119 Publications (Page 5 of 5)
1999
Somatic mutations of the L12a gene in V-kappa(1) light chain deposition disease: potential effects on aberrant protein conformation and deposition.Vidal, Ruben G⋅Goni, Fernando R⋅Stevens, Fred J⋅Aucouturier, Pierre⋅Kumar, A⋅Frangione, Blas⋅Ghiso, Jorge A and Gallo, GThe American journal of pathology, vol. 155, (no. 6), pp. 2009-17, 1999/Dec.
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Somatic mutations of the L12a gene in V-kappa1 light chain deposition disease: Potential effects on aberrant protein conformation and depositionVidal, Ruben⋅Goni, Fernando⋅Stevens, Fred and Aucouturier, PierreThe American Journal of Pathology, vol. 155, (no. 6), pp. 2009, 19991201.
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Somatic Mutations of the L12a Gene in V-{kappa}1 Light Chain Deposition Disease : Potential Effects on Aberrant Protein Conformation andDepositionVidal, Ruben⋅Goni, Fernando⋅Stevens, Fred⋅Aucouturier, Pierre⋅Kumar, Asok⋅Frangione, Blas⋅Ghiso, Jorge and Gallo, GloriaAmerican Journal of Pathology, vol. 155, (no. 6), pp. 2009, 19991201.
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Somatic Mutations of the L12a Gene in V-κ1 Light Chain Deposition DiseaseVidal, Ruben⋅Goñi, Fernando⋅Stevens, Fred⋅Aucouturier, Pierre⋅Kumar, Asok⋅Frangione, Blas⋅Ghiso, Jorge and Gallo, GloriaThe American Journal of Pathology, vol. 155, (no. 6), pp. 2017, 1999-12-00.
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Somatic Mutations of the L12a Gene in V-κ1 Light Chain Deposition Disease : Potential Effects on Aberrant Protein Conformation and DepositionVidal, Ruben⋅Goñi, Fernando⋅Stevens, Fred⋅Aucouturier, Pierre⋅Kumar, Asok⋅Frangione, Blas⋅Ghiso, Jorge and Gallo, GloriaThe American Journal of Pathology, vol. 155, (no. 6), pp. 2017, 1999-12-01.
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1998
Complete Primary Sequences of Two {lambda} Immunoglobulin Light Chains in Myelomas with Nonamyloid (Randall-Type) Light Chain Deposition DiseaseDecourt, Catherine⋅Touchard, Guy⋅Preud'homme, Jean-Louis⋅Vidal, Ruben⋅Beaufils, Helene⋅Diemert, Marie-Claude and Cogne, MichelAmerican Journal of Pathology, vol. 153, (no. 1), pp. 313, 19980701.
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Complete Primary Sequences of Two λ Immunoglobulin Light Chains in Myelomas with Nonamyloid (Randall-Type) Light Chain Deposition DiseaseDecourt, Catherine⋅Touchard, Guy⋅Preud'homme, Jean-Louis⋅Vidal, Ruben⋅Beaufils, Hélène⋅Diemert, Marie-Claude and Cogné, MichelThe American Journal of Pathology, vol. 153, (no. 1), pp. 318, 1998.
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Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues.Jiménez-Huete, A⋅Lievens, P M⋅Vidal, Ruben G⋅Piccardo, Pedro⋅Ghetti, Bernardino⋅Tagliavini, F⋅Frangione, Blas and Prelli, FThe American journal of pathology, vol. 153, (no. 5), pp. 1561-72, 1998/Nov.
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IgG1-kappa biclonal gammopathy associated with multiple myeloma suggests a regulatory mechanism.Pizzolato, M⋅Bragantini, G⋅Bresciani, P⋅Pavlovsky, S⋅Chuba, J⋅Vidal, Ruben G⋅Rostagno Ghiso, Agueda A and Ghiso, Jorge ABritish journal of haematology, vol. 102, (no. 2), pp. 503-8, 1998/Jul.
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1997
Amino-terminal identity of co-existent amyloid and non-amyloid immunoglobulin Kappa light chain deposits. A human disease to study alterations of protein conformationKaplan, B.⋅Vidal, Ruben G⋅Kumar, A.⋅Ghiso, Jorge A⋅Frangione, Blas and Gallo, Gloria RClinical and Experimental Immunology, vol. 110, (no. 3), pp. 472-478, 1997.
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Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly)Garzuly, F⋅Vidal, Ruben G⋅Wisniewski, Thomas M⋅Brittig, F and Budka, HNeurology, vol. 47, (no. 6), pp. 1562-7, 1996/Dec.
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Fibrillary glomerulonephritis related to serum fibrillar immunoglobulin-fibronectin complexesRostagno, Agueda⋅Rostagno Ghiso, Agueda A⋅Vidal, Ruben⋅Vidal, R⋅Kumar, Asok⋅Kumar, A⋅Chuba, J⋅Chuba, Joseph⋅Niederman, G⋅Niederman, George⋅Gold, Leslie I⋅Gold, Leslie⋅Frangione, Blas⋅Frangione, Blas⋅Ghiso, Jorge A⋅Ghiso, Jorge⋅Gallo, Gloria and Gallo, Gloria RAmerican Journal of Kidney Diseases, vol. 28, (no. 5), pp. 684, 1996.
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Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)Vidal, Ruben G⋅Garzuly, F⋅Budka, H⋅Lalowski, M⋅Linke, R P⋅Brittig, F⋅Frangione, Blas and Wisniewski, Thomas MThe American journal of pathology, vol. 148, (no. 2), pp. 361-6, 1996/Feb.
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PrP27-30 is a normal soluble prion protein fragment released by human platelets.Perini, F⋅Vidal, Ruben G⋅Ghetti, Bernardino⋅Tagliavini, F⋅Frangione, Blas and Prelli, FBiochemical and biophysical research communications, vol. 223, (no. 3), pp. 572-7, 1996/Jun/25.
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PRP.sub.27-30Is a Normal Soluble Prion Protein Fragment Released by Human PlateletsPerini, Francesco⋅Perini, Francesco⋅Vidal, Ruben⋅Vidal, Ruben⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Tagliavini, Fabrizio⋅Tagliavini, Fabrizio⋅Frangione, Blas⋅Frangione, Blas⋅Prelli, Frances and Prelli, FrancesBiochemical and Biophysical Research Communications, vol. 223, (no. 3), pp. 572, 19960625.
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1993
Complexes of multiple transcription factors in regulation of keratin synthesisFreedberg, Irwin M⋅Ohtsuki, Mamitaro⋅Magnaldo, Thierry⋅Bernerd, Francoise⋅Vidal, Ruben and Blumenberg, MiroslavJournal of Dermatological Science, vol. 6, (no. 1), pp. 31, 1993.
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1992
Amyloidoma of the CNS. II. Immunohistochemical and biochemical study.Vidal, Ruben G⋅Ghiso, Jorge A⋅Gallo, Gloria R⋅Cohen, M⋅Gambetti, P L and Frangione, BlasNeurology, vol. 42, (no. 10), pp. 2024-8, 1992/Oct.
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