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Nature|January 30, 2007
Organ size is limited by the number of embryonic progenitor cells in the pancreas but not the liverBen Z Stanger, Akemi J Tanaka, Douglas A MeltonDevelopmental Biology|January 18, 2008
Mononuclear muscle cells in Drosophila ovaries revealed by GFP protein trapsAndrew M Hudson, Lisa N Petrella, Akemi J Tanaka, et al.Cold Spring Harbor Molecular Case Studies|February 5, 2020
Phenotypic expansion of autosomal dominant retinitis pigmentosa associated with the D477G mutation in RPE65Ruben Jauregui, Ahra Cho, Jin Kyun Oh, et al.Cold Spring Harbor Molecular Case Studies|November 18, 2018
A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorderAkemi J Tanaka, Kanji Okumoto, Shigehiko Tamura, et al.Cold Spring Harbor Molecular Case Studies|December 15, 2019
Compound heterozygous novel frameshift variants in the PROM1 gene result in Leber congenital amaurosisSara D Ragi, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.Ophthalmic Genetics|February 14, 2020
Progressive RPE atrophy and photoreceptor death in KIZ-associated autosomal recessive retinitis pigmentosaYuchen Lin, Christine L Xu, Mark P Breazzano, et al.Orphanet Journal of Rare Diseases|February 1, 2020
Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing resultsAhra Cho, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.Journal of Cell Science|May 13, 2020
Recent insights into peroxisome biogenesis and associated diseasesYukio Fujiki, Yuichi Abe, Yuuta Imoto, et al.Documenta Ophthalmologica. Advances in Ophthalmology|September 21, 2019
Novel REEP6 gene mutation associated with autosomal recessive retinitis pigmentosaYuchen Lin, Christine L Xu, Gabriel Velez, 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.Pageof 2