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Shubhrajit Roy

Showing results (11-20 of 18) with videos related to

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Journal of Molecular Neuroscience : MN|July 15, 2020
Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in IndiaSubhajit Giri, Arunibha Ghosh, Shubhrajit Roy, et al.
Journal of Molecular Neuroscience : MN|March 27, 2019
A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive DystoniaSubhajit Giri, Tufan Naiya, Shubhrajit Roy, et al.
The Journal of Gene Medicine|July 3, 2019
Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patientsShubhrajit Roy, Sampurna Ghosh, Sreyashi Bhattacharya, et al.
Annals of Human Genetics|October 24, 2017
Influence of Apolipoprotein E polymorphism on susceptibility of Wilson diseaseShubhrajit Roy, Kausik Ganguly, Prosenjit Pal, et al.
Neuromolecular Medicine|July 12, 2018
Potential Role of Brain-Derived Neurotrophic Factor and Dopamine Receptor D2 Gene Variants as Modifiers for the Susceptibility and Clinical Course of Wilson's DiseaseShubhrajit Roy, Prosenjit Pal, Sampurna Ghosh, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 26, 2023
α-lipoic acid ameliorates consequences of copper overload by up-regulating selenoproteins and decreasing redox misbalanceEkaterina Kabin, Yixuan Dong, Shubhrajit Roy, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
NON-REDUNDANT ROLES OF COPPER TRANSPORTERS ATP7A AND ATP7B IN NORADRENERGIC SIGNALINGShubhrajit Roy, Yu Wang, Susan Aja, et al.
Plos Genetics|January 10, 2023
Atp7b-dependent choroid plexus dysfunction causes transient copper deficit and metabolic changes in the developing mouse brainClorissa L Washington-Hughes, Shubhrajit Roy, Herana Kamal Seneviratne, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Molecular Neuroscience : MN|July 15, 2020
Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in IndiaSubhajit Giri, Arunibha Ghosh, Shubhrajit Roy, et al.
Journal of Molecular Neuroscience : MN|March 27, 2019
A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive DystoniaSubhajit Giri, Tufan Naiya, Shubhrajit Roy, et al.
The Journal of Gene Medicine|July 3, 2019
Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patientsShubhrajit Roy, Sampurna Ghosh, Sreyashi Bhattacharya, et al.
Annals of Human Genetics|October 24, 2017
Influence of Apolipoprotein E polymorphism on susceptibility of Wilson diseaseShubhrajit Roy, Kausik Ganguly, Prosenjit Pal, et al.
Neuromolecular Medicine|July 12, 2018
Potential Role of Brain-Derived Neurotrophic Factor and Dopamine Receptor D2 Gene Variants as Modifiers for the Susceptibility and Clinical Course of Wilson's DiseaseShubhrajit Roy, Prosenjit Pal, Sampurna Ghosh, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 26, 2023
α-lipoic acid ameliorates consequences of copper overload by up-regulating selenoproteins and decreasing redox misbalanceEkaterina Kabin, Yixuan Dong, Shubhrajit Roy, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
NON-REDUNDANT ROLES OF COPPER TRANSPORTERS ATP7A AND ATP7B IN NORADRENERGIC SIGNALINGShubhrajit Roy, Yu Wang, Susan Aja, et al.
Plos Genetics|January 10, 2023
Atp7b-dependent choroid plexus dysfunction causes transient copper deficit and metabolic changes in the developing mouse brainClorissa L Washington-Hughes, Shubhrajit Roy, Herana Kamal Seneviratne, et al.
Pageof 2