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M Zatz

Showing results (101-110 of 252) with videos related to

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The Journal of Biological Chemistry|October 10, 1981
Nonpolar lipid methylation. Biosynthesis of fatty acid methyl esters by rat lung membranes using S-adenosylmethionineM Zatz, P A Dudley, Y Kloog, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1975
Rapid changes in rat pineal beta-adrenergic receptor: alterations in l-(3H)alprenolol binding and adenylate cyclaseJ W Kebabian, M Zatz, J A Romero, et al.
American Journal of Medical Genetics|January 1, 1991
Familial occurrence of Duchenne dystrophy through paternal lines in four familiesM Zatz, M R Passos-Bueno, D Rapaport, et al.
American Journal of Medical Genetics|March 9, 1999
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2GM R Passos-Bueno, M Vainzof, E S Moreira, et al.
Journal of Neurochemistry|May 23, 2000
Chick pineal melatonin synthesis: light and cyclic AMP control abundance of serotonin N-acetyltransferase proteinM Zatz, J A Gastel, J R Heath, et al.
The International Journal of Neuroscience|January 1, 1980
Differentiation of chronic schizophrenics with and without ventricular enlargement by the Luria-Nebraska Neuropsychological BatteryC J Golden, B Graber, J A Moses, et al.
American Journal of Medical Genetics|October 6, 1999
Genetic counseling for childless women at risk for Duchenne muscular dystrophyS Eggers, R C Pavanello, M R Passos-Bueno, et al.
Journal of the Neurological Sciences|July 1, 1995
Is dystrophin always altered in Becker muscular dystrophy patients?M Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Human Molecular Genetics|June 1, 1994
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyM R Passos-Bueno, M Vainzof, S K Marie, et al.
Journal De Genetique Humaine|June 1, 1976
Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian studyM Zatz, O Frota-Pessoa, J A Levy, et al.
Pageof 26

Showing results (101-110 of 252) with videos related to

Sort By:
Pageof 26
The Journal of Biological Chemistry|October 10, 1981
Nonpolar lipid methylation. Biosynthesis of fatty acid methyl esters by rat lung membranes using S-adenosylmethionineM Zatz, P A Dudley, Y Kloog, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1975
Rapid changes in rat pineal beta-adrenergic receptor: alterations in l-(3H)alprenolol binding and adenylate cyclaseJ W Kebabian, M Zatz, J A Romero, et al.
American Journal of Medical Genetics|January 1, 1991
Familial occurrence of Duchenne dystrophy through paternal lines in four familiesM Zatz, M R Passos-Bueno, D Rapaport, et al.
American Journal of Medical Genetics|March 9, 1999
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2GM R Passos-Bueno, M Vainzof, E S Moreira, et al.
Journal of Neurochemistry|May 23, 2000
Chick pineal melatonin synthesis: light and cyclic AMP control abundance of serotonin N-acetyltransferase proteinM Zatz, J A Gastel, J R Heath, et al.
The International Journal of Neuroscience|January 1, 1980
Differentiation of chronic schizophrenics with and without ventricular enlargement by the Luria-Nebraska Neuropsychological BatteryC J Golden, B Graber, J A Moses, et al.
American Journal of Medical Genetics|October 6, 1999
Genetic counseling for childless women at risk for Duchenne muscular dystrophyS Eggers, R C Pavanello, M R Passos-Bueno, et al.
Journal of the Neurological Sciences|July 1, 1995
Is dystrophin always altered in Becker muscular dystrophy patients?M Vainzof, M R Passos-Bueno, R C Pavanello, et al.
Human Molecular Genetics|June 1, 1994
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyM R Passos-Bueno, M Vainzof, S K Marie, et al.
Journal De Genetique Humaine|June 1, 1976
Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian studyM Zatz, O Frota-Pessoa, J A Levy, et al.
Pageof 26