Direct Evidence for Epithelial-Mesenchymal Transitions in Breast Cancer von TRIMBOLI, Anthony J, FUKINO, Koichi, OSTROWSKI, Michael C, LEONE, Gustavo, DE BRUIN, Alain, GUO WEI, LEI SHEN, TANNER, Stephan M, CREASAP, Nicholas, ROSOL, Thomas J, ROBINSON, Michael L, ENG, Charis

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Downregulation of Death-Associated Protein Kinase 1 (DAPK1) in Chronic Lymphocytic Leukemia von Raval, Aparna, Tanner, Stephan M., Byrd, John C., Angerman, Elizabeth B., Perko, James D., Chen, Shih-Shih, Hackanson, Björn, Grever, Michael R., Lucas, David M., Matkovic, Jennifer J., Lin, Thomas S., Kipps, Thomas J., Murray, Fiona, Weisenburger, Dennis, Sanger, Warren, Lynch, Jane, Watson, Patrice, Jansen, Mary, Yoshinaga, Yuko, Rosenquist, Richard, de Jong, Pieter J., Coggill, Penny, Beck, Stephan, Lynch, Henry, de la Chapelle, Albert, Plass, Christoph

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Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns von Tanner, Stephan M, Sturm, Amy C, Baack, Elizabeth C, Liyanarachchi, Sandya, de la Chapelle, Albert

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The functional cobalamin (vitamin B12)–intrinsic factor receptor is a novel complex of cubilin and amnionless von Fyfe, John C., Madsen, Mette, Højrup, Peter, Christensen, Erik I., Tanner, Stephan M., de la Chapelle, Albert, He, Qianchuan, Moestrup, Søren K.

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Germline allele-specific expression of DAPK1 in chronic lymphocytic leukemia von Wei, Quan-Xiang, Claus, Rainer, Hielscher, Thomas, Mertens, Daniel, Raval, Aparna, Oakes, Christopher C, Tanner, Stephan M, de la Chapelle, Albert, Byrd, John C, Stilgenbauer, Stephan, Plass, Christoph

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RelA/p65 functions to maintain cellular senescence by regulating genomic stability and DNA repair von Wang, Jingxin, Jacob, Naduparambil K, Ladner, Katherine J, Beg, Amer, Perko, James D, Tanner, Stephan M, Liyanarachchi, Sandya, Fishel, Richard, Guttridge, Denis C

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Heritable polymorphism predisposes to high BAALC expression in acute myeloid leukemia von Eisfeld, Ann-Kathrin, Marcucci, Guido, Liyanarachchi, Sandya, Döhner, Konstanze, Schwind, Sebastian, Maharry, Kati, Leffel, Benjamin, Döhner, Hartmut, Radmacher, Michael D, Bloomfield, Clara D, Tanner, Stephan M, de la Chapelle, Albert

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Acute Myeloid Leukemia with Complex Karyotypes and Abnormal Chromosome 21: Amplification Discloses Overexpression of APP, ETS2, and ERG Genes von Baldus, Claudia D, Liyanarachchi, Sandya, Mrózek, Krzysztof, Auer, Herbert, Tanner, Stephan M, Guimond, Martin, Ruppert, Amy S, Mohamed, Nehad, Davuluri, Ramana V, Caligiuri, Michael A, Bloomfield, Clara D, de la Chapelle, Albert

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Variants in the Netrin-1 Receptor UNC5C Prevent Apoptosis and Increase Risk of Familial Colorectal Cancer von Coissieux, Marie–May, Tomsic, Jerneja, Castets, Marie, Hampel, Heather, Tuupanen, Sari, Andrieu, Nadine, Comeras, Ilene, Drouet, Youenn, Lasset, Christine, Liyanarachchi, Sandya, Mazelin, Laetitia, Puisieux, Alain, Saurin, Jean–Christophe, Scoazec, Jean–Yves, Wang, Qing, Aaltonen, Lauri, Tanner, Stephan M, de la Chapelle, Albert, Bernet, Agnès, Mehlen, Patrick

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Expression Profiling Reveals Fundamental Biological Differences in Acute Myeloid Leukemia with Isolated Trisomy 8 and Normal Cytogenetics von Virtaneva, Kimmo, Wright, Fred A., Tanner, Stephan M., Yuan, Bo, Lemon, William J., Caligiuri, Michael A., Bloomfield, Clara D., de la Chapelle, Albert, Krahe, Ralf

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Hereditary Juvenile Cobalamin Deficiency Caused by Mutations in the Intrinsic Factor Gene von Tanner, Stephan M., Li, Zhongyuan, Perko, James D., Öner, Cihan, Çetin, Mualla, Altay, Çiğdem, Yurtsever, Zekiye, David, Karen L., Faivre, Laurence, Ismail, Essam A., Gräsbeck, Ralph, de la Chapelle, Albert

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Vitamin B12 deficiency in a 15‐year old boy due to mutations in the intrinsic factor gene, GIF von Overgaard, Ulrik M., Tanner, Stephan M., Birgens, Henrik S.

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Juvenile Selective Vitamin B12 Malabsorption: 50 Years After Its Description—10 Years of Genetic Testing von Gräsbeck, Ralph, Tanner, Stephan M

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Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities von Beech, Cameron M, Liyanarachchi, Sandya, Shah, Nidhi P, Sturm, Amy C, Sadiq, May F, de la Chapelle, Albert, Tanner, Stephan M

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BAALC, The Human Member of a Novel Mammalian Neuroectoderm Gene Lineage, is Implicated in Hematopoiesis and Acute Leukemia von Tanner, Stephan M., Austin, Jamie L., Leone, Gustavo, Rush, Laura J., Plass, Christoph, Heinonen, Kristiina, Mrózek, Krzysztof, Sill, Heinz, Knuutila, Sakari, Kolitz, Jonathan E., Archer, Kellie J., Caligiuri, Michael A., Bloomfield, Clara D., de la Chapelle, Albert

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Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the... von Tanner, Stephan M., Li, Zhongyuan, Bisson, Ryan, Acar, Ceren, Öner, Cihan, Öner, Reyhan, Çetin, Mualla, Abdelaal, Mohamed A., Ismail, Essam A., Lissens, Willy, Krahe, Ralf, Broch, Harald, Gräsbeck, Ralph, Chapelle, Albert de la

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Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal Cancer von Valle, Laura, Serena-Acedo, Tarsicio, Liyanarachchi, Sandya, Hampel, Heather, Comeras, Ilene, Li, Zhongyuan, Zeng, Qinghua, Zhang, Hong-Tao, Pennison, Michael J, Sadim, Maureen, Pasche, Boris, Tanner, Stephan M, de la Chapelle, Albert

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miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemia von Eisfeld, Ann-Kathrin, Marcucci, Guido, Maharry, Kati, Schwind, Sebastian, Radmacher, Michael D., Nicolet, Deedra, Becker, Heiko, Mrózek, Krzysztof, Whitman, Susan P., Metzeler, Klaus H., Mendler, Jason H., Wu, Yue-Zhong, Liyanarachchi, Sandya, Patel, Ravi, Baer, Maria R., Powell, Bayard L., Carter, Thomas H., Moore, Joseph O., Kolitz, Jonathan E., Wetzler, Meir, Caligiuri, Michael A., Larson, Richard A., Tanner, Stephan M., de la Chapelle, Albert, Bloomfield, Clara D.

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Molecular cytogenetic characterization of the KG-1 and KG-1a acute myeloid leukemia cell lines by use of spectral karyotyping and fluorescence in situ hybridization von Mrózek, Krzysztof, Tanner, Stephan M., Heinonen, Kristiina, Bloomfield, Clara D.

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Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo von He, Qianchuan, Madsen, Mette, Kilkenney, Adam, Gregory, Brittany, Christensen, Erik I., Vorum, Henrik, Højrup, Peter, Schäffer, Alejandro A., Kirkness, Ewen F., Tanner, Stephan M., de la Chapelle, Albert, Giger, Urs, Moestrup, Søren K., Fyfe, John C.

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