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R C Eisensmith

Showing results (1-10 of 59) with videos related to

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European Journal of Pediatrics|July 1, 1996
Gene therapy for phenylketonuriaR C Eisensmith, S L Woo
American Journal of Human Genetics|December 1, 1992
Updated listing of haplotypes at the human phenylalanine hydroxylase (PAH) locusR C Eisensmith, S L Woo
Thrombosis and Haemostasis|July 1, 1997
Viral vector-mediated gene therapy for hemophilia BR C Eisensmith, S L Woo
Molecular Biology & Medicine|February 1, 1991
Phenylketonuria and the phenylalanine hydroxylase geneR C Eisensmith, S L Woo
Human Mutation|January 1, 1992
Molecular basis of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase geneR C Eisensmith, S L Woo
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Gene therapy for phenylketonuriaR C Eisensmith, S L Woo
Advances in Genetics|January 1, 1995
Molecular genetics of phenylketonuria: from molecular anthropology to gene therapyR C Eisensmith, S L Woo
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|March 29, 2001
An immunomodulatory procedure that stabilizes transgene expression and permits readministration of E1-deleted adenovirus vectorsA I Kuzmin, O Galenko, R C Eisensmith
Pageof 6

Showing results (1-10 of 59) with videos related to

Sort By:
Pageof 6
European Journal of Pediatrics|July 1, 1996
Gene therapy for phenylketonuriaR C Eisensmith, S L Woo
American Journal of Human Genetics|December 1, 1992
Updated listing of haplotypes at the human phenylalanine hydroxylase (PAH) locusR C Eisensmith, S L Woo
Thrombosis and Haemostasis|July 1, 1997
Viral vector-mediated gene therapy for hemophilia BR C Eisensmith, S L Woo
Molecular Biology & Medicine|February 1, 1991
Phenylketonuria and the phenylalanine hydroxylase geneR C Eisensmith, S L Woo
Human Mutation|January 1, 1992
Molecular basis of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase geneR C Eisensmith, S L Woo
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Gene therapy for phenylketonuriaR C Eisensmith, S L Woo
Advances in Genetics|January 1, 1995
Molecular genetics of phenylketonuria: from molecular anthropology to gene therapyR C Eisensmith, S L Woo
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|March 29, 2001
An immunomodulatory procedure that stabilizes transgene expression and permits readministration of E1-deleted adenovirus vectorsA I Kuzmin, O Galenko, R C Eisensmith
Pageof 6