Zobrazeno 1 - 10
of 83
pro vyhledávání: '"A Tiradani"'
Autor:
Mhashilkar, Parag, Altunay, Mine, Berman, Eileen, Dagenhart, David, Fuess, Stuart, Holzman, Burt, Kowalkowski, James, Litvintsev, Dmitry, Lu, Qiming, Moibenko, Alexander, Paterno, Marc, Spentzouris, Panagiotis, Timm, Steven, Tiradani, Anthony, Vaandering, Eric, Hover, John, Bejar, Jose Caballero
HEPCloud is rapidly becoming the primary system for provisioning compute resources for all Fermilab-affiliated experiments. In order to reliably meet the peak demands of the next generation of High Energy Physics experiments, Fermilab must plan to el
Externí odkaz:
http://arxiv.org/abs/1904.08988
Autor:
Altunay, Mine, Dagenhart, W. David, Fuess, Stuart, Holzman, Burt, Kowalkowski, Jim, Litvintsev, Dmitry, Lu, Qiming, Mhashilkar, Parag, Moibenko, Alexander, Paterno, Marc, Spentzouris, Panagiotis, Timm, Steven, Tiradani, Anthony
The next generation of High Energy Physics experiments are expected to generate exabytes of data---two orders of magnitude greater than the current generation. In order to reliably meet peak demands, facilities must either plan to provision enough re
Externí odkaz:
http://arxiv.org/abs/1806.03224
Autor:
Holzman, Burt, Bauerdick, Lothar A. T., Bockelman, Brian, Dykstra, Dave, Fisk, Ian, Fuess, Stuart, Garzoglio, Gabriele, Girone, Maria, Gutsche, Oliver, Hufnagel, Dirk, Kim, Hyunwoo, Kennedy, Robert, Magini, Nicolo, Mason, David, Spentzouris, Panagiotis, Tiradani, Anthony, Timm, Steve, Vaandering, Eric W.
Publikováno v:
Comput Softw Big Sci (2017) 1:1
Historically, high energy physics computing has been performed on large purpose-built computing systems. These began as single-site compute facilities, but have evolved into the distributed computing grids used today. Recently, there has been an expo
Externí odkaz:
http://arxiv.org/abs/1710.00100
Autor:
Vasco Meneghini, Annalisa Lattanzi, Luigi Tiradani, Gabriele Bravo, Francesco Morena, Francesca Sanvito, Andrea Calabria, John Bringas, Jeanne M Fisher‐Perkins, Jason P Dufour, Kate C Baker, Claudio Doglioni, Eugenio Montini, Bruce A Bunnell, Krystof Bankiewicz, Sabata Martino, Luigi Naldini, Angela Gritti
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 5, Pp 489-510 (2016)
Abstract Metachromatic leukodystrophy (MLD) and globoid cell leukodystrophy (GLD or Krabbe disease) are severe neurodegenerative lysosomal storage diseases (LSD) caused by arylsulfatase A (ARSA) and galactosylceramidase (GALC) deficiency, respectivel
Externí odkaz:
https://doaj.org/article/df4a76df4d1e46e5afca6e405d504c4a
Autor:
Hufnagel Dirk, Holzman Burt, Mason David, Mhashilkar Parag, Timm Steven, Tiradani Anthony, Aftab Khan Farrukh, Gutsche Oliver, Bloom Kenneth
Publikováno v:
EPJ Web of Conferences, Vol 214, p 03031 (2019)
The higher energy and luminosity from the LHC in Run 2 have put increased pressure on CMS computing resources. Extrapolating to even higher luminosities (and thus higher event complexities and trigger rates) beyond Run 3, it becomes clear that simply
Externí odkaz:
https://doaj.org/article/fdf91bb9645a45bea922e9531080fae8
Autor:
Eric Wayne Vaandering, W. David Dagenhart, Mine Altunay, Burt Holzman, James B. Kowalkowski, Qiming Lu, E. Berman, Dmitry Litvintsev, S. Fuess, Parag Mhashilkar, Alexander Moibenko, Anthony Tiradani, Steven Timm, Jose Caballero Bejar, Marc Paterno, John Hover, Panagiotis Spentzouris
Publikováno v:
EPJ Web of Conferences, Vol 214, p 03060 (2019)
DOE / OSTI
DOE / OSTI
HEPCloud is rapidly becoming the primary system for provisioning compute resources for all Fermilab-affiliated experiments. In order to reliably meet the peak demands of the next generation of High Energy Physics experiments, Fermilab must plan to el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76260352547f20dd07971eca5a83d91a
https://www.epj-conferences.org/articles/epjconf/pdf/2019/19/epjconf_chep2018_03060.pdf
https://www.epj-conferences.org/articles/epjconf/pdf/2019/19/epjconf_chep2018_03060.pdf
Autor:
Kate C. Baker, Vasco Meneghini, Bruce A. Bunnell, Gabriele Bravo, Angela Gritti, Annalisa Lattanzi, Claudio Doglioni, Sabata Martino, Luigi Tiradani, John Bringas, Luigi Naldini, Eugenio Montini, Andrea Calabria, Francesco Morena, Krystof S. Bankiewicz, Francesca Sanvito, Jason Dufour, Jeanne M. Fisher-Perkins
Publikováno v:
EMBO molecular medicine, vol 8, iss 5
EMBO Molecular Medicine
EMBO Molecular Medicine
Metachromatic leukodystrophy (MLD) and globoid cell leukodystrophy (GLD or Krabbe disease) are severe neurodegenerative lysosomal storage diseases (LSD) caused by arylsulfatase A (ARSA) and galactosylceramidase (GALC) deficiency, respectively. Our pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6882eddb70d8d4146947d15405d21b9f
https://doi.org/10.15252/emmm.201505850
https://doi.org/10.15252/emmm.201505850
Autor:
Parag Mhashilkar, S. Fuess, Anthony Tiradani, Panagiotis Spentzouris, Burt Holzman, Mine Altunay, Steven Timm, Jim Kowalkowski, Dmitry Litvintsev, Marc Paterno, W. Dagenhart, Qiming Lu, Alexander Moibenko
Publikováno v:
CCGrid
The next generation of High Energy Physics experiments are expected to generate exabytes of data---two orders of magnitude greater than the current generation. In order to reliably meet peak demands, facilities must either plan to provision enough re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c20a64b0dc2ff600e4aeb466e20a2a5a
https://doi.org/10.1109/ccgrid.2018.00053
https://doi.org/10.1109/ccgrid.2018.00053
Autor:
Lattanzi Annalisa, Tiradani Luigi, Bravo Gabriele, Morena Francesco, Sanvito Francesca, Calabria Andrea, Bringas John, Fisher Perkins Jeanne M., Dufour Jason P., Baker Kate C., Montini Eugenio, Bunnell Bruce A., Bankiewicz Krystof, Martino Sabata, Naldini Luigi, Gritti Angela, DOGLIONI , CLAUDIO
Metachromatic leukodystrophy (MLD) and globoid cell leukodystrophy (GLD or Krabbe disease) are severe neurodegenerative lysosomal storage diseases (LSD) caused by arylsulfatase A (ARSA) and galactosylceramidase (GALC) deficiency, respectively. Our pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10495::bd752a7d13711d1067af582d45a191fd
Autor:
Rita Marabese, Claudio Bardelli, Luigi Tiradani, Michela Godi, Gianni Bona, Mara Giordano, Simona Mellone, Patricia Momigliano-Richiardi, Simonetta Bellone, Flavia Prodam, Mariacarolina Salerno, Antonella Petri
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 97:E1791-E1797
Context: Mutations within the PROP1 gene represent one of the main causes of familial combined pituitary hormone deficiency (CPHD). However, most of the cases are sporadic with an unknown genetic cause. Objective: The aim of this study was the search
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a4583aa83194347b07a4b26e5289b67
https://doi.org/10.1210/jc.2012-1527
https://doi.org/10.1210/jc.2012-1527