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A Mackey

Showing results (551-560 of 763) with videos related to

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Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Investigative Ophthalmology & Visual Science|May 4, 2010
Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohortRavikanth Metlapally, Chang-Seok Ki, Yi-Ju Li, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Molecular Vision|June 14, 2013
Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association studySeyhan Yazar, Aniket Mishra, Wei Ang, et al.
Disability and Rehabilitation|November 14, 2008
Novel methods for tendon investigationsM Kjaer, H Langberg, J Bojsen-Møller, et al.
Clinical & Experimental Ophthalmology|October 14, 2014
Pterygium and conjunctival ultraviolet autofluorescence in young Australian adults: the Raine studyCharlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
American Journal of Ophthalmology|July 30, 2014
Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort studyCharlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 15, 2010
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern GreeceGeorge Kitsos, Zacharias Petrou, Maria Grigoriadou, et al.
Scientific Reports|October 6, 2020
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt diseaseJason Charng, Di Xiao, Maryam Mehdizadeh, et al.
Pageof 77

Showing results (551-560 of 763) with videos related to

Sort By:
Pageof 77
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Investigative Ophthalmology & Visual Science|May 4, 2010
Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohortRavikanth Metlapally, Chang-Seok Ki, Yi-Ju Li, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Molecular Vision|June 14, 2013
Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association studySeyhan Yazar, Aniket Mishra, Wei Ang, et al.
Disability and Rehabilitation|November 14, 2008
Novel methods for tendon investigationsM Kjaer, H Langberg, J Bojsen-Møller, et al.
Clinical & Experimental Ophthalmology|October 14, 2014
Pterygium and conjunctival ultraviolet autofluorescence in young Australian adults: the Raine studyCharlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
American Journal of Ophthalmology|July 30, 2014
Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort studyCharlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 15, 2010
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern GreeceGeorge Kitsos, Zacharias Petrou, Maria Grigoriadou, et al.
Scientific Reports|October 6, 2020
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt diseaseJason Charng, Di Xiao, Maryam Mehdizadeh, et al.
Pageof 77