Torthaí cuardaigh - Frances Prelli
- 1 - 20 toradh as 28 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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STRUCTURAL UNITS OF HUMAN 7S GAMMA GLOBULIN * de réir Edward C. Franklin, Frances Prelli
Foilsithe / Cruthaithe 1960Artigo -
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Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin. de réir Mordechai Pras, Frances Prelli, E. C. Franklin, B Frangione
Foilsithe / Cruthaithe 1983Artigo -
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A variant of prealbumin from amyloid fibrils in familial polyneuropathy of Jewish origin. de réir Mordechai Pras, E. C. Franklin, Frances Prelli, B Frangione
Foilsithe / Cruthaithe 1981Artigo -
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Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type de réir Jorge Ghiso, Matti Haltia, Frances Prelli, J. C. Novello, Blas Frangione
Foilsithe / Cruthaithe 1990Artigo -
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PRP27–30Is a Normal Soluble Prion Protein Fragment Released by Human Platelets de réir Francesco Perini, Rubén Vidal, Bernardino Ghetti, Fabrizio Tagliavini, Blas Frangione, Frances Prelli
Foilsithe / Cruthaithe 1996Artigo -
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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 amyloidoti... de réir Peter D. Gorevic, Frances Prelli, James R. Wright, Mordechai Pras, Blas Frangione
Foilsithe / Cruthaithe 1989Artigo -
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Blocking the apolipoprotein E/amyloid-β interaction as a potential therapeutic approach for Alzheimer's disease de réir Martin Sadowski, Joanna Pankiewicz, Henrieta Scholtzova, Pankaj Mehta, Frances Prelli, David Quartermain, Thomas Wısnıewskı
Foilsithe / Cruthaithe 2006Artigo -
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Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein de réir Matti Haltia, Frances Prelli, Jorge Ghiso, Sari Kiuru, Hannu Somer, Jorma Palo, Blas Frangione
Foilsithe / Cruthaithe 1990Artigo -
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Mutation in gelsolin gene in Finnish hereditary amyloidosis. de réir Efrat Levy, Matti Haltia, Ivan Fernandez‐Madrid, Olli Koivunen, Jorge Ghiso, Frances Prelli, Blas Frangione
Foilsithe / Cruthaithe 1990Artigo -
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Fibrillogenesis in Alzheimer's disease of amyloid <i>β</i> peptides and apolipoprotein E de réir E. M. Castaño, Frances Prelli, Thomas Wısnıewskı, Adam A. Golabek, Rashmi Kumar, Claudio Soto, Blas Frangione
Foilsithe / Cruthaithe 1995Artigo -
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The length of Amyloid-β in Hereditary Cerebral Hemorrhage with Amyloidosis, Dutch Type de réir Eduardo M. Castaño, Frances Prelli, Claudio Soto, Ronald C. Beavis, Etsuro Matsubara, Mikio Shoji, Blas Frangione
Foilsithe / Cruthaithe 1996Artigo -
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Beta-2 microglobulin is an amyloidogenic protein in man. de réir Peter D. Gorevic, Terence T. Casey, William J. Stone, Carol R. DiRaimondo, Frances Prelli, B Frangione
Foilsithe / Cruthaithe 1985Artigo -
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Endogenous Proteolytic Cleavage of Normal and Disease-Associated Isoforms of the Human Prion Protein in Neural and Non-Neural Tissues de réir Adolfo Jiménez‐Huete, Patricia Lievens, Rubén Vidal, Pedro Piccardo, Bernardino Ghetti, Fabrizio Tagliavini, Blas Frangione, Frances Prelli
Foilsithe / Cruthaithe 1998Artigo -
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Heavy Chain Disease of the µ (γM) Type: Report of the First Case de réir FRANK A. FORTE, Frances Prelli, William J. Yount, Jerry Li, Shaul Kochwa, Edward C. Franklin, Henry G. Kunkel
Foilsithe / Cruthaithe 1970Artigo -
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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. de réir Fabrizio Tagliavini, Frances Prelli, Jorge Ghiso, Orso Bugiani, D. Serban, Stanley B. Prusiner, Martin R. Farlow, Bernardino Ghetti, Blas Frangione
Foilsithe / Cruthaithe 1991Artigo -
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Differential Degradation of Amyloid β Genetic Variants Associated with Hereditary Dementia or Stroke by Insulin-degrading Enzyme de réir Laura Morelli, Ramiro E. Llovera, Silvia A. González, José L. Affranchino, Frances Prelli, Blas Frangione, Jorge Ghiso, Eduardo M. Castaño
Foilsithe / Cruthaithe 2003Artigo -
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Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro. de réir Fabrizio Tagliavini, Frances Prelli, Laura Verga, Giorgio Giaccone, R. Sarma, P D Gorevic, Bernardino Ghetti, F Passerini, Elena Ghibaudi, Gianluigi Forloni
Foilsithe / Cruthaithe 1993Artigo -
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Identification of Distinct N-terminal Truncated Forms of Prion Protein in Different Creutzfeldt-Jakob Disease Subtypes de réir Gianluigi Zanusso, Alessia Farinazzo, Frances Prelli, Michele Fiorini, Matteo Gelati, Sérgio Ferrari, Pier Giorgio Righetti, Nicolo’ Rizzuto, Blas Frangione, Salvatore Monaco
Foilsithe / Cruthaithe 2004Artigo -
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Prion Protein Amyloidosis de réir Bernardino Ghetti, Pedro Piccardo, B Frangione, Orso Bugiani, Giorgio Giaccone, Katherine Young, Frances Prelli, Martin R. Farlow, Stephen R. Dlouhy, Fabrizio Tagliavini
Foilsithe / Cruthaithe 1996Revisão
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Biology
Pathology
Amyloid (mycology)
Chemistry
Biochemistry
Amyloidosis
Disease
Gene
Molecular biology
Genetics
Inorganic chemistry
Prion protein
Enzyme
Internal medicine
Amino acid
Antibody
Fibril
Immunology
Alzheimer's disease
Dementia
Fibrillogenesis
Scrapie
Endocrinology
Gene isoform
Mutation
Organic chemistry
PRNP
Peptide sequence
Protein subunit