Kunimasa Yan

Tokyo, Japan

Last Updated: 09/26/2026

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Found 33 publications

USP40 protects podocytes by deubiquitylating integrin β1.

USP40 protects podocytes by deubiquitylating integrin β1.

Journal: Biochemical and biophysical research communications

Published: March 10, 2026

The O-GlcNAcylation of β-actin Ser199 controls nuclear speckle localization and is dysregulated in diabetes.

The O-GlcNAcylation of β-actin Ser199 controls nuclear speckle localization and is dysregulated in diabetes.

Journal: Histochemistry and cell biology

Published: October 09, 2025

Early-onset urinary calculi in Menkes disease: A rare presentation in a 5-month-old infant.

Early-onset urinary calculi in Menkes disease: A rare presentation in a 5-month-old infant.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: June 11, 2025

Latent Non-typhoidal Salmonella in Macrophages as a Potential Cause of Persistent Appendicitis.

Latent Non-typhoidal Salmonella in Macrophages as a Potential Cause of Persistent Appendicitis.

Journal: Cureus

Published: May 17, 2025

Immunohistochemical Study on O-GlcNAcylation in Diabetic Pathologies: Molecular Mechanisms and Implications.

Immunohistochemical Study on O-GlcNAcylation in Diabetic Pathologies: Molecular Mechanisms and Implications.

Journal: Acta histochemica et cytochemica

Published: April 12, 2025

Macrophage Activation Syndrome as an Atypical Manifestation of Mixed Connective Tissue Disease in a 14-Year-Old Girl: A Case Report.

Macrophage Activation Syndrome as an Atypical Manifestation of Mixed Connective Tissue Disease in a 14-Year-Old Girl: A Case Report.

Journal: Cureus

Published: March 07, 2025

A scalp abscess causes skull destruction, leading to epidural empyema in an infant.

A scalp abscess causes skull destruction, leading to epidural empyema in an infant.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: January 24, 2025

Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II.

Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II.

Journal: JCEM case reports

Published: November 12, 2022

USP40 deubiquitinates HINT1 and stabilizes p53 in podocyte damage.

USP40 deubiquitinates HINT1 and stabilizes p53 in podocyte damage.

Journal: Biochemical and biophysical research communications

Published: April 27, 2022

A Novel Mouse Model of Idiopathic Nephrotic Syndrome Induced by Immunization with the Podocyte Protein Crb2.

A Novel Mouse Model of Idiopathic Nephrotic Syndrome Induced by Immunization with the Podocyte Protein Crb2.

Journal: Journal of the American Society of Nephrology : JASN

Published: January 16, 2022

Podocyte-specific Crb2 knockout mice develop focal segmental glomerulosclerosis.

Podocyte-specific Crb2 knockout mice develop focal segmental glomerulosclerosis.

Journal: Scientific reports

Published: March 29, 2021

A Japanese case of multisystem inflammatory syndrome in children.

A Japanese case of multisystem inflammatory syndrome in children.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: March 12, 2021

Showing 1-12 of 33

Last Updated: 09/26/2026