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

L Beaudet

Showing results (171-180 of 456) with videos related to

Pageof 46
Sort By:
Clinical Genetics|February 1, 1982
Glycogen storage disease: long-term follow-up of nocturnal intragastric feedingV V Michels, A L Beaudet, V E Potts, et al.
Agents and Actions. Supplements|January 1, 1995
Gene targeting for inflammatory cell adhesion moleculesD C Bullard, E T Sandberg, K Scharffetter-Kochanek, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Molecular definition of bovine argininosuccinate synthetase deficiencyJ A Dennis, P J Healy, A L Beaudet, et al.
Birth Defects Original Article Series|January 1, 1976
Cataract in mannosidosisA L Murphree, A L Beaudet, E A Palmer, et al.
Genomics|March 1, 1991
Assignment of the gene for intercellular adhesion molecule-1 (Icam-1) to proximal mouse chromosome 9C M Ballantyne, C A Kozak, W E O'Brien, et al.
The Journal of Pediatrics|June 1, 1977
Cholesterol ester storage disease: clinical, biochemical, and pathological studiesA L Beaudet, G D Ferry, B L Nichols, et al.
Circulation|February 22, 2001
Absence of p-selectin, but not intercellular adhesion molecule-1, attenuates neointimal growth after arterial injury in apolipoprotein e-deficient miceD Manka, R G Collins, K Ley, et al.
Human Gene Therapy|August 1, 1995
Aerosol delivery of a beta-galactosidase adenoviral vector to the lungs of rodentsJ P Katkin, B E Gilbert, C Langston, et al.
Human Gene Therapy|October 27, 2010
Correction of hyperbilirubinemia in gunn rats using clinically relevant low doses of helper-dependent adenoviral vectorsDavid Dimmock, Nicola Brunetti-Pierri, Donna J Palmer, et al.
Human Molecular Genetics|July 13, 1999
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndromeT F Tsai, Y H Jiang, J Bressler, et al.
Pageof 46

Showing results (171-180 of 456) with videos related to

Sort By:
Pageof 46
Clinical Genetics|February 1, 1982
Glycogen storage disease: long-term follow-up of nocturnal intragastric feedingV V Michels, A L Beaudet, V E Potts, et al.
Agents and Actions. Supplements|January 1, 1995
Gene targeting for inflammatory cell adhesion moleculesD C Bullard, E T Sandberg, K Scharffetter-Kochanek, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Molecular definition of bovine argininosuccinate synthetase deficiencyJ A Dennis, P J Healy, A L Beaudet, et al.
Birth Defects Original Article Series|January 1, 1976
Cataract in mannosidosisA L Murphree, A L Beaudet, E A Palmer, et al.
Genomics|March 1, 1991
Assignment of the gene for intercellular adhesion molecule-1 (Icam-1) to proximal mouse chromosome 9C M Ballantyne, C A Kozak, W E O'Brien, et al.
The Journal of Pediatrics|June 1, 1977
Cholesterol ester storage disease: clinical, biochemical, and pathological studiesA L Beaudet, G D Ferry, B L Nichols, et al.
Circulation|February 22, 2001
Absence of p-selectin, but not intercellular adhesion molecule-1, attenuates neointimal growth after arterial injury in apolipoprotein e-deficient miceD Manka, R G Collins, K Ley, et al.
Human Gene Therapy|August 1, 1995
Aerosol delivery of a beta-galactosidase adenoviral vector to the lungs of rodentsJ P Katkin, B E Gilbert, C Langston, et al.
Human Gene Therapy|October 27, 2010
Correction of hyperbilirubinemia in gunn rats using clinically relevant low doses of helper-dependent adenoviral vectorsDavid Dimmock, Nicola Brunetti-Pierri, Donna J Palmer, et al.
Human Molecular Genetics|July 13, 1999
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndromeT F Tsai, Y H Jiang, J Bressler, et al.
Pageof 46