Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Srikanth Singamsetty"'
Autor:
Yoshio Watanabe, Srikanth Singamsetty, Baobo Zou, Lanping Guo, Darko Stefanovski, Laura C Alonso, Adolfo Garcia-Ocana, Christopher P O'Donnell, Bryan J McVerry
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e67716 (2013)
OBJECTIVES:The development of hyperglycemia and the use of early parenteral feeding are associated with poor outcomes in critically ill patients. We therefore examined the impact of exogenous glucose administration on the integrated metabolic functio
Externí odkaz:
https://doaj.org/article/6921dadee4f546eb8cb48fa84fa4d68c
Autor:
Jessica Ludwig, Onkar B. Sawant, Jill Wood, Srikanth Singamsetty, Xuefang Pan, Vera L. Bonilha, Sujata Rao, Alexey V. Pshezhetsky
Publikováno v:
Experimental Eye Research. 229:109433
Autor:
Shan Li, Sean Ekins, Feng Wang, Steven Q. Le, Tsui-Fen Chou, Chelsee Sauni, Brett Lomenick, Xiaoyi Zhang, Patricia I. Dickson, Shih Hsin Kan, Srikanth Singamsetty, Jill Wood, Derek R. Moen
Publikováno v:
Molecular Pharmaceutics. 18:214-227
There is currently no cure or effective treatment available for mucopolysaccharidosis type IIID (MPS IIID, Sanfilippo syndrome type D), a lysosomal storage disorder (LSD) caused by the deficiency of α-N-acetylglucosamine-6-sulfatase (GNS). The clini
Autor:
Tsui-Fen Chou, Feng Wang, Steven Le, Shan Li, Srikanth Singamsetty, Jill Wood, Patricia I. Dickson
Publikováno v:
Molecular Genetics and Metabolism. 135:S31-S32
Autor:
Fen Wang, George A. Lopez, Tsui-Fen Chou, Jill Wood, Patricia I. Dickson, Kai-Wen Cheng, Srikanth Singamsetty
Publikováno v:
Biochem J
Enzyme replacement therapy (ERT) is a scientifically rational and clinically proven treatment for lysosomal storage diseases. Most enzymes used for ERT are purified from the culture supernatant of mammalian cells. However, it is challenging to purify
Autor:
Feng, Wang, Derek R, Moen, Chelsee, Sauni, Shih-Hsin, Kan, Shan, Li, Steven Q, Le, Brett, Lomenick, Xiaoyi, Zhang, Sean, Ekins, Srikanth, Singamsetty, Jill, Wood, Patricia I, Dickson, Tsui-Fen, Chou
Publikováno v:
Mol Pharm
There is currently no cure or effective treatment available for mucopolysaccharidosis type IIID (MPS IIID, Sanfilippo syndrome type D), a lysosomal storage disorder (LSD) caused by the deficiency of α-N-acetylglucosamine-6-sulfatase (GNS). The clini
Publikováno v:
Molecular Genetics and Metabolism. 135:S71
Autor:
Jill Wood, Alexey V. Pshezhetsky, Xuefang Pan, Sujata Rao, Onkar B. Sawant, Srikanth Singamsetty
Publikováno v:
Molecular Genetics and Metabolism. 129:S162-S163
Autor:
Sruti Shiva, Michael J. Jurczak, Catherine Corey, Lanping Guo, Faraaz Ali Shah, Bryan J. McVerry, Srikanth Singamsetty, Christopher P. O'Donnell, Simona Ioja
Publikováno v:
Oxidative Medicine and Cellular Longevity, Vol 2018 (2018)
Oxidative Medicine and Cellular Longevity
Oxidative Medicine and Cellular Longevity
Although acute exposure to hypoxia can disrupt metabolism, longer-term exposure may normalize glucose homeostasis or even improve glucose disposal in the presence of obesity. We examined the effects of two-week exposure to room air (Air), continuous
Autor:
Sruti Shiva, Yoshio Watanabe, Catherine Corey, Lanping Guo, Jesús Tejero, Yinna Wang, Christopher P. O'Donnell, Mark T. Gladwin, Bryan J. McVerry, Srikanth Singamsetty
Publikováno v:
The Journal of Physiology. 593:3135-3145
Nitrite acts as an endocrine source of bioactive nitric oxide, impacting vascular reactivity, angiogenesis and cytoprotection. Nitrite has recently been shown to have a metabolic role although its effects and mechanisms of action in the obese insulin