Satoshi Hara
Yokohama, Japan
Last Updated: 09/26/2026
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Found 62 publications
Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.
Journal: Human genomics
Published: March 21, 2026
Partial reduction of sympathetic noradrenaline synthesis enhanced insulin secretion and cell-cycle-associated activity of pancreatic β cells in mice.
Journal: American journal of physiology. Cell physiology
Published: February 23, 2026
Subperiosteal Orbital Abscess Complicated by Haemophilus influenzae Type c Bacteremia in a Fully Immunized Toddler: A Brief Clinical Study.
Journal: The Journal of craniofacial surgery
Published: January 15, 2026
A Novel Mouse Model of Sympathoadrenal Catecholamine Deficiency by Ablation of the Tyrosine Hydroxylase Gene With Slc6a4-Cre.
Journal: Journal of neurochemistry
Published: October 25, 2025
Transcriptional regulation of the GTP cyclohydrolase I gene via the NF-κB pathway by bacterial and viral immune stimulants.
Journal: Journal of biochemistry
Published: August 22, 2025
Variants of NLRP genes encoding subcortical maternal complex components are linked to biparental placental mesenchymal dysplasia.
Journal: Human genomics
Published: March 23, 2025
Identification of maternal allele sequences of IG-DMR that are essential for neonatal viability.
Journal: PloS one
Published: January 31, 2025
Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.
Journal: Communications biology
Published: August 07, 2024
Comparative Study of Blood Neopterin and Biopterins in Patients with COVID-19 and Secondary Bacterial Infection.
Journal: Journal of clinical medicine
Published: July 03, 2024
Role of NT5DC2 in tyrosine hydroxylase phosphorylation based on the analysis of NT5DC2-binding proteins.
Journal: Biochemical and biophysical research communications
Published: February 06, 2024
Inhibition of QDPR synergistically modulates intracellular tetrahydrobiopterin profiles in cooperation with methotrexate.
Journal: Biochemical and biophysical research communications
Published: January 25, 2024
Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.
Journal: Journal of medical genetics
Published: September 07, 2023
Last Updated: 09/26/2026