Department of Molecular Neurobiology,
Institute for Developmental Research,
Department of Molecular Neurobiology, Institute for Developmental Research
Koh-ichi Nagata has not added Biography.
If you are Koh-ichi Nagata and would like to personalize this page please email our Author Liaison for assistance.
Morphological characterization of mammalian timeless in the mouse brain development.
Neuroscience research Mar, 2015 | Pubmed ID: 25448545
Morphological characterization of Class III phosphoinositide 3-kinase during mouse brain development.
Medical molecular morphology Mar, 2016 | Pubmed ID: 26242203
Schizophrenia susceptibility gene product dysbindin-1 regulates the homeostasis of cyclin D1.
Biochimica et biophysica acta Aug, 2016 | Pubmed ID: 27130439
Role of Class III phosphoinositide 3-kinase in the brain development: possible involvement in specific learning disorders.
Journal of neurochemistry Oct, 2016 | Pubmed ID: 27607605
Autism spectrum disorder-associated genes and the development of dentate granule cells.
Medical molecular morphology Sep, 2017 | Pubmed ID: 28534217
Expression analyses of Phactr1 (phosphatase and actin regulator 1) during mouse brain development.
Neuroscience research Mar, 2018 | Pubmed ID: 28803787
MUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development.
Acta neuropathologica communications Nov, 2017 | Pubmed ID: 29191246
Expression analyses of Dusp22 (Dual-specificity phosphatase 22) in mouse tissues.
Medical molecular morphology Jun, 2018 | Pubmed ID: 29282540
Functions of Rhotekin, an Effector of Rho GTPase, and Its Binding Partners in Mammals.
International journal of molecular sciences Jul, 2018 | Pubmed ID: 30037057
Role of Per3, a circadian clock gene, in embryonic development of mouse cerebral cortex.
Scientific reports Apr, 2019 | Pubmed ID: 30971765
Expression Analyses of POGZ, A Responsible Gene for Neurodevelopmental Disorders, during Mouse Brain Development.
Developmental neuroscience , 2019 | Pubmed ID: 31430754
Spatiotemporally Dependent Vascularization Is Differently Utilized among Neural Progenitor Subtypes during Neocortical Development.
Cell reports Oct, 2019 | Pubmed ID: 31665628
Biochemical and morphological characterization of SEPT1 in mouse brain.
Medical molecular morphology Dec, 2020 | Pubmed ID: 32146512
Neuropathophysiological significance of the c.1449T>C/p.(Tyr64Cys) mutation in the CDC42 gene responsible for Takenouchi-Kosaki syndrome.
Biochemical and biophysical research communications Sep, 2020 | Pubmed ID: 32819561
Heterotrimeric G-protein, Gi1, is involved in the regulation of proliferation, neuronal migration, and dendrite morphology during cortical development in vivo.
Journal of neurochemistry May, 2021 | Pubmed ID: 33025585
Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice.
Nature communications Nov, 2020 | Pubmed ID: 33203851
Expression analyses of PLEKHG2, a Rho family-specific guanine nucleotide exchange factor, during mouse brain development.
Medical molecular morphology Jun, 2021 | Pubmed ID: 33492483
Expression Analyses of Mediator Complex Subunit 13-Like: A Responsible Gene for Neurodevelopmental Disorders during Mouse Brain Development.
Developmental neuroscience , 2021 | Pubmed ID: 33794529
Author Correction: Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice.
Nature communications Jun, 2021 | Pubmed ID: 34140510
Physiological significance of WDR45, a responsible gene for β-propeller protein associated neurodegeneration (BPAN), in brain development.
Scientific reports Nov, 2021 | Pubmed ID: 34799629
The synaptic scaffolding protein CNKSR2 interacts with CYTH2 to mediate hippocampal granule cell development.
The Journal of biological chemistry Dec, 2021 | Pubmed ID: 34800437
Expression Analyses of Rac3, a Rho Family Small GTPase, during Mouse Brain Development.
Developmental neuroscience , 2022 | Pubmed ID: 34839287
Pathophysiological Mechanisms in Neurodevelopmental Disorders Caused by Rac GTPases Dysregulation: What's behind Neuro-RACopathies.
Cells Dec, 2021 | Pubmed ID: 34943902
Functions of CNKSR2 and Its Association with Neurodevelopmental Disorders.
Cells Jan, 2022 | Pubmed ID: 35053419
Impaired Function of PLEKHG2, a Rho-Guanine Nucleotide-Exchange Factor, Disrupts Corticogenesis in Neurodevelopmental Phenotypes.
Cells Feb, 2022 | Pubmed ID: 35203342
Expression Analyses of Cep152, a Responsible Gene Product for Autosomal Recessive Primary Microcephaly, during Mouse Brain Development.
Developmental neuroscience , 2022 | Pubmed ID: 35259752
Gain-of-function p.F28S variant in disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorder.
Journal of medical genetics Mar, 2023 | Pubmed ID: 35595279
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.
Brain : a journal of neurology Sep, 2022 | Pubmed ID: 35851598
Expression Analyses of Polo-Like Kinase 4, a Gene Product Responsible for Autosomal Recessive Microcephaly and Seckel Syndrome, during Mouse Brain Development.
Developmental neuroscience , 2022 | Pubmed ID: 36067731
Deficiency of , a gene related to intellectual disability, causes impaired neuronal development and a mild behavioural phenotype.
Brain communications , 2022 | Pubmed ID: 36106092
Erratic and blood vessel-guided migration of astrocyte progenitors in the cerebral cortex.
Nature communications Nov, 2022 | Pubmed ID: 36323680
Pathophysiological Mechanism of Neurodevelopmental Disorders-Overview.
Cells Dec, 2022 | Pubmed ID: 36552846
Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.
Developmental neuroscience , 2023 | Pubmed ID: 36630934
MED13L and its disease-associated variants influence the dendritic development of cerebral cortical neurons in the mammalian brain.
Journal of neurochemistry May, 2023 | Pubmed ID: 36798993
Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome.
Biomolecules Apr, 2023 | Pubmed ID: 37238632
A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association.
Scientific reports Jun, 2023 | Pubmed ID: 37328543
Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development.
Medical molecular morphology Dec, 2023 | Pubmed ID: 37402055
Expression analysis of type I ARF small GTPases ARF1-3 during mouse brain development.
Molecular biology reports Jan, 2024 | Pubmed ID: 38227057
ACERCA DE JoVE
Copyright © 2024 MyJoVE Corporation. Todos los derechos reservados