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Nishtha Pandey

Showing results (1-10 of 10) with videos related to

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Iscience|June 24, 2022
Model scenarios for cell cycle re-entry in Alzheimer's diseaseNishtha Pandey, P K Vinod
Plos One|June 2, 2018
Mathematical modelling of reversible transition between quiescence and proliferationNishtha Pandey, P K Vinod
Bioinformation|February 21, 2012
Mobility in the structure of E.coli recQ helicase upon substrate binding as seen from molecular dynamics simulationsNishtha Pandey, Savitha Govardhan, Ravi Kant Pathak
Scientific Reports|April 7, 2020
Network-based metabolic characterization of renal cell carcinomaNishtha Pandey, Vinay Lanke, P K Vinod
Biophysical Journal|August 14, 2020
Modeling the Control of Meiotic Cell Divisions: Entry, Progression, and ExitPrakrati Dangarh, Nishtha Pandey, Palakkad Krishnanunni Vinod
Scientific Data|August 26, 2025
A structure-oriented kinetics dataset of enzyme-substrate interactionsSowmya Ramaswamy Krishnan, Nishtha Pandey, Rajgopal Srinivasan, et al.
Human Genetics|November 26, 2008
A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3Arunima Chatterjee, Rajeev Jalvi, Nishtha Pandey, et al.
The Indian Journal of Medical Research|February 14, 2018
Mutations in <i>OTOF, CLDN14</i> & <i>SLC26A4</i> genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, IndiaNishtha Pandey, Tabassum Rashid, Rajeev Jalvi, et al.
Annals of Human Genetics|December 2, 2015
Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and KeratodermaNishtha Pandey, Dennis F Xavier, Arunima Chatterjee, et al.
Plos One|January 14, 2014
Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIEAparna Ganapathy, Nishtha Pandey, C R Srikumari Srisailapathy, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Iscience|June 24, 2022
Model scenarios for cell cycle re-entry in Alzheimer's diseaseNishtha Pandey, P K Vinod
Plos One|June 2, 2018
Mathematical modelling of reversible transition between quiescence and proliferationNishtha Pandey, P K Vinod
Bioinformation|February 21, 2012
Mobility in the structure of E.coli recQ helicase upon substrate binding as seen from molecular dynamics simulationsNishtha Pandey, Savitha Govardhan, Ravi Kant Pathak
Scientific Reports|April 7, 2020
Network-based metabolic characterization of renal cell carcinomaNishtha Pandey, Vinay Lanke, P K Vinod
Biophysical Journal|August 14, 2020
Modeling the Control of Meiotic Cell Divisions: Entry, Progression, and ExitPrakrati Dangarh, Nishtha Pandey, Palakkad Krishnanunni Vinod
Scientific Data|August 26, 2025
A structure-oriented kinetics dataset of enzyme-substrate interactionsSowmya Ramaswamy Krishnan, Nishtha Pandey, Rajgopal Srinivasan, et al.
Human Genetics|November 26, 2008
A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3Arunima Chatterjee, Rajeev Jalvi, Nishtha Pandey, et al.
The Indian Journal of Medical Research|February 14, 2018
Mutations in <i>OTOF, CLDN14</i> & <i>SLC26A4</i> genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, IndiaNishtha Pandey, Tabassum Rashid, Rajeev Jalvi, et al.
Annals of Human Genetics|December 2, 2015
Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and KeratodermaNishtha Pandey, Dennis F Xavier, Arunima Chatterjee, et al.
Plos One|January 14, 2014
Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIEAparna Ganapathy, Nishtha Pandey, C R Srikumari Srisailapathy, et al.
Pageof 1