Yutaka Saikawa
Kanazawa, 9200293, Japan
Last Updated: 09/26/2026
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Found 16 publications
Cellular automata modelling of leukaemic stem cell dynamics in acute myeloid leukaemia: insights into predictive outcomes and targeted therapies.
Journal: Royal Society open science
Published: July 23, 2024
Mesenchymal cells regulate enteric neural crest cell migration via RET-GFRA1b trans-signaling.
Journal: Biochemical and biophysical research communications
Published: February 26, 2024
Tertiary hyperparathyroidism in patients with pseudohypoparathyroidism type 1a.
Journal: Bone reports
Published: January 05, 2022
Spinal rosette-forming glioneuronal tumor: First case in a young child.
Journal: Radiology case reports
Published: September 17, 2021
Exposure to Maternal Immune Activation Causes Congenital Unfolded Protein Response Defects and Increases the Susceptibility to Postnatal Inflammatory Stimulation in Offspring.
Journal: Journal of inflammation research
Published: December 01, 2020
Sinonasal NUT carcinoma: clinicopathological and cytogenetic analysis with autopsy findings.
Journal: Human pathology
Published: August 03, 2017
Gastric Gyri - Pediatric Ménétrier's Disease.
Journal: The New England journal of medicine
Published: February 23, 2017
Interaction between the immune system and acute myeloid leukemia: A model incorporating promotion of regulatory T cell expansion by leukemic cells.
Journal: Bio Systems
Published: January 17, 2017
Role of 18-fluoro-2-deoxyglucose positron emission tomography in detecting acute inflammatory lesions of non-bacterial osteitis in patients with a fever of unknown origin: A comparative study of 18-fluoro-2-deoxyglucose positron emission tomography, bone scan, and magnetic resonance imaging.
Journal: Modern rheumatology
Published: June 21, 2016
A novel MEN1 mutation in a Japanese adolescent with multiple endocrine neoplasia type 1.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: May 19, 2016
A novel frameshift mutation in the TRPS1 gene caused Tricho-rhino-phalangeal syndrome type I and III in a Japanese family.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: February 29, 2016
Last Updated: 09/26/2026