Publications by authors named "Mari Tada"

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An inducible oligodendrocyte dysfunction triggered a pathological cascade of massive microglial activation and neurodegeneration.
Masataka Ise, Norihisa Bizen, Anna Simankova, Kentaro Okuyama, Shinsuke Shibata, Mari Tada

Neurobiol Dis· November 2025

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Quantifying subpercent nuclear TDP-43 loss in cells and ALS cortex using junction-specific cryptic exon RT-qPCR.
Shingo Koide, Ichiko Ikegami, Ryutaro Hanyu, Yuka Mitsuhashi Koike, Takuma Yamagishi, Mari Tada

FEBS Lett· October 2025

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Mitochondrial dysfunction in MED13 variant-associated disease: a case of infantile spasms, cardiomyopathy and hepatomegaly.
Mizuki Harada, Takanori Onuki, Hiromi Nyuzuki, Hisato Suzuki, Kozue Ito, Mari Tada

Hum Genome Var· October 2025

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Late-onset multiple system atrophy: Neuropathological features associated with slow disease progression.
Misato Ozawa, Rie Saito, Takuya Konno, Yasuko Kuroha, Tetsuhiko Ikeda, Mari Tada

Brain Pathol· September 2025

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Association of rare missense variants with Alzheimer's disease in the Japanese population.
Akinori Miyashita, Ai Obinata, Norikazu Hara, Risa Mitsumori, Daita Kaneda, Mari Tada

J Alzheimers Dis· July 2025

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Mutations in the human CSF1R gene impact microglia's maintenance of brain white matter integrity.
Siling Du, Yingyue Zhou, Dian Li, Julia Lier, Marina Cella, Mari Tada

Nat Immunol· July 2025

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TAF15 and Transportin 1 in Intranuclear Inclusions of Neuronal Intranuclear Inclusion Disease.
Yasuo Miki, Yutaka Inoue, Fumiaki Mori, Mari Tada, Mari Yoshida

Neuropathol Appl Neurobiol· June 2025

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Abnormal α-synuclein binds to synaptotagmin 13, impairing extracellular vesicle release in synucleinopathies.
Yasuo Miki, Shuji Shimoyama, Makoto T Tanaka, Hanae Kushibiki, Asa Nakahara, Mari Tada

Transl Neurodegener· June 2025

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Diagnosis of Leptomeningeal Disease in Diffuse Midline Gliomas by Detection of H3F3A K27M Mutation in Circulating Tumor DNA of Cerebrospinal Fluid.
Satoshi Shibuma, Jotaro On, Manabu Natsumeda, Akihide Koyama, Haruhiko Takahashi, Mari Tada

Pediatr Blood Cancer· April 2025

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Novel Aspects of Hereditary Spastic Paraplegia: A Clinicopathologic and Biochemical Study of a Patient With a Heterozygous GCH1 Variant.
Shoko Hongo, Tetsuhiko Ikeda, Mari Tada, Rina Aida, Tetsuo Ozawa

Neuropathol Appl Neurobiol· February 2025

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SMN2 gene copy number affects the incidence and prognosis of motor neuron diseases in Japan.
Tomohiko Ishihara, Akihide Koyama, Naoki Atsuta, Mari Tada, Saori Toyoda

BMC Med Genomics· November 2024

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Case report: Progressive multifocal leukoencephalopathy co-occurring with neurosarcoidosis: early brain biopsy and appropriate therapy for PML resulted in a favorable prognosis.
Qiannan Wang, Shintaro Tsuboguchi, Kouichirou Okamoto, Mari Tada, Akiyoshi Kakita

Front Immunol· October 2024

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Evaluation of specific binding of [C]TZ7774 to the receptor-interacting protein kinase 1 (RIPK1) in the brain.
Takayuki Sakai, Takashi Yamada, Hiroshi Ikenuma, Aya Ogata, Masanori Ichise, Mari Tada

Am J Nucl Med Mol Imaging· October 2024

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Indications for a brain biopsy in neurological diseases of unknown etiology: The role of magnetic resonance imaging findings and liquid biopsy in yielding definitive pathological diagnoses.
Toshiya Kizaki, Masato Kanazawa, Takanobu Ishiguro, Manabu Natsumeda, Mari Tada

J Neurol Sci· August 2024

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A novel PET probe to selectively image heat shock protein 90α/β isoforms in the brain.
Takayuki Sakai, Aya Ogata, Hiroshi Ikenuma, Takashi Yamada, Saori Hattori, Mari Tada

EJNMMI Radiopharm Chem· March 2024

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Successful Multimodal Treatment of Intracranial Growing Teratoma Syndrome with Malignant Features.
Daiken Satake, Manabu Natsumeda, Kaishi Satomi, Mari Tada, Taro Sato

Curr Oncol· March 2024

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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.
Makoto Sainouchi, Shinya Oginezawa, Mari Tada, Tomohiko Ishihara, Osamu Onodera

Neuropathol Appl Neurobiol· February 2024

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Reliable detection of genetic alterations in cyst fluid DNA for the diagnosis of brain tumors.
Jotaro On, Manabu Natsumeda, Haruhiko Takahashi, Akihide Koyama, Satoshi Shibuma, Mari Tada

J Neurooncol· January 2024

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[Case of hereditary Y69H (p.Y89H) transthyretin variant leptomeningeal amyloidosis presenting with drop attacks and recurrent transient language disorder].
Natsumi Saito, Yasuko Kuroha, Arika Hasegawa, Mari Tada, Akiyoshi Kakita

Rinsho Shinkeigaku· October 2023

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Administration of glucocorticoids prior to liquid biopsy dramatically reduces the detection rate of mutation in cerebrospinal fluid of primary CNS lymphoma patients.
Haruhiko Takahashi, Manabu Natsumeda, Jotaro On, Jun Watanabe, Mari Tada

Leuk Lymphoma· June 2023

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Development of a novel PET ligand, [C]GO289 targeting CK2 expressed in the brain.
Aya Ogata, Takashi Yamada, Saori Hattori, Hiroshi Ikenuma, Junichiro Abe, Mari Tada

Bioorg Med Chem Lett· June 2023

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Human early-onset dementia caused by DAP12 deficiency reveals a unique signature of dysregulated microglia.
Yingyue Zhou, Mari Tada, Zhangying Cai, Prabhakar S Andhey, Amanda Swain

Nat Immunol· March 2023

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Publisher Correction: Human early-onset dementia caused by DAP12 deficiency reveals a unique signature of dysregulated microglia.
Yingyue Zhou, Mari Tada, Zhangying Cai, Prabhakar S Andhey, Amanda Swain

Nat Immunol· March 2023

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SYNE1-ataxia: clinicopathologic features of an autopsied patient with novel compound heterozygous mutations.
Rie Saito, Norikazu Hara, Mari Tada, Masatoshi Wakabayashi, Akinori Miyashita

J Neuropathol Exp Neurol· February 2023

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Meningoencephalocele in the Lateral Sphenoid Sinus Showing Malformation of Cortical Development: A Case Report.
Taro Sato, Tetsuya Hiraishi, Mari Tada, Manabu Natsumeda, Jotaro On

NMC Case Rep J· September 2022

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