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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 Population
Dhanasekaran 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 population
Sundaramoorthy 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 Indians
Aditya Saxena, Pradeep Tiwari, Shalu Gupta, et al.
Diabetes Technology & Therapeutics
|
February 28, 2015
Identification of Genetic Variants of Gestational Diabetes in South Indians
Sekar 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 India
Ramasamy 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 setting
Ramasamy 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 channels
Rosa Scala, Yunpeng Li, Jian Gao, et al.
Plos One
|
November 29, 2017
Interaction between TCF7L2 polymorphism and dietary fat intake on high density lipoprotein cholesterol
Dhanasekaran 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 patients
Sundaramoorthy Gopi, Babu Kavitha, Sekar Kanthimathi, et al.
Gene
|
June 19, 2023
A novel mutation in the KCNJ11 gene (p.Val36Glu), predisposes to congenital hyperinsulinemia
Idrees A Shah, Rabiya Rashid, Abid Bhat, et al.
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of 9
Search research articles
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Showing results (51-60 of 86) with videos related to
Sort By:
Page
of 9
Annals of Human Genetics
|
October 5, 2016
Association of rs11643718 SLC12A3 and rs741301 ELMO1 Variants with Diabetic Nephropathy in South Indian Population
Dhanasekaran 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 population
Sundaramoorthy 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 Indians
Aditya Saxena, Pradeep Tiwari, Shalu Gupta, et al.
Diabetes Technology & Therapeutics
|
February 28, 2015
Identification of Genetic Variants of Gestational Diabetes in South Indians
Sekar 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 India
Ramasamy 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 setting
Ramasamy 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 channels
Rosa Scala, Yunpeng Li, Jian Gao, et al.
Plos One
|
November 29, 2017
Interaction between TCF7L2 polymorphism and dietary fat intake on high density lipoprotein cholesterol
Dhanasekaran 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 patients
Sundaramoorthy Gopi, Babu Kavitha, Sekar Kanthimathi, et al.
Gene
|
June 19, 2023
A novel mutation in the KCNJ11 gene (p.Val36Glu), predisposes to congenital hyperinsulinemia
Idrees A Shah, Rabiya Rashid, Abid Bhat, et al.
Page
of 9