Yukiko Kuroda

Brain-specific expression of the nuclear actin-related protein ArpNalpha and its involvement in mammalian SWI/SNF chromatin remodeling complex.

Regulation of TRPC6 channel activity by tyrosine phosphorylation.

Expanding phenotype and clinical heterogeneity in patients with identical mutation of the parkin gene.

Oxidative stress-associated mitochondrial dysfunction in corticosteroid-treated muscle cells.

Amplification of Ca2+ signaling by diacylglycerol-mediated inositol 1,4,5-trisphosphate production.

Involvement of mitochondria in myasthenia gravis complicated with dermatomyositis and rheumatoid arthritis: a case report.

Successful treatment with tacrolimus in a case of refractory dermatomyositis.

Parkin enhances mitochondrial biogenesis in proliferating cells.

Parkin affects mitochondrial function and apoptosis in neuronal and myogenic cells.

Three-dimensional finite-element model of the human temporomandibular joint disc during prolonged clenching.

Inositol 1,4,5-trisphosphate receptor type 1 in granule cells, not in Purkinje cells, regulates the dendritic morphology of Purkinje cells through brain-derived neurotrophic factor production.

Abnormal taste perception in mice lacking the type 3 inositol 1,4,5-trisphosphate receptor.

Phosphorylation of Homer3 by calcium/calmodulin-dependent kinase II regulates a coupling state of its target molecules in Purkinje cells.

Osteoblasts induce Ca2+ oscillation-independent NFATc1 activation during osteoclastogenesis.

[Parkin and mitochondria].

80K-H interacts with inositol 1,4,5-trisphosphate (IP3) receptors and regulates IP3-induced calcium release activity.

Inositol 1,4,5-triphosphate receptor-binding protein released with inositol 1,4,5-triphosphate (IRBIT) associates with components of the mRNA 3' processing machinery in a phosphorylation-dependent manner and inhibits polyadenylation.

Intermittent posterior displacement of the rat mandible in the growth period affects the condylar cancellous bone.

Parkin interacts with Klokin1 for mitochondrial import and maintenance of membrane potential.

The effects of FK506 on refractory inflammatory myopathies.

[Comatose patient with neuroleptic malignant syndrome brought by ambulance].

Cot kinase promotes Ca2+ oscillation/calcineurin-independent osteoclastogenesis by stabilizing NFATc1 protein.

Regulation of osteoclasts by membrane-derived lipid mediators.

Molecular mechanisms of triggering, amplifying and targeting RANK signaling in osteoclasts.

FK506 attenuates thymic output in patients with myasthenia gravis.

De novo duplication of 17p13.1-p13.2 in a patient with intellectual disability and obesity.

Superoxide dismutase as a target of clioquinol-induced neurotoxicity.

Immediate effect of spinal magnetic stimulation on camptocormia in Parkinson's disease.

Refinement of the deletion in 8q22.2-q22.3: the minimum deletion size at 8q22.3 related to intellectual disability and epilepsy.

West syndrome in a patient with Schinzel-Giedion syndrome.

Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.

Microdeletion of 19p13.3 in a girl with Peutz-Jeghers syndrome, intellectual disability, hypotonia, and distinctive features.

Delineation of the KIAA2022 mutation phenotype: two patients with X-linked intellectual disability and distinctive features.

A postzygotic NRAS mutation in a patient with Schimmelpenning syndrome.

IRBIT regulates CaMKIIα activity and contributes to catecholamine homeostasis through tyrosine hydroxylase phosphorylation.

A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability.

Osteogenic capillaries orchestrate growth plate-independent ossification of the malleus.

Osteoprotegerin Regulates Pancreatic β-Cell Homeostasis upon Microbial Invasion.

A Novel method for the simultaneous identification of methylcytosine and hydroxymethylcytosine at a single base resolution.