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

Victor H K Yong

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Frontiers in Neuroscience|November 25, 2021
Loss of Caveolin-1 Impairs Light Flicker-Induced Neurovascular Coupling at the Optic Nerve HeadJing Hong Loo, Ying Shi Lee, Chang Yi Woon, et al.
Investigative Ophthalmology & Visual Science|March 26, 2005
Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucomaTin Aung, Victor H K Yong, Paul T K Chew, et al.
Investigative Ophthalmology & Visual Science|September 28, 2005
Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutationsKelvin Y C Lee, Adrian H C Koh, Tin Aung, et al.
Journal of Glaucoma|June 17, 2008
Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle closure glaucoma in Singaporean subjectsTin Aung, Victor H K Yong, Marcus C C Lim, et al.
Journal of Glaucoma|November 10, 2015
CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma PatientsTan Do, William Shei, Pham Thi Minh Chau, et al.
Molecular Vision|July 24, 2008
Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyesTin Aung, Marcus C C Lim, Tina T L Wong, et al.
Investigative Ophthalmology & Visual Science|April 27, 2007
Lack of association between interleukin-1 gene cluster polymorphisms and glaucoma in Chinese subjectsAlicia C S How, Tin Aung, Xinyi Chew, et al.
Investigative Ophthalmology & Visual Science|January 4, 2008
Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophyJodhbir S Mehta, Eranga N Vithana, Donald T H Tan, et al.
Human Mutation|April 3, 2007
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. OnlineVedam L Ramprasad, Neil D Ebenezer, Tin Aung, et al.
Human Molecular Genetics|November 21, 2007
SLC4A11 mutations in Fuchs endothelial corneal dystrophyEranga N Vithana, Patricio E Morgan, Vedam Ramprasad, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Frontiers in Neuroscience|November 25, 2021
Loss of Caveolin-1 Impairs Light Flicker-Induced Neurovascular Coupling at the Optic Nerve HeadJing Hong Loo, Ying Shi Lee, Chang Yi Woon, et al.
Investigative Ophthalmology & Visual Science|March 26, 2005
Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucomaTin Aung, Victor H K Yong, Paul T K Chew, et al.
Investigative Ophthalmology & Visual Science|September 28, 2005
Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutationsKelvin Y C Lee, Adrian H C Koh, Tin Aung, et al.
Journal of Glaucoma|June 17, 2008
Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle closure glaucoma in Singaporean subjectsTin Aung, Victor H K Yong, Marcus C C Lim, et al.
Journal of Glaucoma|November 10, 2015
CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma PatientsTan Do, William Shei, Pham Thi Minh Chau, et al.
Molecular Vision|July 24, 2008
Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyesTin Aung, Marcus C C Lim, Tina T L Wong, et al.
Investigative Ophthalmology & Visual Science|April 27, 2007
Lack of association between interleukin-1 gene cluster polymorphisms and glaucoma in Chinese subjectsAlicia C S How, Tin Aung, Xinyi Chew, et al.
Investigative Ophthalmology & Visual Science|January 4, 2008
Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophyJodhbir S Mehta, Eranga N Vithana, Donald T H Tan, et al.
Human Mutation|April 3, 2007
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. OnlineVedam L Ramprasad, Neil D Ebenezer, Tin Aung, et al.
Human Molecular Genetics|November 21, 2007
SLC4A11 mutations in Fuchs endothelial corneal dystrophyEranga N Vithana, Patricio E Morgan, Vedam Ramprasad, et al.
Pageof 2