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Tohru Hagiwara

Tohru Hagiwara,Neuroscience

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Tohru Hagiwara

Publications: 1 | Citations: 45

Fields: Neuroscience

Collaborated with 12 co-authors in 2004 | Cited by 182 authors

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Actin mutations are one cause of congenital fibre type disproportion (Citations: 45)

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Journal: Annals of Neurology - ANN NEUROL , vol. 56, no. 5, pp. 689-694, 2004

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Citations (45 times by 45 publications)

Actin Nemaline Myopathy Mouse Reproduces Disease, Suggests Other Actin Disease Phenotypes and Provides Cautionary Note on Muscle Transgene Expression

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Journal: PLOS One , vol. 6, no. 12, 2011

Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin gene (Citations: 1)

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Journal: Neuromuscular Disorders - NEUROMUSCULAR DISORD , vol. 20, no. 6, pp. 363-374, 2010

In Vitro Analysis of Rod Composition and Actin Dynamics in Inherited Myopathies (Citations: 1)

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Journal: Journal of Neuropathology and Experimental Neurology - J NEUROPATHOL EXP NEUROL , vol. 69, no. 5, pp. 429-441, 2010

Mutations of tropomyosin 3 ( TPM3 ) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion

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Journal: Human Mutation - HUM MUTAT , vol. 31, no. 2, pp. 176-183, 2010

Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene ( ACTA1) mutation

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Journal: Neuromuscular Disorders - NEUROMUSCULAR DISORD , vol. 20, no. 8, pp. 531-533, 2010

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