Akihiro Ikeda

Department of Medical Genetics, University of Wisconsin-Madison

Affiliated withUniversity of Wisconsin-Madison

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 1	2023

Other Publications

Article	Year
Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene. Visual neuroscience\| PubMed ID: 17266781	2006
Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum. Molecular and cellular neurosciences\| PubMed ID: 17376701	2007
Effect of destrin mutations on the gene expression profile in vivo. Physiological genomics\| PubMed ID: 18381839	2008
Defects in actin dynamics lead to an autoinflammatory condition through the upregulation of CXCL5. PloS one\| PubMed ID: 18628996	2008
Serum response factor is essential for the proper development of skin epithelium. Mammalian genome : official journal of the International Mammalian Genome Society\| PubMed ID: 20047077	2010
Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration. PLoS genetics\| PubMed ID: 20502676	2010
Gene targeting in the mouse. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 21805269	2011
Genetic basis of age-dependent synaptic abnormalities in the retina. Mammalian genome : official journal of the International Mammalian Genome Society\| PubMed ID: 25273269	2015
Length regulation of mechanosensitive stereocilia depends on very slow actin dynamics and filament-severing proteins. Nature communications\| PubMed ID: 25897778	2015
A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia. Investigative ophthalmology & visual science\| PubMed ID: 26066746	2015
The Significance of the Discordant Occurrence of Lens Tumors in Humans versus Other Species. Ophthalmology\| PubMed ID: 26130328	2015
Syndactyly in a novel Fras1(rdf) mutant results from interruption of signals for interdigital apoptosis. Developmental dynamics : an official publication of the American Association of Anatomists\| PubMed ID: 26813283	2016
Mouse mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies. eLife\| PubMed ID: 27863209	2016
Metabolomics Identifies Metabolic Markers of Maturation in Human Pluripotent Stem Cell-Derived Cardiomyocytes. Theranostics\| PubMed ID: 28656061	2017
The effect of Tmem135 overexpression on the mouse heart. PloS one\| PubMed ID: 30102730	2018
Loss of Chondroitin Sulfate Modification Causes Inflammation and Neurodegeneration in Mice. Genetics\| PubMed ID: 31754016	2020
Long-term evaluation of retinal morphology and function in a mouse model of oxygen-induced retinopathy. Molecular vision\| PubMed ID: 32256029	2020
Metabolic alterations caused by the mutation and overexpression of the gene. Experimental biology and medicine (Maywood, N.J.)\| PubMed ID: 32515224	2020
Modulation of Tmem135 Leads to Retinal Pigmented Epithelium Pathologies in Mice. Investigative ophthalmology & visual science\| PubMed ID: 33064130	2020
Different Human Immune Lineage Compositions Are Generated in Non-Conditioned NBSGW Mice Depending on HSPC Source. Frontiers in immunology\| PubMed ID: 33193358	2020
The Influence of Mitochondrial Dynamics and Function on Retinal Ganglion Cell Susceptibility in Optic Nerve Disease. Cells\| PubMed ID: 34201955	2021
Retinopathy of prematurity shows alterations in Vegfa isoform expression. Pediatric research\| PubMed ID: 34285351	2022
A mutation in transmembrane protein 135 impairs lipid metabolism in mouse eyecups. Scientific reports\| PubMed ID: 35031662	2022
Transmembrane protein 135 regulates lipid homeostasis through its role in peroxisomal DHA metabolism. Communications biology\| PubMed ID: 36599953	2023