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

R L Nussbaum

Showing results (101-110 of 115) with videos related to

Pageof 12
Sort By:
Nucleic Acids Research|September 11, 1992
Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiaeI Okabe, L C Bailey, O Attree, et al.
American Journal of Human Genetics|November 1, 1989
An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometryR E Schnur, B J Trask, G van den Engh, et al.
Genomics|December 1, 1994
Isolation and regional mapping of 110 chromosome 22 STSsT J Hudson, A M Colbert, M P Reeve, et al.
American Journal of Human Genetics|October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21D E Merry, J G Lesko, D M Sosnoski, et al.
The Journal of Clinical Investigation|June 1, 1988
Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIaD M Sosnoski, B S Emanuel, A L Hawkins, et al.
Human Genetics|July 1, 1989
Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37J C Skare, H L Grierson, J L Sullivan, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|June 17, 1998
Contig map of the Parkinson's disease region on 4q21-q23C Lavedan, A Dehejia, B Pike, et al.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
Science (New York, N.Y.)|November 15, 1996
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23M H Polymeropoulos, J J Higgins, L I Golbe, et al.
Neurobiology of Disease|October 21, 1999
Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]H M Mitchison, D J Bernard, N D Greene, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Nucleic Acids Research|September 11, 1992
Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiaeI Okabe, L C Bailey, O Attree, et al.
American Journal of Human Genetics|November 1, 1989
An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometryR E Schnur, B J Trask, G van den Engh, et al.
Genomics|December 1, 1994
Isolation and regional mapping of 110 chromosome 22 STSsT J Hudson, A M Colbert, M P Reeve, et al.
American Journal of Human Genetics|October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21D E Merry, J G Lesko, D M Sosnoski, et al.
The Journal of Clinical Investigation|June 1, 1988
Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIaD M Sosnoski, B S Emanuel, A L Hawkins, et al.
Human Genetics|July 1, 1989
Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37J C Skare, H L Grierson, J L Sullivan, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|June 17, 1998
Contig map of the Parkinson's disease region on 4q21-q23C Lavedan, A Dehejia, B Pike, et al.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
Science (New York, N.Y.)|November 15, 1996
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23M H Polymeropoulos, J J Higgins, L I Golbe, et al.
Neurobiology of Disease|October 21, 1999
Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]H M Mitchison, D J Bernard, N D Greene, et al.
Pageof 12