Michael Deture

Mayo Clinic Jacksonville, Jacksonville, FL, United States 
"Michael Deture"
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Shinohara M, Murray ME, Frank RD, et al. (2016) Impact of sex and APOE4 on cerebral amyloid angiopathy in Alzheimer's disease. Acta Neuropathologica
Tacik P, DeTure M, Hinkle KM, et al. (2015) A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease. Journal of Neuropathology and Experimental Neurology. 74: 1042-52
Prudencio M, Belzil VV, Batra R, et al. (2015) Distinct brain transcriptome profiles in C9orf72-associated and sporadic ALS. Nature Neuroscience. 18: 1175-82
Pottier C, Bieniek KF, Finch N, et al. (2015) Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease. Acta Neuropathologica. 130: 77-92
Tacik P, DeTure M, Lin WL, et al. (2015) A novel tau mutation, p.K317N, causes globular glial tauopathy. Acta Neuropathologica. 130: 199-214
Zhang YJ, Jansen-West K, Xu YF, et al. (2014) Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress. Acta Neuropathologica. 128: 505-24
Carlomagno Y, Zhang Y, Davis M, et al. (2014) Casein kinase II induced polymerization of soluble TDP-43 into filaments is inhibited by heat shock proteins. Plos One. 9: e90452
Kouri N, Carlomagno Y, Baker M, et al. (2014) Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration. Acta Neuropathologica. 127: 271-82
Cook C, Carlomagno Y, Gendron TF, et al. (2014) Acetylation of the KXGS motifs in tau is a critical determinant in modulation of tau aggregation and clearance. Human Molecular Genetics. 23: 104-16
Cook C, Gendron TF, Scheffel K, et al. (2012) Loss of HDAC6, a novel CHIP substrate, alleviates abnormal tau accumulation. Human Molecular Genetics. 21: 2936-45
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