Found: 10
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Exogenous GalR2‐specific peptide agonist as a tool for treating myocardial ischemia/reperfusion injury.
- Published in:
- Fundamental & Clinical Pharmacology, 2023, v. 37, n. 6, p. 1109, doi. 10.1111/fcp.12925
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- Article
Exogenous Galanin Reduces Hyperglycemia and Myocardial Metabolic Disorders Induced by Streptozotocin in Rats.
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- International Journal of Peptide Research & Therapeutics, 2022, v. 28, n. 3, p. 1, doi. 10.1007/s10989-022-10412-2
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- Article
Chimeric Agonist of Galanin Receptor GALR2 Reduces Heart Damage in Rats with Streptozotocin-Induced Diabetes.
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- Biochemistry (00062979), 2022, v. 87, n. 4, p. 346, doi. 10.1134/S0006297922040046
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- Article
Galanin Peptides Alleviate Myocardial Ischemia/Reperfusion Injury by Reducing Reactive Oxygen Species Formation.
- Published in:
- International Journal of Peptide Research & Therapeutics, 2021, v. 27, n. 3, p. 2039, doi. 10.1007/s10989-021-10231-x
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- Article
Correction to: Galanin Peptides Alleviate Myocardial Ischemia/Reperfusion Injury by Reducing Reactive Oxygen Species Formation.
- Published in:
- 2021
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- Correction Notice
Galanin receptors activation modulates myocardial metabolic and antioxidant responses to ischaemia/reperfusion stress.
- Published in:
- Clinical & Experimental Pharmacology & Physiology, 2019, v. 46, n. 12, p. 1174, doi. 10.1111/1440-1681.13164
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- Article
Protective Effects of a Novel Agonist of Galanin Receptors Against Doxorubicin-Induced Cardiotoxicity in Rats.
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- Cardiovascular Toxicology, 2019, v. 19, n. 2, p. 136, doi. 10.1007/s12012-018-9483-x
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- Article
Therapeutic potential of N-terminal fragments of galanin in cardiovascular diseases.
- Published in:
- Pharmakeftiki, 2019, v. 31, n. 2, p. 69
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- Article
Design of peptidase-resistant peptide inhibitors of myosin light chain kinase.
- Published in:
- Journal of Peptide Science, 2016, v. 22, n. 11/12, p. 673, doi. 10.1002/psc.2928
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- Article
Effects of structural analogues of apelin-12 in acute myocardial infarction in rats.
- Published in:
- Journal of Pharmacology & Pharmacotherapeutics, 2013, v. 4, n. 3, p. 198, doi. 10.4103/0976-500X.114600
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- Article