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

A J Mears

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Nature Genetics|November 6, 2001
Nrl is required for rod photoreceptor developmentA J Mears, M Kondo, P K Swain, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
American Journal of Human Genetics|July 1, 1994
Molecular characterization of the marker chromosome associated with cat eye syndromeA J Mears, A M Duncan, M L Budarf, et al.
The Journal of Biological Chemistry|July 31, 2001
Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptorsP K Swain, D Hicks, A J Mears, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
European Journal of Medical Genetics|March 22, 2021
A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesiaK Backman, W E Mears, A Waheeb, et al.
American Journal of Human Genetics|October 30, 1998
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomalyA J Mears, T Jordan, F Mirzayans, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Nature Genetics|November 6, 2001
Nrl is required for rod photoreceptor developmentA J Mears, M Kondo, P K Swain, et al.
American Journal of Human Genetics|March 3, 1999
Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosaA J Mears, L Gieser, D Yan, et al.
American Journal of Human Genetics|July 1, 1994
Molecular characterization of the marker chromosome associated with cat eye syndromeA J Mears, A M Duncan, M L Budarf, et al.
The Journal of Biological Chemistry|July 31, 2001
Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptorsP K Swain, D Hicks, A J Mears, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
European Journal of Medical Genetics|March 22, 2021
A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesiaK Backman, W E Mears, A Waheeb, et al.
American Journal of Human Genetics|October 30, 1998
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomalyA J Mears, T Jordan, F Mirzayans, et al.
Pageof 2