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Perciliz L Tan

Showing results (21-30 of 28) with videos related to

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Nature Genetics|May 21, 2013
A functional variant in the CFI gene confers a high risk of age-related macular degenerationJohannes P H van de Ven, Sara C Nilsson, Perciliz L Tan, et al.
American Journal of Human Genetics|February 13, 2018
Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone FragilityClothilde Esteve, Ludmila Francescatto, Perciliz L Tan, et al.
Ophthalmology|June 19, 2012
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypesLucia Sobrin, Stephan Ripke, Yi Yu, et al.
The New England Journal of Medicine|August 30, 2008
Toll-like receptor 3 and geographic atrophy in age-related macular degenerationZhenglin Yang, Charity Stratton, Peter J Francis, et al.
Nature Genetics|May 12, 2009
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathiesHemant Khanna, Erica E Davis, Carlos A Murga-Zamalloa, et al.
Human Molecular Genetics|June 14, 2011
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYi Yu, Tushar R Bhangale, Jesen Fagerness, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degenerationWei Chen, Dwight Stambolian, Albert O Edwards, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingLot Snijders Blok, Erik Madsen, Jane Juusola, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Nature Genetics|May 21, 2013
A functional variant in the CFI gene confers a high risk of age-related macular degenerationJohannes P H van de Ven, Sara C Nilsson, Perciliz L Tan, et al.
American Journal of Human Genetics|February 13, 2018
Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone FragilityClothilde Esteve, Ludmila Francescatto, Perciliz L Tan, et al.
Ophthalmology|June 19, 2012
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypesLucia Sobrin, Stephan Ripke, Yi Yu, et al.
The New England Journal of Medicine|August 30, 2008
Toll-like receptor 3 and geographic atrophy in age-related macular degenerationZhenglin Yang, Charity Stratton, Peter J Francis, et al.
Nature Genetics|May 12, 2009
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathiesHemant Khanna, Erica E Davis, Carlos A Murga-Zamalloa, et al.
Human Molecular Genetics|June 14, 2011
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYi Yu, Tushar R Bhangale, Jesen Fagerness, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degenerationWei Chen, Dwight Stambolian, Albert O Edwards, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingLot Snijders Blok, Erik Madsen, Jane Juusola, et al.
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