Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Battini Mohan Reddy"'
Autor:
Kumuda Irgam, Battini Sriteja Reddy, Sai Gayathri Hari, Swathi Banapuram, Battini Mohan Reddy
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-13 (2021)
Abstract Background The genetic association studies of type 2 diabetes mellitus (T2DM) hitherto undertaken among the Indian populations are grossly inadequate representation of the ethnic and geographic heterogeneity of the country. In view of this a
Externí odkaz:
https://doaj.org/article/1f2b51f1526f4ce9af4a7236b6f93f2d
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-7 (2020)
Abstract Development of coronary artery disease (CAD) is primarily due to the process of atherosclerosis, however the prognosis of CAD depends on pleiotropic effects of the genes located at 9p21.3 region. Genome wide association studies revealed asso
Externí odkaz:
https://doaj.org/article/c8733a33320d4a5b9c0b2a94b6f417ec
Publikováno v:
Lipids in Health and Disease, Vol 16, Iss 1, Pp 1-9 (2017)
Abstract Background Given the characteristic atherogenic dyslipidemia of south Indian population and crucial role of APOA1, APOC3, APOA4 and APOA5 genes clustered in 11q23.3 chromosomal region in regulating lipoprotein metabolism and cholesterol home
Externí odkaz:
https://doaj.org/article/05b055c3645c4a0d91b242ff24d13345
Autor:
Rayabarapu Pranav Chand, Arramraju Sreenivas Kumar, Kapadia Anuj, Satti Vishnupriya, Battini Mohan Reddy
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0153720 (2016)
In our attempt to comprehensively understand the nature of association of variants at 11q23.3 apolipoprotein gene cluster region, we genotyped a prioritized set of 96 informative SNPs using Fluidigm customized SNP genotyping platform in a sample of 5
Externí odkaz:
https://doaj.org/article/3a46b83b908040f9a79f16782ffc1c0c
Autor:
Kommoju Uma Jyothi, Maruda Jayaraj, Kadarkarai Samy Subburaj, Kotla Jaya Prasad, Irgam Kumuda, Velaga Lakshmi, Battini Mohan Reddy
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60212 (2013)
We attempt to evaluate the nature of association of TCF7L2 gene variants with T2DM, for the first time in the population of Hyderabad, which is considered to be diabetic capital of India. It is a case-control study of the three SNPs of TCF7L2, rs7903
Externí odkaz:
https://doaj.org/article/2e92652d0c5a48488d14655b7d494925
Autor:
Sai Gayathri Hari, Swathi Banapuram, Battini Mohan Reddy, Battini Sriteja Reddy, Kumuda Irgam
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-13 (2021)
BMC Medical Genomics
BMC Medical Genomics
Background The genetic association studies of type 2 diabetes mellitus (T2DM) hitherto undertaken among the Indian populations are grossly inadequate representation of the ethnic and geographic heterogeneity of the country. In view of this and due to
Akademický článek
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Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-7 (2020)
Scientific Reports
Scientific Reports
Development of coronary artery disease (CAD) is primarily due to the process of atherosclerosis, however the prognosis of CAD depends on pleiotropic effects of the genes located at 9p21.3 region. Genome wide association studies revealed association o
Publikováno v:
Gene. 701:113-120
We explored genetic susceptibility profile of the South Indian women with a large set of SNPs and tested if the lack of association of type 2 diabetes genes with PCOS, recently observed in a number of studies, holds true for this Indian population an
Publikováno v:
Journal of biosciences. 44(1)
In this review, we briefly outlined salient features of pathophysiology and results of the genetic association studies hitherto conducted on type 2 diabetes. Primarily focusing on the current status of genomic research, we briefly discussed the limit