119 Publications (Page 2 of 5)
2013
Increased tau phosphorylation and tau truncation, and decreased synaptophysin levels in mutant BRI2/tau transgenic mice.Garringer, Holly⋅Garringer, Holly J⋅Murrell, Jill⋅Murrell, Jill⋅Sammeta, Neeraja⋅Sammeta, Neeraja⋅Gnezda, Anita⋅Gnezda, Anita⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Vidal, Ruben and Vidal, RubenPloS one, vol. 8, (no. 2), pp. e56426, 2013.
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2012
A mutant light-chain ferritin that causes neurodegeneration has enhanced propensity toward oxidative damageBaraibar, Martin A⋅Barbeito, Ana G⋅Muhoberac, Barry B and Vidal, RubenFree Radical Biology and Medicine, vol. 52, (no. 9), pp. 1692-1697, 2012.
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Early-onset Alzheimer's disease associated with PSEN1 L166P mutation: An atypical clinical phenotypeGhetti, Bernardino⋅Ghetti, Bernardino⋅Murrell, Jill⋅Murrell, Jill⋅Boyer, Philip⋅Boyer, Philip⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Vidal, Ruben⋅Vidal, Ruben⋅Hargrave, Kevin⋅Hargrave, Kevin⋅Scott, Kevin⋅Scott, Kevin⋅Silber, Michael⋅Silber, Michael⋅Filley, Christopher⋅Filley, Christopher⋅DeMasters, Bette⋅DeMasters, Bette⋅Iyriboz, Tunc⋅Iyriboz, Tunc⋅Towfighi, Javad and Towfighi, JavadAlzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 8, (no. 4), pp. P665, 2012.
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Generation of a novel murine model of Aβ deposition based on the expression of human wild-type amyloid precursor protein gene.Vidal, Ruben G and Ghetti, BernardinoPrion, vol. 6, (no. 4), pp. 346-9, 2012 Sep-Oct.
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P4‐091: Follow‐up of the first American report of familial Alzheimer’s diseaseGhetti, Bernardino⋅Ghetti, Bernardino⋅Murrell, Jill⋅Murrell, Jill⋅Koeppe, Robert⋅Koeppe, Robert⋅Gilman, Sid⋅Gilman, Sid⋅Fink, John⋅Fink, John⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Albin, Roger⋅Albin, Roger⋅Vidal, Ruben⋅Vidal, Ruben⋅Foster, Norman and Foster, Norman2012-07.
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The Psen1-L166P knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic miceGhetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Vidal, Ruben⋅Vidal, Ruben⋅Vidal, Ruben⋅Sammeta, Neeraja⋅Sammeta, Neeraja⋅Sammeta, Neeraja⋅Garringer, Holly⋅Garringer, Holly⋅Garringer, Holly⋅Sambamurti, Kumar⋅Sambamurti, Kumar⋅Sambamurti, Kumar⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Lamb, Bruce⋅Lamb, Bruce and Lamb, BruceAlzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 8, (no. 4), pp. P86, 2012.
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The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice.Vidal, Ruben⋅Vidal, Ruben G⋅Sammeta, Neeraja⋅Sammeta, Neeraja⋅Garringer, Holly J⋅Garringer, Holly J⋅Sambamurti, Kumar⋅Sambamurti, Kumar⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Lamb, Bruce T⋅Lamb, Bruce T⋅Ghetti, Bernardino and Ghetti, BernardinoFASEB journal : official publication of the Federation of American Societies for Experimental Biology, vol. 26, (no. 7), pp. 2899-910, 2012/Jul.
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2011
Characterization of amyloid deposits in neurodegenerative diseases.Vidal, Ruben G and Ghetti, BernardinoMethods in molecular biology (Clifton, N.J.), vol. 793, pp. 241-58, 2011.
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Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in miceFarrow, Emily G⋅Farrow, Emily⋅Yu, Xijie⋅Yu, Xijie⋅Summers, Lelia⋅Summers, Lelia J⋅Davis, Siobhan⋅Davis, Siobhan I⋅Fleet, James⋅Fleet, James C⋅Allen, Matthew R⋅Allen, Matthew⋅Robling, Alexander⋅Robling, Alexander⋅Stayrook, Keith R⋅Stayrook, Keith⋅Jideonwo, Victoria⋅Jideonwo, Victoria⋅Magers, Martin⋅Magers, Martin J⋅Garringer, Holly⋅Garringer, Holly J⋅Vidal, Ruben⋅Vidal, Ruben⋅Chan, Rebecca J⋅Chan, Rebecca⋅Goodwin, Charles⋅Goodwin, Charles B⋅Hui, Siu L⋅Hui, Siu⋅Peacock, Munro⋅Peacock, Munro⋅White, Kenneth and White, Kenneth EProceedings of the National Academy of Sciences of the United States of America, vol. 108, (no. 46), Nov 15, 2011.
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Iron loading-induced aggregation and reduction of iron incorporation in heteropolymeric ferritin containing a mutant light chain that causes neurodegeneration.Muhoberac, Barry B⋅Baraibar, Martin A and Vidal, RubenBiochimica et biophysica acta, vol. 1812, (no. 4), pp. 544-8, 2011/Apr.
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2010
Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy.Barbeito, Ana G⋅Levade, Thierry⋅Delisle, Marie B⋅Ghetti, Bernardino and Vidal, Ruben GMolecular neurodegeneration, vol. 5, pp. 50, 2010.
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Accumulation of oxidative DNA damage in brain mitochondria in mouse model of hereditary ferritinopathyDeng, Xiaoling⋅Vidal, Ruben and Englander, EllaNeuroscience Letters, vol. 479, (no. 1), pp. 44-48, 2010.
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Memory deficits due to familial British dementia BRI2 mutation are caused by loss of BRI2 function rather than amyloidosis.Tamayev, Robert⋅Tamayev, Robert⋅Tamayev, Robert⋅Giliberto, Luca⋅Giliberto, Luca⋅Giliberto, Luca⋅Li, Wei⋅Li, Wei⋅Li, Wei⋅d'Abramo, Cristina⋅d'Abramo, Cristina⋅d'Abramo, Cristina⋅Arancio, Ottavio⋅Arancio, Ottavio⋅Arancio, Ottavio⋅Vidal, Ruben⋅Vidal, Ruben⋅Vidal, Ruben⋅D'Adamio, Luciano⋅D'Adamio, Luciano and D'Adamio, LucianoThe Journal of neuroscience : the official journal of the Society for Neuroscience, vol. 30, (no. 44), pp. 14915-14924, November 3, 2010.
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Modeling familial British and Danish dementiaGarringer, Holly J⋅Garringer, Holly J⋅Murrell, Jill R⋅Murrell, Jill⋅D'Adamio, Luciano⋅D'Adamio, Luciano⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Vidal, Ruben and Vidal, Ruben GBrain Structure and Function, vol. 214, (no. 2-3), pp. 235-244, 2010.
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P1‐171: A novel tissue culture model of sporadic Creutzfeldt‐Jakob diseasePrelli, Frances⋅Vidal, Ruben and Wisniewski, ThomasAlzheimer's & Dementia, vol. 6, pp. S224, July 2010.
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P3‐156: Cognition and brain structure in Gerstmann‐Straussler‐Scheinker disease (PRNP F198S)Unverzagt, Frederick W⋅Unverzagt, Frederick W⋅Unverzagt, Frederick W⋅Unverzagt, Frederick⋅Unverzagt, Frederick W⋅Farlow, Martin R⋅Farlow, Martin R⋅Farlow, Martin R⋅Farlow, Martin⋅Farlow, Martin R⋅Gao, Sujuan⋅Gao, Sujuan⋅Gao, Sujuan⋅Gao, Sujuan⋅Gao, Sujuan⋅Saykin, Andrew⋅Saykin, Andrew J⋅Saykin, Andrew J⋅Saykin, Andrew J⋅Saykin, Andrew J⋅Murrell, Jill R⋅Murrell, Jill R⋅Murrell, Jill⋅Murrell, Jill R⋅Murrell, Jill R⋅Risacher, Shannon L⋅Risacher, Shannon L⋅Risacher, Shannon⋅Risacher, Shannon L⋅Risacher, Shannon L⋅Lane, Kathleen A⋅Lane, Kathleen A⋅Lane, Kathleen A⋅Lane, Kathleen⋅Lane, Kathleen A⋅West, John D⋅West, John D⋅West, John⋅West, John D⋅West, John D⋅Matthews, Brandy R⋅Matthews, Brandy⋅Matthews, Brandy R⋅Matthews, Brandy R⋅Matthews, Brandy R⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Vidal, Ruben⋅Vidal, Ruben G⋅Vidal, Ruben G⋅Vidal, Ruben G⋅Vidal, Ruben G⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino and Ghetti, BernardinoAlzheimer's & Dementia, vol. 6, pp. S495, July 2010.
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P3‐353: Therapeutic mechanisms of anti‐prion monoclonal antibodiesPankiewicz, Joanna⋅Asuni, Ayodeji⋅Kascak, Richard⋅Kascak, Regina⋅Prelli, Frances⋅Vidal, Ruben and Sadowski, MartinAlzheimer's & Dementia, vol. 6, pp. S555, July 2010.
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S1‐02‐04: Mouse models of British and Danish dementiaVidal, RubenAlzheimer's & Dementia, vol. 6, pp. S66, July 2010.
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Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration.Baraibar, Martin A⋅Baraibar, Martin⋅Muhoberac, Barry⋅Muhoberac, Barry B⋅Garringer, Holly J⋅Garringer, Holly⋅Hurley, Thomas D⋅Hurley, Thomas⋅Vidal, Ruben and Vidal, Ruben GThe Journal of biological chemistry, vol. 285, (no. 3), pp. 1950-6, 2010/Jan/15.
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2009
Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide geneBarbeito, Ana G⋅Garringer, Holly J⋅Baraibar, Martin A⋅Gao, Xiaoying⋅Arredondo, Miguel⋅Arredondo Olguín, Miguel⋅Núñez, Marco T⋅Smith, Mark A⋅Ghetti, Bernardino and Vidal, RubenJournal of Neurochemistry, vol. 109, (no. 4), pp. 1067-1078, May 2009.
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Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2.Vidal, Ruben G⋅Barbeito, Ana G⋅Miravalle, Leticia and Ghetti, BernardinoBrain pathology (Zurich, Switzerland), vol. 19, (no. 1), pp. 58-68, 2009/Jan.
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Cerebral Amyloid Angiopathy and Parenchymal Amyloid Deposition in Transgenic Mice Expressing the Danish Mutant Form of Human BRI2Vidal, Ruben G⋅Barbeito, Ana G⋅Miravalle, Leticia and Ghetti, BernardinoBrain Pathology, vol. 19, pp. 58-68, 2009.
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Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498‐499InsTC)Ory-Magne, Fabienne⋅Ory‐Magne, Fabienne⋅Brefel‐Courbon, Christine⋅Brefel-Courbon, Christine⋅Payoux, Pierre⋅Payoux, Pierre⋅Debruxelles, Sabrina⋅Debruxelles, Sabrina⋅Sibon, Igor⋅Sibon, Igor⋅Goizet, Cyril⋅Goizet, Cyril⋅Labauge, Pierre⋅Labauge, Pierre⋅Menegon, Patrice⋅Menegon, Patrice⋅Uro-Coste, Emmanuelle⋅Uro‐Coste, Emmanuelle⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Delisle, Marie Bernadetle⋅Delisle, Marie Bernadetle⋅Vidal, Ruben⋅Vidal, Ruben⋅Rascol, Olivier and Rascol, OlivierMovement Disorders, vol. 24, (no. 11), pp. 1683, 15 August 2009.
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Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.Xiao, Xiangzhu⋅Miravalle, Leticia⋅Yuan, Jue⋅McGeehan, John⋅Dong, Zhiqian⋅Wyza, Robert⋅Mac Lennan, Gregory⋅Golichowski, Alan M⋅Kneale, Geoff⋅King, Nicholas⋅Kong, Qingzhong⋅Spina, Salvatore⋅Vidal, Ruben G⋅Ghetti, Bernardino⋅Roos, Karen⋅Gambetti, Pierluigi and Zou, Wen QuanThe American journal of pathology, vol. 174, (no. 5), pp. 1602-8, 2009/May.
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Generation and initial characterization of FDD knock in mice.Giliberto, Luca⋅Giliberto, Luca⋅Giliberto, Luca⋅Matsuda, Shuji⋅Matsuda, Shuji⋅Matsuda, Shuji⋅Vidal, Ruben⋅Vidal, Ruben⋅Vidal, Ruben⋅D'Adamio, Luciano⋅D'Adamio, Luciano and D'Adamio, LucianoPloS one, vol. 4, (no. 11), pp. e7900, November 18, 2009.
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