OpenURL Connection Search

Select item for more details and to access through your institution.

Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India.
Published in:
Journal of Molecular Neuroscience, 2021, v. 71, n. 2, p. 325, doi. 10.1007/s12031-020-01653-1
By:
- Giri, Subhajit;
- Ghosh, Arunibha;
- Roy, Shubhrajit;
- Sankhla, Charulata Savant;
- Das, Shyamal Kumar;
- Ray, Kunal;
- Ray, Jharna
Publication type:
Article
A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia.
Published in:
Journal of Molecular Neuroscience, 2019, v. 68, n. 2, p. 214, doi. 10.1007/s12031-019-01301-3
By:
- Giri, Subhajit;
- Naiya, Tufan;
- Roy, Shubhrajit;
- Das, Gautami;
- Wali, Gurusidheshwar M.;
- Das, Shyamal Kumar;
- Ray, Kunal;
- Ray, Jharna
Publication type:
Article
Potential Role of Brain-Derived Neurotrophic Factor and Dopamine Receptor D2 Gene Variants as Modifiers for the Susceptibility and Clinical Course of Wilson’s Disease.
Published in:
NeuroMolecular Medicine, 2018, v. 20, n. 3, p. 401, doi. 10.1007/s12017-018-8501-2
By:
- Roy, Shubhrajit;
- Pal, Prosenjit;
- Ghosh, Sampurna;
- Bhattacharya, Sreyashi;
- Das, Shyamal Kumar;
- Gangopadhyay, Prasanta Kumar;
- Bavdekar, Ashish;
- Ray, Kunal;
- Sengupta, Mainak;
- Ray, Jharna
Publication type:
Article
Influence of <italic>Apolipoprotein E</italic> polymorphism on susceptibility of Wilson disease.
Published in:
Annals of Human Genetics, 2018, v. 82, n. 2, p. 53, doi. 10.1111/ahg.12223
By:
- Roy, Shubhrajit;
- Ganguly, Kausik;
- Pal, Prosenjit;
- Ghosh, Sampurna;
- Das, Shyamal K.;
- Gangopadhyay, Prasanta K.;
- Bavdekar, Ashish;
- Ray, Kunal;
- Sengupta, Mainak;
- Ray, Jharna
Publication type:
Article
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties.
Published in:
Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70366-7
By:
- Roy, Shubhrajit;
- McCann, Courtney J.;
- Ralle, Martina;
- Ray, Kunal;
- Ray, Jharna;
- Lutsenko, Svetlana;
- Jayakanthan, Samuel
Publication type:
Article
Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients.
Published in:
Journal of Gene Medicine, 2019, v. 21, n. 9, p. N.PAG, doi. 10.1002/jgm.3109
By:
- Roy, Shubhrajit;
- Ghosh, Sampurna;
- Bhattacharya, Sreyashi;
- Saha, Arpan;
- Das, Shyamal Kumar;
- Gangopadhyay, Prasanta Kumar;
- Bavdekar, Ashish;
- Ray, Kunal;
- Sengupta, Mainak;
- Ray, Jharna
Publication type:
Article
Missing heritability of Wilson disease: a search for the uncharacterized mutations.
Published in:
Mammalian Genome, 2023, v. 34, n. 1, p. 1, doi. 10.1007/s00335-022-09971-y
By:
- Roy, Shubhrajit;
- Ghosh, Sampurna;
- Ray, Jharna;
- Ray, Kunal;
- Sengupta, Mainak
Publication type:
Article
Mechanism of Cu entry into the brain: many unanswered questions.
Published in:
Neural Regeneration Research, 2024, v. 19, n. 11, p. 2421, doi. 10.4103/1673-5374.393107
By:
- Roy, Shubhrajit;
- Lutsenko, Svetlana
Publication type:
Article
Atp7b-dependent choroid plexus dysfunction Causes transient copper deficit and metabolic changes in the developing mouse brain.
Published in:
PLoS Genetics, 2023, v. 18, n. 1, p. 1, doi. 10.1371/journal.pgen.1010558
By:
- Washington-Hughes, Clorissa L.;
- Roy, Shubhrajit;
- Seneviratne, Herana Kamal;
- Karuppagounder, Senthilkumar S.;
- Morel, Yulemni;
- Jones, Jace W.;
- Zak, Alex;
- Xiao, Tong;
- Boronina, Tatiana N.;
- Cole, Robert N.;
- Bumpus, Namandjé N.;
- Chang, Christopher J.;
- Dawson, Ted M.;
- Lutsenko, Svetlana
Publication type:
Article

Found: 9