Search Results - "Wilgenbus, K K"

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    DMBT1 , a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours by Mollenhauer, Jan, Wiemann, Stefan, Scheurlen, Wolfram, Korn, Bernhard, Hayashi, Yutaka, Wilgenbus, Klaus K, von Deimling, Andreas, Poustka, Annemarie

    Published in Nature genetics (01-09-1997)
    “…Loss of sequences from human chromosome 10q has been associated with the progression of human cancer. Medulloblastoma and glioblastoma multiforme are the most…”
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    CDNA microarray gene expression analysis of B‐cell chronic lymphocytic leukemia proposes potential new prognostic markers involved in lymphocyte trafficking by Stratowa, Christian, Löffler, Gerald, Lichter, Peter, Stilgenbauer, Stephan, Haberl, Peter, Schweifer, Norbert, Döhner, Hartmut, Wilgenbus, Klaus K.

    Published in International journal of cancer (15-02-2001)
    “…Human cancer is characterized by complex molecular perturbations leading to variable clinical behavior, often even in single‐disease entities. We performed a…”
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  3. 3

    Expression of Cx26, Cx32 and Cx43 gap junction proteins in normal and neoplastic human tissues by Wilgenbus, K K, Kirkpatrick, C J, Knuechel, R, Willecke, K, Traub, O

    Published in International journal of cancer (19-06-1992)
    “…This report concerns the expression of the gap-junction proteins Connexin (Cx)26, 32 and 43 in different malignant and non-malignant human tissues…”
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  4. 4

    DNA chip technology ante portas by WILGENBUS, K. K, LICHTER, P

    “…The recent popularity of DNA chip technology has been fostered by the increasing demand for new diagnostic tools which allow the simultaneous analysis of large…”
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    Mapping of chromosomal imbalances in gastric adenocarcinoma revealed amplified protooncogenes MYCN, MET, WNT2, and ERBB2 by Nessling, Michelle, Solinas-Toldo, Sabina, Wilgenbus, Klaus K., Borchard, Franz, Lichter, Peter

    Published in Genes chromosomes & cancer (01-12-1998)
    “…Gastric adenocarcinoma is a malignant tumor with a high incidence and a low survival rate. In order to identify genetic alterations associated with this tumor,…”
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    Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics by Otaño-Joos, M, Mechtersheimer, G, Ohl, S, Wilgenbus, K K, Scheurlen, W, Lehnert, T, Willeke, F, Otto, H F, Lichter, P, Joos, S

    Published in Cytogenetics and cell genetics (01-01-2000)
    “…Leiomyosarcomas comprise a group of malignant soft-tissue tumors with smooth-muscle differentiation. In this study, 14 cases of leiomyosarcoma were screened…”
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    Molecular Characterization of a Genetically Unstable Region Containing the SMS Critical Area and a Breakpoint Cluster for Human PNETs by Wilgenbus, Klaus K., Seranski, Peter, Brown, Angela, Leuchs, Barbara, Mincheva, Antoaneta, Lichter, Peter, Poustka, Annemarie

    Published in Genomics (San Diego, Calif.) (15-05-1997)
    “…Recently we demonstrated the clustering of deletion breakpoints in the pericentromeric region of human chromosome 17p in human primitive neuroectodermal tumors…”
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    Molecular cloning, cDNA sequence, and chromosomal assignment of the human radixin gene and two dispersed pseudogenes by Wilgenbus, K K, Milatovich, A, Francke, U, Furthmayr, H

    Published in Genomics (San Diego, Calif.) (01-04-1993)
    “…Radixin is a cytoskeletal protein that may be important in linking actin to the plasma membrane. Recent cloning of the murine and porcine radixin cDNAs…”
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    Acute lethal necrotising pancreatitis in childhood systemic lupus erythematosus--possible toxicity of immunosuppressive therapy by Kolk, A, Horneff, G, Wilgenbus, K K, Wahn, V, Gerharz, C D

    Published in Clinical and experimental rheumatology (01-05-1995)
    “…We report on a 16 year old girl with a three-year history of systemic lupus erythematosus who developed a case of acute lethal haemorrhagic pancreatitis. She…”
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  12. 12

    Two fetuses with Fryns syndrome without diaphragmatic defects by Wilgenbus, K K, Engers, R, Crombach, G, Majewski, F

    Published in Journal of medical genetics (01-12-1994)
    “…We report two fetuses with Fryns syndrome including the typical facial appearance and distal limb and lung hypoplasia, but no diaphragmatic hernias. The…”
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    Further evidence that acanthosis nigricans maligna is linked to enhanced secretion by the tumour of transforming growth factor alpha by WILGENBUS, K, LENTNER, A, KUCKELKORN, R, HANDT, S, MITTERMAYER, C

    Published in Archives of Dermatological Research (01-09-1992)
    “…The pathogenesis of cutaneous paraneoplastic syndromes is still under discussion. Since many of these syndromes, including acanthosis nigricans, are…”
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  14. 14

    Structure and localization on the X chromosome of the gene coding for the human filopodial protein moesin (MSN) by Wilgenbus, K K, Hsieh, C L, Lankes, W T, Milatovich, A, Francke, U, Furthmayr, H

    Published in Genomics (San Diego, Calif.) (15-01-1994)
    “…Moesin is a member of a recently discovered family of closely related proteins that includes ezrin, radixin, and merlin. It is widely expressed in different…”
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  15. 15

    Ordering of 66 STSs along the entire short arm of human chromosome 17 and chromosome assignment of a transcribed sequence (FMR1L2) homologous to FMR1 by Wilgenbus, K K, Coy, J F, Mincheva, A, Nicolai, H, Solomon, E, Lichter, P, Poustka, A

    Published in Cytogenetics and cell genetics (01-01-1996)
    “…Sixty-four PCR-markers previously assigned to the short arm of chromosome 17 and two newly established STSs were localized on a hybrid cell-YAC clone panel…”
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    Correlation of clinical data with proteomics profiles in 24 patients with B‐cell chronic lymphocytic leukemia by Voss, Tilman, Ahorn, Horst, Haberl, Peter, Döhner, Hartmut, Wilgenbus, Klaus

    Published in International journal of cancer (15-01-2001)
    “…The development of human cancer is caused by complex molecular perturbations leading to variable clinical behavior often even in single disease entities. To…”
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  17. 17

    Gene expression profiling in drug discovery and development by Stratowa, C, Wilgenbus, K K

    Published in Current opinion in molecular therapeutics (01-12-1999)
    “…Recent advances in technology, especially the merger between molecular biology, automation technology and computer science, are rapidly changing the manner in…”
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    Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q) by Scheurlen, Wolfram G., Schwabe, Georg C., Seranski, Peter, Joos, Stefan, Harbott, Jochen, Metzke, Simone, Döhner, Hartmut, Poustka, Annemarie, Wilgenbus, Klaus, Haas, Oskar A.

    Published in Genes chromosomes & cancer (01-07-1999)
    “…Isochromosomes are monocentric or dicentric chromosomes with homologous arms that are attached in a reverse configuration as mirror images. With an incidence…”
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    Eye changes in acanthosis nigricans maligna--possible effect of growth factors in the etiopathogenesis of this paraneoplastic disease picture by Kuckelhorn, R, Wilgenbus, K, Lentner, A, Reim, M

    “…A 64-year-old white male presented to our hospital with hyperplastic tarsal and to a lesser degree bulbar conjunctivae. Approximately one month later the full…”
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