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

P Brooks

Showing results (781-790 of 854) with videos related to

Pageof 86
Sort By:
Human Mutation|March 19, 2013
DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnosticsDimitre R Simeonov, Xinjing Wang, Chen Wang, et al.
American Journal of Ophthalmology|September 10, 2013
Systemic diagnostic testing in patients with apparently isolated uveal colobomaNancy Huynh, Delphine Blain, Tanya Glaser, et al.
Nature Communications|June 21, 2020
Nolz1 expression is required in dopaminergic axon guidance and striatal innervationClement Soleilhavoup, Marco Travaglio, Kieran Patrick, et al.
Cell Reports|July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 MutationsHiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, et al.
Communications Medicine|April 24, 2025
Artificial intelligence assisted clinical fluorescence imaging achieves in vivo cellular resolution comparable to adaptive optics ophthalmoscopyJoanne Li, Jianfei Liu, Vineeta Das, et al.
Ophthalmology Science|November 7, 2022
Investigating Determinants and Evaluating Deep Learning Training Approaches for Visual Acuity in Foveal HypoplasiaVolha V Malechka, Dat Duong, Keyla D Bordonada, et al.
Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Open Biology|November 28, 2019
Loss of CRMP2 O-GlcNAcylation leads to reduced novel object recognition performance in miceVillo Muha, Ritchie Williamson, Rachel Hills, et al.
Rheumatology (Oxford, England)|September 29, 1999
Interpreting the clinical significance of the differential inhibition of cyclooxygenase-1 and cyclooxygenase-2P Brooks, P Emery, J F Evans, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Analysis of ocular hypopigmentation in Rab38cht/cht miceBrian P Brooks, Denise M Larson, Chi-Chao Chan, et al.
Pageof 86

Showing results (781-790 of 854) with videos related to

Sort By:
Pageof 86
Human Mutation|March 19, 2013
DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnosticsDimitre R Simeonov, Xinjing Wang, Chen Wang, et al.
American Journal of Ophthalmology|September 10, 2013
Systemic diagnostic testing in patients with apparently isolated uveal colobomaNancy Huynh, Delphine Blain, Tanya Glaser, et al.
Nature Communications|June 21, 2020
Nolz1 expression is required in dopaminergic axon guidance and striatal innervationClement Soleilhavoup, Marco Travaglio, Kieran Patrick, et al.
Cell Reports|July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 MutationsHiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, et al.
Communications Medicine|April 24, 2025
Artificial intelligence assisted clinical fluorescence imaging achieves in vivo cellular resolution comparable to adaptive optics ophthalmoscopyJoanne Li, Jianfei Liu, Vineeta Das, et al.
Ophthalmology Science|November 7, 2022
Investigating Determinants and Evaluating Deep Learning Training Approaches for Visual Acuity in Foveal HypoplasiaVolha V Malechka, Dat Duong, Keyla D Bordonada, et al.
Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Open Biology|November 28, 2019
Loss of CRMP2 O-GlcNAcylation leads to reduced novel object recognition performance in miceVillo Muha, Ritchie Williamson, Rachel Hills, et al.
Rheumatology (Oxford, England)|September 29, 1999
Interpreting the clinical significance of the differential inhibition of cyclooxygenase-1 and cyclooxygenase-2P Brooks, P Emery, J F Evans, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Analysis of ocular hypopigmentation in Rab38cht/cht miceBrian P Brooks, Denise M Larson, Chi-Chao Chan, et al.
Pageof 86