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Sakae Ikeda

Showing results (21-30 of 33) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 3, 2014
Genetic basis of age-dependent synaptic abnormalities in the retinaHitoshi Higuchi, Erica L Macke, Wei-Hua Lee, et al.
Scientific Reports|January 15, 2022
A mutation in transmembrane protein 135 impairs lipid metabolism in mouse eyecupsMichael Landowski, Vijesh J Bhute, Tetsuya Takimoto, et al.
Physiological Genomics|February 20, 2014
Serum response factor: positive and negative regulation of an epithelial gene expression network in the destrin mutant corneaSharolyn V Kawakami-Schulz, Angela M Verdoni, Shannon G Sattler, et al.
Plos One|August 14, 2018
The effect of Tmem135 overexpression on the mouse heartSarah Aileen Lewis, Tetsuya Takimoto, Shima Mehrvar, et al.
Human Molecular Genetics|April 18, 2003
Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor)Sakae Ikeda, Leslie A Cunningham, Dawnalyn Boggess, et al.
Frontiers in Cell and Developmental Biology|June 19, 2026
Mitofusins are required for specialized mitochondrial morphology and function of rod photoreceptor cellsMichael Landowski, Ryo Hagimori, Purnima Gogoi, et al.
The American Journal of Pathology|April 28, 2005
Spontaneous corneal hem- and lymphangiogenesis in mice with destrin-mutation depend on VEGFR3 signalingClaus Cursiefen, Sakae Ikeda, Patsy M Nishina, et al.
Investigative Ophthalmology & Visual Science|October 16, 2020
Modulation of Tmem135 Leads to Retinal Pigmented Epithelium Pathologies in MiceMichael Landowski, Samuel Grindel, Pawan K Shahi, et al.
Investigative Ophthalmology & Visual Science|June 13, 2015
A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller GliaDennis M Maddox, Gayle B Collin, Akihiro Ikeda, et al.
Genetics|November 23, 2019
Loss of Chondroitin Sulfate Modification Causes Inflammation and Neurodegeneration in <i>skt</i> MiceErica L Macke, Erika Henningsen, Erik Jessen, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 3, 2014
Genetic basis of age-dependent synaptic abnormalities in the retinaHitoshi Higuchi, Erica L Macke, Wei-Hua Lee, et al.
Scientific Reports|January 15, 2022
A mutation in transmembrane protein 135 impairs lipid metabolism in mouse eyecupsMichael Landowski, Vijesh J Bhute, Tetsuya Takimoto, et al.
Physiological Genomics|February 20, 2014
Serum response factor: positive and negative regulation of an epithelial gene expression network in the destrin mutant corneaSharolyn V Kawakami-Schulz, Angela M Verdoni, Shannon G Sattler, et al.
Plos One|August 14, 2018
The effect of Tmem135 overexpression on the mouse heartSarah Aileen Lewis, Tetsuya Takimoto, Shima Mehrvar, et al.
Human Molecular Genetics|April 18, 2003
Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor)Sakae Ikeda, Leslie A Cunningham, Dawnalyn Boggess, et al.
Frontiers in Cell and Developmental Biology|June 19, 2026
Mitofusins are required for specialized mitochondrial morphology and function of rod photoreceptor cellsMichael Landowski, Ryo Hagimori, Purnima Gogoi, et al.
The American Journal of Pathology|April 28, 2005
Spontaneous corneal hem- and lymphangiogenesis in mice with destrin-mutation depend on VEGFR3 signalingClaus Cursiefen, Sakae Ikeda, Patsy M Nishina, et al.
Investigative Ophthalmology & Visual Science|October 16, 2020
Modulation of Tmem135 Leads to Retinal Pigmented Epithelium Pathologies in MiceMichael Landowski, Samuel Grindel, Pawan K Shahi, et al.
Investigative Ophthalmology & Visual Science|June 13, 2015
A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller GliaDennis M Maddox, Gayle B Collin, Akihiro Ikeda, et al.
Genetics|November 23, 2019
Loss of Chondroitin Sulfate Modification Causes Inflammation and Neurodegeneration in <i>skt</i> MiceErica L Macke, Erika Henningsen, Erik Jessen, et al.
Pageof 4