Nishikawa M - Search Results

1

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

Nishikawa M, Hayashi S, Nakayama A, Nishio Y, Shiraki A, Ito H, Maruyama K, Muramatsu Y, Ogi T, Mizuno S, Nagata KI. Nishikawa M, et al. Biochim Biophys Acta Mol Basis Dis. 2025 Jan;1871(1):167520. doi: 10.1016/j.bbadis.2024.167520. Epub 2024 Sep 20. Biochim Biophys Acta Mol Basis Dis. 2025. PMID: 39307291

2

Expression analyses of PLEKHG2, a Rho family-specific guanine nucleotide exchange factor, during mouse brain development.

Nishikawa M, Ito H, Noda M, Hamada N, Tabata H, Nagata KI. Nishikawa M, et al. Med Mol Morphol. 2021 Jun;54(2):146-155. doi: 10.1007/s00795-020-00275-1. Epub 2021 Jan 25. Med Mol Morphol. 2021. PMID: 33492483

3

Expression Analyses of Mediator Complex Subunit 13-Like: A Responsible Gene for Neurodevelopmental Disorders during Mouse Brain Development.

Hamada N, Iwamoto I, Nishikawa M, Nagata KI. Hamada N, et al. Among authors: nishikawa m. Dev Neurosci. 2021;43(1):43-52. doi: 10.1159/000515188. Epub 2021 Apr 1. Dev Neurosci. 2021. PMID: 33794529

4

Expression Analyses of Rac3, a Rho Family Small GTPase, during Mouse Brain Development.

Nishikawa M, Ito H, Noda M, Hamada N, Tabata H, Nagata KI. Nishikawa M, et al. Dev Neurosci. 2022;44(1):49-58. doi: 10.1159/000521168. Epub 2021 Nov 26. Dev Neurosci. 2022. PMID: 34839287

5

Pathophysiological Mechanisms in Neurodevelopmental Disorders Caused by Rac GTPases Dysregulation: What's behind Neuro-RACopathies.

Scala M, Nishikawa M, Nagata KI, Striano P. Scala M, et al. Among authors: nishikawa m. Cells. 2021 Dec 2;10(12):3395. doi: 10.3390/cells10123395. Cells. 2021. PMID: 34943902 Free PMC article. Review.

6

Impaired Function of PLEKHG2, a Rho-Guanine Nucleotide-Exchange Factor, Disrupts Corticogenesis in Neurodevelopmental Phenotypes.

Nishikawa M, Ito H, Tabata H, Ueda H, Nagata KI. Nishikawa M, et al. Cells. 2022 Feb 16;11(4):696. doi: 10.3390/cells11040696. Cells. 2022. PMID: 35203342 Free PMC article.

7

Gain-of-function p.F28S variant in RAC3 disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorder.

Nishikawa M, Scala M, Umair M, Ito H, Waqas A, Striano P, Zara F, Costain G, Capra V, Nagata KI. Nishikawa M, et al. J Med Genet. 2023 Mar;60(3):223-232. doi: 10.1136/jmedgenet-2022-108483. Epub 2022 May 20. J Med Genet. 2023. PMID: 35595279

8

Expression Analyses of Polo-Like Kinase 4, a Gene Product Responsible for Autosomal Recessive Microcephaly and Seckel Syndrome, during Mouse Brain Development.

Hamada N, Iwamoto I, Noda M, Nishikawa M, Nagata KI. Hamada N, et al. Among authors: nishikawa m. Dev Neurosci. 2022;44(6):643-650. doi: 10.1159/000526914. Epub 2022 Sep 6. Dev Neurosci. 2022. PMID: 36067731

9

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

Nishikawa M, Matsuki T, Hamada N, Nakayama A, Ito H, Nagata KI. Nishikawa M, et al. Med Mol Morphol. 2023 Dec;56(4):266-273. doi: 10.1007/s00795-023-00364-x. Epub 2023 Jul 4. Med Mol Morphol. 2023. PMID: 37402055

10

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

Nishikawa M, Nagata KI, Tabata H. Nishikawa M, et al. Methods Mol Biol. 2024;2794:201-209. doi: 10.1007/978-1-0716-3810-1_17. Methods Mol Biol. 2024. PMID: 38630231

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