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LOX-1 mediates inflammatory activation of microglial cells through the p38-MAPK/NF-κB pathways under hypoxic-ischemic conditions

Cell communication and signaling, 2023-06, Vol.21 (1), p.126-126, Article 126

2023

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Low dose resveratrol ameliorates mitochondrial respiratory dysfunction and enhances cellular reprogramming

Mitochondrion, 2017-05, Vol.34, p.43-48

2017

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Interleukin-1beta (IL-1β)-induced Notch ligand Jagged1 suppresses mitogenic action of IL-1β on human dystrophic myogenic cells

PloS one, 2017-12, Vol.12 (12), p.e0188821

2017

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Late-onset MELAS syndrome with mtDNA 14453G→A mutation masquerading as an acute encephalitis: a case report

BMC neurology, 2020-06, Vol.20 (1), p.1-247, Article 247

2020

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Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes

Internal Medicine, 2017/01/01, Vol.56(1), pp.95-99

2017

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Mitochondrial respiratory dysfunction disturbs neuronal and cardiac lineage commitment of human iPSCs

Cell death & disease, 2017-01, Vol.8 (1), p.e2551-e2551

2017

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13q13.3 microdeletion associated with apparently balanced translocation of 46,XX,t(7;13) suggests NBEA involvement

Brain & development (Tokyo. 1979), 2020-09, Vol.42 (8), p.581-586

2020

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Mitochondrial Complex III Deficiency Caused by a Homozygous UQCRC2 Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation

Human mutation, 2013-03, Vol.34 (3), p.446-452

2013

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Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case report

Brain & development (Tokyo. 1979), 2022-09, Vol.44 (8), p.551-557

2022

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A Pilot Study of Soluble Form of LOX-1 as a Novel Biomarker for Neonatal Hypoxic-Ischemic Encephalopathy

The Journal of pediatrics, 2019-03, Vol.206, p.49-55.e3

2019

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Linear cortical cystic lesions: Characteristic MR findings in MELAS patients

Brain & development (Tokyo. 1979), 2021-10, Vol.43 (9), p.931-938

2021

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A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation

Journal of human genetics, 2014-10, Vol.59 (10), p.581-583

2014

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Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan

Brain & development (Tokyo. 1979), 2016-10, Vol.38 (9), p.785-791

2016

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Reactive oxygen species stimulate mitochondrial allele segregation toward homoplasmy in human cells

Molecular biology of the cell, 2016-05, Vol.27 (10), p.1684-1693

2016

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CRIF1 Is Essential for the Synthesis and Insertion of Oxidative Phosphorylation Polypeptides in the Mammalian Mitochondrial Membrane

Cell metabolism, 2012-08, Vol.16 (2), p.274-283

2012

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Neuronal autoantibodies in the cerebrospinal fluid of 148 patients with schizophrenia and 151 healthy controls

Heliyon, 2024-05, Vol.10 (10), p.e30695-e30695, Article e30695

2024

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Increased cerebrospinal fluid fibrinogen in major depressive disorder

Scientific reports, 2015-06, Vol.5 (1), p.11412-11412, Article 11412

2015

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Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice

Human molecular genetics, 2009-10, Vol.18 (19), p.3708-3724

2009

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Abnormality in GABAergic postsynaptic transmission associated with anxiety in Bronx waltzer mice with an Srrm4 mutation

IBRO neuroscience reports, 2024-06, Vol.16, p.67-77

2024

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Artificial oxygen carriers rescue placental hypoxia and improve fetal development in the rat pre-eclampsia model

Scientific reports, 2015-10, Vol.5 (1), p.15271-15271, Article 15271

2015

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Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice

Journal of neuropathology and experimental neurology, 2005-06, Vol.64 (6), p.537-544

2005

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Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy

Human molecular genetics, 2011-10, Vol.20 (19), p.3841-3851

2011

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A loss-of-function mutation in the SLC9A6 gene causes X-linked mental retardation resembling Angelman syndrome

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-12, Vol.156B (7), p.799-807

2011

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Identification of two novel Shank3 transcripts in the developing mouse neocortex

Journal of neurochemistry, 2014-01, Vol.128 (2), p.280-293

2014

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LOX-1 mediates inflammatory activation of microglial cells through the p38-MAPK/NF-κB pathways under hypoxic-ischemic conditions

Low dose resveratrol ameliorates mitochondrial respiratory dysfunction and enhances cellular reprogramming

Interleukin-1beta (IL-1β)-induced Notch ligand Jagged1 suppresses mitogenic action of IL-1β on human dystrophic myogenic cells

Late-onset MELAS syndrome with mtDNA 14453G→A mutation masquerading as an acute encephalitis: a case report

Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes

Mitochondrial respiratory dysfunction disturbs neuronal and cardiac lineage commitment of human iPSCs

13q13.3 microdeletion associated with apparently balanced translocation of 46,XX,t(7;13) suggests NBEA involvement

Mitochondrial Complex III Deficiency Caused by a Homozygous UQCRC2 Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation

Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case report

A Pilot Study of Soluble Form of LOX-1 as a Novel Biomarker for Neonatal Hypoxic-Ischemic Encephalopathy

Linear cortical cystic lesions: Characteristic MR findings in MELAS patients

A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation

Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan

Reactive oxygen species stimulate mitochondrial allele segregation toward homoplasmy in human cells

CRIF1 Is Essential for the Synthesis and Insertion of Oxidative Phosphorylation Polypeptides in the Mammalian Mitochondrial Membrane

Neuronal autoantibodies in the cerebrospinal fluid of 148 patients with schizophrenia and 151 healthy controls

Increased cerebrospinal fluid fibrinogen in major depressive disorder

Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice

Abnormality in GABAergic postsynaptic transmission associated with anxiety in Bronx waltzer mice with an Srrm4 mutation

Artificial oxygen carriers rescue placental hypoxia and improve fetal development in the rat pre-eclampsia model

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice

Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy

Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations

A loss-of-function mutation in the SLC9A6 gene causes X-linked mental retardation resembling Angelman syndrome

Identification of two novel Shank3 transcripts in the developing mouse neocortex

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