Vidal R - Search Results

1

Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations.

Maarouf CL, Daugs ID, Spina S, Vidal R, Kokjohn TA, Patton RL, Kalback WM, Luehrs DC, Walker DG, Castaño EM, Beach TG, Ghetti B, Roher AE. Maarouf CL, et al. Among authors: vidal r. Mol Neurodegener. 2008 Nov 20;3:20. doi: 10.1186/1750-1326-3-20. Mol Neurodegener. 2008. PMID: 19021905 Free PMC article.

2

The human amyloid-beta precursor protein770 mutation V717F generates peptides longer than amyloid-beta-(40-42) and flocculent amyloid aggregates.

Roher AE, Kokjohn TA, Esh C, Weiss N, Childress J, Kalback W, Luehrs DC, Lopez J, Brune D, Kuo YM, Farlow M, Murrell J, Vidal R, Ghetti B. Roher AE, et al. Among authors: vidal r. J Biol Chem. 2004 Feb 13;279(7):5829-36. doi: 10.1074/jbc.M311380200. Epub 2003 Nov 26. J Biol Chem. 2004. PMID: 14645225 Free article.

3

Neurodegeneration caused by proteins with an aberrant carboxyl-terminus.

Vidal R, Delisle MB, Ghetti B. Vidal R, et al. J Neuropathol Exp Neurol. 2004 Aug;63(8):787-800. doi: 10.1093/jnen/63.8.787. J Neuropathol Exp Neurol. 2004. PMID: 15330334 Review.

4

Amino-terminally truncated Abeta peptide species are the main component of cotton wool plaques.

Miravalle L, Calero M, Takao M, Roher AE, Ghetti B, Vidal R. Miravalle L, et al. Among authors: vidal r. Biochemistry. 2005 Aug 16;44(32):10810-21. doi: 10.1021/bi0508237. Biochemistry. 2005. PMID: 16086583

5

Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's disease.

Van Vickle GD, Esh CL, Kokjohn TA, Patton RL, Kalback WM, Luehrs DC, Beach TG, Newel AJ, Lopera F, Ghetti B, Vidal R, Castaño EM, Roher AE. Van Vickle GD, et al. Among authors: vidal r. Mol Med. 2008 Mar-Apr;14(3-4):184-94. doi: 10.2119/2007-00094.vanvickle. Mol Med. 2008. PMID: 18317569 Free PMC article.

6

Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2.

Vidal R, Barbeito AG, Miravalle L, Ghetti B. Vidal R, et al. Brain Pathol. 2009 Jan;19(1):58-68. doi: 10.1111/j.1750-3639.2008.00164.x. Epub 2008 Apr 10. Brain Pathol. 2009. PMID: 18410407 Free PMC article.

7

Modeling familial British and Danish dementia.

Garringer HJ, Murrell J, D'Adamio L, Ghetti B, Vidal R. Garringer HJ, et al. Among authors: vidal r. Brain Struct Funct. 2010 Mar;214(2-3):235-44. doi: 10.1007/s00429-009-0221-9. Epub 2009 Sep 25. Brain Struct Funct. 2010. PMID: 19779737 Free PMC article. Review.

8

Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy.

Barbeito AG, Levade T, Delisle MB, Ghetti B, Vidal R. Barbeito AG, et al. Among authors: vidal r. Mol Neurodegener. 2010 Nov 10;5:50. doi: 10.1186/1750-1326-5-50. Mol Neurodegener. 2010. PMID: 21067605 Free PMC article.

9

Characterization of amyloid deposits in neurodegenerative diseases.

Vidal R, Ghetti B. Vidal R, et al. Methods Mol Biol. 2011;793:241-58. doi: 10.1007/978-1-61779-328-8_16. Methods Mol Biol. 2011. PMID: 21913105

10

Generation of a novel murine model of Aβ deposition based on the expression of human wild-type amyloid precursor protein gene.

Vidal R, Ghetti B. Vidal R, et al. Prion. 2012 Sep-Oct;6(4):346-9. doi: 10.4161/pri.21023. Epub 2012 Aug 9. Prion. 2012. PMID: 22874668 Free PMC article.

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