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Rando Allikmets

Showing results (101-110 of 180) with videos related to

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Human Molecular Genetics|April 28, 2021
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt diseaseWinston Lee, Jana Zernant, Takayuki Nagasaki, et al.
Journal of Medical Genetics|April 28, 2017
Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degenerationJana Zernant, Winston Lee, Frederick T Collison, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 3, 2017
Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt DiseaseTommaso Verdina, Vivienne C Greenstein, Andrea Sodi, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencingJana Zernant, Carl Schubert, Kate M Im, et al.
Ophthalmology|April 10, 2010
Three major loci involved in age-related macular degeneration are also associated with polypoidal choroidal vasculopathyLuiz H Lima, Carl Schubert, Daniela C Ferrara, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
Quantification of peripapillary sparing and macular involvement in Stargardt disease (STGD1)Tomas R Burke, David W Rhee, R Theodore Smith, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 13, 2008
Analysis of major alleles associated with age-related macular degeneration in patients with multifocal choroiditis: strong association with complement factor HDaniela C Ferrara, Joanna E Merriam, K Bailey Freund, et al.
American Journal of Ophthalmology|June 11, 2019
Spectrum of Disease Severity and Phenotype in Choroideremia CarriersRuben Jauregui, Karen Sophia Park, Akemi J Tanaka, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosaB Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, et al.
Clinical Chemistry|June 12, 2004
Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variationsStefania Stenirri, Isabella Fermo, Stefania Battistella, et al.
Pageof 18

Showing results (101-110 of 180) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|April 28, 2021
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt diseaseWinston Lee, Jana Zernant, Takayuki Nagasaki, et al.
Journal of Medical Genetics|April 28, 2017
Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degenerationJana Zernant, Winston Lee, Frederick T Collison, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 3, 2017
Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt DiseaseTommaso Verdina, Vivienne C Greenstein, Andrea Sodi, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencingJana Zernant, Carl Schubert, Kate M Im, et al.
Ophthalmology|April 10, 2010
Three major loci involved in age-related macular degeneration are also associated with polypoidal choroidal vasculopathyLuiz H Lima, Carl Schubert, Daniela C Ferrara, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
Quantification of peripapillary sparing and macular involvement in Stargardt disease (STGD1)Tomas R Burke, David W Rhee, R Theodore Smith, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 13, 2008
Analysis of major alleles associated with age-related macular degeneration in patients with multifocal choroiditis: strong association with complement factor HDaniela C Ferrara, Joanna E Merriam, K Bailey Freund, et al.
American Journal of Ophthalmology|June 11, 2019
Spectrum of Disease Severity and Phenotype in Choroideremia CarriersRuben Jauregui, Karen Sophia Park, Akemi J Tanaka, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosaB Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, et al.
Clinical Chemistry|June 12, 2004
Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variationsStefania Stenirri, Isabella Fermo, Stefania Battistella, et al.
Pageof 18