Genetic Polymorphisms in DRD4 and Risk for Parkinson's Disease Among Eastern Indians
Dipanwita, Sadhukhan, Arindam, Biswas, Atanu, Biswas, Kunal, Ray, Jharna, Ray
Published in Neurology India (01.03.2022)
Published in Neurology India (01.03.2022)
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Gene therapy restores vision in a canine model of childhood blindness
Bennett, Jean, Acland, Gregory M, Aguirre, Gustavo D, Ray, Jharna, Zhang, Qi, Aleman, Tomas S, Cideciyan, Artur V, Pearce-Kelling, Susan E, Anand, Vibha, Zeng, Yong, Maguire, Albert M, Jacobson, Samuel G, Hauswirth, William W
Published in Nature genetics (01.05.2001)
Published in Nature genetics (01.05.2001)
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Ligand and Structure Based Models for the Identification of Beta 2 Adrenergic Receptor Antagonists
Joshi, Jayadev, Dimri, Manali, Ghosh, Subhajit, Shrivastava, Nitisha, Chakraborti, Rina, Sehgal, Neeta, Ray, Jharna, Kumar, Indracanti Prem
Published in Current computer-aided drug design (01.01.2015)
Published in Current computer-aided drug design (01.01.2015)
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Missing heritability of Wilson disease: a search for the uncharacterized mutations
Roy, Shubhrajit, Ghosh, Sampurna, Ray, Jharna, Ray, Kunal, Sengupta, Mainak
Published in Mammalian genome (01.03.2023)
Published in Mammalian genome (01.03.2023)
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Convolvulus pluricaulis extract can modulate synaptic plasticity in rat brain hippocampus
Das, Rishi, Sengupta, Tathagata, Roy, Shubhrajit, Chattarji, Sumantra, Ray, Jharna
Published in Neuroreport (22.05.2020)
Published in Neuroreport (22.05.2020)
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Dopamine β Hydroxylase (DBH) is a potential modifier gene associated with Parkinson's disease in Eastern India
Ghosh, Arunibha, Sadhukhan, Tamal, Giri, Subhajit, Biswas, Arindam, Das, Shyamal Kumar, Ray, Kunal, Ray, Jharna
Published in Neuroscience letters (27.07.2019)
Published in Neuroscience letters (27.07.2019)
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Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties
Roy, Shubhrajit, McCann, Courtney J., Ralle, Martina, Ray, Kunal, Ray, Jharna, Lutsenko, Svetlana, Jayakanthan, Samuel
Published in Scientific reports (10.08.2020)
Published in Scientific reports (10.08.2020)
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Journal Article
Genetic screening of THAP1 in primary dystonia patients of India
Giri, Subhajit, Naiya, Tufan, Equbal, Zaffar, Sankhla, Charulata Savant, Das, Shyamal Kumar, Ray, Kunal, Ray, Jharna
Published in Neuroscience letters (10.01.2017)
Published in Neuroscience letters (10.01.2017)
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Identification of GBA mutations among neurodegenerative disease patients from eastern India
Biswas, Arindam, Sadhukhan, Dipanwita, Biswas, Atanu, Das, Shyamal K., Banerjee, Tapas K, Bal, Partha Sarathi, Pal, Sandip, Ghosh, Amitabha, Ray, Kunal, Ray, Jharna
Published in Neuroscience letters (23.04.2021)
Published in Neuroscience letters (23.04.2021)
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trans -4,4'-Dihydroxystilbene (DHS) inhibits human neuroblastoma tumor growth and induces mitochondrial and lysosomal damages in neuroblastoma cell lines
Saha, Bhaskar, Patro, Birija Sankar, Koli, Mrunesh, Pai, Ganesh, Ray, Jharna, Bandyopadhyay, Sandip K, Chattopadhyay, Subrata
Published in Oncotarget (26.09.2017)
Published in Oncotarget (26.09.2017)
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Journal Article
Evaluation of FGF 20 variants for susceptibility to Parkinson’s disease in Eastern Indians
Sadhukhan, Dipanwita, Das, Gautami, Biswas, Arindam, Ghosh, Soumitra, Das, Shyamal K., Ray, Kunal, Ray, Jharna
Published in Neuroscience letters (14.05.2018)
Published in Neuroscience letters (14.05.2018)
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Journal Article
Primary generalized dystonia due to TOR1A ?GAG mutation in an Indian family with intrafamilial clinical heterogeneity
Giri, Subhajit, Biswas, Arindam, Das, Shyamal, Ray, Kunal, Ray, Jharna
Published in Neurology India (01.05.2019)
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Published in Neurology India (01.05.2019)
Journal Article
A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia
Giri, Subhajit, Naiya, Tufan, Roy, Shubhrajit, Das, Gautami, Wali, Gurusidheshwar M., Das, Shyamal Kumar, Ray, Kunal, Ray, Jharna
Published in Journal of molecular neuroscience (01.06.2019)
Published in Journal of molecular neuroscience (01.06.2019)
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