Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Babu Kavitha"'
Autor:
Babu Kavitha, Sampathkumar Ranganathan, Sundaramoorthy Gopi, Umashankar Vetrivel, Nagarajan Hemavathy, Viswanathan Mohan, Venkatesan Radha
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundHNF1A is an essential component of the transcription factor network that controls pancreatic β-cell differentiation, maintenance, and glucose stimulated insulin secretion (GSIS). A continuum of protein malfunction is caused by variations i
Externí odkaz:
https://doaj.org/article/14d3494cf9024ecf8ef34b3e32eeb811
Autor:
Venkatesan Radha, Bhuvanagiri Ramya, Sundaramoorthy Gopi, Babu Kavitha, Somayajula Preetika, Kalpana Thai, Ranjit Unnikrishnan, Viswanathan Mohan, Prasanna Kumar Gupta
Publikováno v:
Journal of Diabetology, Vol 9, Iss 2, Pp 65-67 (2018)
Neonatal diabetes mellitus (NDM) is a monogenic form of diabetes mellitus that occurs in the first 6 months of life. It is a rare condition with a prevalence of 1 in 100,000–500,000 live births. We report a 3-month-old girl child with high blood gl
Externí odkaz:
https://doaj.org/article/0389530990004ed38db100c7afde76d0
Autor:
Babu, Kavitha, Zhang, Jinbi, Moloney, Stephanie, Pleasants, Tony, McLean, Cameron A., Phua, Sin H., Sheppard, Allan M.
Publikováno v:
In Journal of Proteomics 27 June 2012 75(12):3410-3418
Autor:
Swati Kanodia, Sanket Pendsey, Sundaramoorthy Gopi, Rajesh Kumar, Babu Kavitha, Rajesh Joshi, Sharad Pendsey, Alagarsamy Kannan, Venkatesan Radha, Sekar Kanthimathi, Viswanathan Mohan, Archana Dayal Arya, P Raghupathy
Publikováno v:
Pediatric Diabetes. 22:82-92
Background There are very few reports pertaining to Indian patients with neonatal diabetes mellitus (NDM). Activating or gain of function mutations of KATP channel genes namely KCNJ11 and ABCC8 are most predominant cause of permanent neonatal diabete
Autor:
Babu Kavitha, Kandasamy Balamurugan, Viswanathan Mohan, Zhongying Yang, Venkatesan Radha, Show Ling Shyng
Publikováno v:
Pediatric Diabetes. 20:397-407
BACKGROUND: Gain-of-function of ATP-sensitive K+ (KATP ) channels because of mutations in the genes encoding SUR1 (ABCC8) or Kir6.2 (KCNJ11) is a major cause of neonatal diabetes mellitus (NDM). Our aim is to determine molecular defects in KATP chann
Publikováno v:
Anesthesia: Essays & Researches. Apr-Jun2018, Vol. 12 Issue 2, p313-317. 5p.
Autor:
Babu Kavitha, Viswanathan Mohan, Rakesh Kumar, Rajesh Joshi, Archana Dayal Arya, Sanket Pendsey, Swati Kanodia, Sundaramoorthy Gopi, Sekar Kanthimathi, Alagarsamy Kannan, Sharad Pendsey, P Raghupathy, V Radha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdd8335ca6f89bbfbcfab95f6d9ce39b
https://doi.org/10.1111/pedi.13109/v2/response1
https://doi.org/10.1111/pedi.13109/v2/response1
Autor:
Sundaramoorthy, Gopi, Babu, Kavitha, Sekar, Kanthimathi, Alagarsamy, Kannan, Rakesh, Kumar, Rajesh, Joshi, Swati, Kanodia, Archana Dayal, Arya, Sanket, Pendsey, Sharad, Pendsey, Palany, Raghupathy, Viswanathan, Mohan, Venkatesan, Radha
Publikováno v:
Pediatric diabetesREFERENCES. 22(1)
There are very few reports pertaining to Indian patients with neonatal diabetes mellitus (NDM). Activating or gain of function mutations of KTo identify the genotype-phenotype correlation of KDirect sequencing of all exons of KCNJ11 and ABCC8 genes i
Publikováno v:
In Journal of Colloid And Interface Science 2007 310(1):184-189
Autor:
Babu Kavitha, P. Varalakshmi
Publikováno v:
Communications in Computer and Information Science ISBN: 9789811086021
Cloud computing is a good paradigm which utilizes virtualization technology to isolate the workloads from one another as well as elastic in nature. Cloud providers possessing multiples of Virtual Machines (VM) to perform the full functionality demand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::769807528c388b95c9b08a70742b20f1
https://doi.org/10.1007/978-981-10-8603-8_9
https://doi.org/10.1007/978-981-10-8603-8_9