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 R Osborne

Showing results (1-10 of 22) with videos related to

Pageof 3
Sort By:
Molecular Medicine Today|August 12, 2000
The fruits of the fly genome projectL R Osborne
Molecular Genetics and Metabolism|May 18, 1999
Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorderL R Osborne
Trends in Molecular Medicine|April 5, 2001
'Forkhead' gene expression balanced on a knife-edgeL R Osborne
Anesthesiology|January 1, 1991
Central anticholinergic syndrome following glycopyrrolateD F Grum, L R Osborne
Molecular Medicine Today|September 26, 1997
Resources for human genetics on the World Wide WebL R Osborne, J R Lee, S W Scherer
Biochimica Et Biophysica Acta|December 30, 1994
Lack of inhibition by dideoxy-forskolin and verapamil of DIDS-sensitive volume-activated Cl- secretion in human squamous lung carcinoma epithelial cellsF M Munkonge, L R Osborne, D M Geddes, et al.
Genomics|April 13, 1999
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndromeL R Osborne, T Campbell, A Daradich, et al.
Genomics|May 23, 1998
Assignment of the human CC chemokine MPIF-2/eotaxin-2 (SCYA24) to chromosome 7q11.23H Nomiyama, L R Osborne, T Imai, et al.
Genomics|November 5, 1997
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7L R Osborne, J A Herbrick, T Greavette, et al.
American Journal of Human Genetics|August 1, 1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndromeL R Osborne, S Soder, X M Shi, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Molecular Medicine Today|August 12, 2000
The fruits of the fly genome projectL R Osborne
Molecular Genetics and Metabolism|May 18, 1999
Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorderL R Osborne
Trends in Molecular Medicine|April 5, 2001
'Forkhead' gene expression balanced on a knife-edgeL R Osborne
Anesthesiology|January 1, 1991
Central anticholinergic syndrome following glycopyrrolateD F Grum, L R Osborne
Molecular Medicine Today|September 26, 1997
Resources for human genetics on the World Wide WebL R Osborne, J R Lee, S W Scherer
Biochimica Et Biophysica Acta|December 30, 1994
Lack of inhibition by dideoxy-forskolin and verapamil of DIDS-sensitive volume-activated Cl- secretion in human squamous lung carcinoma epithelial cellsF M Munkonge, L R Osborne, D M Geddes, et al.
Genomics|April 13, 1999
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndromeL R Osborne, T Campbell, A Daradich, et al.
Genomics|May 23, 1998
Assignment of the human CC chemokine MPIF-2/eotaxin-2 (SCYA24) to chromosome 7q11.23H Nomiyama, L R Osborne, T Imai, et al.
Genomics|November 5, 1997
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7L R Osborne, J A Herbrick, T Greavette, et al.
American Journal of Human Genetics|August 1, 1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndromeL R Osborne, S Soder, X M Shi, et al.
Pageof 3