119 Publications (Page 2 of 5)
2013
Increased tau phosphorylation and tau truncation, and decreased synaptophysin levels in mutant BRI2/tau transgenic mice.
Garringer, HollyGarringer, Holly JMurrell, JillMurrell, JillSammeta, NeerajaSammeta, NeerajaGnezda, AnitaGnezda, AnitaGhetti, BernardinoGhetti, BernardinoVidal, Ruben and Vidal, Ruben
PloS one, vol. 8, (no. 2), pp. e56426, 2013. | Journal Article
2012
A mutant light-chain ferritin that causes neurodegeneration has enhanced propensity toward oxidative damage
Baraibar, Martin ABarbeito, Ana GMuhoberac, Barry B and Vidal, Ruben
Free Radical Biology and Medicine, vol. 52, (no. 9), pp. 1692-1697, 2012. | Journal Article
 
Early-onset Alzheimer's disease associated with PSEN1 L166P mutation: An atypical clinical phenotype
Ghetti, BernardinoGhetti, BernardinoMurrell, JillMurrell, JillBoyer, PhilipBoyer, PhilipPiccardo, PedroPiccardo, PedroVidal, RubenVidal, RubenHargrave, KevinHargrave, KevinScott, KevinScott, KevinSilber, MichaelSilber, MichaelFilley, ChristopherFilley, ChristopherDeMasters, BetteDeMasters, BetteIyriboz, TuncIyriboz, TuncTowfighi, Javad and Towfighi, Javad
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 8, (no. 4), pp. P665, 2012. | Journal Article
 
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, Bernardino
Prion, vol. 6, (no. 4), pp. 346-9, 2012 Sep-Oct. | Journal Article
 
P4‐091: Follow‐up of the first American report of familial Alzheimer’s disease
Ghetti, BernardinoGhetti, BernardinoMurrell, JillMurrell, JillKoeppe, RobertKoeppe, RobertGilman, SidGilman, SidFink, JohnFink, JohnMiravalle, LeticiaMiravalle, LeticiaAlbin, RogerAlbin, RogerVidal, RubenVidal, RubenFoster, Norman and Foster, Norman
2012-07. | Journal Article
 
The Psen1-L166P knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice
Ghetti, BernardinoGhetti, BernardinoGhetti, BernardinoVidal, RubenVidal, RubenVidal, RubenSammeta, NeerajaSammeta, NeerajaSammeta, NeerajaGarringer, HollyGarringer, HollyGarringer, HollySambamurti, KumarSambamurti, KumarSambamurti, KumarMiravalle, LeticiaMiravalle, LeticiaMiravalle, LeticiaLamb, BruceLamb, Bruce and Lamb, Bruce
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 8, (no. 4), pp. P86, 2012. | Journal Article
 
The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice.
Vidal, RubenVidal, Ruben GSammeta, NeerajaSammeta, NeerajaGarringer, Holly JGarringer, Holly JSambamurti, KumarSambamurti, KumarMiravalle, LeticiaMiravalle, LeticiaLamb, Bruce TLamb, Bruce TGhetti, Bernardino and Ghetti, Bernardino
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, vol. 26, (no. 7), pp. 2899-910, 2012/Jul. | Journal Article
2011
Characterization of amyloid deposits in neurodegenerative diseases.
Vidal, Ruben G and Ghetti, Bernardino
Methods in molecular biology (Clifton, N.J.), vol. 793, pp. 241-58, 2011. | Journal Article
 
Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice
Farrow, Emily GFarrow, EmilyYu, XijieYu, XijieSummers, LeliaSummers, Lelia JDavis, SiobhanDavis, Siobhan IFleet, JamesFleet, James CAllen, Matthew RAllen, MatthewRobling, AlexanderRobling, AlexanderStayrook, Keith RStayrook, KeithJideonwo, VictoriaJideonwo, VictoriaMagers, MartinMagers, Martin JGarringer, HollyGarringer, Holly JVidal, RubenVidal, RubenChan, Rebecca JChan, RebeccaGoodwin, CharlesGoodwin, Charles BHui, Siu LHui, SiuPeacock, MunroPeacock, MunroWhite, Kenneth and White, Kenneth E
Proceedings of the National Academy of Sciences of the United States of America, vol. 108, (no. 46), Nov 15, 2011. | Journal Article
 
Iron loading-induced aggregation and reduction of iron incorporation in heteropolymeric ferritin containing a mutant light chain that causes neurodegeneration.
Muhoberac, Barry BBaraibar, Martin A and Vidal, Ruben
Biochimica et biophysica acta, vol. 1812, (no. 4), pp. 544-8, 2011/Apr. | Journal Article
2010
Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy.
Barbeito, Ana GLevade, ThierryDelisle, Marie BGhetti, Bernardino and Vidal, Ruben G
Molecular neurodegeneration, vol. 5, pp. 50, 2010. | Journal Article
 
Accumulation of oxidative DNA damage in brain mitochondria in mouse model of hereditary ferritinopathy
Deng, XiaolingVidal, Ruben and Englander, Ella
Neuroscience Letters, vol. 479, (no. 1), pp. 44-48, 2010. | Journal Article
 
Memory deficits due to familial British dementia BRI2 mutation are caused by loss of BRI2 function rather than amyloidosis.
Tamayev, RobertTamayev, RobertTamayev, RobertGiliberto, LucaGiliberto, LucaGiliberto, LucaLi, WeiLi, WeiLi, Weid'Abramo, Cristinad'Abramo, Cristinad'Abramo, CristinaArancio, OttavioArancio, OttavioArancio, OttavioVidal, RubenVidal, RubenVidal, RubenD'Adamio, LucianoD'Adamio, Luciano and D'Adamio, Luciano
The Journal of neuroscience : the official journal of the Society for Neuroscience, vol. 30, (no. 44), pp. 14915-14924, November 3, 2010. | Journal Article
 
Modeling familial British and Danish dementia
Garringer, Holly JGarringer, Holly JMurrell, Jill RMurrell, JillD'Adamio, LucianoD'Adamio, LucianoGhetti, BernardinoGhetti, BernardinoVidal, Ruben and Vidal, Ruben G
Brain Structure and Function, vol. 214, (no. 2-3), pp. 235-244, 2010. | Journal Article
 
P1‐171: A novel tissue culture model of sporadic Creutzfeldt‐Jakob disease
Prelli, FrancesVidal, Ruben and Wisniewski, Thomas
Alzheimer's & Dementia, vol. 6, pp. S224, July 2010. | Journal Article
 
P3‐156: Cognition and brain structure in Gerstmann‐Straussler‐Scheinker disease (PRNP F198S)
Unverzagt, Frederick WUnverzagt, Frederick WUnverzagt, Frederick WUnverzagt, FrederickUnverzagt, Frederick WFarlow, Martin RFarlow, Martin RFarlow, Martin RFarlow, MartinFarlow, Martin RGao, SujuanGao, SujuanGao, SujuanGao, SujuanGao, SujuanSaykin, AndrewSaykin, Andrew JSaykin, Andrew JSaykin, Andrew JSaykin, Andrew JMurrell, Jill RMurrell, Jill RMurrell, JillMurrell, Jill RMurrell, Jill RRisacher, Shannon LRisacher, Shannon LRisacher, ShannonRisacher, Shannon LRisacher, Shannon LLane, Kathleen ALane, Kathleen ALane, Kathleen ALane, KathleenLane, Kathleen AWest, John DWest, John DWest, JohnWest, John DWest, John DMatthews, Brandy RMatthews, BrandyMatthews, Brandy RMatthews, Brandy RMatthews, Brandy RPiccardo, PedroPiccardo, PedroPiccardo, PedroPiccardo, PedroPiccardo, PedroMiravalle, LeticiaMiravalle, LeticiaMiravalle, LeticiaMiravalle, LeticiaMiravalle, LeticiaVidal, RubenVidal, Ruben GVidal, Ruben GVidal, Ruben GVidal, Ruben GGhetti, BernardinoGhetti, BernardinoGhetti, BernardinoGhetti, Bernardino and Ghetti, Bernardino
Alzheimer's & Dementia, vol. 6, pp. S495, July 2010. | Journal Article
 
P3‐353: Therapeutic mechanisms of anti‐prion monoclonal antibodies
Pankiewicz, JoannaAsuni, AyodejiKascak, RichardKascak, ReginaPrelli, FrancesVidal, Ruben and Sadowski, Martin
Alzheimer's & Dementia, vol. 6, pp. S555, July 2010. | Journal Article
 
S1‐02‐04: Mouse models of British and Danish dementia
Vidal, Ruben
Alzheimer's & Dementia, vol. 6, pp. S66, July 2010. | Journal Article
 
Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration.
Baraibar, Martin ABaraibar, MartinMuhoberac, BarryMuhoberac, Barry BGarringer, Holly JGarringer, HollyHurley, Thomas DHurley, ThomasVidal, Ruben and Vidal, Ruben G
The Journal of biological chemistry, vol. 285, (no. 3), pp. 1950-6, 2010/Jan/15. | Journal Article
2009
Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene
Barbeito, Ana GGarringer, Holly JBaraibar, Martin AGao, XiaoyingArredondo, MiguelArredondo Olguín, MiguelNúñez, Marco TSmith, Mark AGhetti, Bernardino and Vidal, Ruben
Journal of Neurochemistry, vol. 109, (no. 4), pp. 1067-1078, May 2009. | Journal Article
 
Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2.
Vidal, Ruben GBarbeito, Ana GMiravalle, Leticia and Ghetti, Bernardino
Brain pathology (Zurich, Switzerland), vol. 19, (no. 1), pp. 58-68, 2009/Jan. | Journal Article
 
Cerebral Amyloid Angiopathy and Parenchymal Amyloid Deposition in Transgenic Mice Expressing the Danish Mutant Form of Human BRI2
Vidal, Ruben GBarbeito, Ana GMiravalle, Leticia and Ghetti, Bernardino
Brain Pathology, vol. 19, pp. 58-68, 2009. | Journal Article
 
Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498‐499InsTC)
Ory-Magne, FabienneOry‐Magne, FabienneBrefel‐Courbon, ChristineBrefel-Courbon, ChristinePayoux, PierrePayoux, PierreDebruxelles, SabrinaDebruxelles, SabrinaSibon, IgorSibon, IgorGoizet, CyrilGoizet, CyrilLabauge, PierreLabauge, PierreMenegon, PatriceMenegon, PatriceUro-Coste, EmmanuelleUro‐Coste, EmmanuelleGhetti, BernardinoGhetti, BernardinoDelisle, Marie BernadetleDelisle, Marie BernadetleVidal, RubenVidal, RubenRascol, Olivier and Rascol, Olivier
Movement Disorders, vol. 24, (no. 11), pp. 1683, 15 August 2009. | Journal Article
 
Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.
Xiao, XiangzhuMiravalle, LeticiaYuan, JueMcGeehan, JohnDong, ZhiqianWyza, RobertMac Lennan, GregoryGolichowski, Alan MKneale, GeoffKing, NicholasKong, QingzhongSpina, SalvatoreVidal, Ruben GGhetti, BernardinoRoos, KarenGambetti, Pierluigi and Zou, Wen Quan
The American journal of pathology, vol. 174, (no. 5), pp. 1602-8, 2009/May. | Journal Article
 
Generation and initial characterization of FDD knock in mice.
Giliberto, LucaGiliberto, LucaGiliberto, LucaMatsuda, ShujiMatsuda, ShujiMatsuda, ShujiVidal, RubenVidal, RubenVidal, RubenD'Adamio, LucianoD'Adamio, Luciano and D'Adamio, Luciano
PloS one, vol. 4, (no. 11), pp. e7900, November 18, 2009. | Journal Article