Curcumin for monoclonal gammopathies. What can we hope for, what should we fear? von Vermorken, A.J.M, Zhu, J, Van de Ven, W.J.M, Andrès, E

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The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly von Debeer, P, Schoenmakers, E F P M, Twal, W O, Argraves, W S, De Smet, L, Fryns, J-P, Van de Ven, W J M

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Curcumin for the prevention of progression in monoclonal gammopathy of undetermined significance: A word of caution von VERMORKEN, A.J.M, ZHU, J, VAN DE VEN, W.J.M, CUI, Y, FRYNS, J.P

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The Vasopressin Precursor Is Not Processed in the Hypothalamus of Wolfram Syndrome Patients with Diabetes Insipidus: Evidence for the Involvement of PC2 and 7B2 von Gabreëls, B. A. Th. F, Swaab, D. F, de Kleijn, D. P. V, Dean, A, Seidah, N. G, Van de Loo, J.-W, Van de Ven, W. J. M, Martens, G. J. M, van Leeuwen, F. W

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Attenuation of the Polypeptide 7B2, Prohormone Convertase PC2, and Vasopressin in the Hypothalamus of Some Prader-Willi Patients: Indications for a Processing Defect von Gabreëls, B. A. Th. F, Swaab, D. F, de Kleijn, D. P. V, Seidah, N. G, Van de Loo, J.-W, Van de Ven, W. J. M, Martens, G. J. M, van Leeuwen, F. W

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Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11) von Debeer, P, Mols, R, Huysmans, C, Devriendt, K, Van de Ven, WJM, Fryns, J-P

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MON-150, a versatile monoclonal antibody against involucrin : characterization and applications von VAN DUIJNHOVEN, L. P, SCHALKWIJK, J, KRANENBORG, M. H. G. C, VAN VLIJMEN-WILLEMS, I. M. J. J, GROENVELD, A, VAN ERP, P. E. J, TIMMER, E. D. J, DE JONGH, G. J, VAN DE VEN, W. J. M

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Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene von Lemmens, Irma, Van de Ven, Wim J. M., Kas, Koen, Zhang, Chang X., Giraud, Sophie, Wautot, Virginie, Buisson, Nathalie, De Witte, Ko, Salandre, Janine, Lenoir, Gilbert, Pugeat, Michel, Calender, Alain, Parente, Fabienne, Quincey, Danielle, Gaudray, Patrick, De Wit, Mireille J., Lips, Cornelis J. M., Höppener, Jo W. M., Khodaei, Shideh, Grant, Abby L., Weber, Günther, Kytölä, Soili, Teh, Bin T., Farnebo, Filip, Phelan, Catherine, Hayward, Nicholas, Larsson, Catharina, Pannett, Anna A. J., Forbes, Simon A., Bassett, J. H. Duncan, Thakker, Rajesh V.

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PLAG1, the main translocation target in pleomorphic adenoma of the salivary glands, is a positive regulator of IGF-II von VOZ, M. L, AGTEN, N. S, VAN DE VEN, W. J. M, KAS, K

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Promoter swapping between the genes for a novel zinc finger protein and beta-catenin in pleiomorphic adenomas with t(3;8)(p21;q12) translocations von Kas, K, Voz, Marianne, Roijer, E, Astrom, A. K, Meyen, E, Stenman, G, Van de Ven, W. J

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Recurrent rearrangements in the high mobility group protein gene, HMGI-C , in benign mesenchymal tumours von Schoenmakers, Eric F.P.M, Wanschura, Sylke, Mols, Raf, Bullerdiek, Jörn, Van den Berghe, Herman, Van de Ven, Wim J.M

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The recurrent translocation t(5;8)(p13;q12) in pleomorphic adenomas results in upregulation of PLAG1 gene expression under control of the LIFR promoter von VOZ, M. L, ASTRÖM, A.-K, KAS, K, MARK, J, STENMAN, G, VAN DE VEN, W. J. M

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Identification of NFIB as recurrent translocation partner gene of HMGIC in pleomorphic adenomas von GEURTS, J. M. W, SCHOENMAKERS, E. F. P. M, RÖIJER, E, ASTRÖM, A.-K, STENMAN, G, VAN DE VEN, W. J. M

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Allelic knockout of novel splice variants of human recombination repair gene RAD51B in t(12;14) uterine leiomyomas von SCHOENMAKERS, E. F. P. M, HUYSMANS, C, VAN DE VEN, W. J. M

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LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family von PETIT, M. M. R, MOLS, R, SCHOENMAKERS, E. F. P. M, MANDAHL, N, VAN DE VEN, W. J. M

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LHFP, a novel translocation partner gene of HMGIC in a lipoma, is a member of a new family of LHFP-like genes von PETIT, M. M. R, SCHOENMAKERS, E. F. P. M, HUYSMANS, C, GEURTS, J. M. W, MANDAHL, N, VAN DE VEN, W. J. M

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Expression of reciprocal hybrid transcripts of HMGIC and FHIT in a pleomorphic adenoma of the parotid gland von GEURTS, J. M. W, SCHOENMAKERS, E. F. P. M, RÖIJER, E, STENMAN, G, VAN DE VEN, W. J. M

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HMGIC, the gene for an architectural transcription factor, is amplified and rearranged in a subset of human sarcomas von BERNER, J.-M, MEZA-ZEPEDA, L. A, KOOLS, P. F. J, FORUS, A, SCHOENMAKERS, E. F. P. M, VAN DE VEN, W. J. M, FODSTAD, Ø, MYKLEBOST, O

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Identification of Three Mutations and Associated Haplotypes in the Protoporphyrinogen Oxidase Gene in South African Families with Variegate Porphyria von Warnich, Louise, Kotze, Maritha J., Groenewald, Ilse M., Groenewald, Johannes Z., van Brakel, Maléne G., van Heerden, Carel J., de Villiers, J. Nico P., van de Ven, Wim J. M., Schoenmakers, Eric F.P.M., Taketani, Shigeru, Retief, Andries E.

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A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostoses von Debeer, P., Baten, E., Huysmans, C., Van de Ven, W.J.M., Fryns, J.-P., Devriendt, K.

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