Výsledky vyhledávání - "Dr. Ruben Vidal"

Akademický článek

Distinct Chemical Determinants are Essential for Achieving Ligands for Superior Optical Detection of Specific Amyloid‐β Deposits in Alzheimer's Disease

Autor: Dr. Xiongyu Wu, Dr. Hamid Shirani, Dr. Ruben Vidal, Dr. Bernardino Ghetti, Prof. Martin Ingelsson, Dr. Therése Klingstedt, Prof. K. Peter R. Nilsson

Publikováno v: ChemistryOpen, Vol 13, Iss 12, Pp n/a-n/a (2024)

Abstract Aggregated forms of different proteins are common hallmarks for several neurodegenerative diseases, including Alzheimer's disease, and ligands that selectively detect specific protein aggregates are vital. Herein, we investigate the molecula

Externí odkaz: https://doaj.org/article/1598e09001f14fe59f903c6615850023

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Akademický článek

A1 reactive astrocytes and a loss of TREM2 are associated with an early stage of pathology in a mouse model of cerebral amyloid angiopathy.

Autor: Taylor, Xavier^1,2 (AUTHOR), Cisternas, Pablo^1,2 (AUTHOR), You, Yanwen^1,2 (AUTHOR), You, Yingjian^1,2 (AUTHOR), Xiang, Shunian³ (AUTHOR), Marambio, Yamil^1,2 (AUTHOR), Zhang, Jie³ (AUTHOR), Vidal, Ruben^1,4 (AUTHOR), Lasagna-Reeves, Cristian A.^1,2 (AUTHOR) clasagna@iu.edu

Publikováno v: Journal of Neuroinflammation. 7/25/2020, Vol. 17 Issue 1, p1-18. 18p.

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Akademický článek

Endoplasmic Reticulum Stress in Tauopathies: Contrasting Human Brain Pathology with Cellular and Animal Models.

Autor: Bocai, Nadia I., Marcora, María S., Belfiori-Carrasco, Lautaro F., Morelli, Laura, Castaño, Eduardo M., Iqbal, Khalid

Publikováno v: Journal of Alzheimer's Disease; 2019, Vol. 68 Issue 2, p439-458, 20p

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Akademický článek

Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene.

Autor: Barbeito, Ana G., Garringer, Holly J., Baraibar, Martin A., Gao, Xiaoying, Arredondo, Miguel, N&;#x00FA;ñez, Marco T., Smith, Mark A., Ghetti, Bernardino, Vidal, Ruben

Publikováno v: Journal of Neurochemistry; May2009, Vol. 109 Issue 4, p1067-1078, 12p, 1 Color Photograph, 5 Graphs

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Akademický článek

A novel mutation (G217D) in the Presenilin 1 gene (PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum.

Autor: Takao, Masaki, Ghetti, Bernardino, Hayakawa, Isao, Ikeda, Eiji, Fukuuchi, Yasuo, Miravalle, Leticia, Piccardo, Pedro, Murrell, Jill R., Glazier, Bradley S., Koto, Atsuo

Publikováno v: Acta Neuropathologica; Aug2002, Vol. 104 Issue 2, p155-170, 16p

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Akademický článek

Ectopic White Matter Neurons, a Developmental Abnormality That May Be Caused by the PSEN1 S169L Mutation in a Case of Familial AD with Myoclonus and Seizures.

Autor: TAKAO, MASAKI, GHETTI, BERNARDINO, MURRELL, JILL R., UNVERZAGT, FREDERICK W., GIACCONE, GIORGIO, TAGLIAVINI, FABRIZIO, BUGIANI, ORSO, PICCARDO, PEDRO, HULETTE, CHRISTINE M., CRAIN, BARBARA J., FARLOW, MARTIN R., HEYMAN, ALBERT

Publikováno v: Journal of Neuropathology & Experimental Neurology; Dec2001, Vol. 60 Issue 12, p1137-1152, 16p

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Akademický článek

Acknowledgments.

Publikováno v: Amyloid; 1998, Vol. 5 Issue 4, p307-307, 1p

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