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

J S Beckmann

Showing results (71-80 of 165) with videos related to

Pageof 17
Sort By:
Neuromuscular Disorders : NMD|June 6, 2000
Calpain3 expression during human cardiogenesisF Fougerousse, L V Anderson, A L Delezoide, et al.
Journal of Dairy Science|November 1, 1990
Parentage identification in the bovine using "deoxyribonucleic acid fingerprints"Y Kashi, E Lipkin, A Darvasi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1971
Purification and in vitro transcription of a transfer RNA geneV Daniel, J S Beckmann, S Sarid, et al.
Circulation Research|January 24, 1998
Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human developmentF Fougerousse, A L Delezoide, M Y Fiszman, et al.
Molecular Biology and Evolution|March 1, 1988
Phylogenetic distribution in the genus Mus of t-complex-specific DNA and protein markers: inferences on the origin of t-haplotypesC Delarbre, Y Kashi, P Boursot, et al.
Neuromuscular Disorders : NMD|November 2, 1999
66th/67th ENMC sponsored international workshop: The limb-girdle muscular dystrophies, 26-28 March 1999, Naarden, The NetherlandsJ S Beckmann, R H Brown, F Muntoni, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 4, 2001
Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscleS Baghdiguian, I Richard, M Martin, et al.
Human Molecular Genetics|November 1, 1992
Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophyI Richard, O Broux, D Hillaire, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 6, 1975
DNA-RNA hybridizationJ O Bishop, J S Beckmann, M S Campo, et al.
Human Molecular Genetics|September 1, 1997
A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase geneH Zouali, E H Hani, A Philippi, et al.
Pageof 17

Showing results (71-80 of 165) with videos related to

Sort By:
Pageof 17
Neuromuscular Disorders : NMD|June 6, 2000
Calpain3 expression during human cardiogenesisF Fougerousse, L V Anderson, A L Delezoide, et al.
Journal of Dairy Science|November 1, 1990
Parentage identification in the bovine using "deoxyribonucleic acid fingerprints"Y Kashi, E Lipkin, A Darvasi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1971
Purification and in vitro transcription of a transfer RNA geneV Daniel, J S Beckmann, S Sarid, et al.
Circulation Research|January 24, 1998
Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human developmentF Fougerousse, A L Delezoide, M Y Fiszman, et al.
Molecular Biology and Evolution|March 1, 1988
Phylogenetic distribution in the genus Mus of t-complex-specific DNA and protein markers: inferences on the origin of t-haplotypesC Delarbre, Y Kashi, P Boursot, et al.
Neuromuscular Disorders : NMD|November 2, 1999
66th/67th ENMC sponsored international workshop: The limb-girdle muscular dystrophies, 26-28 March 1999, Naarden, The NetherlandsJ S Beckmann, R H Brown, F Muntoni, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 4, 2001
Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscleS Baghdiguian, I Richard, M Martin, et al.
Human Molecular Genetics|November 1, 1992
Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophyI Richard, O Broux, D Hillaire, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 6, 1975
DNA-RNA hybridizationJ O Bishop, J S Beckmann, M S Campo, et al.
Human Molecular Genetics|September 1, 1997
A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase geneH Zouali, E H Hani, A Philippi, et al.
Pageof 17