Akihiro Ikeda

Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene.

Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum.

Effect of destrin mutations on the gene expression profile in vivo.

Defects in actin dynamics lead to an autoinflammatory condition through the upregulation of CXCL5.

Serum response factor is essential for the proper development of skin epithelium.

Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration.

Gene targeting in the mouse.

Genetic basis of age-dependent synaptic abnormalities in the retina.

Length regulation of mechanosensitive stereocilia depends on very slow actin dynamics and filament-severing proteins.

A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia.

The Significance of the Discordant Occurrence of Lens Tumors in Humans versus Other Species.

Syndactyly in a novel Fras1(rdf) mutant results from interruption of signals for interdigital apoptosis.

Mouse mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies.

Metabolomics Identifies Metabolic Markers of Maturation in Human Pluripotent Stem Cell-Derived Cardiomyocytes.

The effect of Tmem135 overexpression on the mouse heart.

Loss of Chondroitin Sulfate Modification Causes Inflammation and Neurodegeneration in Mice.

Long-term evaluation of retinal morphology and function in a mouse model of oxygen-induced retinopathy.

Metabolic alterations caused by the mutation and overexpression of the gene.

Modulation of Tmem135 Leads to Retinal Pigmented Epithelium Pathologies in Mice.

Different Human Immune Lineage Compositions Are Generated in Non-Conditioned NBSGW Mice Depending on HSPC Source.

The Influence of Mitochondrial Dynamics and Function on Retinal Ganglion Cell Susceptibility in Optic Nerve Disease.

Retinopathy of prematurity shows alterations in Vegfa isoform expression.

A mutation in transmembrane protein 135 impairs lipid metabolism in mouse eyecups.

Transmembrane protein 135 regulates lipid homeostasis through its role in peroxisomal DHA metabolism.