Association of Fetuin-A with Thr256Ser exon polymorphism of alpha2-Heremans Schmid Glycoprotein (AHSG) gene in type 2 diabetic patients with overt nephropathy.

Keywords : ["schmid glycoprotein ahsg gene", "type diabetic patient", "overt nephropathy", "exon polymorphism", "fetuina", "association"]
Author : D Umapathy
45

Association of Fetuin-A with Thr256Ser exon polymorphism of alpha2-Heremans Schmid Glycoprotein (AHSG) gene in type 2 diabetic patients with overt nephropathy.

Keywords : ["schmid glycoprotein ahsg gene", "type diabetic patient", "overt nephropathy", "exon polymorphism", "fetuina", "association"]
Author : D Umapathy
42

Estradiol overcomes adiponectin-resistance in diabetic mice by regulating skeletal muscle adiponectin receptor 1 expression.

Keywords : ["regulate skeletal muscle adiponectin receptor expression", "estradiol overcome adiponectinresistance", "diabetic mouse"]
Author : S Chattopadhyay
79

Functional Gly297Ser Variant of the Physiological Dysglycemic Peptide Pancreastatin Is a Novel Risk Factor for Cardiometabolic Disorders.

Keywords : ["physiological dysglycemic peptide pancreastatin", "novel risk factor", "functional variant", "cardiometabolic disorder"]
Author : PKR Allu
79

L-Methionine prevents beta-cell damage by modulating the expression of Arx, MafA and regulation of FOXO1 in type 1 diabetic rats.

Keywords : ["lmethionine prevent betacell damage", "type diabetic rat", "arx mafa", "regulation", "modulate", "expression"]
Author : U Navik
59

Association between serum netrin-1, netrin-4 and risk of the acute coronary syndrome in patients with type 2 diabetes mellitus-A pilot study.

Keywords : ["type diabetes mellitusa pilot study", "acute coronary syndrome", "serum", "risk", "patient", "association"]
Author : K Inderjeet
44

Diabetes and pre-diabetes in patients with heart failure and preserved ejection fraction.

Keywords : ["preserve ejection fraction", "heart failure", "prediabete", "patient", "diabetes"]
Author : AM Jackson
99

Lissencephaly-pachygyria spectrum in a North Indian boy with Wolcott-Rallison syndrome due to homozygous deletion of exon 1 in the EIF2AK3 gene.

Keywords : ["wolcottrallison syndrome due", "north indian boy", "lissencephalypachygyria spectrum", "homozygous deletion", "gene", "exon"]
Author : A Gupta
147

WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India.

Keywords : ["geneassociate diabetes phenotype", "southern india", "founder mutation", "identification"]
Author : A Chapla
79

Adverse drug reactions of GLP-1 agonists: A systematic review of case reports.

Keywords : ["adverse drug reaction", "systematic review", "case report", "agonist"]
Author : R Shetty
181