological insigh
97  bioscaffold for delivery of donor syngeneic pancreatic islet cells to reverse hyperglycemia in murin
98 mising treatment option for type 1 diabetes, pancreatic islet cell transformation has been hindered b
99  Drug Administration (FDA) recently endorsed pancreatic islet cell transplantation (ICT) therapy for
100                         The optimal site for pancreatic islet cell transplantation is presently uncle
101 er SOCS proteins can prevent the destruction pancreatic islet cells transplanted beneath the kidney c
102       We also show that for encapsulated rat pancreatic islet cells transplanted into streptozotocin-
103 ession in the RIP1-Tag2 (RT2) mouse model of pancreatic islet cell tumorigenesis.
104 evelopment of renal cell carcinoma (RCC) and pancreatic islet cell tumors (PICT).
105 s after initial screening, she developed two pancreatic islet cell tumors and a premalignant renal cy
106 e reviews the current clinical management of pancreatic islet cell tumors and describes the molecular
107 ly history that describes the development of pancreatic islet cell tumors in four of five female sibl
108 rmore, we conclude that the preponderance of pancreatic islet cell tumors in this family cannot be ex
109 ma are common lesions; pheochromocytomas and pancreatic islet cell tumors occur less frequently but a
110                 Angiogenesis was examined in pancreatic islet cell tumors of RIP-Tag2 transgenic mice
111 e molecular events underlying the biology of pancreatic islet cell tumors will aid the development of
112 e endocrine pancreas, commonly referenced as pancreatic islet cell tumors, are rare, often well diffe
113  VHL gene in the four affected siblings with pancreatic islet cell tumors.
114 cts of RCA I on blood vessels of spontaneous pancreatic islet-cell tumors in RIP-Tag2 transgenic mice
115  (Ppy)-expressing y-cells, one of the rarest pancreatic islet cell-type, remains elusive.
116  the Pax6 gene in mice leads to loss of most pancreatic islet cell types, the functional consequences
117  for the development of beta-cells and other pancreatic islet cell types, we considered it a candidat
118 roD1 are vital for proper differentiation of pancreatic islet cell types.
119                  Juan-Mateu et al. find that pancreatic islet cells utilize a regulatory program, ori
120 e enhancer which directs STF-1 expression to pancreatic islet cells via two functional elements that
121 cose and gut hormones during feeding promote pancreatic islet cell viability in part via the calcium-
122 rmeability coefficient of the golden hamster pancreatic islet cells was determined to be 0.27 microns
123 r permeability coefficient of golden hamster pancreatic islet cells were determined.
124         To validate the approach, single rat pancreatic islet cells were rapidly analyzed with optica
125 ltage-gated potassium (Kv) currents of human pancreatic islet cells were studied by whole-cell patch
126 at amphioxus may have homologs of vertebrate pancreatic islet cells, which express neurogenin3.
127  RIP-mOVA mice expressing chicken OVA in the pancreatic islet cells, which received naive OVA-specifi
128 effectively transduces both human and murine pancreatic islet cells with reporter genes as well as po

 
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