Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Sekar, Kanthimathi"'
Autor:
Visvanathan Gnanaprakash, Dhanasekaran Bodhini, Sekar Kanthimathi, Kumaradas Ginivenisha, Coimbatore Subramanian Shanthirani, Ranjit Mohan Anjana, Viswanathan Mohan, Venkatesan Radha
Publikováno v:
Journal of Diabetology, Vol 10, Iss 1, Pp 29-36 (2019)
Background: Vitamin D deficiency is known to be involved in the development of insulin resistance and type 2 diabetes (T2D), and the functions of Vitamin D are mediated through Vitamin D receptor (VDR). Only a few reports are available in the Asian I
Externí odkaz:
https://doaj.org/article/b722016f18ab46d49adfb49166d356b2
Autor:
Swati Kanodia, Sanket Pendsey, Sundaramoorthy Gopi, Rajesh Kumar, Babu Kavitha, Rajesh Joshi, Sharad Pendsey, Alagarsamy Kannan, Venkatesan Radha, Sekar Kanthimathi, Viswanathan Mohan, Archana Dayal Arya, P Raghupathy
Publikováno v:
Pediatric Diabetes. 22:82-92
Background There are very few reports pertaining to Indian patients with neonatal diabetes mellitus (NDM). Activating or gain of function mutations of KATP channel genes namely KCNJ11 and ABCC8 are most predominant cause of permanent neonatal diabete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::388b4cf2056130d2ff131685468fdb77
https://doi.org/10.1111/pedi.13109
https://doi.org/10.1111/pedi.13109
Autor:
Babu Kavitha, Viswanathan Mohan, Rakesh Kumar, Rajesh Joshi, Archana Dayal Arya, Sanket Pendsey, Swati Kanodia, Sundaramoorthy Gopi, Sekar Kanthimathi, Alagarsamy Kannan, Sharad Pendsey, P Raghupathy, V Radha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdd8335ca6f89bbfbcfab95f6d9ce39b
https://doi.org/10.1111/pedi.13109/v2/response1
https://doi.org/10.1111/pedi.13109/v2/response1
Autor:
Sundaramoorthy, Gopi, Babu, Kavitha, Sekar, Kanthimathi, Alagarsamy, Kannan, Rakesh, Kumar, Rajesh, Joshi, Swati, Kanodia, Archana Dayal, Arya, Sanket, Pendsey, Sharad, Pendsey, Palany, Raghupathy, Viswanathan, Mohan, Venkatesan, Radha
Publikováno v:
Pediatric diabetesREFERENCES. 22(1)
There are very few reports pertaining to Indian patients with neonatal diabetes mellitus (NDM). Activating or gain of function mutations of KTo identify the genotype-phenotype correlation of KDirect sequencing of all exons of KCNJ11 and ABCC8 genes i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b94e26cc3f36bb32688f923b4506b14
https://pubmed.ncbi.nlm.nih.gov/32893419
https://pubmed.ncbi.nlm.nih.gov/32893419
Autor:
Viswanathan Mohan, Aruyerchelvan Bhavatharini, Sekar Kanthimathi, Ram Uma, Manickam Chidambaram, Ranjit Mohan Anjana, Dhanasekaran Bodhini, Samuel Liju, Venkatesan Radha
Publikováno v:
Molecular Genetics and Genomics. 292:585-591
Earlier studies have provided evidence that the gestational diabetes mellitus (GDM) and Type 2 diabetes mellitus (T2DM) share common genetic background. A recent genome wide association study (GWAS) showed a strong association of six novel gene varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::946c3224efd21ca24f83693e6bfc3902
https://doi.org/10.1007/s00438-017-1292-6
https://doi.org/10.1007/s00438-017-1292-6
Autor:
Balakannan Revathi, Natarajan Sathish, Viswanathan Mohan, Manickam Chidambaram, Samuel Liju, Dhanasekaran Bodhini, Saurabh Ghosh, Venkatesan Radha, Dhandapani Laasya, Ranjit Mohan Anjana, Sekar Kanthimathi
Publikováno v:
Annals of Human Genetics. 80:336-341
This study reports on the association of genetic variants selected from previous genome-wide association studies for type 2 diabetic nephropathy in south Indians. Eight variants were genotyped in 601 type 2 diabetic subjects without nephropathy (DM)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95b6d373204d2a847cd758655260f363
https://doi.org/10.1111/ahg.12174
https://doi.org/10.1111/ahg.12174
Autor:
Viswanathan Mohan, Venkatesan Radha, Ranjit Mohan Anjana, Sekar Kanthimathi, Dhandapani Laasya, Samuel Liju
Publikováno v:
Annals of Human Genetics. 80:241-245
Summary Hexokinase domain containing 1 (HKDC1), a novel human hexokinase gene, is known to affect glucose metabolism and was shown to have a strong association with 2-h plasma glucose in pregnant women in a recent genome wide association study. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fe7a1997c2ebe6d0480e2463c020f2e
https://doi.org/10.1111/ahg.12155
https://doi.org/10.1111/ahg.12155
Autor:
Narayanaswamy Srinivasan, Radha, Kandasamy Balamurugan, Swapnil Mahajan, Lise Bjørkhaug, Sekar Kanthimathi, Pål R. Njølstad, Mohan
Publikováno v:
Clinical Genetics. 90:486-495
Maturity-onset diabetes of the young (MODY) is a genetically heterogeneous monogenic form of diabetes characterized by onset of diabetes below 25years of age, autosomal dominant mode of inheritance and primary defect in insulin secretion. Mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5546a25a272cd28702c5da99bd00cfd
https://doi.org/10.1111/cge.12757
https://doi.org/10.1111/cge.12757
Autor:
Kandasamy Balamurugan, Viswanathan Mohan, Vijay Gayathri, Venkatesan Radha, Coimbatore Subramaniyam Shanthirani, Sekar Kanthimathi
Publikováno v:
Annals of Human Genetics. 79:10-19
Summary Heterozygous mutations of the HNF1B gene (HNF1B-MODY or MODY5) are associated with a wide clinical spectrum of renal and extrarenal disease without clear genotype–phenotype correlation. In this study, we investigated the prevalence of HNF1B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49e469d77d07fd29b2630e3a182ad57f
https://doi.org/10.1111/ahg.12093
https://doi.org/10.1111/ahg.12093