Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Stephen H. Smith"'
Autor:
Kai Wang, Stephen H. Smith, Hirotaka Iijima, Zachary R. Hettinger, Adarsh Mallepally, Sanjeev G. Shroff, Fabrisia Ambrosio
Publikováno v:
Advanced Materials. 35
Publikováno v:
Bulletin of Marine Science. 96:785-802
A survey conducted in Fall 2017 by US Navy scientists around the small, uninhabited island of Farallon de Medinilla (FDM) documented severe bleaching related to extended regional heat stress. Three of the dominant scleractinian genera at FDM, Pocillo
Autor:
Stephen H. Smith
Publikováno v:
Irish Theological Quarterly. 85:109-126
In recent years, debate has resumed regarding whether or not the post-resurrection appearances may have been hallucinations or delusions on the part of the disciples. A sub-category of this debate is the question of bereavement hallucinations. Was th
Autor:
Mohun Ramratnam, Guy Salama, Ravi K Sharma, David Wen Rui Wang, Stephen H Smith, Sanjay K Banerjee, Xueyin N Huang, Lindsey M Gifford, Michele L Pruce, Bethann E Gabris, Samir Saba, Sanjeev G Shroff, Ferhaan Ahmad
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0167681 (2016)
Most studies of the mechanisms leading to hereditary dilated cardiomyopathy (DCM) have been performed in reconstituted in vitro systems. Genetically engineered murine models offer the opportunity to dissect these mechanisms in vivo. We generated a ge
Externí odkaz:
https://doaj.org/article/1d85a8f426dd47978e0da7492464e7eb
Autor:
Stephen H. Smith
Publikováno v:
The Heythrop Journal. 61:689-700
Autor:
Stephen H. Smith
Publikováno v:
Neotestamentica. 53:53-78
Autor:
Ferhaan Ahmad, Sanjay K Banerjee, Michele L Lage, Xueyin N Huang, Stephen H Smith, Samir Saba, Jennifer Rager, David A Conner, Andrzej M Janczewski, Kimimasa Tobita, Joseph P Tinney, Ivan P Moskowitz, Antonio R Perez-Atayde, Bradley B Keller, Michael A Mathier, Sanjeev G Shroff, Christine E Seidman, J G Seidman
Publikováno v:
PLoS ONE, Vol 3, Iss 7, p e2642 (2008)
Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mutations, including cardiac troponin T (cTnT, TNNT2). We determined whether TNNT2 mutations cause cardiomyopathies by altering cTnT function or quantity; whether th
Externí odkaz:
https://doaj.org/article/cd3d3ebeca6e44d79a325dd4ab1ab7e6
Autor:
Stephen H Smith, Samir Saba, Guy Salama, David W. Wang, Ferhaan Ahmad, Xueyin N Huang, Sanjeev G. Shroff, Mohun Ramratnam, Ravi K. Sharma, Bethann Gabris, Michele L. Pruce, Lindsey M Gifford, Sanjay K. Banerjee
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 12, p e0167681 (2016)
PLoS ONE, Vol 11, Iss 12, p e0167681 (2016)
Most studies of the mechanisms leading to hereditary dilated cardiomyopathy (DCM) have been performed in reconstituted in vitro systems. Genetically engineered murine models offer the opportunity to dissect these mechanisms in vivo. We generated a ge
Autor:
Donald E. Marx, Stephen H Smith
Publikováno v:
Marine pollution bulletin. 102(1)
Fourteen surveys were conducted at Farallon De Medinilla (a U.S. Department of Defense bombing range in the Mariana Archipelago) between 1997 and 2012; annual surveys were conducted from 1999 through 2012. There was no evidence that the condition of
Autor:
Franklin Fuchs, Stephen H Smith
Publikováno v:
Journal of Molecular and Cellular Cardiology. 34:547-554
Although ATP is the immediate source of energy for muscle contraction other nucleoside triphosphates (NTP) can substitute for ATP as substrates for myosin and as sources of energy for contraction of skinned muscle fibers. However, experiments with sk