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Shubhrajit Roy

Showing results (1-10 of 18) with videos related to

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Neural Regeneration Research|March 25, 2024
Mechanism of Cu entry into the brain: many unanswered questionsShubhrajit Roy, Svetlana Lutsenko
Physiological Reviews|August 22, 2024
Mammalian copper homeostasis: physiological roles and molecular mechanismsSvetlana Lutsenko, Shubhrajit Roy, Peter Tsvetkov
Mutation Research. Reviews in Mutation Research|November 23, 2025
Non-coding RNAs in Wilson's Disease: Plausible drivers of hepatic symptom heterogeneityNeelanjana Sarkar, Arpan Saha, Shubhrajit Roy, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 3, 2022
Missing heritability of Wilson disease: a search for the uncharacterized mutationsShubhrajit Roy, Sampurna Ghosh, Jharna Ray, et al.
Developmental Cell|July 10, 2024
Slc25a3-dependent copper transport controls flickering-induced Opa1 processing for mitochondrial safeguardDaisuke Murata, Shubhrajit Roy, Svetlana Lutsenko, et al.
Neuroreport|April 14, 2020
Convolvulus pluricaulis extract can modulate synaptic plasticity in rat brain hippocampusRishi Das, Tathagata Sengupta, Shubhrajit Roy, et al.
Neuroscience Letters|January 5, 2023
Parkinson's disease-associated 18 bp promoter variant of DJ-1 alters REST binding and regulates its expressionProsenjit Pal, Shubhrajit Roy, Abhishek Chowdhury, et al.
Frontiers in Molecular Biosciences|December 22, 2022
Heterogeneous nuclear ribonucleoprotein hnRNPA2/B1 regulates the abundance of the copper-transporter ATP7A in an isoform-dependent mannerCourtney J McCann, Nesrin M Hasan, Teresita Padilla-Benavides, et al.
Pediatric Neurology|March 29, 2024
An Effort to Identify Genetic Determinants in Siblings With Wilson Disease Manifesting Striking Clinical Heterogeneity: An Exome Profiling Study of Two Indian FamiliesArpan Saha, Shristi Das, Samragni De, et al.
Scientific Reports|August 12, 2020
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their propertiesShubhrajit Roy, Courtney J McCann, Martina Ralle, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Neural Regeneration Research|March 25, 2024
Mechanism of Cu entry into the brain: many unanswered questionsShubhrajit Roy, Svetlana Lutsenko
Physiological Reviews|August 22, 2024
Mammalian copper homeostasis: physiological roles and molecular mechanismsSvetlana Lutsenko, Shubhrajit Roy, Peter Tsvetkov
Mutation Research. Reviews in Mutation Research|November 23, 2025
Non-coding RNAs in Wilson's Disease: Plausible drivers of hepatic symptom heterogeneityNeelanjana Sarkar, Arpan Saha, Shubhrajit Roy, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 3, 2022
Missing heritability of Wilson disease: a search for the uncharacterized mutationsShubhrajit Roy, Sampurna Ghosh, Jharna Ray, et al.
Developmental Cell|July 10, 2024
Slc25a3-dependent copper transport controls flickering-induced Opa1 processing for mitochondrial safeguardDaisuke Murata, Shubhrajit Roy, Svetlana Lutsenko, et al.
Neuroreport|April 14, 2020
Convolvulus pluricaulis extract can modulate synaptic plasticity in rat brain hippocampusRishi Das, Tathagata Sengupta, Shubhrajit Roy, et al.
Neuroscience Letters|January 5, 2023
Parkinson's disease-associated 18 bp promoter variant of DJ-1 alters REST binding and regulates its expressionProsenjit Pal, Shubhrajit Roy, Abhishek Chowdhury, et al.
Frontiers in Molecular Biosciences|December 22, 2022
Heterogeneous nuclear ribonucleoprotein hnRNPA2/B1 regulates the abundance of the copper-transporter ATP7A in an isoform-dependent mannerCourtney J McCann, Nesrin M Hasan, Teresita Padilla-Benavides, et al.
Pediatric Neurology|March 29, 2024
An Effort to Identify Genetic Determinants in Siblings With Wilson Disease Manifesting Striking Clinical Heterogeneity: An Exome Profiling Study of Two Indian FamiliesArpan Saha, Shristi Das, Samragni De, et al.
Scientific Reports|August 12, 2020
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their propertiesShubhrajit Roy, Courtney J McCann, Martina Ralle, et al.
Pageof 2