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

N L Hawes

Showing results (21-30 of 29) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 29 results.
Investigative Ophthalmology & Visual Science|May 14, 1998
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J miceS W John, R S Smith, O V Savinova, et al.
Cytogenetics and Cell Genetics|July 28, 2001
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase geneS A Cook, E C Akeson, C Calvano, et al.
BMC Genetics|February 15, 2001
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J miceM G Anderson, R S Smith, O V Savinova, et al.
Nature Genetics|April 7, 1999
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J miceB Chang, R S Smith, N L Hawes, et al.
Investigative Ophthalmology & Visual Science|September 1, 2000
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescensN L Hawes, B Chang, G S Hageman, et al.
BMC Genetics|November 28, 2001
Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressureB Chang, R S Smith, M Peters, et al.
Nature Genetics|April 1, 1996
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiationM Burmeister, J Novak, M Y Liang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2000
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouseN B Akhmedov, N I Piriev, B Chang, et al.
Vision Research|February 3, 2007
Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase geneB Chang, N L Hawes, M T Pardue, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Investigative Ophthalmology & Visual Science|May 14, 1998
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J miceS W John, R S Smith, O V Savinova, et al.
Cytogenetics and Cell Genetics|July 28, 2001
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase geneS A Cook, E C Akeson, C Calvano, et al.
BMC Genetics|February 15, 2001
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J miceM G Anderson, R S Smith, O V Savinova, et al.
Nature Genetics|April 7, 1999
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J miceB Chang, R S Smith, N L Hawes, et al.
Investigative Ophthalmology & Visual Science|September 1, 2000
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescensN L Hawes, B Chang, G S Hageman, et al.
BMC Genetics|November 28, 2001
Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressureB Chang, R S Smith, M Peters, et al.
Nature Genetics|April 1, 1996
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiationM Burmeister, J Novak, M Y Liang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2000
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouseN B Akhmedov, N I Piriev, B Chang, et al.
Vision Research|February 3, 2007
Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase geneB Chang, N L Hawes, M T Pardue, et al.
Pageof 3