Masashi Nishikawa

Nagoya, Japan

Last Updated: 09/26/2026

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Found 29 publications

An N-terminal CDC42 T43I variant reveals the mechanism of pyrin inflammasome activation.

An N-terminal CDC42 T43I variant reveals the mechanism of pyrin inflammasome activation.

Journal: Science immunology

Published: August 07, 2026

A hypofunctional PREX1 variant (p.Y191C) leads to neurodevelopmental abnormalities and epilepsy by attenuating RAC1 signaling.

A hypofunctional PREX1 variant (p.Y191C) leads to neurodevelopmental abnormalities and epilepsy by attenuating RAC1 signaling.

Journal: Scientific reports

Published: November 04, 2025

PLEKHG2 and the PLEKHG family: Linking Rho family GTPases to neural development and disorders.

PLEKHG2 and the PLEKHG family: Linking Rho family GTPases to neural development and disorders.

Journal: Histology and histopathology

Published: May 02, 2025

Regulation of RHOV signaling by interaction with SH3 domain-containing adaptor proteins and phosphorylation by PKA.

Regulation of RHOV signaling by interaction with SH3 domain-containing adaptor proteins and phosphorylation by PKA.

Journal: Biochemical and biophysical research communications

Published: June 08, 2024

Pathophysiological significance of the p.E31G variant in RAC1 responsible for a neurodevelopmental disorder with microcephaly.

Pathophysiological significance of the p.E31G variant in RAC1 responsible for a neurodevelopmental disorder with microcephaly.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: May 29, 2024

Live Imaging of Migrating Neurons and Glial Progenitors Visualized by in Utero Electroporation.

Live Imaging of Migrating Neurons and Glial Progenitors Visualized by in Utero Electroporation.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: April 17, 2024

Variations associated with neurodevelopmental disorders affect ARF1 function and cortical development.

Variations associated with neurodevelopmental disorders affect ARF1 function and cortical development.

Journal: Journal of biochemistry

Published: January 28, 2024

A Novel Constitutively Active c.98G > C, p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization.

A Novel Constitutively Active c.98G > C, p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization.

Journal: Human mutation

Published: May 17, 2023

Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development.

Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development.

Journal: Medical molecular morphology

Published: May 01, 2023

A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association.

A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association.

Journal: Scientific reports

Published: February 06, 2023

Hyodeoxycholic Acid (HDCA) Prevents Development of Dextran Sulfate Sodium (DSS)-Induced Colitis in Mice: Possible Role of Synergism between DSS and HDCA in Increasing Fecal Bile Acid Levels.

Hyodeoxycholic Acid (HDCA) Prevents Development of Dextran Sulfate Sodium (DSS)-Induced Colitis in Mice: Possible Role of Synergism between DSS and HDCA in Increasing Fecal Bile Acid Levels.

Journal: Biological & pharmaceutical bulletin

Published: October 02, 2022

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.

Journal: Developmental neuroscience

Published: August 07, 2022

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Last Updated: 09/26/2026