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P Hechtman

Showing results (11-20 of 42) with videos related to

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Journal of Bacteriology|November 1, 1970
Neutral amino acid transport in Pseudomonas fluorescensP Hechtman, C R Scriver
American Journal of Human Genetics|June 1, 1994
Four novel PEPD alleles causing prolidase deficiencyP Ledoux, C Scriver, P Hechtman
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
The GM2 gangliosidoses databases: allelic variation at the HEXA, HEXB, and GM2A gene lociP Cordeiro, P Hechtman, F Kaplan
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1984
Synthesis of 4-methylumbelliferyl-beta-D-N-acetylglucosamine-6-sulfate and its use in classification of GM2 gangliosidosis genotypesJ Bayleran, P Hechtman, W Saray
Clinical Genetics|September 1, 1983
A new form of residual hexosaminidase activity in infantile Tay Sachs disease fibroblastsP Hechtman, K Khoo, C Isaacs
Biochimica Et Biophysica Acta|June 20, 1997
Formation of a ternary complex between GM2 activator protein, GM2 ganglioside and hexosaminidase AF Yadao, P Hechtman, F Kaplan
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|August 1, 1985
Substrate binding properties of the human liver hexosaminidase A activator proteinP Hechtman, C Isaacs, L Smith-Jones
American Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P Hechtman
Clinical Genetics|May 1, 1989
The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseP Hechtman, B Boulay, J Bayleran, et al.
Journal of Bacteriology|November 1, 1970
Isolation and properties of a beta-alanine transaminaseless mutant of Pseudomonas fluorescensP Hechtman, C R Scriver, R B Middleton
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Journal of Bacteriology|November 1, 1970
Neutral amino acid transport in Pseudomonas fluorescensP Hechtman, C R Scriver
American Journal of Human Genetics|June 1, 1994
Four novel PEPD alleles causing prolidase deficiencyP Ledoux, C Scriver, P Hechtman
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
The GM2 gangliosidoses databases: allelic variation at the HEXA, HEXB, and GM2A gene lociP Cordeiro, P Hechtman, F Kaplan
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1984
Synthesis of 4-methylumbelliferyl-beta-D-N-acetylglucosamine-6-sulfate and its use in classification of GM2 gangliosidosis genotypesJ Bayleran, P Hechtman, W Saray
Clinical Genetics|September 1, 1983
A new form of residual hexosaminidase activity in infantile Tay Sachs disease fibroblastsP Hechtman, K Khoo, C Isaacs
Biochimica Et Biophysica Acta|June 20, 1997
Formation of a ternary complex between GM2 activator protein, GM2 ganglioside and hexosaminidase AF Yadao, P Hechtman, F Kaplan
Canadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|August 1, 1985
Substrate binding properties of the human liver hexosaminidase A activator proteinP Hechtman, C Isaacs, L Smith-Jones
American Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P Hechtman
Clinical Genetics|May 1, 1989
The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseP Hechtman, B Boulay, J Bayleran, et al.
Journal of Bacteriology|November 1, 1970
Isolation and properties of a beta-alanine transaminaseless mutant of Pseudomonas fluorescensP Hechtman, C R Scriver, R B Middleton
Pageof 5