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G Hoganson

Showing results (1-10 of 17) with videos related to

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FEBS Letters|May 23, 1998
Very-long-chain acyl-CoA dehydrogenase subunit assembles to the dimer form on mitochondrial inner membraneM Souri, T Aoyama, G Hoganson, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1983
Single coronary artery arising anomalously from the pulmonary trunkG Hoganson, E McPherson, P Piper, et al.
Birth Defects Original Article Series|January 1, 1987
Pathological findings in 5,10-methylene tetrahydrofolate reductase deficiencyD R Beckman, G Hoganson, S Berlow, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Altered phosphorylation state of branched-chain 2-oxo acid dehydrogenase in a branched-chain acyltransferase deficient human fibroblast cell lineR S Eisenstein, G Hoganson, R H Miller, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1990
Phylogenetic comparisons of the branched-chain alpha-ketoacid dehydrogenase complexR S Eisenstein, R H Miller, G Hoganson, et al.
Gene|June 15, 1990
The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conservedC S Surowy, G Hoganson, J Gosink, et al.
The Journal of Clinical Investigation|March 1, 1994
Identification of a novel exonic mutation at -13 from 5' splice site causing exon skipping in a girl with mitochondrial acetoacetyl-coenzyme A thiolase deficiencyT Fukao, S Yamaguchi, A Wakazono, et al.
Fetal Diagnosis and Therapy|May 1, 1994
Clinical and pathologic findings in 2 siblings with congenital nephrotic syndromeJ Santolaya, M Farolan, J Czapar, et al.
Birth Defects Original Article Series|January 1, 1987
Glutaric acidemia type II and flavin-dependent enzymes in morphogenesisG Hoganson, S Berlow, E F Gilbert, et al.
American Journal of Medical Genetics|January 15, 1992
Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28)D I Hoar, L L Field, F Beards, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
FEBS Letters|May 23, 1998
Very-long-chain acyl-CoA dehydrogenase subunit assembles to the dimer form on mitochondrial inner membraneM Souri, T Aoyama, G Hoganson, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1983
Single coronary artery arising anomalously from the pulmonary trunkG Hoganson, E McPherson, P Piper, et al.
Birth Defects Original Article Series|January 1, 1987
Pathological findings in 5,10-methylene tetrahydrofolate reductase deficiencyD R Beckman, G Hoganson, S Berlow, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Altered phosphorylation state of branched-chain 2-oxo acid dehydrogenase in a branched-chain acyltransferase deficient human fibroblast cell lineR S Eisenstein, G Hoganson, R H Miller, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1990
Phylogenetic comparisons of the branched-chain alpha-ketoacid dehydrogenase complexR S Eisenstein, R H Miller, G Hoganson, et al.
Gene|June 15, 1990
The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conservedC S Surowy, G Hoganson, J Gosink, et al.
The Journal of Clinical Investigation|March 1, 1994
Identification of a novel exonic mutation at -13 from 5' splice site causing exon skipping in a girl with mitochondrial acetoacetyl-coenzyme A thiolase deficiencyT Fukao, S Yamaguchi, A Wakazono, et al.
Fetal Diagnosis and Therapy|May 1, 1994
Clinical and pathologic findings in 2 siblings with congenital nephrotic syndromeJ Santolaya, M Farolan, J Czapar, et al.
Birth Defects Original Article Series|January 1, 1987
Glutaric acidemia type II and flavin-dependent enzymes in morphogenesisG Hoganson, S Berlow, E F Gilbert, et al.
American Journal of Medical Genetics|January 15, 1992
Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28)D I Hoar, L L Field, F Beards, et al.
Pageof 2