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Showing results (431-440 of 614) with videos related to

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Journal of AOAC International|June 29, 2025
Validation of the OnSite® Gluten Test Kit for Detection of Gluten in Selected Foods and Environmental Surfaces: AOAC Performance Tested MethodSM 012501Meiting Wu, Lora Benoit, Cesar Nadala, et al.
Chemical Communications (Cambridge, England)|April 27, 2013
A fluorescent "2 in 1" proton sensor and polarity probe based on core substituted naphthalene diimideHeather F Higginbotham, Rosalind P Cox, Saman Sandanayake, et al.
The Journal of Biological Chemistry|July 5, 2014
Biophysical optimization of a therapeutic protein by nonstandard mutagenesis: studies of an iodo-insulin derivativeVijay Pandyarajan, Nelson B Phillips, Gabriela P Cox, et al.
Pediatric Research|November 14, 1997
Apoptosis in the brains of infants suffering intrauterine cerebral injuryA D Edwards, X Yue, P Cox, et al.
Neuropediatrics|December 22, 1999
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1F Muntoni, F Goodwin, C Sewry, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Localization of the dihydrolipoamide branched-chain transacylase gene (DBT) of the human branched-chain keto acid dehydrogenase complex to chromosome 1K S Lau, R L Eddy, T B Shows, et al.
The Journal of Biological Chemistry|February 25, 1989
Molecular phenotypes in cultured maple syrup urine disease cells. Complete E1 alpha cDNA sequence and mRNA and subunit contents of the human branched chain alpha-keto acid dehydrogenase complexC W Fisher, J L Chuang, T A Griffin, et al.
Nature Genetics|August 31, 2010
The ratio of human X chromosome to autosome diversity is positively correlated with genetic distance from genesMichael F Hammer, August E Woerner, Fernando L Mendez, et al.
The Journal of Clinical Investigation|September 1, 1991
Maple syrup urine disease in Mennonites. Evidence that the Y393N mutation in E1 alpha impedes assembly of the E1 component of branched-chain alpha-keto acid dehydrogenase complexC R Fisher, J L Chuang, R P Cox, et al.
Biochemical and Biophysical Research Communications|January 31, 1991
A 17-bp insertion and a Phe215----Cys missense mutation in the dihydrolipoyl transacylase (E2) mRNA from a thiamine-responsive maple syrup urine disease patient WG-34C W Fisher, K S Lau, C R Fisher, et al.
Pageof 62

Showing results (431-440 of 614) with videos related to

Sort By:
Pageof 62
Journal of AOAC International|June 29, 2025
Validation of the OnSite® Gluten Test Kit for Detection of Gluten in Selected Foods and Environmental Surfaces: AOAC Performance Tested MethodSM 012501Meiting Wu, Lora Benoit, Cesar Nadala, et al.
Chemical Communications (Cambridge, England)|April 27, 2013
A fluorescent "2 in 1" proton sensor and polarity probe based on core substituted naphthalene diimideHeather F Higginbotham, Rosalind P Cox, Saman Sandanayake, et al.
The Journal of Biological Chemistry|July 5, 2014
Biophysical optimization of a therapeutic protein by nonstandard mutagenesis: studies of an iodo-insulin derivativeVijay Pandyarajan, Nelson B Phillips, Gabriela P Cox, et al.
Pediatric Research|November 14, 1997
Apoptosis in the brains of infants suffering intrauterine cerebral injuryA D Edwards, X Yue, P Cox, et al.
Neuropediatrics|December 22, 1999
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1F Muntoni, F Goodwin, C Sewry, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Localization of the dihydrolipoamide branched-chain transacylase gene (DBT) of the human branched-chain keto acid dehydrogenase complex to chromosome 1K S Lau, R L Eddy, T B Shows, et al.
The Journal of Biological Chemistry|February 25, 1989
Molecular phenotypes in cultured maple syrup urine disease cells. Complete E1 alpha cDNA sequence and mRNA and subunit contents of the human branched chain alpha-keto acid dehydrogenase complexC W Fisher, J L Chuang, T A Griffin, et al.
Nature Genetics|August 31, 2010
The ratio of human X chromosome to autosome diversity is positively correlated with genetic distance from genesMichael F Hammer, August E Woerner, Fernando L Mendez, et al.
The Journal of Clinical Investigation|September 1, 1991
Maple syrup urine disease in Mennonites. Evidence that the Y393N mutation in E1 alpha impedes assembly of the E1 component of branched-chain alpha-keto acid dehydrogenase complexC R Fisher, J L Chuang, R P Cox, et al.
Biochemical and Biophysical Research Communications|January 31, 1991
A 17-bp insertion and a Phe215----Cys missense mutation in the dihydrolipoyl transacylase (E2) mRNA from a thiamine-responsive maple syrup urine disease patient WG-34C W Fisher, K S Lau, C R Fisher, et al.
Pageof 62