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2010, Advances in experimental medicine and biology, ISBN 9789048190591, Volume 690., xvi, 207
Highlighting the role local renin-angiotensin systems (RAS) play in pancreatic disease, this review presents the latest research advances in the field. These... 
Medicine | Pancreatic Diseases | Biology | Research | Renin-angiotensin system | Pancreas | Diseases | Medicine: General Issues | Angiotensins | Physiology | Renin | Kidneys | Pathophysiology
Book
Cellular Physiology and Biochemistry, ISSN 1015-8987, 11/2018, Volume 51, Issue 2, pp. 924 - 937
Journal Article
2010, Advances in experimental medicine and biology, ISBN 9789048190591, Volume 690., xvi, 207
Book
Journal Article
American Journal of Physiology, ISSN 0193-1849, 09/2017, Volume 313, Issue 3, p. E292
Fibroblast growth factor 21 (FGF21) is a potent endocrine regulator with physiological effects on glucose and lipid metabolism and thus garners much attention... 
Fibroblast growth factor | Physiological effects | Adipose tissue | Liver | Lipids | Body weight loss | Glucose | Experiments | Glucose metabolism | Fibroblasts | Dark current | Lipid metabolism | Pancreas | Growth factors | Data points | Health | Diabetes mellitus | Organs | Weight loss | Muscles | Metabolism | Insulin | Light effects | Skeletal muscle | Life span | Klotho protein | Biomarkers | Metabolic disorders
Journal Article
Diabetes, ISSN 0012-1797, 02/2006, Volume 55, Issue 2, pp. 367 - 374
Angiotensin II Type 1 Receptor Blockade Improves β-Cell Function and Glucose Tolerance in a Mouse Model of Type 2 Diabetes Kwan Yi Chu 1 , Tung Lau 1 , Per-Ola... 
SYSTEM | MORTALITY | CHRONIC HEART-FAILURE | ISLET BLOOD-FLOW | PANCREATIC-ISLETS | INHIBITION | ENDOCRINOLOGY & METABOLISM | RANDOMIZED-TRIAL | CARDIOVASCULAR MORBIDITY | HYPERTENSION | INSULIN SENSITIVITY | Insulin-Secreting Cells - physiology | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Diabetes Mellitus, Type 2 - genetics | Gene Expression Regulation | Losartan - pharmacology | Angiotensin II Type 1 Receptor Blockers - pharmacology | Blood Glucose - drug effects | Glucose Intolerance - drug therapy | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Receptor, Angiotensin, Type 1 - genetics | Animals | Insulin-Secreting Cells - drug effects | Receptor, Angiotensin, Type 1 - metabolism | Losartan - therapeutic use | Mice, Obese | Proinsulin - biosynthesis | Insulin-Secreting Cells - cytology | Mice | Diabetes Mellitus, Type 2 - drug therapy | Disease Models, Animal | Proinsulin/biosynthesis | Losartan/pharmacology/therapeutic use | Medical and Health Sciences | Medicin och hälsovetenskap | Angiotensin II Type 1 Receptor Blockers/pharmacology/therapeutic use | Mice; Obese | Diabetes Mellitus; Type 2/drug therapy/genetics | Receptor; Angiotensin; Type 1/genetics/metabolism | Insulin-Secreting Cells/cytology/drug effects/metabolism/physiology | Blood Glucose/drug effects | Insulin/metabolism | Glucose Intolerance/drug therapy | Disease Models; Animal
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 1, p. e0147391
The novel sodium glucose co-transporter 2 (SGLT2) inhibitor empagliflozin has recently been reported to improve glycemic control in streptozotocin-induced type... 
INSULIN | POTENT | DAPAGLIFLOZIN | IMPROVES GLYCEMIC CONTROL | MULTIDISCIPLINARY SCIENCES | RATS | MICE | MELLITUS | KIDNEY | Diabetes Mellitus, Experimental - drug therapy | Benzhydryl Compounds - administration & dosage | Apoptosis - drug effects | Area Under Curve | Diabetes Mellitus, Type 1 - metabolism | Homeostasis | Male | Insulin - blood | Insulin - biosynthesis | Dose-Response Relationship, Drug | RNA, Messenger - biosynthesis | Hypoglycemic Agents - administration & dosage | Glucosides - therapeutic use | Diabetes Mellitus, Experimental - metabolism | Drug Evaluation, Preclinical | Insulin - genetics | Benzhydryl Compounds - therapeutic use | Hypoglycemic Agents - therapeutic use | Glucose Tolerance Test | Glucosides - pharmacology | Mice, Inbred C57BL | RNA, Messenger - genetics | Sodium-Glucose Transporter 2 Inhibitors | Diabetes Mellitus, Type 1 - drug therapy | Hypoglycemic Agents - pharmacology | Organ Size - drug effects | Animals | Glucosides - administration & dosage | Insulin-Secreting Cells - drug effects | Glucose - metabolism | Benzhydryl Compounds - pharmacology | Mice | Insulin-Secreting Cells - pathology | Immunohistochemistry | Cell proliferation | Oxidative stress | Reactive oxygen species | Streptozocin | Diabetes mellitus (insulin dependent) | Glucose | Blood | Hyperglycemia | Rodents | Pancreas | Enzyme-linked immunosorbent assay | Glucose transporter | Kidneys | Diabetes mellitus | Hypoglycemia | Gene expression | Insulin | Studies | Polymerase chain reaction | Glucose tolerance | Regeneration | Inhibitors | Sodium | Insulin resistance | Diabetes | Laboratory animals | Transporter | Apoptosis
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2015, Volume 10, Issue 6, p. e0128216
Angiotensin-converting enzyme 2 (ACE2), its product Angiotensin-(1-7) [Ang-(1-7)], and Ang-(1-7) receptor Mas, have been shown to regulate organogenesis during... 
CONVERTING ENZYME 2 | SYSTEM | ACE2 | ANGIOGENESIS | MULTIDISCIPLINARY SCIENCES | IN-VIVO | ANGIOTENSIN-II RECEPTORS | MICE | FETAL | EXPRESSION | TYPE-2 | Islets of Langerhans - drug effects | Reactive Oxygen Species - metabolism | Receptors, G-Protein-Coupled - metabolism | Peptide Fragments - pharmacology | Insulin - blood | RNA, Messenger - metabolism | Islets of Langerhans - metabolism | Islets of Langerhans - cytology | Peptidyl-Dipeptidase A - metabolism | Female | Angiotensin I - pharmacology | Insulin Secretion | Animals, Newborn | Proto-Oncogene Proteins - metabolism | Glucose Tolerance Test | Peptide Fragments - metabolism | NADPH Oxidases - antagonists & inhibitors | RNA, Messenger - genetics | Enzyme Inhibitors - pharmacology | Gene Expression Regulation, Developmental - drug effects | Islets of Langerhans - embryology | Angiotensin I - metabolism | Mice, Inbred ICR | Pregnancy | Insulin - metabolism | Animals | Signal Transduction - drug effects | Cell Differentiation - drug effects | Embryo, Mammalian - cytology | Cell Proliferation - drug effects | Mice | Oxidative Stress - drug effects | Enzymes | Embryonic development | Pancreatic beta cells | Biological products | RNA | Pregnant women | Angiotensin | Glucose | Dextrose | Cell proliferation | Neonates | Oxidative stress | Reactive oxygen species | Substance abuse treatment | Angiogenesis | Embryogenesis | NOX4 protein | Peptidyl-dipeptidase A | Rodents | Pancreas | Fetuses | Cultures | Gene expression | Insulin | Embryos | Organogenesis | Embryonic growth stage | Glucose tolerance | Stem cells | Insulin resistance | Diabetes | Islets of Langerhans | Laboratory animals | Apoptosis
Journal Article
Clinical Science, ISSN 0143-5221, 01/2019, Volume 133, Issue 1, pp. 101 - 116
G-protein coupled receptor 120 (GPR120) has been shown to act as an omega-3 unsaturated fatty acid sensor and is involved in insulin secretion. However, the... 
MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | OBESITY | INSULIN-RESISTANCE | GLUCOSE | ADIPOSE-TISSUE INFLAMMATION | FATTY-ACID | MOUSE MODEL | GENE-EXPRESSION | SECRETION | MURINE ISLETS
Journal Article
Drug Design, Development and Therapy, ISSN 1177-8881, 07/2014, Volume 8, pp. 1013 - 1027
Journal Article
by Lu, Sheng-Nan and Wang, Jing-Houng and Su, Chien-Wei and Wang, Tsang-En and Dai, Chia-Yen and Chen, Chien-Hung and Chen, Ran-Chou and Yang, Sien-Sing and Hung, Chien-Fu and Huang, Shiu-Feng and Liao, Li-Ying and Wang, Jing-Houng and Lu, Sheng-Nan and Chen, Chien-Hung and Huo, The-Ia and Wu, Cheng-Chung and Lee, Po-Huang and Ting, Chin-Tsung and Lee, Wei-Chen and Chau, Gar-Yang and Hung, Chien-Fu and Wang, Chih-Chi and Lee, King-The and Wang, Jing-Houng and Huang, Yi-Hsiang and Su, Chien-Wei and Ho, Ming-Chih and Lin, Shi-Ming and Huang, Guan-Tarn and Chen, Kuan-Yang and Wang, Tsang-En and Lin, Xi-Zhang and Liao, Li-Ying and Wang, Jing-Houng and Hwang, Jen-I and Chau, Gar-Yang and Chiou, Yi-You and Wang, Chung-Kwe and Hu, Jui-Ting and Lu, Sheng-Nan and Chen, Shinn-Cherng and Hwang, Jen-I and Liang, Po-Chin and Hung, Chien-Fu and Lee, Rheun-Chuan and Wu, Ding-Kwo and Lin, Cheng-Yao and Lin, Chen-Chun and Chen, Ran-Chou and Cheng, Ann-Lii and Hsu, Chiun and Huang, Yi-Hsiang and Chao, Yee and Chen, Li-Tzong and Wang, Po-Ming and Wang, Po-Ming and Hong, Ji-Hong and Hsu, Hsuan-Chih and Chen, Shang-Wen and Leung, Stephen Wan and Cheng, Jason Chia-Hsien and Lin, Chen-Chun and Hung, Chien-Fu and Wu, Jaw-Ching and Su, Chien-Wei and Lin, Shi-Ming and Wu, Chun-Ying and Hsu, Yao-Chun and Hsu, Chao-Wei and Ni, Yen-Hsuan and Su, Chien-Wei and Chen, Chien-Hung and Wu, Cheng-Chung and Lin, Shi-Ming and Hwang, Jen-I and Hsu, Chiun and Chen, Shang-Wen and Lin, Chih-Lin and Drafting group and Surveillance group and Target therapy/systemic therapy group and Radiotherapy group and Diagnosis group and Staging group and Local ablation group and Surgery group and TACE/TARE/HAI group and Prevention group and TACE TARE HAI Grp and Surg Grp and Radiotherapy Grp and Surveillance Grp and Drafting Grp and Local Ablation Grp and Staging Grp and Prevention Grp and Diag Grp and Target Therapy Systemic Therapy Gr
Journal of the Formosan Medical Association, ISSN 0929-6646, 05/2018, Volume 117, Issue 5, pp. 381 - 403
Journal Article