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SARS-CoV-2 infection status in corneal preservation solution and COVID-19 prevalence after corneal transplantation

Scientific reports, 2024-02, Vol.14 (1), p.3766-3766, Article 3766

2024

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Simultaneous Vitreoretinal Surgery and Sclerokeratoplasty for Keratoglobus with Intraocular Hemorrhage and Extensive Corneal Rupture

Case reports in ophthalmology, 2022-03, Vol.13 (1), p.220-226

2022

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Improving the effect of NaOCl pretreatment on bonding to caries-affected dentin using self-etch adhesives

Journal of dentistry, 2009-10, Vol.37 (10), p.769-775

2009

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Fracture toughness of human dentin

Journal of biomedical materials research, 2003-09, Vol.66A (3), p.507-512

2003

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Penetration of silver nitrate into bleached enamel, dentin, and cementum

Quintessence international (Berlin, Germany : 1985), 2007-03, Vol.38 (3), p.e183

2007

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Shear bond strength of current adhesive systems to enamel, dentin and dentin-enamel junction region

Operative dentistry, 2003-09, Vol.28 (5), p.585-590

2003

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Improvement of Bonding to Caries-affected Dentin

The Japanese Journal of Conservative Dentistry, 2008/08/31, Vol.51(4), pp.396-402

2008

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Simultaneous Vitreoretinal Surgery and Sclerokeratoplasty for Keratoglobus with Intraocular Hemorrhage and Extensive Corneal Rupture

Case reports in ophthalmology, 2022, Vol.13 (1), p.220-226

2022

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う蝕象牙質に対する2ステップ・セルフエッチ接着システムの接着性能の改良

日本歯科保存学雑誌, 2008/08/31, Vol.51(4), pp.396-402

2008

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Heterotrimeric G‐protein, Gi1, is involved in the regulation of proliferation, neuronal migration, and dendrite morphology during cortical development in vivo

Journal of neurochemistry, 2021-05, Vol.157 (4), p.1167-1181

2021

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Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development

Scientific reports, 2016-08, Vol.6 (1), p.30805-30805, Article 30805

2016

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Neuropathophysiological significance of the c.1449T>C/p.(Tyr64Cys) mutation in the CDC42 gene responsible for Takenouchi-Kosaki syndrome

Biochemical and biophysical research communications, 2020-09, Vol.529 (4), p.1033-1037

2020

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MED13L and its disease‐associated variants influence the dendritic development of cerebral cortical neurons in the mammalian brain

Journal of neurochemistry, 2023-05, Vol.165 (3), p.334-347

2023

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Heterotrimeric G‐protein, Gi1, is involved in the regulation of proliferation, neuronal migration, and dendrite morphology during cortical development in vivo

Journal of neurochemistry, 2020-10, Vol.157 (4)

2020

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Analyses of Conditional Knockout Mice for Pogz , a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the Brain

Cells (Basel, Switzerland), 2024-03, Vol.13 (6), p.540

2024

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Expression Analyses of C-Terminal-Binding Protein 1 (CtBP1) during Mouse Brain Development

Developmental neuroscience, 2024-08, Vol.46 (4), p.262-272

2024

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Expression Analyses of Cep152, a Responsible Gene Product for Autosomal Recessive Primary Microcephaly, during Mouse Brain Development

Developmental neuroscience, 2022-05, Vol.44 (3), p.162-170

2022

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Expression analysis of type I ARF small GTPases ARF1-3 during mouse brain development

Molecular biology reports, 2024-12, Vol.51 (1), p.106-106, Article 106

2024

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

Developmental neuroscience, 2021-05, Vol.43 (1), p.43-52

2021

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

Developmental neuroscience, 2022-01, Vol.44 (6), p.643-650

2022

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MUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Acta neuropathologica communications, 2017-11, Vol.5 (1), p.92-92, Article 92

2017

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Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

Molecular autism, 2015-10, Vol.6 (1), p.56-56, Article 56

2015

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Interleukin-1 and Tumor Necrosis Factor-α Trigger Restriction of Hepatitis B Virus Infection via a Cytidine Deaminase Activation-induced Cytidine Deaminase (AID)

The Journal of biological chemistry, 2013-11, Vol.288 (44), p.31715-31727

2013

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De novo PHACTR1 mutations in West syndrome and their pathophysiological effects

Brain (London, England : 1878), 2018-11, Vol.141 (11), p.3098-3114

2018

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Analyses of Conditional Knockout Mice for IPogz/I, a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the Brain

Cells (Basel, Switzerland), 2024-03, Vol.13 (6)

2024

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SARS-CoV-2 infection status in corneal preservation solution and COVID-19 prevalence after corneal transplantation

Simultaneous Vitreoretinal Surgery and Sclerokeratoplasty for Keratoglobus with Intraocular Hemorrhage and Extensive Corneal Rupture

Improving the effect of NaOCl pretreatment on bonding to caries-affected dentin using self-etch adhesives

Fracture toughness of human dentin

Penetration of silver nitrate into bleached enamel, dentin, and cementum

Shear bond strength of current adhesive systems to enamel, dentin and dentin-enamel junction region

Improvement of Bonding to Caries-affected Dentin

Simultaneous Vitreoretinal Surgery and Sclerokeratoplasty for Keratoglobus with Intraocular Hemorrhage and Extensive Corneal Rupture

う蝕象牙質に対する2ステップ・セルフエッチ接着システムの接着性能の改良

Heterotrimeric G‐protein, Gi1, is involved in the regulation of proliferation, neuronal migration, and dendrite morphology during cortical development in vivo

Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development

Neuropathophysiological significance of the c.1449T>C/p.(Tyr64Cys) mutation in the CDC42 gene responsible for Takenouchi-Kosaki syndrome

MED13L and its disease‐associated variants influence the dendritic development of cerebral cortical neurons in the mammalian brain

Heterotrimeric G‐protein, Gi1, is involved in the regulation of proliferation, neuronal migration, and dendrite morphology during cortical development in vivo

Analyses of Conditional Knockout Mice for Pogz , a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the Brain

Expression Analyses of C-Terminal-Binding Protein 1 (CtBP1) during Mouse Brain Development

Expression Analyses of Cep152, a Responsible Gene Product for Autosomal Recessive Primary Microcephaly, during Mouse Brain Development

Expression analysis of type I ARF small GTPases ARF1-3 during mouse brain development

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

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

MUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development

Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

Interleukin-1 and Tumor Necrosis Factor-α Trigger Restriction of Hepatitis B Virus Infection via a Cytidine Deaminase Activation-induced Cytidine Deaminase (AID)

De novo PHACTR1 mutations in West syndrome and their pathophysiological effects

Analyses of Conditional Knockout Mice for IPogz/I, a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the Brain

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