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Colocalization of 14-3-3 Proteins with SOD1 in Lewy Body-Like Hyaline Inclusions in Familial Amyotrophic Lateral Sclerosis Cases and the Animal Model

• Authors : Okamoto, Yoko; Shirakashi, Yoshitomo; Ihara, Masafumi

Subjects: biology; neuroscience; neurobiology of disease and regeneration

• Source: Okamoto, Yoko, Yoshitomo Shirakashi, Masafumi Ihara, Makoto Urushitani, Miki Oono, Yasuhiro Kawamoto, Hirofumi Yamashita, et al. 2011. Colocalization of 14-3-3 Proteins with SOD1 in Lewy Body-Like

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Protein Expression Redirects Vesicular Stomatitis Virus RNA Synthesis to Cytoplasmic Inclusions

• Authors : Heinrich, Bianca Susanne; Cureton, David Kirk; Rahmeh, Amal Ali

Subjects: virology; viral replication and gene regulation

• Source: Heinrich, Bianca S., David K. Cureton, Amal A. Rahmeh, and Sean P. J. Whelan. 2010. Protein expression redirects vesicular stomatitis virus RNA synthesis to cytoplasmic

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Physiological and Pathological Role of Alpha-Synuclein in Parkinson’s Disease through Iron Mediated Oxidative Stress; The Role of a Putative Iron-Responsive Element

• Authors : Olivares, David; Huang, Xudong; Branden, Lars

Subjects: Parkinson's disease; Alzheimer's disease; \(\alpha\)-syn

• Source: Olivares, David, Xudong Huang, Lars Branden, Nigel H. Greig, and Jack T. Rogers. 2009. Physiological and pathological role of alpha-synuclein in Parkinson’s disease through iron mediated oxidative

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Bi-Abundance Ionisation Structure of the Wolf–Rayet Planetary Nebula PB 8

• Authors : Danehkar, Ashkbiz

• Source: Quick submit: 2018-05-06T01:52:44-0400Danehkar, A. 2018. “Bi-Abundance Ionisation Structure of the Wolf–Rayet Planetary Nebula PB 8.” Publications of the Astronomical Society of Australia

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Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation

• Authors : Kiely, Aoife P.; Ling, Helen; Asi, Yasmine T.

Subjects: Parkinson’s disease; Multiple system atrophy; α-synuclein

• Source: Kiely, A. P., H. Ling, Y. T. Asi, E. Kara, C. Proukakis, A. H. Schapira, H. R. Morris, et al. 2015. “Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA

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Migalastat improves diarrhea in patients with Fabry disease: clinical-biomarker correlations from the phase 3 FACETS trial

• Authors : Schiffmann, Raphael; Bichet, Daniel G.; Jovanovic, Ana

Subjects: Amenable mutation; Diarrhea; Fabry disease

• Source: Schiffmann, R., D. G. Bichet, A. Jovanovic, D. A. Hughes, R. Giugliani, U. Feldt-Rasmussen, S. P. Shankar, et al. 2018. “Migalastat improves diarrhea in patients with Fabry disease:

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Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington’s disease

• Authors : Bragg, Robert M.; Coffey, Sydney R.; Weston, Rory M.

• Source: Bragg, R. M., S. R. Coffey, R. M. Weston, S. A. Ament, J. P. Cantle, S. Minnig, C. C. Funk, et al. 2017. “Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and

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Genetic Variants in GAPDH Confer Susceptibility to Sporadic Parkinson’s Disease in a Chinese Han Population

• Authors : Liu, Ling; Xiong, Nian; Zhang, Ping

• Source: Liu, Ling, Nian Xiong, Ping Zhang, Chunnuan Chen, Jinsha Huang, Guoxin Zhang, Xiaoyun Xu, Yan Shen, Zhicheng Lin, and Tao Wang. 2015. “Genetic Variants in GAPDH Confer Susceptibility to Sporadic

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Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging

• Authors : Ghetti, B; Oblak, A L; Boeve, B F

Subjects: FTDP-17; tau aggregation; neurofibrillary tangle

• Source: Ghetti, B, A L Oblak, B F Boeve, K A Johnson, B C Dickerson, and M Goedert. 2014. “Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a

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Deciphering Amyotrophic Lateral Sclerosis: What Phenotype, Neuropathology and Genetics Are Telling Us about Pathogenesis

• Authors : Ravits, John; Appel, Stanley; Baloh, Robert H.

Subjects: ALS; PLS; PMA

• Source: Quick submit: 2013-08-02T09:54:05-04:00Ravits, John, Stanley Appel, Robert H. Baloh, Richard Barohn, Benjamin Rix Brooks, Lauren Elman, Mary Kay Floeter, et al. 2013. Deciphering amyotrophic

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