Suchergebnisse - "Beck, Goichi"

PubPharm (61)

1

RGMa collapses the neuronal actin barrier against disease-implicated protein and exacerbates ALS

enthalten in: Science advances | 2023

von Shimizu, M. | Shiraishi, N. | Tada, S. | +18

CommentIn: Nat Rev Neurol. 2024 Jan;20(1):1. - PMID 38049641

2

Neuropathology of spinocerebellar ataxia type 8 : Common features and unique tauopathy

enthalten in: Neuropathology : official journal of the Japanese Society of Neuropathology | 2023

von Yonenobu, Y. | Beck, G. | Kido, K. | +11

3

RNA interference in late-stage hereditary transthyretin amyloidosis : a clinicopathological study

enthalten in: Journal of neurology | 2023

von Beck, G. | Yonenobu, Y. | Kawai, M. | +11

4

A heterozygous splicing variant IVS9-7A > T in intron 9 of the MAPT gene in a patient with right-temporal variant frontotemporal dementia with atypical 4 repeat tauopathy

enthalten in: Acta neuropathologica communications | 2023

von Mori, K. | Shigenobu, K. | Beck, G. | +14

5

A heterozygous splicing variant IVS9-7A > T in intron 9 of the MAPT gene in a patient with right-temporal variant frontotemporal dementia with atypical 4 repeat tauopathy

enthalten in: Acta Neuropathologica Communications | 2023

von Mori, K. | Shigenobu, K. | Beck, G. | +14

6

An autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau

enthalten in: Neuropathology : official journal of the Japanese Society of Neuropathology | 2023

von Beck, G. | Yamashita, R. | Kido, K. | +8

CommentIn: Neuropathology. 2023 Dec;43(6):500-502. - PMID 37194404

7

Human induced pluripotent stem cell line (ONHi001-A) generated from a patient with infantile neuroaxonal dystrophy having PLA2G6 c.517C > T (p.Q173X) and c.1634A > G (p.K545R) compound heterozygous mutations

enthalten in: Stem cell research | 2023

von Fukusumi, H. | Togo, K. | Beck, G. | +7

8

Phosphatidylinositol-3,4,5-trisphosphate interacts with alpha-synuclein and initiates its aggregation and formation of Parkinson's disease-related fibril polymorphism

enthalten in: Acta neuropathologica | 2023

von Choong, C. | Aguirre, C. | Kakuda, K. | +22

9

RNA interference in late-stage hereditary transthyretin amyloidosis: a clinicopathological study

enthalten in: Journal of neurology | 2023

von Beck, G. | Yonenobu, Y. | Kawai, M. | +11

10

RNA interference in late-stage hereditary transthyretin amyloidosis: a clinicopathological study

enthalten in: Journal of neurology | 2023

von Beck, G. | Yonenobu, Y. | Kawai, M. | +11

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