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S Packman

Showing results (21-30 of 98) with videos related to

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American Journal of Human Genetics|October 1, 1991
Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferaseJ K Reichardt, S Packman, S L Woo
Neurology|August 1, 1982
Brain pyruvate carboxylase and the pathophysiology of biotin-dependent diseasesJ E Sander, S Packman, J J Townsend
European Journal of Respiratory Diseases. Supplement|January 1, 1983
Response to almitrine bismesylate in a child with a central alveolar hypoventilation syndromeC J Newth, S Packman, R T Bachand
Biochemical and Biophysical Research Communications|November 1, 1972
A comparison of globin genes in duck reticulocytes and liver cellsS Packman, H Aviv, J Ross, et al.
Journal of the American Academy of Dermatology|July 1, 1983
Alopecia and periorificial dermatitis in biotin-responsive multiple carboxylase deficiencyM L Williams, S Packman, M J Cowan
Journal of Inherited Metabolic Disease|January 5, 2002
A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosisA Seyda, K Chun, S Packman, et al.
The Journal of Clinical Investigation|May 1, 1987
Metallothionein messenger RNA regulation in the mottled mouse and Menkes kinky hair syndromeS Packman, R D Palmiter, M Karin, et al.
The Journal of Biological Chemistry|September 25, 1978
Purification and properties of cystathionine beta-synthase from human liver. Evidence for identical subunitsJ Kraus, S Packman, B Fowler, et al.
The Journal of Clinical Investigation|March 1, 1978
Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblastsB Fowler, J Kraus, S Packman, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolismC Jakobs, L Sweetman, W L Nyhan, et al.
Pageof 10

Showing results (21-30 of 98) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|October 1, 1991
Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferaseJ K Reichardt, S Packman, S L Woo
Neurology|August 1, 1982
Brain pyruvate carboxylase and the pathophysiology of biotin-dependent diseasesJ E Sander, S Packman, J J Townsend
European Journal of Respiratory Diseases. Supplement|January 1, 1983
Response to almitrine bismesylate in a child with a central alveolar hypoventilation syndromeC J Newth, S Packman, R T Bachand
Biochemical and Biophysical Research Communications|November 1, 1972
A comparison of globin genes in duck reticulocytes and liver cellsS Packman, H Aviv, J Ross, et al.
Journal of the American Academy of Dermatology|July 1, 1983
Alopecia and periorificial dermatitis in biotin-responsive multiple carboxylase deficiencyM L Williams, S Packman, M J Cowan
Journal of Inherited Metabolic Disease|January 5, 2002
A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosisA Seyda, K Chun, S Packman, et al.
The Journal of Clinical Investigation|May 1, 1987
Metallothionein messenger RNA regulation in the mottled mouse and Menkes kinky hair syndromeS Packman, R D Palmiter, M Karin, et al.
The Journal of Biological Chemistry|September 25, 1978
Purification and properties of cystathionine beta-synthase from human liver. Evidence for identical subunitsJ Kraus, S Packman, B Fowler, et al.
The Journal of Clinical Investigation|March 1, 1978
Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblastsB Fowler, J Kraus, S Packman, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolismC Jakobs, L Sweetman, W L Nyhan, et al.
Pageof 10