Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Vainzof

Showing results (21-30 of 85) with videos related to

Pageof 9
Sort By:
Human Molecular Genetics|January 1, 1993
Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?M Vainzof, R I Takata, M R Passos-Bueno, et al.
American Journal of Medical Genetics|March 17, 2001
Mutations in the caveolin-3 gene: When are they pathogenic?F de Paula, M Vainzof, A L Bernardino, et al.
Journal of the Neurological Sciences|October 1, 1993
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotypeM Vainzof, M R Passos-Bueno, R I Takata, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Muscle & Nerve|May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathyJ Gurgel-Giannetti, M-L Bang, U Reed, et al.
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics|August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial casesM Zatz, D Sumita, S Campiotto, et al.
American Journal of Human Genetics|July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12E S Moreira, M Vainzof, S K Marie, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|January 1, 1993
Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?M Vainzof, R I Takata, M R Passos-Bueno, et al.
American Journal of Medical Genetics|March 17, 2001
Mutations in the caveolin-3 gene: When are they pathogenic?F de Paula, M Vainzof, A L Bernardino, et al.
Journal of the Neurological Sciences|October 1, 1993
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotypeM Vainzof, M R Passos-Bueno, R I Takata, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Muscle & Nerve|May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathyJ Gurgel-Giannetti, M-L Bang, U Reed, et al.
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics|August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial casesM Zatz, D Sumita, S Campiotto, et al.
American Journal of Human Genetics|July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12E S Moreira, M Vainzof, S K Marie, et al.
Pageof 9