Sakae Ikeda

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

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.

Effects of the conjugation of whey proteins with gellan polysaccharides on surfactant-induced competitive displacement from the air-water interface.

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

Stabilization of milk proteins in acidic conditions by pectic polysaccharides extracted from soy flour.

The effect of Tmem135 overexpression on the mouse heart.

Rheological characteristics and supramolecular structure of the exopolysaccharide produced by Lactobacillus fermentum MTCC 25067.

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

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

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

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.