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au.\*:("TANNER, Stephan M")

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Juvenile Selective Vitamin B12 Malabsorption: 50 Years After Its Description-10 Years of Genetic TestingGRÄSBECK, Ralph; TANNER, Stephan M.Pediatric research. 2011, Vol 70, Num 3, pp 222-228, issn 0031-3998, 7 p.Article

Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene, GIFOVERGAARD, Ulrik M; TANNER, Stephan M; BIRGENS, Henrik S et al.British journal of haematology. 2010, Vol 150, Num 3, pp 369-371, issn 0007-1048, 3 p.Article

Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo. CommentaryQIANCHUAN HE; MADSEN, Mette; DE LA CHAPELLE, Albert et al.Blood. 2005, Vol 106, Num 4, issn 0006-4971, 1146, 1447-1453 [8 p.]Article

Molecular profiling of chronic lymphocytic leukaemia : genetics meets epigenetics to identify predisposing genesPLASS, Christoph; BYRD, John C; RAVAL, Aparna et al.British journal of haematology. 2007, Vol 139, Num 5, pp 744-752, issn 0007-1048, 9 p.Article

Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in JordanAL-ALAMI, Jamil R; TANNER, Stephan M; TAYEH, Marwan K et al.Saudi medical journal. 2005, Vol 26, Num 7, pp 1061-1064, issn 0379-5284, 4 p.Article

Infrequent Detection of Germline Allele-Specific Expression of TGFBR1 in Lymphoblasts and Tissues of Colon Cancer PatientsGUDA, Kishore; NATALE, Leanna; WILLIS, Joseph et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 12, issn 0008-5472, 4959-4961 [3 p.]Article

Direct Evidence for Epithelial-Mesenchymal Transitions in Breast CancerTRIMBOLI, Anthony J; FUKINO, Koichi; OSTROWSKI, Michael C et al.Cancer research (Baltimore). 2008, Vol 68, Num 3, pp 937-945, issn 0008-5472, 9 p.Article

Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal CancerVALLE, Laura; SERENA-ACEDO, Tarsicio; PASCHE, Boris et al.Science (Washington, D.C.). 2008, Vol 321, Num 5894, pp 1361-1365, issn 0036-8075, 5 p.Article

Allele-specific expression of TGFBR1 in colon cancer patientsTOMSIC, Jerneja; GUDA, Kishore; LIYANARACHCHI, Sandya et al.Carcinogenesis (New York. Print). 2010, Vol 31, Num 10, pp 1800-1804, issn 0143-3334, 5 p.Article

Imerslund-Gräsbeck syndrome in a 15-year-old German girl caused by compound heterozygous mutations in CUBNHAUCK, Fabian H; TANNER, Stephan M; HENKER, Jobst et al.European journal of pediatrics. 2008, Vol 167, Num 6, pp 671-675, issn 0340-6199, 5 p.Article

A high-density SNP genome-wide linkage search of 206 families identifies susceptibility loci for chronic lymphocytic leukemiaTANNER, Stephan M; BYRD, John C; MARTI, Gerald E et al.Blood. 2007, Vol 110, Num 9, issn 0006-4971, 3094-3095, 3326-3333 [10 p.]Article

The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionlessFYFE, John C; MADSEN, Mette; HØJRUP, Peter et al.Blood. 2004, Vol 103, Num 5, pp 1573-1579, issn 0006-4971, 7 p.Article

miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemiaEISFELD, Ann-Kathrin; MARCUCCI, Guido; MENDLER, Jason H et al.Blood. 2012, Vol 120, Num 2, pp 249-258, issn 0006-4971, 10 p.Article

Differential gene expression in patients genetically predisposed to pancreatic cancerZERVOS, Emmanuel E; TANNER, Stephan M; OSBORNE, Dana A et al.The Journal of surgical research. 2006, Vol 135, Num 2, pp 317-322, issn 0022-4804, 6 p.Article

Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemiaTANNER, Stephan M; AMINOFF, Maria; WRIGHT, Fred A et al.Nature genetics. 2003, Vol 33, Num 3, pp 426-429, issn 1061-4036, 4 p.Article

BAALC expression predicts clinical outcome of de novo acute myeloid leukemia patients with normal cytogenetics: a Cancer and Leukemia Group B studyBALDUS, Claudia D; TANNER, Stephan M; ALLEN, Steven L et al.Blood. 2003, Vol 102, Num 5, pp 1613-1618, issn 0006-4971, 6 p.Article

Aberrant promoter methylation of previously unidentified target genes is a common abnormality in medulloblastomas : Implications for tumor biology and potential clinical utilityFRÜHWALD, Michael C; O'DORISIO, M. Sue; ZUNYAN DAI et al.Oncogene (Basingstoke). 2001, Vol 20, Num 36, pp 5033-5042, issn 0950-9232Article

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