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Odity Mukherjee

Showing results (21-30 of 31) with videos related to

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Dementia and Geriatric Cognitive Disorders|January 22, 2011
Apolipoprotein E polymorphism and dementia: a hospital-based study from southern IndiaSrikala Bharath, Meera Purushottam, Odity Mukherjee, et al.
Journal of Affective Disorders|June 13, 2015
Cellular models to study bipolar disorder: A systematic reviewBiju Viswanath, Sam P Jose, Alessio Squassina, et al.
ACS Chemical Neuroscience|February 29, 2024
A Toxicogenic Interaction between Intracellular Amyloid-β and Apolipoprotein-EArpan Dey, Aditi Verma, Uchit Bhaskar, et al.
Stem Cell Research|January 4, 2019
Derivation of iPSC lines from two patients with familial Alzheimer's disease from IndiaAshaq H Najar, K M Sneha, Aparna Ashok, et al.
Psychiatric Genetics|August 31, 2007
Serotonergic candidate genes and puerperal psychosis: an association studyH B Kiran Kumar, Meera Purushottam, Shobana Kubendran, et al.
Pharmacogenomics|March 18, 2009
Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatmentMeenal Gupta, Pallav Bhatnagar, Sandeep Grover, et al.
Alzheimer Disease and Associated Disorders|March 6, 2007
Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutationMaria I Behrens, Odity Mukherjee, Pang-hsien Tu, et al.
Human Mutation|January 10, 2008
Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementiaOdity Mukherjee, Jun Wang, Michael Gitcho, et al.
Genetic Epidemiology|November 20, 2009
The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16Ping An, Odity Mukherjee, Pritam Chanda, et al.
Annals of Neurology|September 20, 2006
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulinOdity Mukherjee, Pau Pastor, Nigel J Cairns, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Dementia and Geriatric Cognitive Disorders|January 22, 2011
Apolipoprotein E polymorphism and dementia: a hospital-based study from southern IndiaSrikala Bharath, Meera Purushottam, Odity Mukherjee, et al.
Journal of Affective Disorders|June 13, 2015
Cellular models to study bipolar disorder: A systematic reviewBiju Viswanath, Sam P Jose, Alessio Squassina, et al.
ACS Chemical Neuroscience|February 29, 2024
A Toxicogenic Interaction between Intracellular Amyloid-β and Apolipoprotein-EArpan Dey, Aditi Verma, Uchit Bhaskar, et al.
Stem Cell Research|January 4, 2019
Derivation of iPSC lines from two patients with familial Alzheimer's disease from IndiaAshaq H Najar, K M Sneha, Aparna Ashok, et al.
Psychiatric Genetics|August 31, 2007
Serotonergic candidate genes and puerperal psychosis: an association studyH B Kiran Kumar, Meera Purushottam, Shobana Kubendran, et al.
Pharmacogenomics|March 18, 2009
Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatmentMeenal Gupta, Pallav Bhatnagar, Sandeep Grover, et al.
Alzheimer Disease and Associated Disorders|March 6, 2007
Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutationMaria I Behrens, Odity Mukherjee, Pang-hsien Tu, et al.
Human Mutation|January 10, 2008
Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementiaOdity Mukherjee, Jun Wang, Michael Gitcho, et al.
Genetic Epidemiology|November 20, 2009
The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16Ping An, Odity Mukherjee, Pritam Chanda, et al.
Annals of Neurology|September 20, 2006
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulinOdity Mukherjee, Pau Pastor, Nigel J Cairns, et al.
Pageof 4