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Publications by Popp, Susanne

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Number of items: 13.

Journal article

Manoir, Stanislas du; Speicher, Michael R.; Joos, Stefan; Schröck, Evelin; Popp, Susanne; Döhner, Hartmut; Kovacs, Gyula; Robert-Nicoud, Michel; Lichter, Peter; Cremer, Thomas (1993): Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. In: Human Genetics, Vol. 90, No. 6: pp. 590-610 [PDF, 2MB]

Popp, Susanne; Jauch, Anna; Schindler, Detlev; Speicher, Michael R.; Lengauer, Christoph; Donis-Keller, Helen; Riethman, Harold C.; Cremer, Thomas (1993): A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones. In: Human Genetics, Vol. 92, No. 6: pp. 527-532 [PDF, 2MB]

Lengauer, Christoph; Speicher, Michael R.; Popp, Susanne; Jauch, Anna; Taniwaki, Masafumi; Nagaraja, Ramaiah; Riethman, Harold C.; Donis-Keller, Helen; D'Urso, Michele; Schlessinger, David; Cremer, Thomas (1993): Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probes. In: Human Molecular Genetics, Vol. 2: pp. 505-512 [PDF, 1MB]

Taniwaki, Masafumi; Speicher, Michael R.; Lengauer, Christoph; Jauch, Anna; Popp, Susanne; Cremer, Thomas (1993): Characterization of two marker chromosomes in a patient with acute nonlymphocytic leukemia by two-color fluorescence in situ hybridization. In: Cancer Genetics and Cytogenetics, Vol. 70, No. 2: pp. 99-102 [PDF, 471kB]

Wessman, M.; Popp, Susanne; Ruutu, Tapani; Volin, L.; Cremer, Thomas; Knuutila, Sakari (1993): Detection of residual host cells after bone marrow transplantation using non-isotopic in situ hybridization. In: Bone Marrow Transplantation, Vol. 11: pp. 279-284 [PDF, 3MB]

Tiainen, Marianne; Knuutila, Sakari; Popp, Susanne; Emmerich, Patricia; Cremer, Thomas; Parlier, Valerie; Jotterand Bellomo, Martine; Ruutu, Tapani (1992): Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies. In: Genes, Chromosomes and Cancer, Vol. 4, No. 2: pp. 135-140 [PDF, 661kB]

Popp, Susanne; Cremer, Thomas (1992): Development of a Biological Dosimeter for Translocation Scoring Based on Two-Color Fluorescence in Situ Hybridization of Chromosome Subsets. In: Journal of Radiation Research, Vol. 33: pp. 61-70 [PDF, 536kB]

Popp, Susanne; Jauch, Anna; Qiu, Jing Ying; Smialek, Barbara; Cremer, Thomas; Becher, Reinhard (1991): Translocation (8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization. In: Cancer Genetics and Cytogenetics, Vol. 57, No. 1: pp. 103-107 [PDF, 295kB]

Popp, Susanne; Scholl, Hans Peter; Loos, Peter; Jauch, Anna; Stelzer, Ernst; Cremer, Christoph; Cremer, Thomas (1990): Distribution of chromosome 18 and X centric heterochromatin in the interphase nucleus of cultured human cells. In: Experimental Cell Research, Vol. 189, No. 1: pp. 1-12 [PDF, 5MB]

Cremer, Thomas; Popp, Susanne; Emmerich, Patricia; Lichter, Peter; Cremer, Christoph (1990): Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization. In: Cytometry, Vol. 11, No. 1: pp. 110-118 [PDF, 1MB]

Popp, Susanne; Remm, B.; Hausmann, Michael; Lührs, H.; van Kaick, G.; Cremer, Thomas; Cremer, Christoph (1990): Towards a cumultative biological dosimeter based on chromosome painting and digital image analysis. In: Kerntechnik, Vol. 55, No. 4: pp. 204-210 [PDF, 2MB]

Book Section

Cremer, Christoph; Hausmann, Michael; Popp, Susanne; Cremer, Thomas (1993): Analyse von Strahlenschäden in menschlichen Metaphasechromosomen nach fluoreszenz in situ Hybridisierung. In: Arndt, Dietrich (ed.) : Zytogenetische Methoden. BGA-Schriften, Vol. 3. München: MMV. pp. 27-32 [PDF, 1MB]

Cremer, Thomas; Lichter, Peter; Popp, Susanne; Schröck, Evelin; Jauch, Anna; Manoir, Stanislas du; Joos, Stefan; Lengauer, Christoph; Scherthan, Harry; Ried, Thomas; Speicher, Michael R. (1993): Detection of genetic imbalances in tumor genomes by fluorescence in situ hybridization with tumor genomic DNA and subregional DNA probes. In: Obe, Günter; Natarajan, Adayapalam T. (eds.) : Chromosomal alterations. Berlin u.a.: Springer. pp. 42-49 [PDF, 1MB]

This list was generated on Thu Dec 5 05:31:19 2019 CET.