Miwa Yamazaki
Izumi, 5941101, Japan
Last Updated: 09/26/2026
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Found 17 publications
A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: March 13, 2023
Osteocytes and the pathogenesis of hypophosphatemic rickets.
Journal: Frontiers in endocrinology
Published: July 28, 2022
Extracellular Phosphate, Inflammation and Cytotoxicity.
Journal: Advances in experimental medicine and biology
Published: March 15, 2022
Growth-related skeletal changes and alterations in phosphate metabolism.
Journal: Bone
Published: February 03, 2022
Clonal osteoblastic cell lines with CRISPR/Cas9-mediated ablation of Pit1 or Pit2 show enhanced mineralization despite reduced osteogenic gene expression.
Journal: Bone
Published: December 24, 2020
Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients.
Journal: Calcified tissue international
Published: September 12, 2019
CREB activation in hypertrophic chondrocytes is involved in the skeletal overgrowth in epiphyseal chondrodysplasia Miura type caused by activating mutations of natriuretic peptide receptor B.
Journal: Human molecular genetics
Published: August 24, 2018
Phosphate as a Signaling Molecule and Its Sensing Mechanism.
Journal: Physiological reviews
Published: August 16, 2018
Extracellular Phosphate Induces the Expression of Dentin Matrix Protein 1 Through the FGF Receptor in Osteoblasts.
Journal: Journal of cellular biochemistry
Published: February 19, 2016
Last Updated: 09/26/2026