Search Results - "Oberthur, A"

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    Integrated genomic profiling identifies two distinct molecular subtypes with divergent outcome in neuroblastoma with loss of chromosome 11q by Fischer, M, Bauer, T, Oberthür, A, Hero, B, Theissen, J, Ehrich, M, Spitz, R, Eils, R, Westermann, F, Brors, B, König, R, Berthold, F

    Published in Oncogene (11-02-2010)
    “…Imbalances in chromosome 11q occur in approximately 30% of primary neuroblastoma and are associated with poor outcome. It has been suggested that 11q loss…”
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    Risk estimation of neuroblastoma patients using molecular markers by Fischer, M, Spitz, R, Oberthür, A, Westermann, F, Berthold, F

    Published in Klinische Pädiatrie (01-05-2008)
    “…The pediatric tumor neuroblastoma is a heterogeneous disease: Patients' clinical courses can range from spontaneous regression to fatal progression of the…”
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    Cloning and characterization of a porcine protein kinase gene and relationship to a class of heat shock proteins by König, B, Seehaus, B, Bangsow, T, Oberthür, A, Henninger, J, Weber, P, Schepelmann, S, Wollny, E, Gassen, H G

    Published in DNA and cell biology (01-11-1997)
    “…We have determined the genomic sequence of a porcine protein kinase (PPK) gene, including 1,844 bp upstream of the transcription initiation site. The gene…”
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    Identification of a gene selectively expressed in the brain, which encodes a putative transmembrane protein and a soluble cytoplasmic isoform by Bangsow, Thorsten, Schepelmann, Silke, Martin, Carmen, May, Monika, Oberthür, Angela, Perl, Sabine, Knüpfer, Ellen, Zinke, Holger, Gassen, Hans G.

    Published in European journal of biochemistry (15-08-1998)
    “…Subtractive cloning procedures led to the identification of a variety of transcripts expressed in mammalian brain. However, little is known about the encoded…”
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    Smith-Lemli-Opitz syndrome--case report, diagnostics and therapeutic options by Oberthür, A, Heller, R, Vogel, M, Körber, F, Rahimi, G, Hoopmann, M, Emmel, M, Roth, B, Vierzig, A

    “…Smith-Lemli-Opitz syndrome (SLOS) is an autosomal-recessive disease characterised by the combination of (foetal) growth retardation, mental retardation and a…”
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