20 results on '"Pramanik, Asmita"'
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2. New paradigms in purinergic receptor ligand discovery
3. Corrigendum to “New paradigms in purinergic receptor ligand discovery” [Neuropharmacology 230 (2023) 109503]
4. Serine protease inhibitors rich Coccinia grandis (L.) Voigt leaf extract induces protective immune responses in murine visceral leishmaniasis
5. Multifaceted Role of Matrix Metalloproteases on Human Diseases
6. Autophagic Proteases: Functional and Pathophysiological Aspects
7. Synthesis and pharmacological characterization of multiply substituted 2H-chromene derivatives as P2Y6 receptor antagonists
8. Pathophysiological Aspects of Lipoprotein-Associated Phospholipase A2: A Brief Overview
9. Alicyclic Ring Size Variation of 4‑Phenyl-2-naphthoic Acid Derivatives as P2Y14 Receptor Antagonists.
10. Polyphenolic Compounds Inhibit Osteoclast Differentiation While Reducing Autophagy through Limiting ROS and the Mitochondrial Membrane Potential
11. Coccinia grandis (L.) Voigt Leaf Extract Exhibits Antileishmanial Effect Through Pro-inflammatory Response: An In Vitro Study
12. Alicyclic Ring Size Variation of 4-Phenyl-2-naphthoic Acid Derivatives as P2Y14Receptor Antagonists
13. Dental pulp–derived stem cells inhibit osteoclast differentiation by secreting osteoprotegerin and deactivating AKT signalling in myeloid cells
14. White jute (Corchorus capsularis L.) leaf extract has potent leishmanicidal activity against Leishmania donovani
15. Coccinia grandis (L.) Voigt Leaf Extract Exhibits Antileishmanial Effect Through Pro-inflammatory Response: An In Vitro Study
16. Alicyclic Ring Size Variation of 4-Phenyl-2-naphthoic Acid Derivatives as P2Y 14 Receptor Antagonists.
17. Synthesis and pharmacological characterization of multiply substituted 2H-chromene derivatives as P2Y 6 receptor antagonists.
18. Antiproteolytic and leishmanicidal activity of Coccinia grandis (L.) Voigt leaf extract against Leishmania donovani promastigotes.
19. Vascular aneurysms: a perspective.
20. Effect of m-calpain in PKCalpha-mediated proliferation of pulmonary artery smooth muscle cells by low dose of ouabain.
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