-
1
-
-
0033304603
-
The glucagon-like peptides
-
Kieffer T.J., and Habener J.F. The glucagon-like peptides. Endocr. Rev. 20 (1999) 876-913
-
(1999)
Endocr. Rev.
, vol.20
, pp. 876-913
-
-
Kieffer, T.J.1
Habener, J.F.2
-
4
-
-
67651173077
-
Incretin-based therapies for type 2 diabetes mellitus
-
Lovshin J.A., and Drucker D.J. Incretin-based therapies for type 2 diabetes mellitus. Nat. Rev. Endocrinol. 5 (2009) 262-269
-
(2009)
Nat. Rev. Endocrinol.
, vol.5
, pp. 262-269
-
-
Lovshin, J.A.1
Drucker, D.J.2
-
5
-
-
66749102158
-
Clinical review: The extrapancreatic effects of glucagon-like peptide-1 and related peptides
-
Abu-Hamdah R., et al. Clinical review: The extrapancreatic effects of glucagon-like peptide-1 and related peptides. J. Clin. Endocrinol Metab. 94 (2009) 1843-1852
-
(2009)
J. Clin. Endocrinol Metab.
, vol.94
, pp. 1843-1852
-
-
Abu-Hamdah, R.1
-
6
-
-
12244281855
-
Circulation and degradation of GIP and GLP-1
-
Deacon C.F. Circulation and degradation of GIP and GLP-1. Horm. Metab. Res. 36 (2004) 761-765
-
(2004)
Horm. Metab. Res.
, vol.36
, pp. 761-765
-
-
Deacon, C.F.1
-
7
-
-
24944436267
-
Neutral endopeptidase 24.11 and dipeptidyl peptidase IV are both mediators of the degradation of glucagon-like peptide 1 in the anaesthetised pig
-
Plamboeck A., et al. Neutral endopeptidase 24.11 and dipeptidyl peptidase IV are both mediators of the degradation of glucagon-like peptide 1 in the anaesthetised pig. Diabetologia. 48 (2005) 1882-1890
-
(2005)
Diabetologia.
, vol.48
, pp. 1882-1890
-
-
Plamboeck, A.1
-
8
-
-
33644618433
-
The biology of incretin hormones
-
Drucker D.J. The biology of incretin hormones. Cell Metab. 3 (2006) 153-165
-
(2006)
Cell Metab.
, vol.3
, pp. 153-165
-
-
Drucker, D.J.1
-
9
-
-
33846006173
-
The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes
-
Drucker D.J., and Nauck M.A. The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes. Lancet 368 (2006) 1696-1705
-
(2006)
Lancet
, vol.368
, pp. 1696-1705
-
-
Drucker, D.J.1
Nauck, M.A.2
-
10
-
-
0027473729
-
Pancreatic beta-cells are rendered glucose-competent by the insulinotropic hormone glucagon-like peptide-1(7-37)
-
Holz IV G.G., et al. Pancreatic beta-cells are rendered glucose-competent by the insulinotropic hormone glucagon-like peptide-1(7-37). Nature 361 (1993) 362-365
-
(1993)
Nature
, vol.361
, pp. 362-365
-
-
Holz IV, G.G.1
-
11
-
-
22044446844
-
A human glucagon-like peptide-1 receptor polymorphism results in reduced agonist responsiveness
-
Beinborn M., et al. A human glucagon-like peptide-1 receptor polymorphism results in reduced agonist responsiveness. Regul. Pept. 130 (2005) 1-6
-
(2005)
Regul. Pept.
, vol.130
, pp. 1-6
-
-
Beinborn, M.1
-
12
-
-
0028803336
-
Both subcutaneously and intravenously administered glucagon-like peptide I are rapidly degraded from the NH2-terminus in type II diabetic patients and in healthy subjects
-
Deacon C.F., et al. Both subcutaneously and intravenously administered glucagon-like peptide I are rapidly degraded from the NH2-terminus in type II diabetic patients and in healthy subjects. Diabetes 144 (1995) 1126-1131
-
(1995)
Diabetes
, vol.144
, pp. 1126-1131
-
-
Deacon, C.F.1
-
13
-
-
0033303516
-
Glucagon-like peptide-1-(7-36)amide is transformed to glucagon-like peptide-1-(9-36)amide by dipeptidyl peptidase IV in the capillaries supplying the L cells of the porcine intestine
-
Hansen L., et al. Glucagon-like peptide-1-(7-36)amide is transformed to glucagon-like peptide-1-(9-36)amide by dipeptidyl peptidase IV in the capillaries supplying the L cells of the porcine intestine. Endocrinology 140 (1999) 5356-5363
-
(1999)
Endocrinology
, vol.140
, pp. 5356-5363
-
-
Hansen, L.1
-
14
-
-
0027475050
-
Neutral endopeptidase 24.11: structure, inhibition, and experimental and clinical pharmacology
-
Roques B.P., et al. Neutral endopeptidase 24.11: structure, inhibition, and experimental and clinical pharmacology. Pharmacol. Rev. 45 (1993) 87-146
-
(1993)
Pharmacol. Rev.
, vol.45
, pp. 87-146
-
-
Roques, B.P.1
-
15
-
-
0029111540
-
Characterisation of the processing by human neutral endopeptidase 24.11 of GLP-1(7-36) amide and comparison of the substrate specificity of the enzyme for other glucagon-like peptides
-
Hupe-Sodmann K., et al. Characterisation of the processing by human neutral endopeptidase 24.11 of GLP-1(7-36) amide and comparison of the substrate specificity of the enzyme for other glucagon-like peptides. Regul. Pept. 58 (1995) 149-156
-
(1995)
Regul. Pept.
, vol.58
, pp. 149-156
-
-
Hupe-Sodmann, K.1
-
16
-
-
35348948499
-
Lack of hepatocellular CD10 along bile canaliculi is physiologic in early childhood and persistent in Alagille syndrome
-
Byrne J.A., et al. Lack of hepatocellular CD10 along bile canaliculi is physiologic in early childhood and persistent in Alagille syndrome. Lab. Invest. 87 (2007) 1138-1148
-
(2007)
Lab. Invest.
, vol.87
, pp. 1138-1148
-
-
Byrne, J.A.1
-
17
-
-
0036342717
-
Glucagon-like peptide-1 augments insulin-mediated glucose uptake in the obese state
-
Egan J.M., et al. Glucagon-like peptide-1 augments insulin-mediated glucose uptake in the obese state. J. Clin. Endocrinol. Metab. (2002) 3768-3773
-
(2002)
J. Clin. Endocrinol. Metab.
, pp. 3768-3773
-
-
Egan, J.M.1
-
18
-
-
0031756220
-
Insulinotropic hormone glucagon-like peptide-1-(7-37) appears not to augment insulin-mediated glucose uptake in young men during euglycemia
-
Ryan A.S., et al. Insulinotropic hormone glucagon-like peptide-1-(7-37) appears not to augment insulin-mediated glucose uptake in young men during euglycemia. J. Clin. Endocrinol. Metab. 83 (1998) 2399-2404
-
(1998)
J. Clin. Endocrinol. Metab.
, vol.83
, pp. 2399-2404
-
-
Ryan, A.S.1
-
19
-
-
34249741098
-
Glucagon-like peptide-1 gene therapy in obese diabetic mice results in long-term cure of diabetes by improving insulin sensitivity and reducing hepatic gluconeogenesis
-
Lee Y.S., et al. Glucagon-like peptide-1 gene therapy in obese diabetic mice results in long-term cure of diabetes by improving insulin sensitivity and reducing hepatic gluconeogenesis. Diabetes 56 (2007) 1671-1679
-
(2007)
Diabetes
, vol.56
, pp. 1671-1679
-
-
Lee, Y.S.1
-
20
-
-
33644803761
-
Exendin-4, a glucagon-like protein-1 (GLP-1) receptor agonist, reverses hepatic steatosis in ob/ob mice
-
Ding X., et al. Exendin-4, a glucagon-like protein-1 (GLP-1) receptor agonist, reverses hepatic steatosis in ob/ob mice. Hepatology 43 (2006) 173-181
-
(2006)
Hepatology
, vol.43
, pp. 173-181
-
-
Ding, X.1
-
21
-
-
54949146796
-
Gene therapy for diabetes: metabolic effects of helper-dependent adenoviral exendin 4 expression in a diet-induced obesity mouse model
-
Samson S.L., et al. Gene therapy for diabetes: metabolic effects of helper-dependent adenoviral exendin 4 expression in a diet-induced obesity mouse model. Mol. Ther. 16 (2008) 1805-1812
-
(2008)
Mol. Ther.
, vol.16
, pp. 1805-1812
-
-
Samson, S.L.1
-
22
-
-
0038445987
-
Cell signaling of the GLP-1 action in liver
-
Redondo A., et al. Cell signaling of the GLP-1 action in liver. Mol. Cell Endocrinol. 204 (2003) 43-50
-
(2003)
Mol. Cell Endocrinol.
, vol.204
, pp. 43-50
-
-
Redondo, A.1
-
23
-
-
28144441354
-
Active metabolite of GLP-1 mediates myocardial glucose uptake and improves left ventricular performance in conscious dogs with dilated cardiomyopathy
-
Nikolaidis L.A., et al. Active metabolite of GLP-1 mediates myocardial glucose uptake and improves left ventricular performance in conscious dogs with dilated cardiomyopathy. Am. J. Physiol. Heart Circ. Physiol. 289 (2005) H2401-H2408
-
(2005)
Am. J. Physiol. Heart Circ. Physiol.
, vol.289
-
-
Nikolaidis, L.A.1
-
24
-
-
43249089631
-
Cardioprotective and vasodilatory actions of glucagon-like peptide 1 receptor are mediated through both glucagon-like peptide 1 receptor-dependent and -independent pathways
-
Ban K., et al. Cardioprotective and vasodilatory actions of glucagon-like peptide 1 receptor are mediated through both glucagon-like peptide 1 receptor-dependent and -independent pathways. Circulation 117 (2008) 2340-2350
-
(2008)
Circulation
, vol.117
, pp. 2340-2350
-
-
Ban, K.1
-
25
-
-
69549089903
-
The cardioprotective and inotropic components of postconditioning effects of GLP-1 and GLP-1(9-36)a in an isolated rat heart
-
Ossum A., et al. The cardioprotective and inotropic components of postconditioning effects of GLP-1 and GLP-1(9-36)a in an isolated rat heart. Pharmacol. Res. 60 (2009) 411-417
-
(2009)
Pharmacol. Res.
, vol.60
, pp. 411-417
-
-
Ossum, A.1
-
26
-
-
38149083367
-
Protective effects of GLP-1 analogues exendin-4 and GLP-1(9-36) amide against ischemia-reperfusion injury in rat heart
-
Sonne D.P., et al. Protective effects of GLP-1 analogues exendin-4 and GLP-1(9-36) amide against ischemia-reperfusion injury in rat heart. Regul. Pept. 146 (2008) 243-249
-
(2008)
Regul. Pept.
, vol.146
, pp. 243-249
-
-
Sonne, D.P.1
-
27
-
-
33646369165
-
Cell-permeable, mitochondrial-targeted, peptide antioxidants
-
Szeto H. Cell-permeable, mitochondrial-targeted, peptide antioxidants. AAPS J. 21 (2006) E277-283
-
(2006)
AAPS J.
, vol.21
-
-
Szeto, H.1
-
28
-
-
0036073195
-
A highly potent peptide analgesic that protects against ischemia-reperfusion-induced myocardial stunning
-
Wu D., et al. A highly potent peptide analgesic that protects against ischemia-reperfusion-induced myocardial stunning. Am. J. Physiol. Heart Circ. Physiol. 283 (2002) H783-791
-
(2002)
Am. J. Physiol. Heart Circ. Physiol.
, vol.283
-
-
Wu, D.1
-
29
-
-
28944431505
-
A potent opiate agonist protects against myocardial stunning during myocardial ischemia and reperfusion in rats
-
Song W., et al. A potent opiate agonist protects against myocardial stunning during myocardial ischemia and reperfusion in rats. Coron. Artery Dis. 16 (2005) 407-410
-
(2005)
Coron. Artery Dis.
, vol.16
, pp. 407-410
-
-
Song, W.1
-
30
-
-
52049093652
-
GLP-1 and related peptides cause concentration-dependent relaxation of rat aorta through a pathway involving KATP and cAMP
-
Green B.D., et al. GLP-1 and related peptides cause concentration-dependent relaxation of rat aorta through a pathway involving KATP and cAMP. Arch. Biochem. Biophys. 478 (2008) 136-142
-
(2008)
Arch. Biochem. Biophys.
, vol.478
, pp. 136-142
-
-
Green, B.D.1
-
31
-
-
68349084564
-
Endothelial dysfunction induced by triglycerides is not restored by exenatide in rat conduit arteries ex vivo
-
Nathanson D., et al. Endothelial dysfunction induced by triglycerides is not restored by exenatide in rat conduit arteries ex vivo. Regul. Pept. 157 (2009) 8-13
-
(2009)
Regul. Pept.
, vol.157
, pp. 8-13
-
-
Nathanson, D.1
-
32
-
-
46249133023
-
Glucagon-like peptide-1 (9-36) amide, cleavage product of glucagon-like peptide-1 (7-36) is a glucoregulatory peptide
-
Elahi D., et al. Glucagon-like peptide-1 (9-36) amide, cleavage product of glucagon-like peptide-1 (7-36) is a glucoregulatory peptide. Obesity 16 (2008) 1501-1509
-
(2008)
Obesity
, vol.16
, pp. 1501-1509
-
-
Elahi, D.1
-
33
-
-
0038359686
-
Effects of GLP-1-(7-37), and GLP-1-(9-36)NH2 on intravenous glucose tolerance and glucose-induced insulin secretion in healthy humans
-
Vahl T.P., et al. Effects of GLP-1-(7-37), and GLP-1-(9-36)NH2 on intravenous glucose tolerance and glucose-induced insulin secretion in healthy humans. J. Clin. Endocrinol. Metab. 88 (2003) 1772-1779
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 1772-1779
-
-
Vahl, T.P.1
-
34
-
-
0032452225
-
Regulatory interactions between lipids and carbohydrates: the glucose fatty acid cycle after 35 years
-
Randle P.J. Regulatory interactions between lipids and carbohydrates: the glucose fatty acid cycle after 35 years. Diabetes Metab. Rev. 14 (1998) 263-283
-
(1998)
Diabetes Metab. Rev.
, vol.14
, pp. 263-283
-
-
Randle, P.J.1
-
35
-
-
34748898831
-
Glucagon-like peptide-1 (GLP-1) receptors expressed on nerve terminals in the portal vein mediate the effects of endogenous GLP-1 on glucose tolerance in rats
-
Vahl T.P., et al. Glucagon-like peptide-1 (GLP-1) receptors expressed on nerve terminals in the portal vein mediate the effects of endogenous GLP-1 on glucose tolerance in rats. Endocrinology 148 (2007) 4965-4973
-
(2007)
Endocrinology
, vol.148
, pp. 4965-4973
-
-
Vahl, T.P.1
-
36
-
-
52649164094
-
Exenatide can reduce glucose independent of islet hormones or gastric emptying
-
Inonut V., et al. Exenatide can reduce glucose independent of islet hormones or gastric emptying. Am. J. Physiol. Endocrinol. Metab. 295 (2008) E269-277
-
(2008)
Am. J. Physiol. Endocrinol. Metab.
, vol.295
-
-
Inonut, V.1
-
37
-
-
50949094723
-
Arcuate glucagon-line peptide 1 receptors regulate glucose homeostasis but not food intake
-
Sandoval D.A., et al. Arcuate glucagon-line peptide 1 receptors regulate glucose homeostasis but not food intake. Diabetes 57 (2008) 2046-2054
-
(2008)
Diabetes
, vol.57
, pp. 2046-2054
-
-
Sandoval, D.A.1
-
38
-
-
0034639946
-
The hepatic vagal reception of intraportal GLP-1 is via receptor different from the pancreatic GLP-1 receptor
-
Nishizawa M., et al. The hepatic vagal reception of intraportal GLP-1 is via receptor different from the pancreatic GLP-1 receptor. J. Auton. Nerv. Syst. 80 (2000) 14-21
-
(2000)
J. Auton. Nerv. Syst.
, vol.80
, pp. 14-21
-
-
Nishizawa, M.1
-
39
-
-
27444441940
-
Insulin secretion-independent effects of GLP-1 on canine liver glucose metabolism do not involve portal vein GLP-1 receptors
-
Dardevet D., et al. Insulin secretion-independent effects of GLP-1 on canine liver glucose metabolism do not involve portal vein GLP-1 receptors. Am. J. Physiol Gastrointest. Liver Physiol. 289 (2005) G806-814
-
(2005)
Am. J. Physiol Gastrointest. Liver Physiol.
, vol.289
-
-
Dardevet, D.1
-
40
-
-
0029027409
-
Glucagon-like peptide-1 binding to rat hepatic membranes
-
Villanueva-Penacarillo M.L., et al. Glucagon-like peptide-1 binding to rat hepatic membranes. J. Endocrinol. 146 (1995) 183-189
-
(1995)
J. Endocrinol.
, vol.146
, pp. 183-189
-
-
Villanueva-Penacarillo, M.L.1
-
41
-
-
20444406125
-
In vitro transdifferentiation of hepatoma cells into functional pancreatic cells
-
Li W.C., et al. In vitro transdifferentiation of hepatoma cells into functional pancreatic cells. Mech. Dev. 122 (2005) 837-847
-
(2005)
Mech. Dev.
, vol.122
, pp. 837-847
-
-
Li, W.C.1
-
42
-
-
70450235041
-
Exendin-4 promotes liver cell proliferation and enhances PDX-1-induced liver to pancreas transdifferentiation
-
Aviv V., et al. Exendin-4 promotes liver cell proliferation and enhances PDX-1-induced liver to pancreas transdifferentiation. J. Biol. Chem. 284 (2009) 33509-33520
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 33509-33520
-
-
Aviv, V.1
-
43
-
-
0030013475
-
Tissue distribution of messenger ribonucleic acid encoding the rat glucagon-like peptide-1 receptor
-
Bullock B.P., et al. Tissue distribution of messenger ribonucleic acid encoding the rat glucagon-like peptide-1 receptor. Endocrinology 137 (1996) 2968-2978
-
(1996)
Endocrinology
, vol.137
, pp. 2968-2978
-
-
Bullock, B.P.1
-
44
-
-
0025728406
-
Absence of insulinotropic glucagon-like peptide-1(7-37) receptors on isolated rat liver hepatocytes
-
Blackmore P.F., et al. Absence of insulinotropic glucagon-like peptide-1(7-37) receptors on isolated rat liver hepatocytes. FEBS Lett. 283 (1991) 7-10
-
(1991)
FEBS Lett.
, vol.283
, pp. 7-10
-
-
Blackmore, P.F.1
-
45
-
-
36849040001
-
Incretin receptors for glucagon-like peptide 1 and glucose-dependent insulinotropic polypeptide are essential for the sustained metabolic actions of vildagliptin in mice
-
Flock G., et al. Incretin receptors for glucagon-like peptide 1 and glucose-dependent insulinotropic polypeptide are essential for the sustained metabolic actions of vildagliptin in mice. Diabetes 56 (2007) 3006-3013
-
(2007)
Diabetes
, vol.56
, pp. 3006-3013
-
-
Flock, G.1
-
46
-
-
34250635159
-
GLP-1 receptor expression in human tumors and human normal tissues: potential for in vitro targeting
-
Korner M., et al. GLP-1 receptor expression in human tumors and human normal tissues: potential for in vitro targeting. J. Nucl. Med. 48 (2007) 736-743
-
(2007)
J. Nucl. Med.
, vol.48
, pp. 736-743
-
-
Korner, M.1
-
47
-
-
10344242925
-
Kinase signaling cascades in the mitochondrion: a matter of life or death
-
Horbinski C., and Chu C.T. Kinase signaling cascades in the mitochondrion: a matter of life or death. Free Radic. Biol. Med. 38 (2005) 2-11
-
(2005)
Free Radic. Biol. Med.
, vol.38
, pp. 2-11
-
-
Horbinski, C.1
Chu, C.T.2
-
48
-
-
0037423304
-
Essential role of A-kinase anchor protein 121 for cAMP signaling to mitochondria
-
Affaitati A., et al. Essential role of A-kinase anchor protein 121 for cAMP signaling to mitochondria. J. Biol. Chem. 278 (2003) 4286-4294
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 4286-4294
-
-
Affaitati, A.1
-
49
-
-
0346434149
-
Rapid accumulation of Akt in mitochondria following phosphatidylinositol 3kinase activation
-
Bijur G.N., and Jope R.S. Rapid accumulation of Akt in mitochondria following phosphatidylinositol 3kinase activation. J. Neurochem. 87 (2003) 1427-1435
-
(2003)
J. Neurochem.
, vol.87
, pp. 1427-1435
-
-
Bijur, G.N.1
Jope, R.S.2
-
50
-
-
4544363024
-
Identification of the growth hormone-releasing peptide binding site in CD36: a photoaffinity cross-linking study
-
Demers A., et al. Identification of the growth hormone-releasing peptide binding site in CD36: a photoaffinity cross-linking study. Biochem. J. 382 (2004) 417-424
-
(2004)
Biochem. J.
, vol.382
, pp. 417-424
-
-
Demers, A.1
-
51
-
-
0346003785
-
A CD36-initiated signaling cascade mediates inflammatory effects of beta-amyloid
-
Moore K.J., et al. A CD36-initiated signaling cascade mediates inflammatory effects of beta-amyloid. J. Biol. Chem. 277 (2002) 47373-47379
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 47373-47379
-
-
Moore, K.J.1
-
52
-
-
34447508335
-
Thrombospondin-1 inhibits nitric oxide signaling via CD36 by inhibiting myristic acid uptake
-
Isenberg J.S., et al. Thrombospondin-1 inhibits nitric oxide signaling via CD36 by inhibiting myristic acid uptake. J. Biol. Chem. 282 (2007) 15404-15415
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 15404-15415
-
-
Isenberg, J.S.1
-
53
-
-
0024317055
-
The mitochondrial targeting function of randomly generated peptide sequences correlates with predicted helical amphiphilicity
-
Lemire B.D., et al. The mitochondrial targeting function of randomly generated peptide sequences correlates with predicted helical amphiphilicity. J. Biol. Chem. 264 (1989) 20205-20215
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 20205-20215
-
-
Lemire, B.D.1
-
54
-
-
10044257654
-
Mitochondrial targeting sequence of the influenza A virus PB1-F2 protein and its function in mitochondria
-
Yamada H., et al. Mitochondrial targeting sequence of the influenza A virus PB1-F2 protein and its function in mitochondria. FEBS Lett. 578 (2004) 331-336
-
(2004)
FEBS Lett.
, vol.578
, pp. 331-336
-
-
Yamada, H.1
-
55
-
-
33646256570
-
Intracellular targeting of truncated secretory peptides in the mammalian heart and brain
-
Brun C., et al. Intracellular targeting of truncated secretory peptides in the mammalian heart and brain. FASEB J. 20 (2006) 732-734
-
(2006)
FASEB J.
, vol.20
, pp. 732-734
-
-
Brun, C.1
-
56
-
-
34248640428
-
Lysine propionylation and butyrylation are novel post-translational modifications in histones
-
Chen Y., et al. Lysine propionylation and butyrylation are novel post-translational modifications in histones. Mol. Cell Proteomics. 6 (2007) 812-819
-
(2007)
Mol. Cell Proteomics.
, vol.6
, pp. 812-819
-
-
Chen, Y.1
-
57
-
-
53349177067
-
Palmitoylation of stathmin family proteins domain A controls Golgi versus mitochondrial subcellular targeting
-
Chauvin S., et al. Palmitoylation of stathmin family proteins domain A controls Golgi versus mitochondrial subcellular targeting. Biol. Cell 100 (2008) 577-589
-
(2008)
Biol. Cell
, vol.100
, pp. 577-589
-
-
Chauvin, S.1
-
58
-
-
34648820054
-
Pathogenesis and management issues for non-alcoholic fatty liver disease
-
Duvnjak M., et al. Pathogenesis and management issues for non-alcoholic fatty liver disease. World J. Gastroenterol. 13 (2007) 4539-4550
-
(2007)
World J. Gastroenterol.
, vol.13
, pp. 4539-4550
-
-
Duvnjak, M.1
-
59
-
-
34547444891
-
Mechanistic insights into diabetes mellitus and oxidative stress
-
Maiese K., et al. Mechanistic insights into diabetes mellitus and oxidative stress. Curr. Med. Chem. 14 (2007) 1729-1738
-
(2007)
Curr. Med. Chem.
, vol.14
, pp. 1729-1738
-
-
Maiese, K.1
-
60
-
-
34248370974
-
Lipids in the heart: a source of fuel and a source of toxins
-
Park T.S., et al. Lipids in the heart: a source of fuel and a source of toxins. Curr. Opin. Lipidol. 18 (2007) 277-282
-
(2007)
Curr. Opin. Lipidol.
, vol.18
, pp. 277-282
-
-
Park, T.S.1
|