K
Kinnari N. Mistry
Researcher at Sardar Patel University
Publications - 36
Citations - 307
Kinnari N. Mistry is an academic researcher from Sardar Patel University. The author has contributed to research in topics: Diabetes mellitus & Type 2 diabetes. The author has an hindex of 10, co-authored 35 publications receiving 267 citations. Previous affiliations of Kinnari N. Mistry include Aribas.
Papers
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Journal ArticleDOI
In silico analysis of single nucleotide polymorphism (SNP) in human TNF-α gene.
Brijesh Dabhi,Kinnari N. Mistry +1 more
TL;DR: It is suggested that P84L and A94T variants of TNF-α could directly or indirectly destabilize the amino acid interactions and hydrogen bond networks thus explaining the functional deviations of protein to some extent.
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Non-enzymatic glycosylation of immunoglobulins in diabetic nephropathy.
TL;DR: Glycosylation of IgG is an equivalent marker for advanced glycosylated hemoglobin as GHb and may have some role to play in the on onset of diabetic nephropathy by altering their immunoreactivity leading to microvascular complications.
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Oxidative stress and its association with TNF-α-308 G/C and IL-1α-889 C/T gene polymorphisms in patients with diabetes and diabetic nephropathy.
Brijesh Dabhi,Kinnari N. Mistry +1 more
TL;DR: The higher serum levels of oxidative stress markers in diabetic patients with nephropathy suggest the possible role of oxidative Stress in West Indian population.
In vitro anti-diabetic and anti-inflammatory activity of stem bark of bauhinia purpurea
TL;DR: The results obtained indicate that the extracts of Bauhinia purpurea stem bark possessed significant level of activity; the highest concentration of extract was high effective as an anti-diabetic and anti-inflammatory agent.
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Non enzymatic glycosylation of IgG and their urinary excretion in patients with diabetic nephropathy
Kinnari N. Mistry,Kiran Kalia +1 more
TL;DR: Serum IgG, glycosylation of IgG and urinary IgG excretion were increased significantly in diabetic patients compared to healthy controls, which were further increase significantly in chronic renal failure patients with respect to the clinical stage of nephropathy.