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of 5
pro vyhledávání: '"Philippa Rogers"'
Autor:
Peter A. Kropp, Philippa Rogers, Sydney E. Kelly, Rebecca McWhirter, Willow D. Goff, Ian M. Levitan, David M. Miller, Andy Golden
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 2 (2023)
Externí odkaz:
https://doaj.org/article/7fad760d19074a22ad90ec75e984d5ed
Autor:
Peter A Kropp, Jing Wu, Michael Reidy, Sanjay Shrestha, Kyle Rhodehouse, Philippa Rogers, Michael N Sack, Andy Golden
Publikováno v:
PLoS Genetics, Vol 17, Iss 8, p e1009771 (2021)
Multiple Mitochondrial Dysfunctions Syndrome 1 (MMDS1) is a rare, autosomal recessive disorder caused by mutations in the NFU1 gene. NFU1 is responsible for delivery of iron-sulfur clusters (ISCs) to recipient proteins which require these metallic co
Externí odkaz:
https://doaj.org/article/eebc84e01da84107a8a3c5604eb644ba
Autor:
Michael Reidy, Andy Golden, Sanjay Shrestha, Philippa Rogers, Kyle Rhodehouse, Peter A. Kropp, Michael N. Sack, Jing Wu
Publikováno v:
PLoS Genetics, Vol 17, Iss 8, p e1009771 (2021)
PLoS Genetics
PLoS Genetics
Multiple Mitochondrial Dysfunctions Syndrome 1 (MMDS1) is a rare, autosomal recessive disorder caused by mutations in the NFU1 gene. NFU1 is responsible for delivery of iron-sulfur clusters (ISCs) to recipient proteins which require these metallic co
Autor:
Kevin Cleary, Julius Cuong Pham, Linda Matthew, Philippa Rogers, Sukhmeet S Panesar, Joyce A. Wahr, Andrew D. Shore, Lindsay H. Harris, Peter J. Pronovost
Publikováno v:
American Journal of Medical Quality. 29:61-69
The objective was to compare the characteristics of medication errors reported to 2 national error reporting systems by conducting a cross-sectional analysis of errors reported from adult intensive care units to the UK National Reporting and Learning
Autor:
Philippa Rogers
Publikováno v:
Labour History. :229