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C Deshpande

Showing results (31-40 of 41) with videos related to

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Cureus|December 22, 2025
An Open Label, Randomized, Comparative Bioavailability Study of BioTurm™ Extract Versus Curcuma longa Extract With Piperine in Healthy Adult VolunteersVineet K Malhotra, Anil C Deshpande, Sanjay Tamoli, et al.
Clinical and Experimental Dermatology|October 1, 2013
Homozygous variegate porphyria presenting with developmental and language delay in childhoodV A E Pinder, S T Holden, C Deshpande, et al.
Marine Pollution Bulletin|March 19, 2023
Material flow analysis of commercial fishing gears in TaiwanChing-Tuan Su, Falk Schneider, Paritosh C Deshpande, et al.
The American Journal of Cardiology|August 30, 2008
A clinical risk score for prediction of stent thrombosisKenneth W Baran, John M Lasala, David A Cox, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|May 19, 2004
The effect of poly(ethylene glycol) molecular architecture on cellular interaction and uptake of DNA complexesMangesh C Deshpande, Martyn C Davies, Martin C Garnett, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|February 19, 2011
A clinical risk score for the prediction of very late stent thrombosis in drug eluting stent patientsKenneth W Baran, John M Lasala, David A Cox, et al.
The American Journal of Cardiology|March 31, 2009
One-year outcomes from the TAXUS express stent versus cypher stentManuel Mayor, Amir Z Malik, Robert J Minor, et al.
Diagnostic Cytopathology|November 22, 2011
Evaluation of EGFR mutation status in cytology specimens: an institutional experienceD L Aisner, C Deshpande, Z Baloch, et al.
Journal of Medical Genetics|January 20, 2017
Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with <i>de novo</i>, heterozygous, loss-of-function mutations in <i>ASXL3</i> and review of published literatureM Balasubramanian, J Willoughby, A E Fry, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 27, 2020
De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 femalesD L Polla, E J Bhoj, J B G M Verheij, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Cureus|December 22, 2025
An Open Label, Randomized, Comparative Bioavailability Study of BioTurm™ Extract Versus Curcuma longa Extract With Piperine in Healthy Adult VolunteersVineet K Malhotra, Anil C Deshpande, Sanjay Tamoli, et al.
Clinical and Experimental Dermatology|October 1, 2013
Homozygous variegate porphyria presenting with developmental and language delay in childhoodV A E Pinder, S T Holden, C Deshpande, et al.
Marine Pollution Bulletin|March 19, 2023
Material flow analysis of commercial fishing gears in TaiwanChing-Tuan Su, Falk Schneider, Paritosh C Deshpande, et al.
The American Journal of Cardiology|August 30, 2008
A clinical risk score for prediction of stent thrombosisKenneth W Baran, John M Lasala, David A Cox, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|May 19, 2004
The effect of poly(ethylene glycol) molecular architecture on cellular interaction and uptake of DNA complexesMangesh C Deshpande, Martyn C Davies, Martin C Garnett, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|February 19, 2011
A clinical risk score for the prediction of very late stent thrombosis in drug eluting stent patientsKenneth W Baran, John M Lasala, David A Cox, et al.
The American Journal of Cardiology|March 31, 2009
One-year outcomes from the TAXUS express stent versus cypher stentManuel Mayor, Amir Z Malik, Robert J Minor, et al.
Diagnostic Cytopathology|November 22, 2011
Evaluation of EGFR mutation status in cytology specimens: an institutional experienceD L Aisner, C Deshpande, Z Baloch, et al.
Journal of Medical Genetics|January 20, 2017
Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with <i>de novo</i>, heterozygous, loss-of-function mutations in <i>ASXL3</i> and review of published literatureM Balasubramanian, J Willoughby, A E Fry, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 27, 2020
De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 femalesD L Polla, E J Bhoj, J B G M Verheij, et al.
Pageof 5