Page last updated: 2024-09-03

angiotensin ii, des-phe(8)- and Non-alcoholic Fatty Liver Disease

angiotensin ii, des-phe(8)- has been researched along with Non-alcoholic Fatty Liver Disease in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's2 (100.00)2.80

Authors

AuthorsStudies
Ajambo, M; Albdeirat, L; Albekairi, N; Ali, R; Alotaibi, H; Amanya, G; Attia, H; Badr, A; Elayeete, S; Ghaffar, A; Harris, JR; Hussain, R; Kadobera, D; Khan, A; Kwesiga, B; Li, K; Li, X; Mwanje, W; Nampeera, R; Nansikombi, HT; Naseem, S; Nsubuga, EJ; Rajab, R; Riolexus, AA; Soliman, A1
Cao, X; Liu, JY; Shi, TT; Song, LN; Xin, Z; Yang, JK; Zhang, YC1

Trials

1 trial(s) available for angiotensin ii, des-phe(8)- and Non-alcoholic Fatty Liver Disease

ArticleYear
    IJID regions, 2022, Volume: 3

    Topics: Angiotensin I; Angiotensin-Converting Enzyme 2; Animals; Anti-Inflammatory Agents; Antioxidants; Biomarkers; Cyprinidae; DNA Damage; Flavonoids; Fresh Water; Fructose; Gills; Insecticides; Non-alcoholic Fatty Liver Disease; Oxidative Stress; Peptide Fragments; Peptidyl-Dipeptidase A; Pyridines; Rats; Receptors, G-Protein-Coupled; Renin-Angiotensin System; Water; Water Pollutants, Chemical

2022

Other Studies

1 other study(ies) available for angiotensin ii, des-phe(8)- and Non-alcoholic Fatty Liver Disease

ArticleYear
Angiotensin-(1-7), the product of ACE2 ameliorates NAFLD by acting through its receptor Mas to regulate hepatic mitochondrial function and glycolipid metabolism.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020, Volume: 34, Issue:12

    Topics: Angiotensin I; Angiotensin-Converting Enzyme 2; Animals; Cell Line, Tumor; Down-Regulation; Glycolipids; Hep G2 Cells; Humans; Insulin Resistance; Lipid Metabolism; Liver; Male; Mice; Mice, Inbred C57BL; Mitochondria; Non-alcoholic Fatty Liver Disease; Peptide Fragments; Proto-Oncogene Mas; Proto-Oncogene Proteins; Receptors, G-Protein-Coupled; Signal Transduction

2020