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Venkatesan Radha

Showing results (21-30 of 86) with videos related to

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Frontiers in Endocrinology|July 3, 2023
Molecular characterization and re-interpretation of <i>HNF1A</i> variants identified in Indian MODY subjects towards precision medicineBabu Kavitha, Sampathkumar Ranganathan, Sundaramoorthy Gopi, et al.
The American Journal of Cardiology|April 26, 2006
Association of lipoprotein lipase Hind III and Ser 447 Ter polymorphisms with dyslipidemia in Asian IndiansVenkatesan Radha, Viswanathan Mohan, Ramprakash Vidya, et al.
Diabetes Technology & Therapeutics|June 15, 2011
GLUT4 gene polymorphisms and their association with type 2 diabetes in south IndiansDhanasekaran Bodhini, Venkatesan Radha, Saurabh Ghosh, et al.
Clinical Genetics|November 27, 2024
The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal CommunityVandana Jain, Venkatesan Radha, Viswanathan Mohan, et al.
Metabolism: Clinical and Experimental|March 31, 2005
Association of low adiponectin levels with the metabolic syndrome--the Chennai Urban Rural Epidemiology Study (CURES-4)Viswanathan Mohan, Raj Deepa, Rajendra Pradeepa, et al.
Metabolic Syndrome and Related Disorders|December 1, 2009
A haplotype at the UCP1 gene locus contributes to genetic risk for type 2 diabetes in Asian Indians (CURES-72)Karani S Vimaleswaran, Venkatesan Radha, Saurabh Ghosh, et al.
Diabetes Technology & Therapeutics|December 24, 2010
Uncoupling protein 2 and 3 gene polymorphisms and their association with type 2 diabetes in asian indiansKarani S Vimaleswaran, Venkatesan Radha, Saurabh Ghosh, et al.
Hormone Research in Paediatrics|September 9, 2025
Neonatal Diabetes: 20-Year Experience from a Tertiary Care Pediatric Diabetes Clinic in North IndiaRakesh Kumar, Devi Dayal, Arun George, et al.
The Journal of the Association of Physicians of India|June 24, 2025
Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with <i>LIPE</i> Gene Defect: A Case ReportViswanathan Mohan, Varun Anil Damle, Akshay Vikas Patil, et al.
Medical Sciences (Basel, Switzerland)|April 23, 2025
Congenital Hyperinsulinism India Association: An Approach to Address the Challenges and Opportunities of a Rare DiseaseJaikumar B Contractor, Venkatesan Radha, Krati Shah, et al.
Pageof 9

Showing results (21-30 of 86) with videos related to

Sort By:
Pageof 9
Frontiers in Endocrinology|July 3, 2023
Molecular characterization and re-interpretation of <i>HNF1A</i> variants identified in Indian MODY subjects towards precision medicineBabu Kavitha, Sampathkumar Ranganathan, Sundaramoorthy Gopi, et al.
The American Journal of Cardiology|April 26, 2006
Association of lipoprotein lipase Hind III and Ser 447 Ter polymorphisms with dyslipidemia in Asian IndiansVenkatesan Radha, Viswanathan Mohan, Ramprakash Vidya, et al.
Diabetes Technology & Therapeutics|June 15, 2011
GLUT4 gene polymorphisms and their association with type 2 diabetes in south IndiansDhanasekaran Bodhini, Venkatesan Radha, Saurabh Ghosh, et al.
Clinical Genetics|November 27, 2024
The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal CommunityVandana Jain, Venkatesan Radha, Viswanathan Mohan, et al.
Metabolism: Clinical and Experimental|March 31, 2005
Association of low adiponectin levels with the metabolic syndrome--the Chennai Urban Rural Epidemiology Study (CURES-4)Viswanathan Mohan, Raj Deepa, Rajendra Pradeepa, et al.
Metabolic Syndrome and Related Disorders|December 1, 2009
A haplotype at the UCP1 gene locus contributes to genetic risk for type 2 diabetes in Asian Indians (CURES-72)Karani S Vimaleswaran, Venkatesan Radha, Saurabh Ghosh, et al.
Diabetes Technology & Therapeutics|December 24, 2010
Uncoupling protein 2 and 3 gene polymorphisms and their association with type 2 diabetes in asian indiansKarani S Vimaleswaran, Venkatesan Radha, Saurabh Ghosh, et al.
Hormone Research in Paediatrics|September 9, 2025
Neonatal Diabetes: 20-Year Experience from a Tertiary Care Pediatric Diabetes Clinic in North IndiaRakesh Kumar, Devi Dayal, Arun George, et al.
The Journal of the Association of Physicians of India|June 24, 2025
Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with <i>LIPE</i> Gene Defect: A Case ReportViswanathan Mohan, Varun Anil Damle, Akshay Vikas Patil, et al.
Medical Sciences (Basel, Switzerland)|April 23, 2025
Congenital Hyperinsulinism India Association: An Approach to Address the Challenges and Opportunities of a Rare DiseaseJaikumar B Contractor, Venkatesan Radha, Krati Shah, et al.
Pageof 9