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S L Woo

Showing results (41-50 of 528) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Population genetics of phenylketonuriaR C Eisensmith, S L Woo
Journal of Inherited Metabolic Disease|January 1, 1996
Somatic gene therapy for phenylketonuria and other hepatic deficienciesR C Eisensmith, S L Woo
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 26, 2001
Auto-regulated hepatic insulin gene expression in type 1 diabetic ratsR Chen, M L Meseck, S L Woo
Journal of Inherited Metabolic Disease|January 1, 1984
The possibility for prenatal diagnosis of PKU by linkage analyses based on phenylalanine hydroxylase locus specific DNA-polymorphismsS L Woo, J H Robson, F Güttler
Annual Review of Genetics|January 1, 1988
Mendelian hyperphenylalaninemiaC R Scriver, S Kaufman, S L Woo
Somatic Cell and Molecular Genetics|March 1, 1987
Selection for phenylalanine hydroxylase activity in cells transformed with recombinant retrovirusesF D Ledley, T Hahn, S L Woo
Journal of Agricultural and Food Chemistry|January 1, 1982
Chemical phosphorylation of bovine beta-lactoglobulinS L Woo, L K Creamer, T Richardson
Biochemical and Biophysical Research Communications|July 16, 1980
Cloning of the rabbit uteroglobin structural geneT Chandra, S L Woo, D W Bullock
Lancet (London, England)|March 9, 1985
Prenatal diagnosis of classic phenylketonuria by DNA analysisA S Lidsky, F Güttler, S L Woo
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
Pageof 53

Showing results (41-50 of 528) with videos related to

Sort By:
Pageof 53
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Population genetics of phenylketonuriaR C Eisensmith, S L Woo
Journal of Inherited Metabolic Disease|January 1, 1996
Somatic gene therapy for phenylketonuria and other hepatic deficienciesR C Eisensmith, S L Woo
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 26, 2001
Auto-regulated hepatic insulin gene expression in type 1 diabetic ratsR Chen, M L Meseck, S L Woo
Journal of Inherited Metabolic Disease|January 1, 1984
The possibility for prenatal diagnosis of PKU by linkage analyses based on phenylalanine hydroxylase locus specific DNA-polymorphismsS L Woo, J H Robson, F Güttler
Annual Review of Genetics|January 1, 1988
Mendelian hyperphenylalaninemiaC R Scriver, S Kaufman, S L Woo
Somatic Cell and Molecular Genetics|March 1, 1987
Selection for phenylalanine hydroxylase activity in cells transformed with recombinant retrovirusesF D Ledley, T Hahn, S L Woo
Journal of Agricultural and Food Chemistry|January 1, 1982
Chemical phosphorylation of bovine beta-lactoglobulinS L Woo, L K Creamer, T Richardson
Biochemical and Biophysical Research Communications|July 16, 1980
Cloning of the rabbit uteroglobin structural geneT Chandra, S L Woo, D W Bullock
Lancet (London, England)|March 9, 1985
Prenatal diagnosis of classic phenylketonuria by DNA analysisA S Lidsky, F Güttler, S L Woo
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
Pageof 53