Catechins and Derived Procyanidins in Red and White Sorghum: Their Contributions to Antioxidant Activity von Bröhan, M., Jerkovic, V., Wilmotte, R., Collin, S.

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Homing Phenotypes of Tumor-Specific CD8 T Cells Are Predetermined at the Tumor Site by Crosspresenting APCs von Calzascia, Thomas, Masson, Frédérick, Di Berardino-Besson, Wilma, Contassot, Emmanuel, Wilmotte, Rick, Aurrand-Lions, Michel, Rüegg, Curzio, Dietrich, Pierre-Yves, Walker, Paul R.

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B7-homolog i expression by human glioma : a new mechanism of immune evasion von WILMOTTE, Rick, BURKHARDT, Karim, KINDLER, Vincent, BELKOUCH, Marie-Claude, DUSSEX, Géraldine, DE TRIBOLET, Nicolas, WALKER, Paul R, DIETRICH, Pierre-Yves

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Arachidonylethanolamide Induces Apoptosis of Human Glioma Cells through Vanilloid Receptor-1 von CONTASSOT, EMMANUEL, WILMOTTE, RICK, TENAN, MIRNA, BELKOUCH, MARIE-CLAUDE, SCHNÜRIGER, VALÉRIE, DE TRIBOLET, NICOLAS, BOURKHARDT, KARIM, DIETRICH, PIERRE-YVES

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Cutting Edge: Cross-Presentation as a Mechanism for Efficient Recruitment of Tumor-Specific CTL to the Brain von Calzascia, Thomas, Di Berardino-Besson, Wilma, Wilmotte, Rick, Masson, Frederick, Tribolet, Nicolas de, Dietrich, Pierre-Yves, Walker, Paul R

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Detection of Pneumocystis carinii DNA by PCR amplification in various rat organs in experimental pneumocystosis von RABODONIRINA, M, WILMOTTE, R, DANNAOUI, E, PERSAT, F, BAYLE, G, MOJON, M

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Two distinct truncated variants of ankyrin associated with hereditary spherocytosis von Hayette, S., Carré, G., Bozon, M., Alloisio, N., Maillet, P., Wilmotte, R., Pascal, O., Reynaud, J., Reman, O., Stéphan, J.‐L., Morlé, L., Delaunay, J.

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Absence of association between HPV DNA, TP53 codon 72 polymorphism, and risk of oesophageal cancer in a high-risk area of China von PEIXOTO GUIMARAES, Denise, SHI HSIN LU, SNIJDERS, Peter, WILMOTTE, Rick, HERRERO, Rolando, LENOIR, Gilbert, MONTESANO, Ruggero, MEIJER, Chris J. L. M, WALBOOMERS, Jan, HAINAUT, Pierre

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TP53 Polymorphism, HPV Infection, and Risk of Cervical Cancer von KLUG, Stefanie J, WILMOTTE, Rick, WALBOOMERS, Jan M. M, MUNOZ, Nubia, SANTOS, Carlos, ALMONTE, Maribel, HERRERO, Rolando, GUERRERO, Ivonne, CACERES, Eduardo, PEIXOTO-GUIMARAES, Denise, LENOIR, Gilbert, HAINAUT, Pierre

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Mycobacterium avium complex strains from AIDS patients belong to a homogeneous group ascribed by rRNA typing methods von Peillon, R., Drouet, E., Wilmotte, R., Cotte, L., Panteix, G., de Montclos, H.

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B7-homolog 1 expression by human glioma: a new mechanism of immune evasion von Wilmotte, Rick, Burkhardt, Karim, Kindler, Vincent, Belkouch, Marie-Claude, Dussex, Géraldine, Tribolet, Nicolas de, Walker, Paul R, Dietrich, Pierre-Yves

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A deletional frameshift mutation of the β-spectrin gene associated with elliptocytosis in spectrin Tokyo (β220/216) von KANZAKI, A, RABODONIRINA, M, NAKAMURA, H, MISHIMA, T, MARLE, L, DELAUNAY, J, YAWATA, Y, WILMOTTE, R, WADA, H, ATA, K, YAMADA, O, AKATSUKA, J, IYORI, H, HORIGUCHI, M

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Arachidony lethanolamide Induces Apoptosis of Human Glioma Cells through Vanilloid Receptor-1 von Contassot, E, Wilmotte, R, Tenan, M, Belkouch, M-C, Schnuriger, V, De Tribolet, N, Bourkhardt, K, Dietrich, P-Y

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Prevalent Skipping of an Individual Exon Accounts for Shortened Protein 4.1 Presles von Feddal, S., Hayette, S., Baklouti, F., Rimokh, R., Wilmotte, R., Magaud, J.P., Maréchal, J., Benz, E.J., Girot, R., Delaunay, J., Morlé, L.

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Cross-Presentation as a Mechanism for Efficient Recruitment of Tumor-Specific CTL to the Brain von Calzascia, T, Di Berardino-Besson, W, Wilmotte, R, Masson, F, De Tribolet, N, Dietrich, P-Y, Walker, PR

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αI/65 hereditary elliptocytosis in Southern Italy : evidence for an African origin von MIRAGLIA DEL GIUDICE, E, DUCLUZEAU, M. T, ALLOISIO, N, WILMOTTE, R, DELAUNAY, J, PERROTTA, S, CUTILLO, S, IOLASCON, A

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Mutation at position -12 of intron 45 (c-->t) plays a prevalent role in the partial skipping of exon 46 from the transcript of allele alphaLELY in erythroid cells von Wilmotte, R, Marechal, J, Delaunay, J

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PREVENTIVE AND CURATIVE PEROXOMETALLATE BASED COMPOSITION, NOTABLY PHARMACEUTICAL COMPOSITION von LORENZO, Fr‚d‚ric, CHRETIEN, Denis Olivier, WILMOTTE, R‚mi

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Mutation at position −12 of intron 45 (c → t) plays a prevalent role in the partial skipping of exon 46 from the transcript of allele αLELY in erythroid cells von Wilmotte, Rick, Marechal, Joëlle, Delaunay, Jean

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The Exon 46-Encoded Sequence Is Essential for Stability of Human Erythroid α-Spectrin and Heterodimer Formation von Wilmotte, Rick, Harper, Sandra L., Ursitti, Jeanine A., Maréchal, Joëlle, Delaunay, Jean, Speicher, David W.

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