Human health implications of nanomaterial exposure von Papp, Thilo, Schiffmann, Dietmar, Weiss, Dieter, Castranova, Vince, Vallyathan, Val, Rahman, Qamar

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Mutational analysis of the BRAF gene in human congenital and dysplastic melanocytic naevi von Papp, Thilo, Schipper, Holger, Kumar, Krishan, Schiffmann, Dietmar, Zimmermann, Regina

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Mutational analysis of Chk1, Chk2, Apaf1 and Rb1 in human malignant melanoma cell lines von Papp, Thilo, Niemetz, Annett, Dosdahl, Nils, Kumar, Krishan, Schiffmann, Dietmar

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Reduction of chrysotile asbestos-induced genotoxicity in human peripheral blood lymphocytes by garlic extract von Bhattacharya, Kunal, Yadava, Santosh, Papp, Thilo, Schiffmann, Dietmar, Rahman, Qamar

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Mutational analysis of Chkl, Chk2, Apaf1 and Rb1 in human malignant melanoma cell lines von PAPP, Thilo, NIEMETZ, Annett, DOSDAHL, Nils, KUMAR, Krishan, SCHIFFMANN, Dietmar

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Lack of p53 mutations and loss of heterozygosity in non-cultured human melanocytic lesions von PAPP, T, JAFARI, M, SCHIFFMANN, D

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Analysis of ras mutations in human melanocytic lesions : activation of the ras gene seems to be associated with the nodular type of human malignant melanoma von JAFARI, M, PAPP, T, KIRCHNER, S, DIENER, U, HENSCHLER, D, BURG, G, SCHIFFMANN, D

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Detection of hyperdiploidy and chromosome breakage affecting the 1 (1cen-q12) region in lentigo malignant melanoma (LMM), superficial spreading melanoma (SSM) and congenital nevus... von Dopp, Elke, Papp, Thilo, Schiffmann, Dietmar

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Lack ofp53 mutations and loss of heterozygosity in non-cultured human melanocytic lesions von Papp, Thilo, Jafari, Mehrdad, Schiffmann, Dietmar

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Differentiation Between Papillary and Nonpapillary Renal Cell Carcinomas by DNA Analysis von Kovacs, Gyula, Wilkens, Ludwig, Papp, Thilo, Riese, Werner de

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Mutational analysis of the N-ras,p53,p16INK4a ,CDK4, and MC1R genes in human congenital melanocytic naevi von Papp, Thilo, Pemsel, Heidi, Zimmermann, Regina, Bastrop, Ralf, Weiss, Dieter G, Schiffmann, Dietmar

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Mutation screening method comprises coupling single strand conformation polymorphism (SSCP) and denaturing gradient gel electrophoresis (DGGE) von PAPP, THILO

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Acil and BstNI/Cfrl detect all possible activating point mutations at codons 13 and 61 of the human H-ras oncogene von Papp, Thilo, Jafari, Mehrdad, Kopp, Corinna, Schiffmann, Dietmar

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Cloning of PCR fragments with a modified M13mp18 T-vector von Papp, Thilo, Kirchner, Stephan, Diener, Ulrike, Jafari, Mehrdad, Golka, Antje, Schiffmann, Dietmar

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Aci l and Bst NI/ Cfr l detect all possible activating point mutations at codons 13 and 61 of the human H-ras oncogene von Papp, Thilo, Jafari, Mehrdad, Kopp, Corinna, Schiffmann, Dietmar

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Modified ASRA facilitates the characterization of activating point mutations in tumors, in which cancer cells constitute only a minor part of the investigated tissue von Papp, T, Jafari, M, Diener, U, Dudley, N, Schiffmann, D

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Analysis ofras mutations in human melanocytic lesions: activation of theras gene seems to be associated with the nodular type of human malignant melanoma von Jafari, Mehrdad, Papp, Thilo, Kirchner, Stephan, Kiener, Ulrike, Henschler, Dietrich, Burg, Günter, Schiffmann, Dietmar

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Simultaneous detection of homozygous deletion and point mutations in tumor suppressor genes p16 and p53 by multiplex-PCR/SSCP analysis von Papp, Thilo, Pemsel, Heidi, Weiss, Dieter G., Schiffmann, Dietmar

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AciI and BstNI/CfrI detect all possible activating point mutations at codons 13 and 61 of the human H-ras oncogene von PAPP, T, FAJARI, M, KOPP, C, SCHIFFMANN, D

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Verfahren zur Kopplung von SSCP und DGGE zur verbesserten Erkennung von Punktmutationen von PAPP, THILO

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