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I D Wexler

Showing results (11-20 of 22) with videos related to

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FEBS Letters|November 21, 1988
Nucleotide sequence of a cDNA for the dihydrolipoamide acetyltransferase component of human pyruvate dehydrogenase complexT J Thekkumkara, L Ho, I D Wexler, et al.
The Journal of Nutrition|October 4, 2000
The association between two common mutations C677T and A1298C in human methylenetetrahydrofolate reductase gene and the risk for diabetic nephropathy in type II diabetic patientsV Shpichinetsky, I Raz, Y Friedlander, et al.
Pediatric Research|August 1, 1992
A mutation in the E1 alpha subunit of pyruvate dehydrogenase associated with variable expression of pyruvate dehydrogenase complex deficiencyI D Wexler, S G Hemalatha, T C Liu, et al.
Pediatric Research|May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous familiesI D Wexler, D S Kerr, Y Du, et al.
Pediatric Pulmonology|November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patientsA Barak, I D Wexler, O Efrati, et al.
Kidney International|August 1, 2000
Renal nitric oxide production during the early phase of experimental diabetes mellitusS Keynan, B Hirshberg, N Levin-Iaina, et al.
Human Molecular Genetics|February 1, 1995
Pyruvate dehydrogenase complex deficiency due to a point mutation (P188L) within the thiamine pyrophosphate binding loop of the E1 alpha subunitS G Hemalatha, D S Kerr, I D Wexler, et al.
Neurology|December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutationsI D Wexler, S G Hemalatha, J McConnell, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Heterogeneous expression of protein and mRNA in pyruvate dehydrogenase deficiencyI D Wexler, D S Kerr, L Ho, et al.
Human Mutation|January 1, 1992
Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha geneH H Dahl, G K Brown, R M Brown, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
FEBS Letters|November 21, 1988
Nucleotide sequence of a cDNA for the dihydrolipoamide acetyltransferase component of human pyruvate dehydrogenase complexT J Thekkumkara, L Ho, I D Wexler, et al.
The Journal of Nutrition|October 4, 2000
The association between two common mutations C677T and A1298C in human methylenetetrahydrofolate reductase gene and the risk for diabetic nephropathy in type II diabetic patientsV Shpichinetsky, I Raz, Y Friedlander, et al.
Pediatric Research|August 1, 1992
A mutation in the E1 alpha subunit of pyruvate dehydrogenase associated with variable expression of pyruvate dehydrogenase complex deficiencyI D Wexler, S G Hemalatha, T C Liu, et al.
Pediatric Research|May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous familiesI D Wexler, D S Kerr, Y Du, et al.
Pediatric Pulmonology|November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patientsA Barak, I D Wexler, O Efrati, et al.
Kidney International|August 1, 2000
Renal nitric oxide production during the early phase of experimental diabetes mellitusS Keynan, B Hirshberg, N Levin-Iaina, et al.
Human Molecular Genetics|February 1, 1995
Pyruvate dehydrogenase complex deficiency due to a point mutation (P188L) within the thiamine pyrophosphate binding loop of the E1 alpha subunitS G Hemalatha, D S Kerr, I D Wexler, et al.
Neurology|December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutationsI D Wexler, S G Hemalatha, J McConnell, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Heterogeneous expression of protein and mRNA in pyruvate dehydrogenase deficiencyI D Wexler, D S Kerr, L Ho, et al.
Human Mutation|January 1, 1992
Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha geneH H Dahl, G K Brown, R M Brown, et al.
Pageof 3