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 M Hunt

Showing results (161-170 of 185) with videos related to

Pageof 19
Sort By:
Journal of Medical Genetics|September 3, 2002
Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)I A Aligianis, T Forshew, S Johnson, et al.
Nature Genetics|February 1, 1994
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortionK Evans, A Fryer, C Inglehearn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
The Journal of Physiology|July 4, 2001
Visual responses of ganglion cells of a New-World primate, the capuchin monkey, Cebus apellaB B Lee, L C Silveira, E S Yamada, et al.
Human Molecular Genetics|September 1, 1995
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qR E Kelsell, B F Godley, K Evans, et al.
The British Journal of Ophthalmology|January 30, 1999
Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6qM B Reichel, R E Kelsell, J Fan, et al.
Human Gene Therapy|February 11, 1998
Adeno-associated virus gene transfer to mouse retinaR R Ali, M B Reichel, M De Alwis, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Genomic organization and amplification of the human desmosomal cadherin genes DSC1 and DSC3, encoding desmocollin types 1 and 3N V Whittock, D M Hunt, L Rickman, et al.
Current Eye Research|September 24, 1998
Absence of p53 delays apoptotic photoreceptor cell death in the rds mouseR R Ali, M B Reichel, N Kanuga, et al.
Human Molecular Genetics|December 15, 2000
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophyS E Wilkie, R J Newbold, E Deery, et al.
Pageof 19

Showing results (161-170 of 185) with videos related to

Sort By:
Pageof 19
Journal of Medical Genetics|September 3, 2002
Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)I A Aligianis, T Forshew, S Johnson, et al.
Nature Genetics|February 1, 1994
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortionK Evans, A Fryer, C Inglehearn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
The Journal of Physiology|July 4, 2001
Visual responses of ganglion cells of a New-World primate, the capuchin monkey, Cebus apellaB B Lee, L C Silveira, E S Yamada, et al.
Human Molecular Genetics|September 1, 1995
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qR E Kelsell, B F Godley, K Evans, et al.
The British Journal of Ophthalmology|January 30, 1999
Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6qM B Reichel, R E Kelsell, J Fan, et al.
Human Gene Therapy|February 11, 1998
Adeno-associated virus gene transfer to mouse retinaR R Ali, M B Reichel, M De Alwis, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Genomic organization and amplification of the human desmosomal cadherin genes DSC1 and DSC3, encoding desmocollin types 1 and 3N V Whittock, D M Hunt, L Rickman, et al.
Current Eye Research|September 24, 1998
Absence of p53 delays apoptotic photoreceptor cell death in the rds mouseR R Ali, M B Reichel, N Kanuga, et al.
Human Molecular Genetics|December 15, 2000
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophyS E Wilkie, R J Newbold, E Deery, et al.
Pageof 19