Ngā hua rapu - Frances Prelli

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

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

    I whakaputaina 1960
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    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. mā Mordechai Pras, Frances Prelli, E. C. Franklin, B Frangione

    I whakaputaina 1983
    Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    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. mā Mordechai Pras, E. C. Franklin, Frances Prelli, B Frangione

    I whakaputaina 1981
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type

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

    I whakaputaina 1990
    Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    PRP27–30Is a Normal Soluble Prion Protein Fragment Released by Human Platelets

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

    I whakaputaina 1996
    Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    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... mā Peter D. Gorevic, Frances Prelli, James R. Wright, Mordechai Pras, Blas Frangione

    I whakaputaina 1989
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  7. 7
    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 mā Martin Sadowski, Joanna Pankiewicz, Henrieta Scholtzova, Pankaj Mehta, Frances Prelli, David Quartermain, Thomas Wısnıewskı

    I whakaputaina 2006
    Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    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 mā Matti Haltia, Frances Prelli, Jorge Ghiso, Sari Kiuru, Hannu Somer, Jorma Palo, Blas Frangione

    I whakaputaina 1990
    Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    Mutation in gelsolin gene in Finnish hereditary amyloidosis.

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

    I whakaputaina 1990
    Whiwhi kuputuhi katoa
    Artigo
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  10. 10
    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 mā E. M. Castaño, Frances Prelli, Thomas Wısnıewskı, Adam A. Golabek, Rashmi Kumar, Claudio Soto, Blas Frangione

    I whakaputaina 1995
    Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    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 mā Eduardo M. Castaño, Frances Prelli, Claudio Soto, Ronald C. Beavis, Etsuro Matsubara, Mikio Shoji, Blas Frangione

    I whakaputaina 1996
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Beta-2 microglobulin is an amyloidogenic protein in man.

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

    I whakaputaina 1985
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    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 mā Adolfo Jiménez‐Huete, Patricia Lievens, Rubén Vidal, Pedro Piccardo, Bernardino Ghetti, Fabrizio Tagliavini, Blas Frangione, Frances Prelli

    I whakaputaina 1998
    Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    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. mā Sjoerd G. van Duinen, Eduardo M. Castaño, Frances Prelli, G. Th. A. M. Bots, W Luyendijk, Blas Frangione

    I whakaputaina 1987
    Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    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 mā FRANK A. FORTE, Frances Prelli, William J. Yount, Jerry Li, Shaul Kochwa, Edward C. Franklin, Henry G. Kunkel

    I whakaputaina 1970
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  16. 16
    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. mā Fabrizio Tagliavini, Frances Prelli, Jorge Ghiso, Orso Bugiani, D. Serban, Stanley B. Prusiner, Martin R. Farlow, Bernardino Ghetti, Blas Frangione

    I whakaputaina 1991
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  17. 17
    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 mā Laura Morelli, Ramiro E. Llovera, Silvia A. González, José L. Affranchino, Frances Prelli, Blas Frangione, Jorge Ghiso, Eduardo M. Castaño

    I whakaputaina 2003
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  18. 18
    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. mā Fabrizio Tagliavini, Frances Prelli, Laura Verga, Giorgio Giaccone, R. Sarma, P D Gorevic, Bernardino Ghetti, F Passerini, Elena Ghibaudi, Gianluigi Forloni

    I whakaputaina 1993
    Whiwhi kuputuhi katoa
    Artigo
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  19. 19
    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 mā Gianluigi Zanusso, Alessia Farinazzo, Frances Prelli, Michele Fiorini, Matteo Gelati, Sérgio Ferrari, Pier Giorgio Righetti, Nicolo’ Rizzuto, Blas Frangione, Salvatore Monaco

    I whakaputaina 2004
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  20. 20
    Prion Protein Amyloidosis

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

    I whakaputaina 1996
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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