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

B M Ross

Showing results (41-50 of 58) with videos related to

Pageof 6
Sort By:
Brain Research|September 17, 1993
Alterations in the activity of adenylate cyclase and high affinity GTPase in Alzheimer's diseaseB M Ross, M McLaughlin, M Roberts, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|January 2, 2007
Biomarkers of oxidative stress in schizophrenic and control subjectsJ Young, S B McKinney, B M Ross, et al.
Human Molecular Genetics|September 1, 1994
Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictionsK Petrukhin, S Lutsenko, I Chernov, et al.
Lipids|April 1, 1997
Phospholipid biosynthetic enzymes in human brainB M Ross, A Moszczynska, J K Blusztajn, et al.
The Journal of Clinical Investigation|April 1, 1995
Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recoveryJ C Plumier, B M Ross, R W Currie, et al.
Annals of Neurology|July 1, 1997
Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologuesC H Wang, T A Carter, K Das, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2000
Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1B M Ross, K Eder, A Moszczynska, et al.
Human Molecular Genetics|August 11, 1999
Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformationO I Buiakova, J Xu, S Lutsenko, et al.
American Journal of Human Genetics|January 1, 1995
Refinement of the spinal muscular atrophy locus by genetic and physical mappingC H Wang, P W Kleyn, E Vitale, et al.
Human Molecular Genetics|March 1, 1996
Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophyC H Wang, J Xu, T A Carter, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Brain Research|September 17, 1993
Alterations in the activity of adenylate cyclase and high affinity GTPase in Alzheimer's diseaseB M Ross, M McLaughlin, M Roberts, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|January 2, 2007
Biomarkers of oxidative stress in schizophrenic and control subjectsJ Young, S B McKinney, B M Ross, et al.
Human Molecular Genetics|September 1, 1994
Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictionsK Petrukhin, S Lutsenko, I Chernov, et al.
Lipids|April 1, 1997
Phospholipid biosynthetic enzymes in human brainB M Ross, A Moszczynska, J K Blusztajn, et al.
The Journal of Clinical Investigation|April 1, 1995
Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recoveryJ C Plumier, B M Ross, R W Currie, et al.
Annals of Neurology|July 1, 1997
Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologuesC H Wang, T A Carter, K Das, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2000
Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1B M Ross, K Eder, A Moszczynska, et al.
Human Molecular Genetics|August 11, 1999
Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformationO I Buiakova, J Xu, S Lutsenko, et al.
American Journal of Human Genetics|January 1, 1995
Refinement of the spinal muscular atrophy locus by genetic and physical mappingC H Wang, P W Kleyn, E Vitale, et al.
Human Molecular Genetics|March 1, 1996
Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophyC H Wang, J Xu, T A Carter, et al.
Pageof 6