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

D G Green

Showing results (81-90 of 85) with videos related to

Pageof 9
Sort By:
You have reached the last page of results.This site can display upto 85 results.
Journal of Neurobiology|January 20, 2000
Partial rescue of the ocular retardation phenotype by genetic modifiersC Bone-Larson, S Basu, J D Radel, et al.
Artificial Life|May 12, 2001
Open problems in artificial lifeM A Bedau, J S McCaskill, N H Packard, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2001
Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell lossP A Sieving, M L Fowler, R A Bush, et al.
Genomics|September 15, 1994
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locusS A Keller, J M Jones, A Boyle, et al.
Molecular Genetics and Metabolism|March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutantsD A Pillers, R G Weleber, D G Green, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
Journal of Neurobiology|January 20, 2000
Partial rescue of the ocular retardation phenotype by genetic modifiersC Bone-Larson, S Basu, J D Radel, et al.
Artificial Life|May 12, 2001
Open problems in artificial lifeM A Bedau, J S McCaskill, N H Packard, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 24, 2001
Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell lossP A Sieving, M L Fowler, R A Bush, et al.
Genomics|September 15, 1994
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locusS A Keller, J M Jones, A Boyle, et al.
Molecular Genetics and Metabolism|March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutantsD A Pillers, R G Weleber, D G Green, et al.
Pageof 9