Authors:
Ronco, PM
Alyanakian, MA
Mougenot, B
Aucouturier, P
Citation: Pm. Ronco et al., Light chain deposition disease: A model of glomerulosclerosis defined at the molecular level, J AM S NEPH, 12(7), 2001, pp. 1558-1565
Authors:
Aucouturier, P
Geissmann, F
Damotte, D
Saborio, GP
Meeker, HC
Kascsak, R
Kascsak, R
Carp, RI
Wisniewski, T
Citation: P. Aucouturier et al., Infected splenic dendritic cells are sufficient for prion transmission to the CNS in mouse scrapie, J CLIN INV, 108(5), 2001, pp. 703-708
Authors:
Wisniewski, T
Sigurdsson, EM
Aucouturier, P
Frangione, B
Citation: T. Wisniewski et al., Conformation as therapeutic target in the prionoses and other neurodegenerative conditions, METH MOL M, 59, 2001, pp. 223-236
Citation: P. Ronco et al., Plasma cell dyscrasia-related glomerulopathies and Fanconi's syndrome: a molecular approach, J NEPHROL, 13, 2000, pp. S34-S44
Authors:
Soto, C
Kascsak, RJ
Saborio, GP
Aucouturier, P
Wisniewski, T
Prelli, F
Kascsak, R
Mendez, E
Harris, DA
Ironside, J
Tagliavini, F
Carp, RI
Frangione, B
Citation: C. Soto et al., Reversion of prion protein conformational changes by synthetic beta-sheet breaker peptides, LANCET, 355(9199), 2000, pp. 192-197
Authors:
Messiaen, T
Deret, S
Mougenot, B
Bridoux, F
Dequiedt, P
Dion, JJ
Makdassi, R
Meeus, F
Pourrat, J
Touchard, G
Vanhille, P
Zaoui, P
Aucouturier, P
Ronco, PM
Citation: T. Messiaen et al., Adult Fanconi syndrome secondary to light chain gammopathy - Clinicopathologic heterogeneity and unusual features in 11 patients, MEDICINE, 79(3), 2000, pp. 135-154
Authors:
Moulin, B
Deret, S
Mariette, X
Kourilsky, O
Imai, H
Dupouet, L
Marcellin, L
Kolb, I
Aucouturier, P
Brouet, JC
Ronco, PM
Mougenot, B
Citation: B. Moulin et al., Nodular glomerulosclerosis with deposition of monoclonal immunoglobulin heavy chains lacking C(H)1, J AM S NEPH, 10(3), 1999, pp. 519-528
Authors:
Aucouturier, P
Kascsak, RJ
Frangione, B
Wisniewski, T
Citation: P. Aucouturier et al., Biochemical and conformational variability of human prion strains in sporadic Creutzfeldt-Jakob disease, NEUROSCI L, 274(1), 1999, pp. 33-36
Authors:
Deret, S
Denoroy, L
Lamarine, M
Vidal, R
Mougenot, B
Frangione, B
Stevens, FJ
Ronco, PM
Aucouturier, P
Citation: S. Deret et al., Kappa light chain-associated Fanconi's syndrome: molecular analysis of monoclonal immunoglobulin light chains from patients with and without intracellular crystals, PROTEIN ENG, 12(4), 1999, pp. 363-369
Authors:
Roussel, A
Spinelli, S
Deret, S
Navaza, J
Aucouturier, P
Cambillau, C
Citation: A. Roussel et al., The structure of an entire noncovalent immunoglobulin kappa light-chain dimer (Bence-Jones protein) reveals a weak and unusual constant domains association, EUR J BIOCH, 260(1), 1999, pp. 192-199
Authors:
Haddad, E
Le Deist, F
Aucouturier, P
Cavazzana-Calvo, M
Blanche, S
De Saint Basile, G
Fischer, A
Citation: E. Haddad et al., Long-term chimerism and B-cell function after bone marrow transplantation in patients with severe combined immunodeficiency with B cells: A single-center study of 22 patients, BLOOD, 94(8), 1999, pp. 2923-2930
Authors:
Vidal, R
Goni, F
Stevens, F
Aucouturier, P
Kumar, A
Frangione, B
Ghiso, J
Gallo, G
Citation: R. Vidal et al., Somatic mutations of the l12a gene in V-kappa(1) light chain deposition disease - Potential effects on aberrant protein conformation and deposition, AM J PATH, 155(6), 1999, pp. 2009-2017