Binukumar Bk

Mall Road
New Delhi, DL 110007, India

Last Updated: 09/26/2026

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Found 11 publications

First Indian Case of Wilson's Disease With a Chinese-specific ATP7B Variant: Clinical and Genetic Insights.

First Indian Case of Wilson's Disease With a Chinese-specific ATP7B Variant: Clinical and Genetic Insights.

Journal: Journal of clinical and experimental hepatology

Published: July 22, 2025

Identification and Functional Validation of Novel Pathogenic Variants in Primary Immunodeficiencies.

Identification and Functional Validation of Novel Pathogenic Variants in Primary Immunodeficiencies.

Journal: European journal of immunology

Published: November 21, 2024

Unprecedented Co-occurrence: Identification of a Pathogenic Genetic Variant in the KMT2B Gene in a Wilson Disease Patient with a Pathogenic ATP7B Mutation.

Unprecedented Co-occurrence: Identification of a Pathogenic Genetic Variant in the KMT2B Gene in a Wilson Disease Patient with a Pathogenic ATP7B Mutation.

Journal: Annals of neurosciences

Published: December 12, 2023

Cdk5-Mediated Brain Unfolded Protein Response Upregulation Associated with Cognitive Impairments in Type 2 Diabetes and Ameliorative Action of NAC.

Cdk5-Mediated Brain Unfolded Protein Response Upregulation Associated with Cognitive Impairments in Type 2 Diabetes and Ameliorative Action of NAC.

Journal: ACS chemical neuroscience

Published: July 19, 2023

Understanding the roles and regulation of mitochondrial microRNAs (MitomiRs) in neurodegenerative diseases: Current status and advances.

Understanding the roles and regulation of mitochondrial microRNAs (MitomiRs) in neurodegenerative diseases: Current status and advances.

Journal: Mechanisms of ageing and development

Published: December 27, 2022

Editorial: Apoptosis, autophagy, and mitophagy dysfunction in Alzheimer's disease: Evolving emergence and mechanisms.

Editorial: Apoptosis, autophagy, and mitophagy dysfunction in Alzheimer's disease: Evolving emergence and mechanisms.

Journal: Frontiers in molecular neuroscience

Published: September 21, 2022

GPi-DBS for KMT2B-Associated Dystonia: Systematic Review and Meta-Analysis.

GPi-DBS for KMT2B-Associated Dystonia: Systematic Review and Meta-Analysis.

Journal: Movement disorders clinical practice

Published: June 19, 2021

Mitochondrial Dysfunction and Mitophagy Closely Cooperate in Neurological Deficits Associated with Alzheimer's Disease and Type 2 Diabetes.

Mitochondrial Dysfunction and Mitophagy Closely Cooperate in Neurological Deficits Associated with Alzheimer's Disease and Type 2 Diabetes.

Journal: Molecular neurobiology

Published: October 30, 2020

WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson's Disease.

WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson's Disease.

Journal: Scientific reports

Published: March 07, 2020

Overexpression of the Cdk5 inhibitory peptide in motor neurons rescue of amyotrophic lateral sclerosis phenotype in a mouse model.

Overexpression of the Cdk5 inhibitory peptide in motor neurons rescue of amyotrophic lateral sclerosis phenotype in a mouse model.

Journal: Human molecular genetics

Published: February 23, 2019

The interaction of Munc 18 (p67) with the p10 domain of p35 protects in vivo Cdk5/p35 activity from inhibition by TFP5, a peptide derived from p35.

The interaction of Munc 18 (p67) with the p10 domain of p35 protects in vivo Cdk5/p35 activity from inhibition by TFP5, a peptide derived from p35.

Journal: Molecular biology of the cell

Published: December 23, 2015

Showing 1-11 of 11

Last Updated: 09/26/2026