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 Zatz

Showing results (211-220 of 252) with videos related to

Pageof 26
Sort By:
Journal of Neural Transmission (Vienna, Austria : 1996)|May 9, 2001
No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patientsA L Nishimura, J R Oliveira, P A Otto, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1994
[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)]U C Reed, M R Passos-Bueno, S K Nagahashi-Marie, et al.
Human Molecular Genetics|November 1, 1993
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysisM R Passos-Bueno, J R Oliveira, E Bakker, et al.
Biochemical and Biophysical Research Communications|July 11, 2001
Characterization of human skeletal muscle Ankrd2A Pallavicini, S Kojić, C Bean, et al.
Neuromuscular Disorders : NMD|April 22, 2004
A novel stop codon mutation in the PMP22 gene associated with a variable phenotypeK T Abe, A M M Lino, M T A Hirata, et al.
American Journal of Human Genetics|November 1, 1992
Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence riskM R Passos-Bueno, E Bakker, A L Kneppers, et al.
Protein Expression and Purification|June 2, 2007
A mutation in human VAP-B--MSP domain, present in ALS patients, affects the interaction with other cellular proteinsM Mitne-Neto, C R R Ramos, D C Pimenta, et al.
Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Molecular Psychiatry|October 17, 1998
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's diseaseJ R Oliveira, R M Gallindo, L G Maia, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Pageof 26

Showing results (211-220 of 252) with videos related to

Sort By:
Pageof 26
Journal of Neural Transmission (Vienna, Austria : 1996)|May 9, 2001
No evidence of association between the D10S1423 locus and Alzheimer disease in Brazilian patientsA L Nishimura, J R Oliveira, P A Otto, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1994
[Myotonic dystrophy: study of clinico-genetic correlation in a pair of relatives (father-son)]U C Reed, M R Passos-Bueno, S K Nagahashi-Marie, et al.
Human Molecular Genetics|November 1, 1993
Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysisM R Passos-Bueno, J R Oliveira, E Bakker, et al.
Biochemical and Biophysical Research Communications|July 11, 2001
Characterization of human skeletal muscle Ankrd2A Pallavicini, S Kojić, C Bean, et al.
Neuromuscular Disorders : NMD|April 22, 2004
A novel stop codon mutation in the PMP22 gene associated with a variable phenotypeK T Abe, A M M Lino, M T A Hirata, et al.
American Journal of Human Genetics|November 1, 1992
Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence riskM R Passos-Bueno, E Bakker, A L Kneppers, et al.
Protein Expression and Purification|June 2, 2007
A mutation in human VAP-B--MSP domain, present in ALS patients, affects the interaction with other cellular proteinsM Mitne-Neto, C R R Ramos, D C Pimenta, et al.
Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Molecular Psychiatry|October 17, 1998
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's diseaseJ R Oliveira, R M Gallindo, L G Maia, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Pageof 26