Daichi Sato
Sendai, Japan
Last Updated: 09/26/2026
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Found 9 publications
A Japanese Case of Infantile Liver Failure Syndrome Type 2 With Novel NBAS Variants.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: January 27, 2026
Comprehensive genetic analysis for identification of monogenic disorders and selection of appropriate treatments in pediatric patients with persistent thrombocytopenia.
Journal: Pediatric hematology and oncology
Published: September 25, 2024
Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood.
Journal: European journal of medical genetics
Published: June 25, 2023
Two-year crizotinib monotherapy induced durable complete response of pediatric ALK-positive inflammatory myofibroblastic tumor.
Journal: Pediatric blood & cancer
Published: January 13, 2023
Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia-telangiectasia caused by novel compound heterozygous variants in ATM.
Journal: International journal of hematology
Published: March 30, 2021
A pediatric case of osteosarcoma and tuberous sclerosis complex with a novel germline mutation in the TSC2 gene and a somatic mutation in the TP53 gene.
Journal: Pediatric blood & cancer
Published: January 06, 2021
The C-terminal region of the yeast monocarboxylate transporter Jen1 acts as a glucose signal-responding degron recognized by the α-arrestin Rod1.
Journal: The Journal of biological chemistry
Published: November 22, 2017
The mechanism of the glycosylase reaction with hOGG1 base-excision repair enzyme: concerted effect of Lys249 and Asp268 during excision of 8-oxoguanine.
Journal: Nucleic acids research
Published: November 29, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026