Canlyniadau Chwilio - Frances Prelli

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  1. 1
    STRUCTURAL UNITS OF HUMAN 7S GAMMA GLOBULIN *

    STRUCTURAL UNITS OF HUMAN 7S GAMMA GLOBULIN * gan Edward C. Franklin, Frances Prelli

    Cyhoeddwyd 1960
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    Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin.

    Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin. gan Mordechai Pras, Frances Prelli, E. C. Franklin, B Frangione

    Cyhoeddwyd 1983
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    A variant of prealbumin from amyloid fibrils in familial polyneuropathy of Jewish origin.

    A variant of prealbumin from amyloid fibrils in familial polyneuropathy of Jewish origin. gan Mordechai Pras, E. C. Franklin, Frances Prelli, B Frangione

    Cyhoeddwyd 1981
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    Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type

    Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type gan Jorge Ghiso, Matti Haltia, Frances Prelli, J. C. Novello, Blas Frangione

    Cyhoeddwyd 1990
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    PRP27–30Is a Normal Soluble Prion Protein Fragment Released by Human Platelets

    PRP27–30Is a Normal Soluble Prion Protein Fragment Released by Human Platelets gan Francesco Perini, Rubén Vidal, Bernardino Ghetti, Fabrizio Tagliavini, Blas Frangione, Frances Prelli

    Cyhoeddwyd 1996
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    Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy.

    Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidoti... gan Peter D. Gorevic, Frances Prelli, James R. Wright, Mordechai Pras, Blas Frangione

    Cyhoeddwyd 1989
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    Blocking the apolipoprotein E/amyloid-β interaction as a potential therapeutic approach for Alzheimer's disease

    Blocking the apolipoprotein E/amyloid-β interaction as a potential therapeutic approach for Alzheimer's disease gan Martin Sadowski, Joanna Pankiewicz, Henrieta Scholtzova, Pankaj Mehta, Frances Prelli, David Quartermain, Thomas Wısnıewskı

    Cyhoeddwyd 2006
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    Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein

    Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein gan Matti Haltia, Frances Prelli, Jorge Ghiso, Sari Kiuru, Hannu Somer, Jorma Palo, Blas Frangione

    Cyhoeddwyd 1990
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    Mutation in gelsolin gene in Finnish hereditary amyloidosis.

    Mutation in gelsolin gene in Finnish hereditary amyloidosis. gan Efrat Levy, Matti Haltia, Ivan Fernandez‐Madrid, Olli Koivunen, Jorge Ghiso, Frances Prelli, Blas Frangione

    Cyhoeddwyd 1990
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    Fibrillogenesis in Alzheimer's disease of amyloid <i>β</i> peptides and apolipoprotein E

    Fibrillogenesis in Alzheimer's disease of amyloid <i>β</i> peptides and apolipoprotein E gan E. M. Castaño, Frances Prelli, Thomas Wısnıewskı, Adam A. Golabek, Rashmi Kumar, Claudio Soto, Blas Frangione

    Cyhoeddwyd 1995
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    The length of Amyloid-β in Hereditary Cerebral Hemorrhage with Amyloidosis, Dutch Type

    The length of Amyloid-β in Hereditary Cerebral Hemorrhage with Amyloidosis, Dutch Type gan Eduardo M. Castaño, Frances Prelli, Claudio Soto, Ronald C. Beavis, Etsuro Matsubara, Mikio Shoji, Blas Frangione

    Cyhoeddwyd 1996
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    Beta-2 microglobulin is an amyloidogenic protein in man.

    Beta-2 microglobulin is an amyloidogenic protein in man. gan Peter D. Gorevic, Terence T. Casey, William J. Stone, Carol R. DiRaimondo, Frances Prelli, B Frangione

    Cyhoeddwyd 1985
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    Endogenous Proteolytic Cleavage of Normal and Disease-Associated Isoforms of the Human Prion Protein in Neural and Non-Neural Tissues

    Endogenous Proteolytic Cleavage of Normal and Disease-Associated Isoforms of the Human Prion Protein in Neural and Non-Neural Tissues gan Adolfo Jiménez‐Huete, Patricia Lievens, Rubén Vidal, Pedro Piccardo, Bernardino Ghetti, Fabrizio Tagliavini, Blas Frangione, Frances Prelli

    Cyhoeddwyd 1998
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    Hereditary cerebral hemorrhage with amyloidosis in patients of Dutch origin is related to Alzheimer disease.

    Hereditary cerebral hemorrhage with amyloidosis in patients of Dutch origin is related to Alzheimer disease. gan Sjoerd G. van Duinen, Eduardo M. Castaño, Frances Prelli, G. Th. A. M. Bots, W Luyendijk, Blas Frangione

    Cyhoeddwyd 1987
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    Heavy Chain Disease of the µ (γM) Type: Report of the First Case

    Heavy Chain Disease of the µ (γM) Type: Report of the First Case gan FRANK A. FORTE, Frances Prelli, William J. Yount, Jerry Li, Shaul Kochwa, Edward C. Franklin, Henry G. Kunkel

    Cyhoeddwyd 1970
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    Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.

    Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58. gan Fabrizio Tagliavini, Frances Prelli, Jorge Ghiso, Orso Bugiani, D. Serban, Stanley B. Prusiner, Martin R. Farlow, Bernardino Ghetti, Blas Frangione

    Cyhoeddwyd 1991
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    Differential Degradation of Amyloid β Genetic Variants Associated with Hereditary Dementia or Stroke by Insulin-degrading Enzyme

    Differential Degradation of Amyloid β Genetic Variants Associated with Hereditary Dementia or Stroke by Insulin-degrading Enzyme gan Laura Morelli, Ramiro E. Llovera, Silvia A. González, José L. Affranchino, Frances Prelli, Blas Frangione, Jorge Ghiso, Eduardo M. Castaño

    Cyhoeddwyd 2003
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    Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.

    Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro. gan Fabrizio Tagliavini, Frances Prelli, Laura Verga, Giorgio Giaccone, R. Sarma, P D Gorevic, Bernardino Ghetti, F Passerini, Elena Ghibaudi, Gianluigi Forloni

    Cyhoeddwyd 1993
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    Identification of Distinct N-terminal Truncated Forms of Prion Protein in Different Creutzfeldt-Jakob Disease Subtypes

    Identification of Distinct N-terminal Truncated Forms of Prion Protein in Different Creutzfeldt-Jakob Disease Subtypes gan Gianluigi Zanusso, Alessia Farinazzo, Frances Prelli, Michele Fiorini, Matteo Gelati, Sérgio Ferrari, Pier Giorgio Righetti, Nicolo’ Rizzuto, Blas Frangione, Salvatore Monaco

    Cyhoeddwyd 2004
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    Prion Protein Amyloidosis

    Prion Protein Amyloidosis gan Bernardino Ghetti, Pedro Piccardo, B Frangione, Orso Bugiani, Giorgio Giaccone, Katherine Young, Frances Prelli, Martin R. Farlow, Stephen R. Dlouhy, Fabrizio Tagliavini

    Cyhoeddwyd 1996
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