Hiroko Shimbo
Yokohama, 2320066, Japan
Last Updated: 09/26/2026
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Found 33 publications
Effects of SLC6A8 mutation-induced creatine deficiency on cellular function in fibroblasts.
Journal: Scientific reports
Published: February 28, 2025
Development of a novel liquid chromatography-tandem mass spectrometry based enzymatic assay of 5,10-methylenetetrahydrofolate reductase.
Journal: Scientific reports
Published: February 18, 2025
Impact of feeding age on cognitive impairment in mice with Disrupted-In-Schizophrenia 1 (Disc1) mutation under a high sucrose diet.
Journal: Behavioural brain research
Published: July 29, 2024
Minocycline prevents early age-related cognitive decline in a mouse model of intellectual disability caused by ZBTB18/RP58 haploinsufficiency.
Journal: Journal of neuroinflammation
Published: February 27, 2024
Disease specific brain capillary angiopathy in schizophrenia, bipolar disorder, and Alzheimer's disease.
Journal: Journal of psychiatric research
Published: January 20, 2023
The ATRX splicing variant c.21-1G>A is asymptomatic.
Journal: Human genome variation
Published: July 07, 2022
The mouse model of intellectual disability by ZBTB18/RP58 haploinsufficiency shows cognitive dysfunction with synaptic impairment.
Journal: Molecular psychiatry
Published: March 27, 2022
High-sucrose diets contribute to brain angiopathy with impaired glucose uptake and psychosis-related higher brain dysfunctions in mice.
Journal: Science advances
Published: November 10, 2021
Pyridoxal in the Cerebrospinal Fluid May Be a Better Indicator of Vitamin B6-dependent Epilepsy Than Pyridoxal 5'-Phosphate.
Journal: Pediatric neurology
Published: July 09, 2020
A novel method for isolating lymphatic endothelial cells from lymphatic malformations and detecting PIK3CA somatic mutation in these isolated cells.
Journal: Surgery today
Published: April 30, 2020
Cyclocreatine Transport by SLC6A8, the Creatine Transporter, in HEK293 Cells, a Human Blood-Brain Barrier Model Cell, and CCDSs Patient-Derived Fibroblasts.
Journal: Pharmaceutical research
Published: November 29, 2019
MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet gene.
Journal: Brain & development
Published: November 27, 2018
Last Updated: 09/26/2026