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A Mackey

Showing results (451-460 of 763) with videos related to

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Journal of Clinical Microbiology|September 28, 2012
Multicenter clinical evaluation of the portrait toxigenic C. difficile assay for detection of toxigenic Clostridium difficile strains in clinical stool specimensBlake W Buchan, Tami-Lea A Mackey, Judy A Daly, et al.
Journal of Glaucoma|May 19, 2021
Physical Activity and Cardiovascular Fitness During Childhood and Adolescence: Association With Retinal Nerve Fibre Layer Thickness in Young AdulthoodSamantha Sze-Yee Lee, Joanne McVeigh, Leon Straker, et al.
Investigative Ophthalmology & Visual Science|May 28, 2010
Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shapeLi Tang, Todd E Scheetz, David A Mackey, et al.
The British Journal of Ophthalmology|July 11, 2006
Nail-patella syndrome and its association with glaucoma: a review of eight familiesZ Mimiwati, D A Mackey, J E Craig, et al.
Plos One|September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern AustraliaAlpana Dave, Kate Laurie, Sandra E Staffieri, et al.
Inorganic Chemistry|December 11, 2012
Selective synthesis, isolation, and crystallographic characterization of LaSc2N@I(h)-C80Steven Stevenson, Coralie B Rose, Juliya S Maslenikova, et al.
Mitochondrion|July 21, 2020
OXPHOS bioenergetic compensation does not explain disease penetrance in Leber hereditary optic neuropathyM Isabel G Lopez Sanchez, Nicole J Van Bergen, Lisa S Kearns, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 14, 2007
No association between variations in the WDR36 gene and primary open-angle glaucomaJohn H Fingert, Wallace L M Alward, Young H Kwon, et al.
JAMA Ophthalmology|November 23, 2013
Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohortsPirro G Hysi, Omar A Mahroo, Phillippa Cumberland, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of diseaseN J Marchbank, J E Craig, J P Leek, et al.
Pageof 77

Showing results (451-460 of 763) with videos related to

Sort By:
Pageof 77
Journal of Clinical Microbiology|September 28, 2012
Multicenter clinical evaluation of the portrait toxigenic C. difficile assay for detection of toxigenic Clostridium difficile strains in clinical stool specimensBlake W Buchan, Tami-Lea A Mackey, Judy A Daly, et al.
Journal of Glaucoma|May 19, 2021
Physical Activity and Cardiovascular Fitness During Childhood and Adolescence: Association With Retinal Nerve Fibre Layer Thickness in Young AdulthoodSamantha Sze-Yee Lee, Joanne McVeigh, Leon Straker, et al.
Investigative Ophthalmology & Visual Science|May 28, 2010
Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shapeLi Tang, Todd E Scheetz, David A Mackey, et al.
The British Journal of Ophthalmology|July 11, 2006
Nail-patella syndrome and its association with glaucoma: a review of eight familiesZ Mimiwati, D A Mackey, J E Craig, et al.
Plos One|September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern AustraliaAlpana Dave, Kate Laurie, Sandra E Staffieri, et al.
Inorganic Chemistry|December 11, 2012
Selective synthesis, isolation, and crystallographic characterization of LaSc2N@I(h)-C80Steven Stevenson, Coralie B Rose, Juliya S Maslenikova, et al.
Mitochondrion|July 21, 2020
OXPHOS bioenergetic compensation does not explain disease penetrance in Leber hereditary optic neuropathyM Isabel G Lopez Sanchez, Nicole J Van Bergen, Lisa S Kearns, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 14, 2007
No association between variations in the WDR36 gene and primary open-angle glaucomaJohn H Fingert, Wallace L M Alward, Young H Kwon, et al.
JAMA Ophthalmology|November 23, 2013
Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohortsPirro G Hysi, Omar A Mahroo, Phillippa Cumberland, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of diseaseN J Marchbank, J E Craig, J P Leek, et al.
Pageof 77