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Hyaluronic Acid Suppresses the Reduction of α2(VI) Collagen Gene Expression Caused by Interleukin-1β in Cultured Rabbit Articular Chondrocytes

The Tohoku Journal of Experimental Medicine, 1999, Vol.187(1), pp.1-13

1999

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Effects of the existence of nitric oxide and the degradation of extracellular matrix on CD44 mRNA expression in cultured chondrocytes

Journal of bone and mineral metabolism, 1998-01, Vol.16 (3), p.178-185

1998

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Hyaluronic acid suppresses the reduction of alpha2(VI) collagen gene expression caused by interleukin-1beta in cultured rabbit articular chondrocytes

Tohoku journal of experimental medicine, 1999-01, Vol.187 (1), p.1-13

1999

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Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS

BMC bioinformatics, 2023-05, Vol.24 (1), p.206-206, Article 206

2023

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Journal of Medicinal Chemistry Collection: Drug Discovery in Japan

Journal of medicinal chemistry, 2024-10, Vol.67 (19), p.16923-16924

2024

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Non-genetically modified models exhibit TARDBP mRNA increase due to perturbed TDP-43 autoregulation

Neurobiology of disease, 2019-10, Vol.130, p.104534-104534, Article 104534

2019

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Hemiplegic-type ALS: clinicopathological features of two autopsied patients

Journal of neurology, neurosurgery and psychiatry, 2021-09, Vol.92 (9), p.1014-1016

2021

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Endogenous human retrovirus-K is not increased in the affected tissues of Japanese ALS patients

Neuroscience research, 2022-05, Vol.178, p.78-82

2022

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Slow disease progression and characteristic TDP‐43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a TARDBP G357S variant

Neuropathology and applied neurobiology, 2024-02, Vol.50 (1), p.e12966-n/a

2024

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Decreased number of Gemini of coiled bodies and U12 snRNA level in amyotrophic lateral sclerosis

Human molecular genetics, 2013-10, Vol.22 (20), p.4136-4147

2013

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TDP-43 differentially propagates to induce antero- and retrograde degeneration in the corticospinal circuits in mouse focal ALS models

Acta neuropathologica, 2023-10, Vol.146 (4), p.611-629

2023

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Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43

Nucleic acids research, 2016-07, Vol.44 (12), p.5820-5836

2016

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Phosphorylated TDP-43 aggregates in skeletal and cardiac muscle are a marker of myogenic degeneration in amyotrophic lateral sclerosis and various conditions

Acta neuropathologica communications, 2019-10, Vol.7 (1), p.165-165, Article 165

2019

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Age-related demethylation of the TDP-43 autoregulatory region in the human motor cortex

Communications biology, 2021-09, Vol.4 (1), p.1107-1107, Article 1107

2021

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Hemiplegic-type ALS: clinicopathological features of two autopsied patients

Journal of neurology, neurosurgery and psychiatry, 2021-09, Vol.92 (9), p.1014-1016

2021

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Inappropriate interpretation of non‐pathogenic HTRA1 variant as pathogenic

Annals of clinical and translational neurology, 2023-07, Vol.10 (7), p.1261-1262

2023

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Alteration of POLDIP3 splicing associated with loss of function of TDP-43 in tissues affected with ALS

PloS one, 2012-08, Vol.7 (8), p.e43120-e43120

2012

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SMN2 gene copy number affects the incidence and prognosis of motor neuron diseases in Japan

BMC medical genomics, 2024-11, Vol.17 (1), p.1-7, Article 263

2024

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Machine Learning Approach for the Prediction of Age-Specific Probability of SCA3 and DRPLA by Survival Curve Analysis

Neurology. Genetics, 2023-06, Vol.9 (3), p.e200075-e200075

2023

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Performance of a Real-time PCR–based Approach and Droplet Digital PCR in Detecting Human Parechovirus Type 3 RNA

Journal of clinical virology, 2016-11, Vol.84, p.27-31

2016

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Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patients

Journal of neurology, neurosurgery and psychiatry, 2023-10, Vol.94 (10), p.816-824

2023

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Accelerated DNA Methylation Age of the TARDBP 3’UTR in the Motor Cortex is Associated with Age of Sporadic ALS Onset. (P1-1.Virtual)

Neurology, 2022-05, Vol.98 (18_supplement)

2022

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A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features

Acta neuropathologica communications, 2021-06, Vol.9 (1), p.1-9, Article 106

2021

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Robustness and Vulnerability of the Autoregulatory System That Maintains Nuclear TDP-43 Levels: A Trade-off Hypothesis for ALS Pathology Based on in Silico Data

Frontiers in neuroscience, 2018-02, Vol.12, p.28-28

2018

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Efficacy and Safety of Ultrahigh-Dose Methylcobalamin in Early-Stage Amyotrophic Lateral Sclerosis: A Randomized Clinical Trial

JAMA neurology, 2022-06, Vol.79 (6), p.575

2022

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Hyaluronic Acid Suppresses the Reduction of α2(VI) Collagen Gene Expression Caused by Interleukin-1β in Cultured Rabbit Articular Chondrocytes

Effects of the existence of nitric oxide and the degradation of extracellular matrix on CD44 mRNA expression in cultured chondrocytes

Hyaluronic acid suppresses the reduction of alpha2(VI) collagen gene expression caused by interleukin-1beta in cultured rabbit articular chondrocytes

Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS

Journal of Medicinal Chemistry Collection: Drug Discovery in Japan

Non-genetically modified models exhibit TARDBP mRNA increase due to perturbed TDP-43 autoregulation

Hemiplegic-type ALS: clinicopathological features of two autopsied patients

Endogenous human retrovirus-K is not increased in the affected tissues of Japanese ALS patients

Slow disease progression and characteristic TDP‐43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a TARDBP G357S variant

Decreased number of Gemini of coiled bodies and U12 snRNA level in amyotrophic lateral sclerosis

TDP-43 differentially propagates to induce antero- and retrograde degeneration in the corticospinal circuits in mouse focal ALS models

Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43

Phosphorylated TDP-43 aggregates in skeletal and cardiac muscle are a marker of myogenic degeneration in amyotrophic lateral sclerosis and various conditions

Age-related demethylation of the TDP-43 autoregulatory region in the human motor cortex

Hemiplegic-type ALS: clinicopathological features of two autopsied patients

Inappropriate interpretation of non‐pathogenic HTRA1 variant as pathogenic

Alteration of POLDIP3 splicing associated with loss of function of TDP-43 in tissues affected with ALS

SMN2 gene copy number affects the incidence and prognosis of motor neuron diseases in Japan

Machine Learning Approach for the Prediction of Age-Specific Probability of SCA3 and DRPLA by Survival Curve Analysis

Performance of a Real-time PCR–based Approach and Droplet Digital PCR in Detecting Human Parechovirus Type 3 RNA

Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patients

Accelerated DNA Methylation Age of the TARDBP 3’UTR in the Motor Cortex is Associated with Age of Sporadic ALS Onset. (P1-1.Virtual)

A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features

Robustness and Vulnerability of the Autoregulatory System That Maintains Nuclear TDP-43 Levels: A Trade-off Hypothesis for ALS Pathology Based on in Silico Data

Efficacy and Safety of Ultrahigh-Dose Methylcobalamin in Early-Stage Amyotrophic Lateral Sclerosis: A Randomized Clinical Trial

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