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Kunal Ray

Showing results (81-90 of 113) 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.
Neuromolecular Medicine|May 29, 2019
Role of Apolipoprotein E, Cathepsin D, and Brain-Derived Neurotrophic Factor in Parkinson's Disease: A Study from Eastern IndiaProsenjit Pal, Tamal Sadhukhan, Subhadip Chakraborty, et al.
Neurology India|April 27, 2021
Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian PopulationTania Saha, Somrita Roy, Rajashree Chakraborty, et al.
The Indian Journal of Medical Research|January 16, 2004
DNA linkage based diagnosis of Wilson disease in asymptomatic siblingsA Gupta, R Neogi, M Mukherjea, et al.
Disease Markers|June 12, 2012
Evaluation of the role of LRRK2 gene in Parkinson's disease in an East Indian cohortTamal Sadhukhan, Mansi Vishal, Gautami Das, et al.
Parkinsonism & Related Disorders|October 14, 2011
Role of glutathione S-transferase T1, M1 and P1 polymorphisms in Indian Parkinson's disease patientsArindam Biswas, Tamal Sadhukhan, Kaumudee Bose, 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.
Parkinsonism & Related Disorders|January 16, 2013
Genetic study on frontotemporal lobar degeneration in IndiaGautami Das, Tamal Sadhukhan, Dipanwita Sadhukhan, et al.
Journal of the Indian Medical Association|May 6, 2005
Genetics and bioinformatics of primary open angle glaucoma: an Indian perspectiveKunal Ray, Sanjay Kumar Daulat Thakur, Arun Kumar Banerjee, et al.
BMC Molecular Biology|March 16, 2007
Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent changeMoulinath Acharya, Suddhasil Mookherjee, Ashima Bhattacharjee, et al.
Pageof 12

Showing results (81-90 of 113) with videos related to

Sort By:
Pageof 12
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.
Neuromolecular Medicine|May 29, 2019
Role of Apolipoprotein E, Cathepsin D, and Brain-Derived Neurotrophic Factor in Parkinson's Disease: A Study from Eastern IndiaProsenjit Pal, Tamal Sadhukhan, Subhadip Chakraborty, et al.
Neurology India|April 27, 2021
Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian PopulationTania Saha, Somrita Roy, Rajashree Chakraborty, et al.
The Indian Journal of Medical Research|January 16, 2004
DNA linkage based diagnosis of Wilson disease in asymptomatic siblingsA Gupta, R Neogi, M Mukherjea, et al.
Disease Markers|June 12, 2012
Evaluation of the role of LRRK2 gene in Parkinson's disease in an East Indian cohortTamal Sadhukhan, Mansi Vishal, Gautami Das, et al.
Parkinsonism & Related Disorders|October 14, 2011
Role of glutathione S-transferase T1, M1 and P1 polymorphisms in Indian Parkinson's disease patientsArindam Biswas, Tamal Sadhukhan, Kaumudee Bose, 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.
Parkinsonism & Related Disorders|January 16, 2013
Genetic study on frontotemporal lobar degeneration in IndiaGautami Das, Tamal Sadhukhan, Dipanwita Sadhukhan, et al.
Journal of the Indian Medical Association|May 6, 2005
Genetics and bioinformatics of primary open angle glaucoma: an Indian perspectiveKunal Ray, Sanjay Kumar Daulat Thakur, Arun Kumar Banerjee, et al.
BMC Molecular Biology|March 16, 2007
Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent changeMoulinath Acharya, Suddhasil Mookherjee, Ashima Bhattacharjee, et al.
Pageof 12