Search Results - "Kadakol, Gurushantappa"

Assessment of Glu504 Lys Genotype and Single Nucleotide Polymorphisms in Exon 12 and 13 of ALDH2 Gene in Alcoholic Liver Cirrhosis patients in Northern Karnataka,India: A Cross-sectional Study by Biradar, Siddanagouda M, Reddy, Y Sethu, Bulagouda, Rudragouda S, Kadakol, Gurushantappa S

“…Introduction: Alcoholic Liver Disease (ALD) is one of the most significant issues affecting the world today and is the principal cause of atleast 60 of the…”
Get full text

Chemokine Receptor Gene (CCR5) Polymorphism in Acute Coronary Syndrome: A Cross-sectional Study by Prashanth, MR, Badiger, Sharan, Kadakol, Gurushantappa

“…Introduction: Acute coronary syndrome is a multifactorial disease with a complex pathogenesis, mainly resulting from the interplay of genetic and environmental…”
Get full text

Mutation Analysis of Exon 1 in the Hemoglobin Subunit Beta (HBB) Gene in Beta-Thalassemia by Kumar, K Sharath, Patil, Mallanagouda M, Bulagouda, Rudragouda, Kadakol, Gurushantappa S

“…Introduction Thalassemia is a widely prevalent monogenic hematological disorder found worldwide. It exists in two forms: alpha- and beta-thalassemia…”
Get full text

Molecular basis of β-thalassemia in Karnataka, India by Kulkarni, Gururaj D, Kulkarni, Suyamindra S, Kadakol, Gurushantappa S, Kulkarni, Bhushan B, Kyamangoudar, Prakashgouda H, Lakkakula, Bhaskar V K S, Thangaraj, Kumarasamy, Shepur, Tipperudra A, Kulkarni, Muralidhar L, Gai, Pramod B

“…In β-thalassemia, point mutations in the β-globin gene are largely responsible for either decreased or no β-globin synthesis. The β-globin gene has three exons…”
Get more information

Macrophage Migration Inhibitory Factor Gene Polymorphism in Acute Coronary Syndrome by M J, Likitha, Badiger, Sharan, Kadakol, Gurushantappa S

“…Background Acute coronary syndrome (ACS) is a result of the interplay between genetic and environmental risk factors. A unique cytokine macrophage migration…”
Get full text

63 Clinical Cytological Study on Klinefelter Syndrome by Siddanagouda M Biradar, Rudragouda S Bulagouda, Gurushantappa Kadakol

“…Klinefelter Syndrome is a chromosomal disorder with addition of X sex chromosome (47XXY) in males. A patient attended to our hospital with loss of secondary…”
Get full text

Clinical & Cytological Study on Klinefelter Syndrome by Biradar, Siddanagouda M, Bulagouda, Rudragouda S, Kadakol, Gurushantappa

“…Case Report A 20-year-old married male was brought to our superspeciality Centre, Sri В M Patii Medical College and Research Institute, Vijayapur Karnataka,…”
Get full text

Variation in Exon 29 of the NOS1 Gene Does Not Contribute to Parkinson’s Disease in the North Karnataka Population by Bulagouda, Rudragouda, Hegde, Smita, Hegde, Rajat, Hiremath, Ashwini, Wali, G M, Kadakol, Gurushantappa S

“…Introduction: Nitric oxide (NO) overproduction has been found to have neurotoxic effects on the brain. Moreover, in…”
Get full text