508 Publications (Page 17 of 21)
1998
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.
Piccardo, PedroDlouhy, Stephen RLievens, P MYoung, KBird, Thomas DNochlin, DavidDickson, Dennis WVinters, Harry VZimmerman, T RMackenzie, IanKish, S JAng, L CDe Carli, CPocchiari, MBrown, PGibbs, C JGajdusek, D CBugiani, OIronside, J. WTagliavini, F and Ghetti, Bernardino
Journal of Neuropathology and Experimental Neurology, vol. 57, (no. 10), pp. 979-88, 1998/Oct. | Journal Article
1997
A possible role for tyrosine kinases in the regulation of the neuronal dopamine transporter in mouse striatum
Simon, Jay RBare, DJGhetti, Bernardino and Richter, Judith A
Neuroscience Letters, vol. 224, (no. 3), pp. 201-205, 1997. | Journal Article
 
Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice.
Verina, TVerina, TatyanaNorton, JamesNorton, J ASorbel, J JSorbel, JeffreyTriarhou, LazarosTriarhou, L CLaferty, DLaferty, DonaldRichter, J ARichter, JudithSimon, JaySimon, J RGhetti, B and Ghetti, Bernardino
Experimental brain research, vol. 113, (no. 1), pp. 5-12, January 1997. | Journal Article
 
Decreased IGF-I gene expression during the apoptosis of Purkinje cells in pcd mice
Zhang, WeiGhetti, Bernardino and Lee, Wei-Hua
Developmental Brain Research, vol. 98, (no. 2), pp. 176, 1997. | Journal Article
 
Diverse cell death pathways result from a single missense mutation in weaver mouse.
Migheli, APiva, RWei, Jian JunAttanasio, ACasolino, SHodes, M EDlouhy, S RBayer, S A and Ghetti, B
The American journal of pathology, vol. 151, (no. 6), pp. 1629-38, 1997/Dec. | Journal Article
 
Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments
Spillantini, Maria GGoedert, M.Crowther, RAMurrell, Jill RFarlow, Martin R and Ghetti, Bernardino
Proceedings of the National Academy of Sciences, USA, vol. 94, (no. 8), pp. 4113-4118, 1997. | Journal Article
 
Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.
Murrell, Jill RKoller, DForoud, TGoedert, MSpillantini, M GEdenberg, H JFarlow, M R and Ghetti, B
American journal of human genetics. , vol. 61, (no. 5), pp. 1131-8, 1997/Nov. | Journal Article
 
Gerstmann–Sträussler–Scheinker disease with the PRNP P102L mutation and valine at codon 129
Young, KatherineClark, H.BrentPiccardo, PedroDlouhy, Stephen R and Ghetti, Bernardino
Molecular Brain Research, vol. 44, (no. 1), pp. 150, 1997. | Journal Article
 
In Situ Hybridization Analysis of Girk2 Expression in the Developing Central Nervous System in Normal and Weaver Mice
Wei, JianjunWei, Jian JunDlouhy, S RDlouhy, StephenBayer, ShirleyBayer, SPiva, RPiva, RobertoVerina, TatyanaVerina, TWang, YWang, YiFeng, YFeng, YueDupree, BrendaDupree, BHodes, M EHodes, MGhetti, Bernardino and Ghetti, B
Journal of Neuropathology and Experimental Neurology, vol. 56, (no. 7), pp. 771, 1997-July. | Journal Article
 
In vitro evidence that the reduction in mesencepalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interaction
Won, LisaGhetti, BernardinoHeller, Barbara and Heller, A
Experimental Brain Research, vol. 115, (no. 1), pp. 179, 19970600. | Journal Article
 
Lack of apolipoprotein E dramatically reduces amyloid β-peptide deposition
Little, Sheila PPiccardo, PedroDodel, Richard CAltstiel, LarryJohnstone, Edward MBales, Kelly RVerina, TatyanaHyslop, PaulPaul, Steven MCummins, David JDu, YanshengBender, Mark and Ghetti, Bernardino
Nature Genetics, vol. 17, (no. 3), pp. 264, 199711. | Journal Article
 
Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana Kindred (F198S)
Unverzagt, Frederick WUNVERZAGT, FREDERICK WUNVERZAGT, FREDERICK WFarlow, Martin RFarlow, M RFARLOW, MARTIN RNORTON, JAMESNorton, JNORTON, JAMESDLOUHY, STEPHEN RDlouhy, S RDLOUHY, STEPHEN RYoung, KYOUNG, KATHERINEYOUNG, KATHERINEGhetti, BernardinoGhetti, B and GHETTI, BERNARDINO
Journal of the International Neuropsychological Society, vol. 3, (no. 2), pp. 178, 19970301. | Journal Article
 
Subacute sclerosing panencephalitis manifesting as viral retinitis: clinical and histopathologic findings.
Park, D WBoldt, H. CMassicotte, S JAkang, E ERoos, K LBodnar, APless, JGhetti, B and Pascuzzi, R M
American journal of ophthalmology, vol. 123, (no. 4), pp. 533-42, 1997/Apr. | Journal Article
 
Subacute sclerosis panencephalitis manifesting as viral retinitis: clinical and histopathologic findings
Park, DonaldRoos, KarenMassicotte, StephenBodnar, AdrianaPascuzzi, RobertAkang, EffiongBoldt, H.Pless, JohnPark, DonaldRoos, KarenMassicotte, StephenBodnar, AdrianaAkang, EffiongBoldt, H.Pless, JohnGhetti, BernardinoGhetti, Bernardino and Pascuzzi, Robert
American Journal of Ophthalmology, vol. 123, (no. 4), pp. 533, 19970401. | Journal Article
1996
Cloning a cDNA for Carbonyl Reductase (Cbr) from Mouse Cerebellum: Murine Genes That Express Cbr Map to Chromosomes 16 and 11
Wei, JianjunWei, Jian JunDlouhy, S. RDlouhy, Stephen RHara, AkiraHara, A.Ghetti, B.Ghetti, BernardinoHodes, M.E and Hodes, ME
Genomics, vol. 34, (no. 1), pp. 148, 1996-05-15. | Journal Article
 
Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease
Parchi, PieroParchi, PieroParchi, P.Parchi, PieroCastellani, R.Castellani, RudolphCastellani, RudolphCastellani, RudolphCapellari, SabinaCapellari, SabinaCapellari, S.Capellari, SabinaGhetti, B.Ghetti, BernardinoGhetti, BernardinoGhetti, BernardinoYoung, KatherineYoung, KatherineYoung, KatherineYoung, K.Chen, Shu GChen, Shu GChen, S. G.Chen, Shu G.Farlow, M.Farlow, MartinFarlow, MartinFarlow, MartinDickson, Dennis WDickson, Dennis W.Dickson, Dennis WDickson, D. W.Sima, Anders A. F.Sima, A. A.Sima, Anders A. FSima, Anders A. FTrojanowski, John QTrojanowski, J. Q.Trojanowski, John QTrojanowski, John Q.Petersen, Robert BPetersen, R. B.Petersen, Robert BPetersen, Robert B.Gambetti, PierluigiGambetti, PierluigiGambetti, P. and Gambetti, Pierluigi
Annals of Neurology, vol. 39, (no. 6), pp. 778, June 1996. | Journal Article
 
Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain.
Bayer, S AWills, K VWei, Jian JunFeng, YDlouhy, S RHodes, M EVerina, T and Ghetti, B
Brain research. Developmental brain research, vol. 96, (no. 1-2), pp. 130-7, 1996/Oct/23. | Journal Article
 
Prion protein amyloidosis.
Ghetti, BernardinoPiccardo, PFrangione, BBugiani, OGiaccone, GYoung, KPrelli, FFarlow, M RDlouhy, S R and Tagliavini, F
Brain Pathology (Zurich, Switzerland), vol. 6, (no. 2), pp. 127-45, 1996/Apr. | Journal Article
 
Prion Protein Amyloidosis
Ghetti, BernardinoPiccardo, PedroFrangione, BiasBugiani, OrsoGiaccone, GiorgioYoung, KatherinePrelli, FrancesFarlow, Martin RDlouhy, Stephen R and Tagliavini, Fabrizio
Brain Pathology, vol. 6, (no. 2), pp. 145, April 1996. | Journal Article
 
Prion protein hereditary amyloidosis: Parenchymal and vascular
Ghetti, BernardinoPiccardo, PedroFrangione, BlasBugiani, O.Giaccone, G.Young, K.Prelli, F.Farlow, MRDlouhy, S. R and Tagliavini, F.
Seminars in Virology, vol. 7, (no. 3), pp. 189-200, 1996. | Journal Article
 
Proteinase-K-Resistant Prion Protein Isoforms in Gerstmann-Straussler-Scheinker Disease (Indiana Kindred)
Piccardo, PedroPiccardo, PedroSeiler, CharlesSeiler, CharlesDlouhy, StephenDlouhy, StephenYoung, KatherineYoung, KatherineFarlow, MartinFarlow, MartinPrelli, FrancesPrelli, FrancesFrangione, BlasFrangione, BlasBugiani, OrsoBugiani, OrsoTagliavini, FabrizioTagliavini, FabrizioGhetti, Bernardino and Ghetti, Bernardino
Journal of Neuropathology and Experimental Neurology, vol. 55, (no. 11), pp. 1163, 1996-November. | Journal Article
 
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).
Piccardo, PedroSeiler, CDlouhy, Stephen RYoung, KFarlow, Martin RPrelli, FFrangione, BlasBugiani, OTagliavini, F and Ghetti, Bernardino
Journal of neuropathology and experimental neurology, vol. 55, (no. 11), pp. 1157-63, 1996/Nov. | Journal Article
 
PrP27-30 is a normal soluble prion protein fragment released by human platelets.
Perini, FVidal, Ruben GGhetti, BernardinoTagliavini, FFrangione, Blas and Prelli, F
Biochemical and biophysical research communications, vol. 223, (no. 3), pp. 572-7, 1996/Jun/25. | Journal Article
 
PRP.sub.27-30Is a Normal Soluble Prion Protein Fragment Released by Human Platelets
Perini, FrancescoPerini, FrancescoVidal, RubenVidal, RubenGhetti, BernardinoGhetti, BernardinoTagliavini, FabrizioTagliavini, FabrizioFrangione, BlasFrangione, BlasPrelli, Frances and Prelli, Frances
Biochemical and Biophysical Research Communications, vol. 223, (no. 3), pp. 572, 19960625. | Journal Article
 
The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2
Tong, YanheTong, YWei, JianjunWei, Jian JunZhang, ShengwenZhang, SStrong, Judith AStrong, J ADlouhy, S RDlouhy, Stephen RHodes, M.EHodes, M EGhetti, BGhetti, BernardinoYu, Lei and Yu, L
FEBS Letters, vol. 390, (no. 1), pp. 68, 1996. | Journal Article