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Results:
1-13
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Results: 13
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:
Fischer, EA
Verpont, MC
Garrett-Sinha, LA
Ronco, PM
Rossert, JA
Citation: Ea. Fischer et al., Klf6 is a zinc finger protein expressed in a cell-specific manner during kidney development, J AM S NEPH, 12(4), 2001, pp. 726-735
Authors:
Bland, R
Zehnder, D
Hughes, SV
Ronco, PM
Stewart, PM
Hewison, M
Citation: R. Bland et al., Regulation of vitamin D-1 alpha-hydroxylase in a human cortical collectingduct cell line, KIDNEY INT, 60(4), 2001, pp. 1277-1286
Authors:
Lelongt, B
Bengatta, S
Delauche, M
Lund, LR
Werb, Z
Ronco, PM
Citation: B. Lelongt et al., Matrix metalloproteinase 9 protects mice from anti-glomerular basement membrane nephritis through its fibrinolytic activity, J EXP MED, 193(7), 2001, pp. 793-802
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
Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases
Authors:
Denamur, E
Bocquet, N
Mougenot, B
Da Silva, F
Martinat, L
Loirat, C
Elion, J
Bensman, A
Ronco, PM
Citation: E. Denamur et al., Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases, J AM S NEPH, 10(10), 1999, pp. 2219-2223
Authors:
Ronco, PM
Aucouturier, P
Citation: Pm. Ronco et P. Aucouturier, The molecular bases of plasma cell dyscrasia-related renal diseases, NEPH DIAL T, 14, 1999, pp. 4-8
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:
Ronco, PM
Harrington, JT
Preud'homme, JL
Cordonnier, D
Laville, M
Deray, G
Clauvel, JP
Lesavre, P
Rossert, J
Sraer, JD
Esnault, V
Combe, C
Piette, JC
Touchard, G
Moulin, B
Rondeau, E
Citation: Pm. Ronco et al., Paraneoplastic glomerulopathies: New insights into an old entity, KIDNEY INT, 56(1), 1999, pp. 355-377
Authors:
Piedagnel, R
Murphy, G
Ronco, PM
Lelong, B
Citation: R. Piedagnel et al., Matrix metalloproteinase 2 (MMP2) and MMP9 are produced by kidney collecting duct principal cells but are differentially regulated by SV40 large-T, arginine vasopressin, and epidermal growth factor, J BIOL CHEM, 274(3), 1999, pp. 1614-1620
Authors:
Tattevin, P
Fischer, EA
Ronco, PM
Rossert, JA
Vasseur, E
Mougenot, B
Citation: P. Tattevin et al., Granulomatous nephritis in an AIDS patient treated with combination antiretroviral therapy and infection with Mycobacterium avium, AM J MED, 107(6), 1999, pp. 642-643
Authors:
Debiec, H
Christensen, EI
Ronco, PM
Citation: H. Debiec et al., The cell adhesion molecule L1 is developmentally regulated in the renal epithelium and is involved in kidney branching morphogenesis, J CELL BIOL, 143(7), 1998, pp. 2067-2079
Risultati:
1-13
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