Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rajasekhar Moka"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 3, Pp GR01-GR04 (2017)
Gerbode defects are rare Ventricular Septal Defects (VSD) constituting approximately one percent cases of congenital heart diseases. The genetic predispositions towards the Gerbode Defect (GD) have remained an unexplored area of study till date. We
Externí odkaz:
https://doaj.org/article/155d53b4d65f4d8ca9c0a9c2e7715e3e
Publikováno v:
Journal of Human Reproductive Sciences, Vol 6, Iss 2, Pp 129-132 (2013)
Aim: The objective of this study was to correlate the genotype, of female patients, withshort stature and primary amenorrhea. Materials and Methods: One hundred and forty-six subjects were recruited during 2005-2012. Microscopic and automated karyoty
Externí odkaz:
https://doaj.org/article/f52070c421f64959a65ab863a7d311da
Publikováno v:
In Gene Reports June 2023 31
Autor:
Prabodh Kumar, Ganesh Paramasivam, Tom Devasia, Mukund Prabhu, Maneesh K. Rai, K. Prakashini, Sandeep Mallya, Dinesh Reghunathan, A. Megha, Krishnananda Nayak, Rajasekhar Moka
Publikováno v:
Indian Journal of Clinical Biochemistry.
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. :188-191
Objective: Intellectual disability is the most common developmental disorder that originates before the age of 18 years and is characterized by limitation in intellectual functioning and adaptive behaviour. The fact that >30 to 50% of all causes are
Autor:
Nidhya Teresa Joseph, Rajasekhar Moka
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. :98-103
Objective: Arsenic has cytotoxic as well as mutagenic effect in human health due to its indirect effect on oxidative stress on the cells. We aimed to find out the effect of gallic acid (GA), a well-known natural antioxidant in ameliorating in heavy m
Autor:
Kapaettu Satyamoorthy, Kanive Parashiva Guruprasad, Sharath Mohan Bhat, Mangala Hegde, Rajasekhar Moka, Manjunath B. Joshi, L Ramachandra
Publikováno v:
Biology of the cellREFERENCES. 114(2)
Background information Excessive angiogenesis characterized by leaky, tortuous and chaotic vasculature is one of the hallmarks of cancers and is significantly correlated to poor prognosis. Disorganized angiogenesis leads to poor perfusion of anti-can
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. :100-103
Objective: Cardiac septal defects (CSDs), the most common human congenital heart malformations are complex and heterogeneous. Progress in molecular biology has helped to identify many genes responsible for cardiac morphogenesis. However, etiologic fa
Autor:
Tom Devasia, Prabodh Kumar, Krishnananda Nayak, Rajasekhar Moka, Manjunath B. Joshi, A. Megha, Prakashini K, Ganesh Paramasivam
Publikováno v:
Circulation. Genomic and precision medicine. 13(3)
Publikováno v:
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences, Vol 6, Iss 2, Pp 129-132 (2013)
Journal of Human Reproductive Sciences, Vol 6, Iss 2, Pp 129-132 (2013)
Aim: The objective of this study was to correlate the genotype, of female patients, withshort stature and primary amenorrhea. Materials and Methods: One hundred and forty-six subjects were recruited during 2005-2012. Microscopic and automated karyoty