ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy von Müllenbach, R, Bennett, A, Tetlow, N, Patel, N, Hamilton, G, Cheng, F, Chambers, J, Howard, R, Taylor-Robinson, S D, Williamson, C

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ABCB4 gene sequence variation in women with intrahepatic cholestasis of pregnancy von Müllenbach, R, Linton, K J, Wiltshire, S, Weerasekera, N, Chambers, J, Elias, E, Higgins, C F, Johnston, D G, McCarthy, M I, Williamson, C

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369 PHENOTYPIC AND EXPRESSION QUANTITATIVE TRAIT LOCI (P/EQTLS) AFFECTING LIVER FIBROSIS BY GENOME-WIDE ASSOCIATION ANALYSIS IN RECOMBINANT INBRED MOUSE LINES von Hall, R, Müllenbach, R, Huss, S, Alberts, R, Schughart, K, Hochrath, K, Weber, S.N, Williams, R.W, Lammert, F

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381 DLL4 AND JAGGED-1 PROVIDE OPPOSING EFFECTS IN LIVER FIBROSIS von Liu, Y, Shen, Z, Xu, M.-Y, Meyer, C, Müller, A, Munker, S, Li, Q, Ilkavets, I, Stump, C, Müllenbach, R, Zimmer, V, Lammert, F, Mertens, P.R, Li, J, Li, Y.-M, Lu, L.-G, Dooley, S, Weng, H.-L

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Severe hepatocellular dysfunction in obstetric cholestasis related to combined genetic variation in hepatobiliary transporters von Zimmer, V, Krawczyk, M, Mahler, M, Weber, S N, Müllenbach, R, Lammert, F

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120 IFN-G INHIBITS HEPATIC PROGENITOR CELL ACTIVATION IN CHRONIC LIVER DAMAGE von Weng, H.-L, Radaeva, S, Liu, Y, Li, Q, Shen, H, Müllenbach, R, Zimmer, V, Lammert, F, Mertens, P, Zakhari, S, Dooley, S, Gao, B

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Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome : evidence for a common mechanism of chromosome breakage von JONES, C, MÜLLENBACH, R, GROSSFELD, P, AUER, R, FAVIER, R, CHIEN, K, JAMES, M, TUNNACLIFFE, A, COTTER, F

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An efficient salt-chloroform extraction of DNA from blood and tissues von Müllenbach, R, Lagoda, P J, Welter, C

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Extranodal Marginal Zone B-Cell Lymphoma Genotyping by Alu - Polymerase Chain Reaction von Bertoni, Francesco, Müllenbach, Roman, Broggini, Massimo, Roggero, Enrico, Cavalli, Franco, Cotter, Finbarr E., Zucca, Emanuele

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Cosmid-derived transcripts and sequence tags mapped to three subregions of human chromosome 22 von Pusch, Carsten, Müllenbach, Roman, Gött, Peter, Schmitt, Holger, Wang, Zhili, Roe, Bruce, Blin, Nikolaus

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A 5.5-Mb High-Resolution Integrated Map of Distal 11q13 von Merscher, Sandra, Bekri, Soumeya, de Leeuw, Bertie, Pedeutour, Florence, Grosgeorge, Josiane, Shows, Thomas B., Müllenbach, Roman, Paslier, Denis Le, Nowak, Norma J., Gaudray, Patrick

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PCR expression analysis of the estrogen-inducible gene BCEI in gastrointestinal and other human tumors von Wundrack, I, Müllenbach, R, Welter, C, Seitz, G, Blin, N

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Role for CCG-trinucleotide repeats in the pathogenesis of chronic lymphocytic leukemia von Auer, Rebecca L., Jones, Christopher, Mullenbach, Roman A., Syndercombe-Court, Denise, Milligan, Donald W., Fegan, Christopher D., Cotter, Finbarr E.

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Expressed sequences within pericentromeric heterochromatin of human chromosome 22 von Blin, N, Scholz, M, Wissinger, B, Müllenbach, R, Pusch, C

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DNA fingerprinting of low-grade extranodal marginal zone B-cell lymphoma (of MALT type) von Bertoni, F., Müllenbach, R., Roggero, E., De Boni, M., Cavalli, F., Cotter, F.E., Zucca, E.

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Distribution and linkage of repetitive clusters from the heterochromatic region of human chromosome 22 von Müllenbach, R, Pusch, C, Holzmann, K, Suijkerbuijk, R, Blin, N

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Debrisoquine hydroxylase gene polymorphism in meningioma von Wundrack, I, Meese, E, Müllenbach, R, Blin, N

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A polymorphic DNA probe (D22S263) mapping to 22q12.1-q13.1 von FALDEY, A, MÜLLENBACH, R, HERZOG, R, BLIN, N

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A non-alphoid repetitive DNA sequence from human chromosome 21 von MÜLLENBACH, R, LUTZ, S, HOLZMANN, K, DOOLEY, S, BLIN, N

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Patient Blood Management in der Herzchirurgie von Meybohm, P., Muellenbach, R. M., Keller, H., Fichtlscherer, S., Papadopoulos, N., Spahn, D. R., Greinacher, A., Zacharowski, K.

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