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Y Indo

Showing results (11-20 of 51) with videos related to

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Progress in Clinical and Biological Research|January 1, 1990
Molecular cloning and nucleotide sequence of cDNA encoding the rat long chain acyl-CoA dehydrogenase precursorY Indo, H Ozasa, Y Ikeda, et al.
Progress in Clinical and Biological Research|January 1, 1992
Molecular cloning and nucleotide sequence of cDNAs encoding human long chain acyl-CoA dehydrogenase and assignment of its gene to chromosome 2Y Indo, T Yang-Feng, R Glassberg, et al.
The Journal of Clinical Investigation|September 1, 1990
Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutationI Yokota, Y Indo, P M Coates, et al.
Genomics|March 1, 1992
Molecular cloning and nucleotide sequence of cDNAs encoding human long-chain acyl-CoA dehydrogenase and assignment of the location of its gene (ACADL) to chromosome 2Y Indo, T Yang-Feng, R Glassberg, et al.
Genomics|November 1, 1991
Molecular cloning and nucleotide sequence of cDNAs encoding human long-chain acyl-CoA dehydrogenase and assignment of the location of its gene (ACADL) to chromosome 2Y Indo, T Yang-Feng, R Glassberg, et al.
Seikagaku. the Journal of Japanese Biochemical Society|February 1, 1992
[Maple syrup urine disease: molecular pathology of the branched chain alpha-keto acid dehydrogenase complex]Y Nobukuni, H Mitsubuchi, Y Indo, et al.
American Journal of Medical Genetics|June 19, 1998
Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypesT Kawano, Y Indo, H Nakazato, et al.
The Journal of Clinical Investigation|July 1, 1987
Altered kinetic properties of the branched-chain alpha-keto acid dehydrogenase complex due to mutation of the beta-subunit of the branched-chain alpha-keto acid decarboxylase (E1) component in lymphoblastoid cells derived from patients with maple syrup urine diseaseY Indo, A Kitano, F Endo, et al.
Human Genetics|September 1, 1988
Maple syrup urine disease: a possible biochemical basis for the clinical heterogeneityY Indo, I Akaboshi, Y Nobukuni, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A structural abnormality of E1 component of the branched-chain alpha-keto acid dehydrogenase complex in maple syrup urine diseaseY Indo, A Kitano, I Akaboshi, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Progress in Clinical and Biological Research|January 1, 1990
Molecular cloning and nucleotide sequence of cDNA encoding the rat long chain acyl-CoA dehydrogenase precursorY Indo, H Ozasa, Y Ikeda, et al.
Progress in Clinical and Biological Research|January 1, 1992
Molecular cloning and nucleotide sequence of cDNAs encoding human long chain acyl-CoA dehydrogenase and assignment of its gene to chromosome 2Y Indo, T Yang-Feng, R Glassberg, et al.
The Journal of Clinical Investigation|September 1, 1990
Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutationI Yokota, Y Indo, P M Coates, et al.
Genomics|March 1, 1992
Molecular cloning and nucleotide sequence of cDNAs encoding human long-chain acyl-CoA dehydrogenase and assignment of the location of its gene (ACADL) to chromosome 2Y Indo, T Yang-Feng, R Glassberg, et al.
Genomics|November 1, 1991
Molecular cloning and nucleotide sequence of cDNAs encoding human long-chain acyl-CoA dehydrogenase and assignment of the location of its gene (ACADL) to chromosome 2Y Indo, T Yang-Feng, R Glassberg, et al.
Seikagaku. the Journal of Japanese Biochemical Society|February 1, 1992
[Maple syrup urine disease: molecular pathology of the branched chain alpha-keto acid dehydrogenase complex]Y Nobukuni, H Mitsubuchi, Y Indo, et al.
American Journal of Medical Genetics|June 19, 1998
Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypesT Kawano, Y Indo, H Nakazato, et al.
The Journal of Clinical Investigation|July 1, 1987
Altered kinetic properties of the branched-chain alpha-keto acid dehydrogenase complex due to mutation of the beta-subunit of the branched-chain alpha-keto acid decarboxylase (E1) component in lymphoblastoid cells derived from patients with maple syrup urine diseaseY Indo, A Kitano, F Endo, et al.
Human Genetics|September 1, 1988
Maple syrup urine disease: a possible biochemical basis for the clinical heterogeneityY Indo, I Akaboshi, Y Nobukuni, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A structural abnormality of E1 component of the branched-chain alpha-keto acid dehydrogenase complex in maple syrup urine diseaseY Indo, A Kitano, I Akaboshi, et al.
Pageof 6