Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Patrick Putnam"'
Autor:
Muhammad Tariq, Thanh-Tam Le, Patrick Putnam, Steven Kindel, Mehdi Keddache, Stephanie M. Ware
Publikováno v:
Cardiogenetics, Vol 2, Iss 1, Pp e7-e7 (2012)
Pediatric cardiomyopathy is a genetically heterogeneous disease associated with significant morbidity. Although identification of underlying etiology is important for management, therapy, and screening of at risk family members, molecular diagnosis i
Externí odkaz:
https://doaj.org/article/559b6dbb7f6144e78ec72a5578381b5f
Autor:
Rachel Sheridan, Kristin Lampe, Shiva Kumar Shanmukhappa, Patrick Putnam, Mehdi Keddache, Senad Divanovic, Jorge Bezerra, Kasper Hoebe
Publikováno v:
PLoS ONE, Vol 6, Iss 7, p e21979 (2011)
Using a small scale ENU mutagenesis approach we identified a recessive germline mutant, designated Lampe1 that exhibited growth retardation and spontaneous hepatosteatosis. Low resolution mapping based on 20 intercrossed Lampe1 mice revealed linkage
Externí odkaz:
https://doaj.org/article/33e71703d69d4f61ae6f46f632937462
Publikováno v:
Simulation Modelling Practice and Theory. 28:55-64
Time Warp synchronized parallel discrete event simulators are organized to operate asynchronously and aggressively without explicit synchronization between the concurrently executing simulation objects. In place of an explicit synchronization mechani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae936e8ff206896bbd1e275d5bb701d6
https://doi.org/10.1016/j.simpat.2012.05.011
https://doi.org/10.1016/j.simpat.2012.05.011
Autor:
Mehdi Keddache, Steven J. Kindel, Patrick Putnam, Thanh-Tam Le, Muhammad Tariq, Stephanie M. Ware
Publikováno v:
Cardiogenetics; Volume 2; Issue 1; Pages: e7
Cardiogenetics, Vol 2, Iss 1 (2012)
Cardiogenetics, Vol 2, Iss 1, Pp e7-e7 (2012)
Cardiogenetics, Vol 2, Iss 1 (2012)
Cardiogenetics, Vol 2, Iss 1, Pp e7-e7 (2012)
Pediatric cardiomyopathy is a genetically heterogeneous disease associated with significant morbidity. Although identification of underlying etiology is important for management, therapy, and screening of at risk family members, molecular diagnosis i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96a4498e54ff93b81ba82449c5ec119b
Autor:
Jorge A. Bezerra, Shiva Kumar Shanmukhappa, Mehdi Keddache, Kasper Hoebe, Patrick Putnam, Kristin Lampe, Senad Divanovic, Rachel Sheridan
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 7, p e21979 (2011)
PLoS ONE, Vol 6, Iss 7, p e21979 (2011)
Using a small scale ENU mutagenesis approach we identified a recessive germline mutant, designated Lampe1 that exhibited growth retardation and spontaneous hepatosteatosis. Low resolution mapping based on 20 intercrossed Lampe1 mice revealed linkage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80439d8a2b677f0f3108ef3345987d36
http://europepmc.org/articles/PMC3131302
http://europepmc.org/articles/PMC3131302
Publikováno v:
BMC Bioinformatics
Background In recent years genetic data analysis has seen a rapid increase in the scale of data to be analyzed. Schadt et al (NRG 11:647–657, 2010) offered that with data sets approaching the petabyte scale, data related challenges such as formatti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d6eea21715e19b551d0ef4ea19ff38c