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1 tivity display decreased insulin content and impaired insulin secretion.
2 sregulated cytosolic zinc homeostasis led to impaired insulin secretion.
3 permanent reduction in islet vascularity and impaired insulin secretion.
4 s ubiquitination and degradation and thus in impaired insulin secretion.
5  from Isl-1(L/L); Pdx1-CreER(Tm) mice showed impaired insulin secretion.
6 tance, indicating a plausible effect through impaired insulin secretion.
7  cassette (ABC) transporter ABCA1 results in impaired insulin secretion.
8 (Glp1r-/-) mice become hyperglycaemic due to impaired insulin secretion.
9  and apoptosis, decreased proliferation, and impaired insulin secretion.
10 ulated to be one of the main contributors to impaired insulin secretion.
11 ochondrial proteins, reduced respiration and impaired insulin secretion.
12 e strains developed glucose intolerance with impaired insulin secretion.
13 age 39 years and in two adult offspring with impaired insulin secretion.
14 xpression as well as reduced cAMP levels and impaired insulin secretion.
15 xpression and pancreatic insulin content and impaired insulin secretion.
16        Mitochondrial dysfunction resulted in impaired insulin secretion.
17 tes, are glucose intolerant, possibly due to impaired insulin secretion.
18 ell mass, increased beta-cell apoptosis, and impaired insulin secretion.
19 resentation of the specific peptide, or have impaired insulin secretion.
20 slet amyloid and leads to beta-cell loss and impaired insulin secretion.
21  levels leads to both insulin resistance and impaired insulin secretion.
22 s of the young [MODY]-3) is characterized by impaired insulin secretion.
23 hich results in reduced ADCY5 expression and impaired insulin secretion.
24          Type 2 diabetes is characterized by impaired insulin secretion.
25 ssociated with selective beta-cell death and impaired insulin secretion.
26 es is characterized by hyperglycaemia due to impaired insulin secretion and aberrant glucagon secreti
27 R-7a in beta cells developed diabetes due to impaired insulin secretion and beta cell dedifferentiati
28 e, early-onset hyperglycemia associated with impaired insulin secretion and beta-cell death.
29 ucible ablation of LDB1 in mature beta cells impaired insulin secretion and glucose homeostasis.
30 renergic receptor (beta(2)AR) in age-related impaired insulin secretion and glucose homeostasis.
31 ing one or both HNF-3alpha alleles also show impaired insulin secretion and glucose intolerance after
32 t had increased body weight and fat mass and impaired insulin secretion and glucose regulation compar
33 -type (beta(2)AR(+/+)) littermates developed impaired insulin secretion and glucose tolerance.
34 tire Nnt gene in C57BL/6J mice rescues their impaired insulin secretion and glucose-intolerant phenot
35 locus for fasting insulin levels, acting via impaired insulin secretion and increased islet disruptio
36          At presentation, they have markedly impaired insulin secretion and insulin action, but inten
37 n receptor provides a potential link between impaired insulin secretion and insulin resistance.
38 t mice exhibited abnormal glucose tolerance, impaired insulin secretion, and changes in islet gene ex
39 ession of human IAPP causes beta-cell death, impaired insulin secretion, and diabetes mellitus.
40  mass, decreased pancreatic insulin content, impaired insulin secretion, and exacerbated glucose into
41 Asna1(beta-/-) mice develop hypoinsulinemia, impaired insulin secretion, and glucose intolerance that
42 s (T2D) is hallmarked by insulin resistance, impaired insulin secretion, and increased hepatic glucos
43                                              Impaired insulin secretion assessed by this index predic
44 0(-/-) mice exhibited increased weight gain, impaired insulin secretion, augmented accumulation of in
45                     Loss of ABCG1 expression impaired insulin secretion both in vivo and in vitro, bu
46  2, the blockade of GLP-1 action resulted in impaired insulin secretion but limited deterioration of
47 played a pathological glucose tolerance with impaired insulin secretion but normal peripheral insulin
48                                              Impaired insulin secretion, but not insulin resistance,
49 ) is characterized by insulin resistance and impaired insulin secretion, but the mechanisms underlyin
50  with NIDDM and 2) did not contribute to the impaired insulin secretion characteristic of NIDDM in Ca
51 -cell mass, decreased glucose tolerance, and impaired insulin secretion compared with WT mice 28 days
52                             This resulted in impaired insulin secretion, decreased beta-cell mass, an
53  macroencapsulated islets have significantly impaired insulin secretion despite achieving normal fed
54                          Tcf7(-/-) mice show impaired insulin secretion, deterioration of glucose tol
55 on might, as in the mouse model, result from impaired insulin secretion due a failure of insulin cont
56 lopment of peripheral insulin resistance and impaired insulin secretion due to pancreatic beta-cell f
57 ral role for the channel might contribute to impaired insulin secretion in diabetes.
58    Increased dietary fat was associated with impaired insulin secretion in hIAPP transgenic (P = 0.05
59              Both doses of BPA significantly impaired insulin secretion in male but not female F1 and
60 mber of risk alleles and type 2 diabetes and impaired insulin secretion in normoglycemic subjects (P
61 n in clonal MIN6 and INS1(832/13) beta-cells impaired insulin secretion in response to glucose plus f
62    This form of diabetes is characterized by impaired insulin secretion in response to glucose, but w
63 stingly, hepatic GK knock-out mice also have impaired insulin secretion in response to glucose.
64          Type 2 diabetes is characterized by impaired insulin secretion in response to increased meta
65 levated glucose levels may contribute to the impaired insulin secretion in severe type II diabetes me
66 h increased mortality, but the mechanisms of impaired insulin secretion in this disease remain unclea
67  affirmed, leading to a novel hypothesis for impaired insulin secretion in type 2 diabetes and follow
68                 The 1339A mice have markedly impaired insulin secretion in vivo and disrupted islet m
69 ion of beta-cell cholesterol homeostasis and impaired insulin secretion increase adiposity, reduce sk
70                                              Impaired insulin secretion is a characteristic of non-in
71 ough the physiological explanation as to why impaired insulin secretion is not accompanied by elevate
72 annels by oleoyl-CoA might contribute to the impaired insulin secretion observed in non-insulin-depen
73          Notably, pyruvate fully rescues the impaired insulin secretion of fission-deficient beta-cel
74 ns in this gene that might contribute to the impaired insulin secretion of NIDDM.
75      Hyperglycemia and/or insulin resistance impaired insulin secretion only from human islets in viv
76  of its overexpression elsewhere, results in impaired insulin secretion, reduced beta cell number and
77 iabetes, but also the insulin resistance and impaired insulin secretion seen in type 2 diabetes.
78                             This resulted in impaired insulin secretion, thereby connecting different
79 eveloped glucose intolerance attributable to impaired insulin secretion, together with reduced alpha-
80 y the biochemical mechanisms responsible for impaired insulin secretion, we used (31)P NMR measured m
81 n elderly men than elderly women, indicating impaired insulin secretion, whereas disposition indexes
82        Islets from donors with T2D exhibited impaired insulin secretion, which was more pronounced in
83 e beta cell-intrinsic NIK activation present impaired insulin secretion with DIO.
84           FAK-deficient beta-cells exhibited impaired insulin secretion with normal glucose sensing a

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