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 R Lupski

Showing results (61-70 of 209) with videos related to

Pageof 21
Sort By:
Molecular & General Genetics : MGG|January 1, 1982
Cloning and characterization of the Escherichia coli chromosomal region surrounding the dnaG Gene, with a correlated physical and genetic map of dnaG generated via transposon Tn5 mutagenesisJ R Lupski, B L Smiley, F R Blattner, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1986
A temperature-dependent pBR322 copy number mutant resulting from a Tn5 position effectJ R Lupski, S J Projan, L S Ozaki, et al.
American Journal of Medical Genetics|March 31, 1997
Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratoryL G Shaffer, G M Kennedy, A S Spikes, et al.
Journal of Bacteriology|July 1, 1997
Characterization of mutations affecting the Escherichia coli essential GTPase era that suppress two temperature-sensitive dnaG allelesR A Britton, B S Powell, D L Court, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1AC D Kashork, K S Chen, J R Lupski, et al.
Pediatric Neurology|April 20, 1999
Congenital hypomyelinating neuropathy: two patients with long-term follow-upJ P Phillips, L E Warner, J R Lupski, et al.
Investigative Ophthalmology & Visual Science|November 1, 2001
Null missense ABCR (ABCA4) mutations in a family with stargardt disease and retinitis pigmentosaN F Shroyer, R A Lewis, A N Yatsenko, et al.
American Journal of Medical Genetics|August 1, 1991
Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2)J R Lupski, C Langston, R Friedman, et al.
Neurogenetics|August 29, 2001
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathyC F Boerkoel, H Takashima, C A Bacino, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 13, 1984
Structure and organization of genes for sporozoite surface antigensG N Godson, J Ellis, J R Lupski, et al.
Pageof 21

Showing results (61-70 of 209) with videos related to

Sort By:
Pageof 21
Molecular & General Genetics : MGG|January 1, 1982
Cloning and characterization of the Escherichia coli chromosomal region surrounding the dnaG Gene, with a correlated physical and genetic map of dnaG generated via transposon Tn5 mutagenesisJ R Lupski, B L Smiley, F R Blattner, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1986
A temperature-dependent pBR322 copy number mutant resulting from a Tn5 position effectJ R Lupski, S J Projan, L S Ozaki, et al.
American Journal of Medical Genetics|March 31, 1997
Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratoryL G Shaffer, G M Kennedy, A S Spikes, et al.
Journal of Bacteriology|July 1, 1997
Characterization of mutations affecting the Escherichia coli essential GTPase era that suppress two temperature-sensitive dnaG allelesR A Britton, B S Powell, D L Court, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1AC D Kashork, K S Chen, J R Lupski, et al.
Pediatric Neurology|April 20, 1999
Congenital hypomyelinating neuropathy: two patients with long-term follow-upJ P Phillips, L E Warner, J R Lupski, et al.
Investigative Ophthalmology & Visual Science|November 1, 2001
Null missense ABCR (ABCA4) mutations in a family with stargardt disease and retinitis pigmentosaN F Shroyer, R A Lewis, A N Yatsenko, et al.
American Journal of Medical Genetics|August 1, 1991
Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2)J R Lupski, C Langston, R Friedman, et al.
Neurogenetics|August 29, 2001
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathyC F Boerkoel, H Takashima, C A Bacino, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 13, 1984
Structure and organization of genes for sporozoite surface antigensG N Godson, J Ellis, J R Lupski, et al.
Pageof 21