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La ricerca find articoli where authors phrase all words ' WILGENBUS KK' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 12 riferimenti
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    1. Stratowa, C; Loffler, G; Lichter, P; Stilgenbauer, S; Haberl, P; Schweifer, N; Dohner, H; Wilgenbus, KK
      cDNA microarray gene expression analysis of B-cell chronic lymphocytic leukemia proposes potential new prognostic markers involved in lymphocyte trafficking

      INTERNATIONAL JOURNAL OF CANCER
    2. Otano-Joos, M; Mechtersheimer, G; Ohl, S; Wilgenbus, KK; Scheurlen, W; Lehnert, T; Willeke, F; Otto, HF; Lichter, P; Joos, S
      Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics

      CYTOGENETICS AND CELL GENETICS
    3. Wilgenbus, KK; Lichter, P
      DNA chip technology ante portas

      JOURNAL OF MOLECULAR MEDICINE-JMM
    4. NESSLING M; SOLINASTOLDO S; WILGENBUS KK; BORCHARD F; LICHTER P
      MAPPING OF CHROMOSOMAL IMBALANCES IN GASTRIC ADENOCARCINOMA REVEALED AMPLIFIED PROTOONCOGENES MYCN, MET, WNT2, AND ERBB2

      Genes chromosomes & cancer (Print)
    5. MOLLENHAUER J; WIEMANN S; SCHEURLEN W; KORN B; HAYASHI Y; WILGENBUS KK; VONDEIMLING A; POUSTKA A
      DMBT1, A NEW MEMBER OF THE SRCR SUPERFAMILY, ON CHROMOSOME 10Q25.3-26.1 IS DELETED IN MALIGNANT BRAIN-TUMORS

      Nature genetics
    6. SCHEURLEN WG; SERANSKI P; MINCHEVA A; KUHL J; SORENSEN N; KRAUSS J; LICHTER P; POUSTKA A; WILGENBUS KK
      HIGH-RESOLUTION DELETION MAPPING OF CHROMOSOME ARM 17P IN CHILDHOOD PRIMITIVE NEUROECTODERMAL TUMORS REVEALS A COMMON CHROMOSOMAL DISRUPTION WITHIN THE SMITH-MAGENIS REGION, AN UNSTABLE REGION IN CHROMOSOME BAND 17P11.2

      Genes, chromosomes & cancer
    7. WILGENBUS KK; SERANSKI P; BROWN A; LEUCHS B; MINCHEVA A; LICHTER P; POUSTKA A
      MOLECULAR CHARACTERIZATION OF A GENETICALLY UNSTABLE REGION CONTAINING THE SMS CRITICAL AREA AND A BREAKPOINT CLUSTER FOR HUMAN PNETS

      Genomics
    8. WILGENBUS KK; COY JF; MINCHEVA A; NICOLAI H; SOLOMON E; LICHTER P; POUSTKA A
      ORDERING OF 66 STSS ALONG THE ENTIRE SHORT ARM OF HUMAN-CHROMOSOME-17AND CHROMOSOME ASSIGNMENT OF A TRANSCRIBED SEQUENCE (FMR1L2) HOMOLOGOUS TO FMR1

      Cytogenetics and cell genetics
    9. KOLK A; HORNEFF G; WILGENBUS KK; WAHN V; GERHARZ CD
      ACUTE LETHAL NECROTIZING PANCREATITIS IN CHILDHOOD SYSTEMIC LUPUS-ERYTHEMATOSUS - POSSIBLE TOXICITY OF IMMUNOSUPPRESSIVE THERAPY

      Clinical and experimental rheumatology
    10. WILGENBUS KK; HSIEH CL; LANKES WT; MILATOVICH A; FRANCKE U; FURTHMAYR H
      STRUCTURE AND LOCALIZATION ON THE X-CHROMOSOME OF THE GENE CODING FORTHE HUMAN FILOPODIAL PROTEIN MOESIN (MSN)

      Genomics
    11. WILGENBUS KK; ENGERS R; CROMBACH G; MAJEWSKI F
      2 FETUSES WITH FRYNS-SYNDROME WITHOUT DIAPHRAGMATIC DEFECTS

      Journal of Medical Genetics
    12. AMIEVA MR; WILGENBUS KK; FURTHMAYR H
      RADIXIN IS A COMPONENT OF HEPATOCYTE MICROVILLI IN-SITU

      Experimental cell research


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/08/20 alle ore 11:14:13