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C Haworth

Showing results (131-140 of 143) with videos related to

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The New Phytologist|November 22, 2016
Informing models through empirical relationships between foliar phosphorus, nitrogen and photosynthesis across diverse woody species in tropical forests of PanamaRichard J Norby, Lianhong Gu, Ivan C Haworth, et al.
Human Molecular Genetics|March 1, 1995
A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type IC R Greenberg, D Reimer, R Singal, et al.
American Journal of Human Genetics|November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiencyAndreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|November 1, 1993
Vitamin D deficiency in a Manitoba communityJ B Lebrun, M E Moffatt, R J Mundy, et al.
Paediatrics & Child Health|January 5, 2010
Congenital rickets caused by maternal vitamin D deficiencyA Micheil Innes, Molly M Seshia, Chitra Prasad, et al.
American Journal of Human Genetics|June 19, 1998
Amerindian pyruvate carboxylase deficiency is associated with two distinct missense mutationsM A Carbone, N MacKay, M Ling, et al.
The Journal of Pediatrics|January 1, 1991
Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindredsJ C Haworth, F A Booth, A E Chudley, et al.
Molecular Genetics and Metabolism|February 5, 2002
Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, CanadaC R Greenberg, A N Prasad, L A Dilling, et al.
Molecular Genetics and Metabolism|May 15, 2001
Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.
Molecular Genetics and Metabolism|February 17, 2009
The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populationsCheryl R Greenberg, Louise A Dilling, G Robert Thompson, et al.
Pageof 15

Showing results (131-140 of 143) with videos related to

Sort By:
Pageof 15
The New Phytologist|November 22, 2016
Informing models through empirical relationships between foliar phosphorus, nitrogen and photosynthesis across diverse woody species in tropical forests of PanamaRichard J Norby, Lianhong Gu, Ivan C Haworth, et al.
Human Molecular Genetics|March 1, 1995
A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type IC R Greenberg, D Reimer, R Singal, et al.
American Journal of Human Genetics|November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiencyAndreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|November 1, 1993
Vitamin D deficiency in a Manitoba communityJ B Lebrun, M E Moffatt, R J Mundy, et al.
Paediatrics & Child Health|January 5, 2010
Congenital rickets caused by maternal vitamin D deficiencyA Micheil Innes, Molly M Seshia, Chitra Prasad, et al.
American Journal of Human Genetics|June 19, 1998
Amerindian pyruvate carboxylase deficiency is associated with two distinct missense mutationsM A Carbone, N MacKay, M Ling, et al.
The Journal of Pediatrics|January 1, 1991
Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindredsJ C Haworth, F A Booth, A E Chudley, et al.
Molecular Genetics and Metabolism|February 5, 2002
Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, CanadaC R Greenberg, A N Prasad, L A Dilling, et al.
Molecular Genetics and Metabolism|May 15, 2001
Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.
Molecular Genetics and Metabolism|February 17, 2009
The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populationsCheryl R Greenberg, Louise A Dilling, G Robert Thompson, et al.
Pageof 15