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Venkatesan Radha

Showing results (51-60 of 86) with videos related to

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Annals of Human Genetics|October 5, 2016
Association of rs11643718 SLC12A3 and rs741301 ELMO1 Variants with Diabetic Nephropathy in South Indian PopulationDhanasekaran Bodhini, Manickam Chidambaram, Samuel Liju, et al.
Journal of Diabetes and Its Complications|October 1, 2021
Insulin gene mutations linked to permanent neonatal diabetes mellitus in Indian populationSundaramoorthy Gopi, Palanisamy Gowri, Jayant Kumar Panda, et al.
Frontiers in Endocrinology|October 24, 2024
Exploring lipodystrophy gene expression in adipocytes: unveiling insights into the pathogenesis of insulin resistance, type 2 diabetes, and clustering diseases (metabolic syndrome) in Asian IndiansAditya Saxena, Pradeep Tiwari, Shalu Gupta, et al.
Diabetes Technology & Therapeutics|February 28, 2015
Identification of Genetic Variants of Gestational Diabetes in South IndiansSekar Kanthimathi, Manickam Chidambaram, Samuel Liju, et al.
Primary Care Diabetes|April 13, 2023
Prevalence, clinical features and complications of common forms of Maturity Onset Diabetes of the Young (MODY) seen at a tertiary diabetes centre in south IndiaRamasamy Aarthy, Kathryn Aston-Mourney, Anandakumar Amutha, et al.
Scientific Reports|July 14, 2023
Identification of appropriate biochemical parameters and cut points to detect Maturity Onset Diabetes of Young (MODY) in Asian Indians in a clinic settingRamasamy Aarthy, Kathryn Aston-Mourney, Anandakumar Amutha, et al.
Diabetes|April 24, 2025
Paradoxical maturity-onset diabetes of the young (MODY) arising from loss-of-function mutations in ATP-sensitive potassium channelsRosa Scala, Yunpeng Li, Jian Gao, et al.
Plos One|November 29, 2017
Interaction between TCF7L2 polymorphism and dietary fat intake on high density lipoprotein cholesterolDhanasekaran Bodhini, Szilvia Gaal, Israa Shatwan, et al.
Pediatric Diabetes|September 7, 2020
Genotype-phenotype correlation of K<sub>ATP</sub> channel gene defects causing permanent neonatal diabetes in Indian patientsSundaramoorthy Gopi, Babu Kavitha, Sekar Kanthimathi, et al.
Gene|June 19, 2023
A novel mutation in the KCNJ11 gene (p.Val36Glu), predisposes to congenital hyperinsulinemiaIdrees A Shah, Rabiya Rashid, Abid Bhat, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Annals of Human Genetics|October 5, 2016
Association of rs11643718 SLC12A3 and rs741301 ELMO1 Variants with Diabetic Nephropathy in South Indian PopulationDhanasekaran Bodhini, Manickam Chidambaram, Samuel Liju, et al.
Journal of Diabetes and Its Complications|October 1, 2021
Insulin gene mutations linked to permanent neonatal diabetes mellitus in Indian populationSundaramoorthy Gopi, Palanisamy Gowri, Jayant Kumar Panda, et al.
Frontiers in Endocrinology|October 24, 2024
Exploring lipodystrophy gene expression in adipocytes: unveiling insights into the pathogenesis of insulin resistance, type 2 diabetes, and clustering diseases (metabolic syndrome) in Asian IndiansAditya Saxena, Pradeep Tiwari, Shalu Gupta, et al.
Diabetes Technology & Therapeutics|February 28, 2015
Identification of Genetic Variants of Gestational Diabetes in South IndiansSekar Kanthimathi, Manickam Chidambaram, Samuel Liju, et al.
Primary Care Diabetes|April 13, 2023
Prevalence, clinical features and complications of common forms of Maturity Onset Diabetes of the Young (MODY) seen at a tertiary diabetes centre in south IndiaRamasamy Aarthy, Kathryn Aston-Mourney, Anandakumar Amutha, et al.
Scientific Reports|July 14, 2023
Identification of appropriate biochemical parameters and cut points to detect Maturity Onset Diabetes of Young (MODY) in Asian Indians in a clinic settingRamasamy Aarthy, Kathryn Aston-Mourney, Anandakumar Amutha, et al.
Diabetes|April 24, 2025
Paradoxical maturity-onset diabetes of the young (MODY) arising from loss-of-function mutations in ATP-sensitive potassium channelsRosa Scala, Yunpeng Li, Jian Gao, et al.
Plos One|November 29, 2017
Interaction between TCF7L2 polymorphism and dietary fat intake on high density lipoprotein cholesterolDhanasekaran Bodhini, Szilvia Gaal, Israa Shatwan, et al.
Pediatric Diabetes|September 7, 2020
Genotype-phenotype correlation of K<sub>ATP</sub> channel gene defects causing permanent neonatal diabetes in Indian patientsSundaramoorthy Gopi, Babu Kavitha, Sekar Kanthimathi, et al.
Gene|June 19, 2023
A novel mutation in the KCNJ11 gene (p.Val36Glu), predisposes to congenital hyperinsulinemiaIdrees A Shah, Rabiya Rashid, Abid Bhat, et al.
Pageof 9