Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sailaja Maddhuri"'
Autor:
Shilpa Reddy, Sailaja Maddhuri, Pratibha Nallari, Venkateshwari Ananthapur, Srinivas Kalyani, Murali Krishna, Nirmala Cherkuri, Sireesha Patibandala
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-11 (2021)
Abstract Background Type 1 diabetes mellitus (TIDM) is a polygenic disorder with the involvement of several genetic and environmental risk factors. Mutation in genes namely ABCC8 and KCNJ11 disrupt the potentiality of KATP channel and regulates the s
Externí odkaz:
https://doaj.org/article/c48c1a6b15ac42bb8e21574b29aca806
Autor:
Sailaja Maddhuri, Srinivas Kalyani, Pratibha Nallari, Nirmala Cherkuri, Sireesha Patibandala, Shilpa Reddy, Venkateshwari Ananthapur, Murali Krishna
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-11 (2021)
Background Type 1 diabetes mellitus (TIDM) is a polygenic disorder with the involvement of several genetic and environmental risk factors. Mutation in genes namely ABCC8 and KCNJ11 disrupt the potentiality of KATP channel and regulates the secretion
Autor:
N. Pratibha Nallari, Amaresh Rao Malempati, Sailaja Maddhuri, Suresh Gudala, Chandana Lakkaraju, Hema Prasad Mundluru
Publikováno v:
Meta Gene. 15:16-22
Myocyte enhancer factor-2A (MEF2A), encoding a member of the MEF2 family of transcription factors, has been identified for primary CAD and MI without other accompanying clinical feature. It plays a role in vascular ontogeny and shows its predominant
Autor:
HemaPrasad Mundluru, Pratibha Nallari, ChaitanyaKumar Bhukya, Sailaja Maddhuri, Jyothy Akka, Sunitha Tella, PardhanandanaReddy Penagaluru, Priyanka Pallapolu
Publikováno v:
International Journal of Advanced Research. 4:539-546
Autor:
Gudlla Suresh, Hema Prasad Mundluru, Srinivas Bandaru, Priyanka Pallapollu, Akka Jyothy, Amaresh Rao Mallempati, Sailaja Maddhuri
Publikováno v:
Folia Cardiologica. 11:272-278
Introduction. The present investigation is pursued to study the possible association of –463G>A and –129G>A polymorphism in MPO gene and assessment of plasma MPO levels with the risk of developing coronary artery disease. Material and methods. A
Autor:
Sailaja Maddhuri, Praveen Kumar Vemuri, Jahnavi Tatineni, Jharna Puppala, Vijaya Lakshmi Bodiga
Publikováno v:
Research Journal of Pharmacy and Technology. 13:599
The present study aims to evaluate the possible association of PPP3R1 gene polymorphism (CnB 5I/5D) in clinical presentation of mental retardation (MR). A total of 100 children with idiopathic mental retardation in the age group of 5-16 years from bo
Autor:
Pratibha Nallari, Hema Prasad Mundluru, Amaresh Rao Malempati, Vinod Cingeetham, Sailaja Maddhuri, Chaitanya Kumar Bhukya, Srinivas Bandaru, M.L.N. Deepika
Publikováno v:
Gene. 632
Calcineurin, a serine/threonine phosphatase is a calcium dependent protein which on activation triggers transcriptional up regulation of inflammatory genes associated with inflammation in the arteries and progressive formation of plaques in CAD. The