Balasundaram Padmanabhan

Hosur Main Road
Bengaluru, KA 560029, India

Last Updated: 09/26/2026

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Found 38 publications

Neuroprotective Potential of Nardostachys jatamansi Extract via Keap1-Nrf2 Pathway Regulation in Parkinson's Disease.

Neuroprotective Potential of Nardostachys jatamansi Extract via Keap1-Nrf2 Pathway Regulation in Parkinson's Disease.

Journal: Applied biochemistry and biotechnology

Published: July 03, 2026

BET Bromodomain Targeting by NSAIDs: Structural, Biophysical, and Computational Insights.

BET Bromodomain Targeting by NSAIDs: Structural, Biophysical, and Computational Insights.

Journal: Proteins

Published: March 22, 2026

Structure and Molecular Basis for Inhibiting Human SOD1 Aggregation by a Promising Decan Derivative Modulator: A Potential Therapeutic Strategy for Treating Amyotrophic Lateral Sclerosis (ALS).

Structure and Molecular Basis for Inhibiting Human SOD1 Aggregation by a Promising Decan Derivative Modulator: A Potential Therapeutic Strategy for Treating Amyotrophic Lateral Sclerosis (ALS).

Journal: ACS chemical neuroscience

Published: October 23, 2025

Parkinson's disease-specific α-Synuclein variants potentially drive Lewy body formation by engaging in promiscuous and non-functional interactions.

Parkinson's disease-specific α-Synuclein variants potentially drive Lewy body formation by engaging in promiscuous and non-functional interactions.

Journal: Communications biology

Published: September 16, 2025

Structural and functional insights into the nuclear role of Parkinson's disease-associated α-synuclein as a histone chaperone.

Structural and functional insights into the nuclear role of Parkinson's disease-associated α-synuclein as a histone chaperone.

Journal: Communications biology

Published: December 02, 2024

Structural Basis for the Essential Role of Ca2+ in the Lytic Activity of Staphylococcus aureus PlyGRCS Endolysin Targeting Methicillin-Resistant Staphylococcus aureus.

Structural Basis for the Essential Role of Ca2+ in the Lytic Activity of Staphylococcus aureus PlyGRCS Endolysin Targeting Methicillin-Resistant Staphylococcus aureus.

Journal: Proteins

Published: August 05, 2024

Tau-S214 Phosphorylation Inhibits Fyn Kinase Interaction and Increases the Decay Time of NMDAR-mediated Current.

Tau-S214 Phosphorylation Inhibits Fyn Kinase Interaction and Increases the Decay Time of NMDAR-mediated Current.

Journal: Journal of molecular biology

Published: August 17, 2023

Structural insights into the modulation Of SOD1 aggregation By a fungal metabolite Phialomustin-B: Therapeutic potential in ALS.

Structural insights into the modulation Of SOD1 aggregation By a fungal metabolite Phialomustin-B: Therapeutic potential in ALS.

Journal: PloS one

Published: July 18, 2023

Neuroanatomical zones of human traumatic brain injury reveal significant differences in protein profile and protein oxidation: Implications for secondary injury events.

Neuroanatomical zones of human traumatic brain injury reveal significant differences in protein profile and protein oxidation: Implications for secondary injury events.

Journal: Journal of neurochemistry

Published: June 03, 2023

Structural and biochemical insights into the bacteriophage PlyGRCS endolysin targeting methicillin-resistant Staphylococcus aureus (MRSA) and serendipitous discovery of its interaction with a cold shock protein C (CspC).

Structural and biochemical insights into the bacteriophage PlyGRCS endolysin targeting methicillin-resistant Staphylococcus aureus (MRSA) and serendipitous discovery of its interaction with a cold shock protein C (CspC).

Journal: Protein science : a publication of the Protein Society

Published: April 06, 2023

High-affinity binding of celastrol to monomeric α-synuclein mitigates in vitro aggregation.

High-affinity binding of celastrol to monomeric α-synuclein mitigates in vitro aggregation.

Journal: Journal of biomolecular structure & dynamics

Published: February 06, 2023

Structural and biochemical insights into purine-based drug molecules in hBRD2 delineate a unique binding mode opening new vistas in the design of inhibitors of the BET family.

Structural and biochemical insights into purine-based drug molecules in hBRD2 delineate a unique binding mode opening new vistas in the design of inhibitors of the BET family.

Journal: Acta crystallographica. Section D, Structural biology

Published: December 06, 2022

Showing 1-12 of 38

Last Updated: 09/26/2026