Shubhrajit Roy

35, Ballygunge Circular Road
Kolkata, WB 700019, India

Last Updated: 09/26/2026

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Found 18 publications

NON-REDUNDANT ROLES OF COPPER TRANSPORTERS ATP7A AND ATP7B IN NORADRENERGIC SIGNALING.

NON-REDUNDANT ROLES OF COPPER TRANSPORTERS ATP7A AND ATP7B IN NORADRENERGIC SIGNALING.

Journal: bioRxiv : the preprint server for biology

Published: February 06, 2026

Non-coding RNAs in Wilson's Disease: Plausible drivers of hepatic symptom heterogeneity.

Non-coding RNAs in Wilson's Disease: Plausible drivers of hepatic symptom heterogeneity.

Journal: Mutation research. Reviews in mutation research

Published: July 26, 2025

Mammalian copper homeostasis: physiological roles and molecular mechanisms.

Mammalian copper homeostasis: physiological roles and molecular mechanisms.

Journal: Physiological reviews

Published: August 22, 2024

An Effort to Identify Genetic Determinants in Siblings With Wilson Disease Manifesting Striking Clinical Heterogeneity: An Exome Profiling Study of Two Indian Families.

An Effort to Identify Genetic Determinants in Siblings With Wilson Disease Manifesting Striking Clinical Heterogeneity: An Exome Profiling Study of Two Indian Families.

Journal: Pediatric neurology

Published: December 06, 2023

α-lipoic acid ameliorates consequences of copper overload by up-regulating selenoproteins and decreasing redox misbalance.

α-lipoic acid ameliorates consequences of copper overload by up-regulating selenoproteins and decreasing redox misbalance.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 26, 2023

Mechanism of Cu entry into the brain: many unanswered questions.

Mechanism of Cu entry into the brain: many unanswered questions.

Journal: Neural regeneration research

Published: August 06, 2023

Slc25a3-dependent copper transport controls flickering-induced Opa1 processing for mitochondrial safeguard.

Slc25a3-dependent copper transport controls flickering-induced Opa1 processing for mitochondrial safeguard.

Journal: Developmental cell

Published: December 12, 2022

Missing heritability of Wilson disease: a search for the uncharacterized mutations.

Missing heritability of Wilson disease: a search for the uncharacterized mutations.

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: November 06, 2022

Parkinson's disease-associated 18 bp promoter variant of DJ-1 alters REST binding and regulates its expression.

Parkinson's disease-associated 18 bp promoter variant of DJ-1 alters REST binding and regulates its expression.

Journal: Neuroscience letters

Published: October 25, 2022

Heterogeneous nuclear ribonucleoprotein hnRNPA2/B1 regulates the abundance of the copper-transporter ATP7A in an isoform-dependent manner.

Heterogeneous nuclear ribonucleoprotein hnRNPA2/B1 regulates the abundance of the copper-transporter ATP7A in an isoform-dependent manner.

Journal: Frontiers in molecular biosciences

Published: October 11, 2022

Atp7b-dependent choroid plexus dysfunction causes transient copper deficit and metabolic changes in the developing mouse brain.

Atp7b-dependent choroid plexus dysfunction causes transient copper deficit and metabolic changes in the developing mouse brain.

Journal: PLoS genetics

Published: July 20, 2022

Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India.

Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India.

Journal: Journal of molecular neuroscience : MN

Published: April 26, 2020

Showing 1-12 of 18

Last Updated: 09/26/2026