Human heavy chain disease protein WIS: implications for the organization of immunoglobulin genes.

Por Franklin, E C, Prelli, F, Frangione, B
Publicado em 1979

Human lambda light-chain constant region gene CMor lambda: the primary structure of lambda VI Bence Jones protein Mor.

Por Frangione, B, Moloshok, T, Prelli, F, Solomon, A
Publicado em 1985

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

Por Pras, M, Prelli, F, Franklin, E C, Frangione, B
Publicado em 1983

Interchain and Intrachain Disulfide Bridges of a Human Immunoglobulin M: Detection of a Unique Fragment

Por Frangione, B., Prelli, F., Mihaesco, C., Franklin, E. C.
Publicado em 1971

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

Por Ghiso, J, Haltia, M, Prelli, F, Novello, J, Frangione, B
Publicado em 1990

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

Por Gorevic, P D, Prelli, F C, Wright, J, Pras, M, Frangione, B
Publicado em 1989

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

Por van Duinen, S G, Castaño, E M, Prelli, F, Bots, G T, Luyendijk, W, Frangione, B
Publicado em 1987

Fibrillogenesis in Alzheimer's disease of amyloid beta peptides and apolipoprotein E.

Por Castano, E M, Prelli, F, Wisniewski, T, Golabek, A, Kumar, R A, Soto, C, Frangione, B
Publicado em 1995

Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin.

Por Haltia, M., Ghiso, J., Prelli, F., Gallo, G., Kiuru, S., Somer, H., Palo, J., Frangione, B.
Publicado em 1990

Beta-2 microglobulin is an amyloidogenic protein in man.

Por Gorevic, P D, Casey, T T, Stone, W J, DiRaimondo, C R, Prelli, F C, Frangione, B
Publicado em 1985

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.

Por Tagliavini, F, Prelli, F, Ghiso, J, Bugiani, O, Serban, D, Prusiner, S B, Farlow, M R, Ghetti, B, Frangione, B
Publicado em 1991

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

Por Tagliavini, F, Prelli, F, Verga, L, Giaccone, G, Sarma, R, Gorevic, P, Ghetti, B, Passerini, F, Ghibaudi, E, Forloni, G
Publicado em 1993

Polymerization of intact beta 2-microglobulin in tissue causes amyloidosis in patients on chronic hemodialysis.

Por Gorevic, P D, Munoz, P C, Casey, T T, DiRaimondo, C R, Stone, W J, Prelli, F C, Rodrigues, M M, Poulik, M D, Frangione, B
Publicado em 1986

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Por Ghetti, B, Piccardo, P, Spillantini, M G, Ichimiya, Y, Porro, M, Perini, F, Kitamoto, T, Tateishi, J, Seiler, C, Frangione, B, Bugiani, O, Giaccone, G, Prelli, F, Goedert, M, Dlouhy, S R, Tagliavini, F
Publicado em 1996