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R Rozen

Showing results (101-110 of 154) with videos related to

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Genomics|May 1, 1994
Assignment of the gene (UQCRFS1) for the Rieske iron-sulfur protein subunit of the mitochondrial cytochrome bc1 complex to the 22q13 and 19q12-q13.1 regions of the human genomeA M Duncan, L Anderson, C Duff, et al.
American Journal of Medical Genetics|November 1, 1986
Clinical application of DNA analysis in a family with OTC deficiencyR E McClead, R Rozen, J Fox, et al.
Molecular Genetics and Metabolism|February 3, 2000
Methylenetetrahydrofolate reductase 677 C --> T polymorphism, plasma folate, vitamin B(12) concentrations, and risk of preeclampsia among black African women from ZimbabweA Rajkovic, K Mahomed, R Rozen, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 1999
Cerebral vascular complication and hyperhomocysteinemia in a cystinotic uremic childA Merouani, J Genest, R Rozen, et al.
The Journal of Biological Chemistry|July 25, 1984
Regulation and expression of carbamyl phosphate synthetase I mRNA in developing rat liver and Morris hepatoma 5123DJ Ryall, R A Rachubinski, M Nguyen, et al.
Kidney International|July 2, 1998
Molecular genetics of cystinuria: mutation analysis of SLC3A1 and evidence for another gene in type I (silent) phenotypeI Saadi, X Z Chen, M Hediger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 29, 1998
Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)P Goyette, A Pai, R Milos, et al.
Nature Structural Biology|April 14, 1999
The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemiaB D Guenther, C A Sheppard, P Tran, et al.
Journal of Inherited Metabolic Disease|April 17, 2008
Mefolinate (5-methyltetrahydrofolate), but not folic acid, decreases mortality in an animal model of severe methylenetetrahydrofolate reductase deficiencyD Li, N Karp, Q Wu, et al.
Human Mutation|February 19, 2000
Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuriaS Sibani, B Christensen, E O'Ferrall, et al.
Pageof 16

Showing results (101-110 of 154) with videos related to

Sort By:
Pageof 16
Genomics|May 1, 1994
Assignment of the gene (UQCRFS1) for the Rieske iron-sulfur protein subunit of the mitochondrial cytochrome bc1 complex to the 22q13 and 19q12-q13.1 regions of the human genomeA M Duncan, L Anderson, C Duff, et al.
American Journal of Medical Genetics|November 1, 1986
Clinical application of DNA analysis in a family with OTC deficiencyR E McClead, R Rozen, J Fox, et al.
Molecular Genetics and Metabolism|February 3, 2000
Methylenetetrahydrofolate reductase 677 C --> T polymorphism, plasma folate, vitamin B(12) concentrations, and risk of preeclampsia among black African women from ZimbabweA Rajkovic, K Mahomed, R Rozen, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 1999
Cerebral vascular complication and hyperhomocysteinemia in a cystinotic uremic childA Merouani, J Genest, R Rozen, et al.
The Journal of Biological Chemistry|July 25, 1984
Regulation and expression of carbamyl phosphate synthetase I mRNA in developing rat liver and Morris hepatoma 5123DJ Ryall, R A Rachubinski, M Nguyen, et al.
Kidney International|July 2, 1998
Molecular genetics of cystinuria: mutation analysis of SLC3A1 and evidence for another gene in type I (silent) phenotypeI Saadi, X Z Chen, M Hediger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 29, 1998
Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)P Goyette, A Pai, R Milos, et al.
Nature Structural Biology|April 14, 1999
The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemiaB D Guenther, C A Sheppard, P Tran, et al.
Journal of Inherited Metabolic Disease|April 17, 2008
Mefolinate (5-methyltetrahydrofolate), but not folic acid, decreases mortality in an animal model of severe methylenetetrahydrofolate reductase deficiencyD Li, N Karp, Q Wu, et al.
Human Mutation|February 19, 2000
Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuriaS Sibani, B Christensen, E O'Ferrall, et al.
Pageof 16