Sie verwenden einen veralteten Browser, welcher von dieser Website nicht unterstützt wird.
Mit dem Benutzen der Webseite erklären Sie sich der Nutzung von Cookies einverstanden. Weitere Pflichtangaben finden Sie in unserer Datenschutzerklärung. Akzeptieren
Zur Startseite Zur Hauptnavigation Zum Inhalt Zum Kontakt Zur Suche Zur Sitemap
+A-
ENDE
  Menü
Institut für Humangenetik
  Menü
Institut für Humangenetik / Publikationen / 2006

2006

  • Balci S, Engiz O, Aktas D, Vargel I, Beksac MS, Mrasek K, Vermeesch J, Liehr T. Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies. Am J Med Genet A 2006, 140A:628-632
  • Barber JCK, Zhang S, Friend N, Collins AL, Maloney VK, Hastings R, Farren B, Barnicoat A, Polityko AD, Rumyantseva NK, Starke H, Ye S. Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenet Genome Res. 2006, 114:351-358.
  • Bindl R, Bornhöft B, Müller C, Bruchhaus H.: Eine besondere mittelalterliche Bestattung aus der Marienkirche zu Mühlhausen/Thür.
    Mühlhäuser Beiträge 2006, 29:22-34
  • Bindl R, Braun S, Uerlings H, Koppe T, Bruchhaus H: . Methoden der Altersschätzung anhand des Os coxae. Bulletin der Schweizerischen Gesellschaft für Anthropologie 2006, 12:1-12.
  • Bosy-Westphal A, Kromeyer-Hauschild K, Pirlich M, Schlattmann A, Scholz GH, Müller MJ. Körperzusammensetzung . Was kann man wie und mit welchem Wert in der Praxis messen? Aktuel Ernaehr Med 2006, 31:189-195
  • Brecevic L, Michel S, Starke H, Müller K, Kosyakova N, Mrasek K, Weise A, Liehr T. Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Cytogenet Genome Res 2006, 114:270-273.
  • Bruchhaus H, Birkenbeil S, Neumann R, Neubert A, Northe A, Schleier P, Thiele K, Uerlings H. "Löcher im Schädel" - Überlegungen zu einem altbekannten Phänomen (Archäologie und Anthropologie), In: Frühe Spuren der Gewalt - Schädelverletzungen und Wundversorgung an prähistorischen Menschenresten aus interdisziplinärer Sicht ,Hrsg.: Jürgen Piek und Thomas Terberger, Beiträge zur Ur- und Frühgeschichte Mecklenburg-Vorpommerns 2006, 41:115-122
  • Diegmann J, Tomiuk S, Sanjmyatav J, Junker K, Hindermann W, von Eggeling F. Comparative transcriptional and functional profiling of clear cell and papillary renal cell carcinoma. Int J Mol Med 2006, 18:395-403.
  • Diegmann J, Junker K, Loncarevic IF, Michel S, Schimmel B, von Eggeling F. Immune escape for renal cell carcinoma: CD70 mediates apoptosis in lymphocytes. Neoplasia 2006, 8:933-938.
  • Dufke A, Singer S, Borell-Kost S, Stötter M, Pflumm DA, Mau-Holzmann UA, Starke H, Mrasek K, Enders H. De novo structural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies. Cytogenet Genome Res 2006, 114:342-350.
  • Ernst G, Melle C, Schimmel B, Bleul A, von Eggeling F. Proteohistography--Direct Analysis of Tissue with High Sensitivity and High Spatial Resolution Using ProteinChip Technology. J Histochem Cytochem 2006, 54:13-17.
  • Escher N, Spies-Weisshart B, Kaatz M, Melle C, Bleul A, Driesch D, Wollina U, von Eggeling F. Identification of HNP3 as a tumour marker in CD4+ and CD4- lymphocytes of patients with cutaneous T-cell lymphoma. Eur J Cancer 2006,42:249-255.
  • Gross M , Starke M, Trifonov V, Claussen U, Liehr T, Weise A. A molecular cytogenetic study of chromosome evolution in chimpanzee. Cytogenet Genome Res 2006, 112:67-75.
  • Hering A, Guratowska M, Bucsky P, Claussen U, Decker J, Ernst G, Hoeppner W, Michel S, Neumann H, Parlowsky T, Loncarevic I. Characteristic genomic imbalances in pediatric pheochromocytoma. Genes Chromosomes Cancer 2006, 45:602-607.
  • Iourov IY, Liehr T, Vorsanova SG, Kolotii AD, Yurov YB. Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res 2006,14:223-229.
  • Karst C, Trifonov V, Romanenko SA, Claussen U, Mrasek K, Michel S, Avner P, Liehr T. Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes. Int J Mol Med 2006, 17:209-213.
  • Karst C, Gross M, Haase D, Wedding U, Höffken K, Liehr T, Mkrtchyan H. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches. Int J Oncol 2006, 28:891-897.
  • Knoll N, Weise A, Claussen U, Sendt W, Marian B, Glei M, Pool-Zobel BL. 2-Dodecylcyclobutanone, a radiolytic product of palmitic acid, is genotoxic in primary human colon cells and in cells from preneoplastic lesions. Mutat Res 2006, 594:10-19.
  • Knöbel Y, Glei M, Weise A, Osswald K, Schäferhenrich A, Richter KK, Claussen U, Pool-Zobel BL. Uranyl Nitrilotriacetate, a Stabilized Salt of Uranium, is Genotoxic in Nontransformed Human Colon Cells and in the Human Colon Adenoma Cell Line LT97. Toxicol Sci 2006, 93:286-297.
  • Korsten-Reck U, Kromeyer-Hauschild K, Korsten K, Rücker G, Dickhuth HH, Berg A. Freiburg Intervention Trial for Obese Children (FITOC) - Ergebnisse einer Beobachtungsstudie. Deutsche Zeitschrift für Sportmedizin 2006, 2:36-41
  • Kriegova E, Melle C, Kolek V, Hutyrova B, Mrazek F, Bleul A, du Bois RM, von Eggeling F, Petrek M. Protein profiles of bronchoalveolar lavage fluid from patients with pulmonary sarcoidosis. Am J Respir Crit Care Med 2006, 173:1145-1154.
  • Junker K, von Eggeling F, Müller J, Steiner T, Schubert J. [Identification of biomarkers and therapeutic targets for renal cell cancer using ProteinChip technology.] Urologe A 2006, 45:305-315. (German)
  • Liehr T. Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line. Genet Med 2006, 8:459-462.
  • Liehr T. Preface to the special issue Multicolor FISH in Human Cytogenetics. Cytogenet Genome Res 2006, 114:187-188.
  • Liehr T, Gross M, Karst C, Glaser M, Mrasek K, Starke H, Weise A, Mkrtchyan H, Kuechler A. FISH banding in tumor cytogenetics. Cancer Genet Cytogenet 2006, 164:88-89.
  • Liehr T, Mrasek K, Weise A, Dufke A, Rodríguez L, Martínez Guardia N, Sanchís A, Vermeesch JR, Ramel C, Polityko A, Haas O, Anderson J, Claussen U, von Eggeling F, Starke H. Small supernumerary marker chromosomes - progress towards a genotype-phenotype correlation. Cytogenet Genome Res 2006, 112:23-34.
  • Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR. Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC. Am J Med Genet A 2006, 140A:46-51.
  • Liehr T, Starke H, Heller a, Kosyakova n, Mrasek k, Gross m, Karst c, Glaser m, Fickelscher i, Kuechler a, Trifonov v, Romanenko sa, Weise a. Multicolor fluorescence in situ hybridization (FISH) applied for FISH-banding. Cytogenet Genome Res 2006, 114:240-244.
  • Melle C, Bogumil R, Ernst G, Schimmel B, Bleul A, von Eggeling F. Detection and identification of heat shock protein 10 as a biomarker in colorectal cancer by protein profiling. Proteomics 2006, 6:2600-2608.
  • Melle C, Camacho JA, Surber R, Betge S, Von Eggeling F, Zimmer T. Region-specific alterations of global protein expression in the remodelled rat myocardium. Int J Mol Med 2006, 18:1207-1215.
  • Melle C, Ernst G, Schimmel B, Bleul A, Mothes H, Kaufmann R, Settmacher U, Von Eggeling F. Different expression of calgizzarin (S100A11) in normal colonic epithelium, adenoma and colorectal carcinoma. Int J Oncol 2006, 28:195-200.
  • Mitter D, Buiting K, von Eggeling F, Kuechler A, Liehr T, Mau-Holzmann UA, Prott EC, Wieczorek D, Gillessen-Kaesbach G. Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR. Am J Med Genet A 2006, 140A:2039-2049.
  • Mkrtchyan H, Glaser M, Gross M, Wedding U, Höffken K, Liehr T, Karst C, Aroutiounian R. Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2). Cytogenet Genome Res 2006, 114:270-273.
  • Müller U, Ernst G, Melle C, Guthke R, von Eggeling F. Convergence of the proteomic pattern in cancer. Bioinformatics 2006, 22:1293-1296.
  • Papadopoulou E, Sifakis S, Sarri C, Gyftodimou J, Liehr T, Mrasek K, Kalmanti M, Petersen MB. A report of pure 7p duplication syndrome and review of the literature. Am J Med Genet A 2006, 140A:2802-2806.
  • Reichelt O, Müller J, von Eggeling F, Driesch D, Wunderlich H, Schubert J, Grone HJ, Stein G, Ott U, Junker K. Prediction of renal allograft rejection by urinary protein analysis using ProteinChip Arrays (surface-enhanced laser desorption/ionization time-of-flight mass spectrometry). Urology 2006, 67:472-475.
  • Rudolph C, Liehr T, Steinemann D, Emura M, Daibata M, Matsuo Y, Emi N, Abe M, Lai R, Mrasek K, Claussen U, Schlegelberger B. Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanisms. Cytogenet Genome Res 2006, 112:213-221.
  • Sarri C, Gyftodimou Y, Grigoriadou M, Pandelia E, Kalogirou S, Kokotas H, Mrasek K, Weise A, Petersen MB. Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face Cytogenet Genome Res 2006, 114:330-337.
  • Schilling S, Keller U, Sprung CN, Weise A, Grabenbauer GG, Sauer R, Distel L. Breakpoint locations within chromosomes 1, 2, and 4 of patients with increased radiosensitivity. Cancer Genet Cytogenet 2006, 168:1-10.
  • Scholl S, Muller R, Clement JH, Loncarevic IF, Bohmer FD, Höffken K. ATRA can enhance apoptosis that is induced by Flt3 tyrosine kinase inhibition in Flt3-ITD positive cells. Leuk Res 2006, 30:633-642.
  • Siegfried W, Kromeyer-Hauschild K, Zabel G, Siegfried A, Wabitsch M, Holl RW. Stationäre Langzeittherapie der extremen junvenilen Adipositas MMW Fortschr Med 2006, 148:147-151.
  • Siegfried W, Kromeyer-Hauschild K, Zabel G, Siegfried A, Wabitsch M, Holl MW. Studie zur stationären Langzeittherapie der extremen juvenilen Adipositas- Jeder Zweite nimmt langfristig ab. MMW Fortschr Med 2006, 35-36:39-41.
  • Stankiewicz P, Kuechler A, Eller CD, Sahoo T, Baldermann C, Lieser U, Hesse M, Glaser C, Hagemann M, Yatsenko SA, Liehr T, Horsthemke B, Claussen U, Marahrens Y, Lupski JR, Hansmann I. Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation. Am J Med Genet A 2006, 140A:442-452
  • Strehl S, König M, Meyer C, Schneider B, Harbott J, Jager U, von Bergh AR, Loncarevic IF, Jarosova M, Schmidt HH, Moore SD, Marschalek R, Haas OA. Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants. Genes Chromosomes Cancer 2006, 45:1041-1049.
  • Sun F, Oliver-Bonet M, Liehr T, Starke H, Turek P, Ko E, Rademaker A, Martin RH. Variation in MLH1 distribution in recombination maps for individual chromosomes from human males. Hum Mol Genet 2006, 15:2376-2391.
  • Sun F, Oliver-Bonet M, Liehr T, Starke H, Turek P, Ko E, Rademaker A, Martin RH. Analysis of non-crossover bivalents in pachytene cells from 10 normal men. Hum Reprod 2006, 21:2335-2339.
  • Tönnies H, Gerlach A, Heineking B, Starke H, Neitzel H, Neumann LM. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13 Cytogenet Genome Res 2006, 114:325-329.

 

Bücher/ Books

 
T Liehr (Ed.) Special Issue: Multicolor-FISH in Human Cytogenetics, Cytogenet Genome Res. 2006;114(3-4)
T Liehr (Ed.) Special Issue: Multicolor-FISH in Human Cytogenetics, Cytogenet Genome Res. 2006;114(3-4)