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M Zatz

Showing results (191-200 of 252) with videos related to

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Journal of Medical Genetics|February 1, 1993
Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?M Zatz, H Vallada, M S Melo, et al.
Neuropediatrics|December 1, 1995
Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterationsM Vainzof, S K Marie, U C Reed, et al.
Journal of the Neurological Sciences|February 1, 1991
Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the proteinM Vainzof, E E Zubrzycka-Gaarn, D Rapaport, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumoursT S Zorick, Z Mustacchi, S Y Bando, et al.
Genomics|April 1, 1996
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2pR Bashir, S Keers, T Strachan, et al.
American Journal of Human Genetics|January 1, 1995
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesM Zatz, S K Marie, M R Passos-Bueno, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different agesM Vainzof, R C Pavanello, I Pavanello, et al.
Stem Cells International|May 23, 2015
Human Mesenchymal Stromal Cells Transplantation May Enhance or Inhibit 4T1 Murine Breast Adenocarcinoma through Different ApproachesT Jazedje, A L Ribeiro, M Pellati, et al.
American Journal of Medical Genetics|December 18, 1998
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriersD R Sumita, M Vainzof, S Campiotto, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Pageof 26

Showing results (191-200 of 252) with videos related to

Sort By:
Pageof 26
Journal of Medical Genetics|February 1, 1993
Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?M Zatz, H Vallada, M S Melo, et al.
Neuropediatrics|December 1, 1995
Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterationsM Vainzof, S K Marie, U C Reed, et al.
Journal of the Neurological Sciences|February 1, 1991
Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the proteinM Vainzof, E E Zubrzycka-Gaarn, D Rapaport, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumoursT S Zorick, Z Mustacchi, S Y Bando, et al.
Genomics|April 1, 1996
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2pR Bashir, S Keers, T Strachan, et al.
American Journal of Human Genetics|January 1, 1995
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesM Zatz, S K Marie, M R Passos-Bueno, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different agesM Vainzof, R C Pavanello, I Pavanello, et al.
Stem Cells International|May 23, 2015
Human Mesenchymal Stromal Cells Transplantation May Enhance or Inhibit 4T1 Murine Breast Adenocarcinoma through Different ApproachesT Jazedje, A L Ribeiro, M Pellati, et al.
American Journal of Medical Genetics|December 18, 1998
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriersD R Sumita, M Vainzof, S Campiotto, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Pageof 26