Uwe Claussen

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Erlecke Jörn; Hartmann Isabell; Hoffmann Martin; Kroll Torsten; Starke Heike; Heller Anita; Gloria Alexander; Sayer Herbert G; Johannes Tilman; Claussen Uwe; Liehr Thomas; Loncarevic Ivan F
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells.
Kosyakova Nadezda; Weise Anja; Mrasek Kristin; Claussen Uwe; Liehr Thomas; Nelle Heike
The hierarchically organized splitting of chromosomal bands for all human chromosomes.
Weise Anja; Mrasek Kristin; Fickelscher Ina; Claussen Uwe; Cheung Sau Wai; Cai Wei Wen; Liehr Thomas; Kosyakova Nadezda
Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set.

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2009: Erlecke Jörn; Hartmann Isabell; Hoffmann Martin; Kroll Torsten; Starke Heike; Heller Anita; Gloria Alexander; Sayer Herbert G; Johannes Tilman; Claussen Uwe; Liehr Thomas; Loncarevic Ivan F
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells.
Molecular Cytogenetics 2009;2():12.
2009: Kosyakova Nadezda; Weise Anja; Mrasek Kristin; Claussen Uwe; Liehr Thomas; Nelle Heike
The hierarchically organized splitting of chromosomal bands for all human chromosomes.
Molecular Cytogenetics 2009;2():4.
2008: Weise Anja; Mrasek Kristin; Fickelscher Ina; Claussen Uwe; Cheung Sau Wai; Cai Wei Wen; Liehr Thomas; Kosyakova Nadezda
Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2008;56(5):487-93.
2008: Weise A; Gross M; Mrasek K; Mkrtchyan H; Horsthemke B; Jonsrud C; Von Eggeling F; Hinreiner S; Witthuhn V; Claussen U; Liehr T
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level.
International journal of molecular medicine 2008;21(2):189-200.
2007: Knöbel Y; Weise A; Glei M; Sendt W; Claussen U; Pool-Zobel B L
Ferric iron is genotoxic in non-transformed and preneoplastic human colon cells.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 2007;45(5):804-11.
2007: Melle Christian; Ernst Günther; Escher Niko; Hartmann Daniel; Schimmel Bettina; Bleul Annett; Thieme Heike; Kaufmann Roland; Felix Klaus; Friess Helmut M; Settmacher Utz; Hommann Merten; Richter Konrad K; Daffner Wolfgang; Täubig Horst; Manger Thomas; Claussen Uwe; von Eggeling Ferdinand
Protein profiling of microdissected pancreas carcinoma and identification of HSP27 as a potential serum marker.
Clinical chemistry 2007;53(4):629-35.
2007: Glei Michael; Schaeferhenrich Anja; Claussen Uwe; Kuechler Alma; Liehr Thomas; Weise Anja; Marian Brigitte; Sendt Wolfgang; Pool-Zobel Beatrice L
Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genes.
Toxicological sciences : an official journal of the Society of Toxicology 2007;96(2):279-84.
2007: Weise Anja; Gross Madeleine; Schmidt Sabine; Reichelt Franziska; Claussen Uwe; Liehr Thomas
New aspects of chromosomal evolution in the gorilla and the orangutan.
International journal of molecular medicine 2007;19(3):437-43.
2007: Melle Christian; Ernst Günther; Scheibner Olaf; Kaufmann Roland; Schimmel Bettina; Bleul Annett; Settmacher Utz; Hommann Merten; Claussen Uwe; von Eggeling Ferdinand
Identification of specific protein markers in microdissected hepatocellular carcinoma.
Journal of proteome research 2007;6(1):306-15.
2007: Felka T; Lemke J; Lemke C; Michel S; Liehr T; Claussen U
DNA degradation during maturation of erythrocytes - molecular cytogenetic characterization of Howell-Jolly bodies.
Cytogenetic and genome research 2007;119(1-2):2-8.
2006: Knöbel Yuonne; Glei Michael; Weise Anja; Osswald Kerstin; Schäferhenrich Anja; Richter Konrad Klaus; Claussen Uwe; Pool-Zobel Beatrice Louise
Uranyl nitrilotriacetate, a stabilized salt of uranium, is genotoxic in nontransformed human colon cells and in the human colon adenoma cell line LT97.
Toxicological sciences : an official journal of the Society of Toxicology 2006;93(2):286-97.
2006: Hering Antje; Guratowska Monika; Bucsky Peter; Claussen Uwe; Decker Jochen; Ernst Guenther; Hoeppner Wolfgang; Michel Susanne; Neumann Hartmut; Parlowsky Thomas; Loncarevic Ivan
Characteristic genomic imbalances in pediatric pheochromocytoma.
Genes, chromosomes & cancer 2006;45(6):602-7.
2006: Stankiewicz Pawel; Kuechler Alma; Eller C Daniel; Sahoo Trilochan; Baldermann Christiane; Lieser Ulla; Hesse Martin; Gläser Christiane; Hagemann Monika; Yatsenko Svetlana A; Liehr Thomas; Horsthemke Bernhard; Claussen Uwe; Marahrens York; Lupski James R; Hansmann Ingo
Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.
American journal of medical genetics. Part A 2006;140(5):442-52.
2006: Karst Constanze; Trifonov Vladimir; Romanenko Svetlana A; Claussen Uwe; Mrasek Kristin; Michel Susanne; Avner Philip; Liehr Thomas
Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes.
International journal of molecular medicine 2006;17(2):209-13.
2006: Knoll Nadine; Weise Anja; Claussen Uwe; Sendt Wolfgang; Marian Brigitte; Glei Michael; Pool-Zobel Beatrice L
2-Dodecylcyclobutanone, a radiolytic product of palmitic acid, is genotoxic in primary human colon cells and in cells from preneoplastic lesions.
Mutation research 2006;594(1-2):10-9.
2006: Gross M; Starke H; Trifonov V; Claussen U; Liehr T; Weise A
A molecular cytogenetic study of chromosome evolution in chimpanzee.
Cytogenetic and genome research 2006;112(1-2):67-75.
2006: Liehr T; Mrasek K; Weise A; Dufke A; Rodríguez L; Martínez Guardia N; Sanchís A; Vermeesch J R; Ramel C; Polityko A; Haas O A; Anderson J; Claussen U; von Eggeling F; Starke H
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
Cytogenetic and genome research 2006;112(1-2):23-34.
2005: Kautenburger Tanja; Beyer-Sehlmeyer Gabriele; Festag Grit; Haag Natja; Kühler Stephanie; Küchler Alma; Weise Anja; Marian Brigitte; Peters Wilbert H M; Liehr Thomas; Claussen Uwe; Pool-Zobel Beatrice L
The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells.
Journal of cancer research and clinical oncology 2005;131(10):692-700.
2005: Weise Anja; Liehr Thomas; Claussen Uwe; Halbhuber Karl-Jürgen
Increased efficiency of fluorescence in situ hybridization (FISH) using the microwave.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(10):1301-3.
2005: Melle Christian; Ernst Günther; Schimmel Bettina; Bleul Annett; Kaufmann Roland; Hommann Merten; Richter Konrad K; Daffner Wolfgang; Settmacher Utz; Claussen Uwe; von Eggeling Ferdinand
Characterization of pepsinogen C as a potential biomarker for gastric cancer using a histo-proteomic approach.
Journal of proteome research 2005;4(5):1799-804.
2005: Karst Constanze; Heller Anita; Claussen Uwe; Gebhart Erich; Liehr Thomas
Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia.
International journal of oncology 2005;27(2):355-9.
2005: Melle Christian; Ernst Günther; Schimmel Bettina; Bleul Annett; Thieme Heike; Kaufmann Roland; Mothes Henning; Settmacher Utz; Claussen Uwe; Halbhuber Karl-Jürgen; Von Eggeling Ferdinand
Discovery and identification of alpha-defensins as low abundant, tumor-derived serum markers in colorectal cancer.
Gastroenterology 2005;129(1):66-73.
2005: Schmidt S; Claussen U; Liehr T; Weise A
Evolution versus constitution: differences in chromosomal inversion.
Human genetics 2005;117(2-3):213-9.
2005: Trifonov Vladimir; Karst Constanze; Claussen Uwe; Mrasek Kristin; Michel Susanne; Avner Philip; Liehr Thomas
Microdissection-derived murine mcb probes from somatic cell hybrids.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(6):791-2.
2005: Schreyer Isolde; Neumann Annett; Beensen Volkmar; Eichhorn Karl-Heinz; Heller Anita; Claussen Uwe; Liehr Thomas
Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotype.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):365-6.
2005: Kuechler Alma; Ziegler Monika; Blank Cornelia; Rommel Birgit; Bullerdiek Joern; Ahrens Jochen; Claussen Uwe; Liehr Thomas
A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):355-7.
2005: Busch Anne; Michel Susanne; Hoppe Constance; Driesch Dominik; Claussen Uwe; von Eggeling Ferdinand
Proteome analysis of maternal serum samples for trisomy 21 pregnancies using ProteinChip arrays and bioinformatics.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):341-3.
2005: Junker Kerstin; Gneist Jana; Melle Christian; Driesch Dominik; Schubert Joerg; Claussen Uwe; Von Eggeling Ferdinand
Identification of protein pattern in kidney cancer using ProteinChip arrays and bioinformatics.
International journal of molecular medicine 2005;15(2):285-90.
2005: Liehr T; Mrasek K; Starke H; Claussen U; Schreiber G
Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
Cytogenetic and genome research 2005;111(2):179-81.
2005: Polityko A; Starke H; Rumyantseva N; Claussen U; Liehr T; Raskin S
Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.
Cytogenetic and genome research 2005;111(2):171-4.
2005: Claussen U
Chromosomics.
Cytogenetic and genome research 2005;111(2):101-6.
2005: Weise A; Starke H; Mrasek K; Claussen U; Liehr T
New insights into the evolution of chromosome 1.
Cytogenetic and genome research 2005;108(1-3):217-22.
2004: Liehr Thomas; Heller Anita; Eichhorn Karl-Heinz; Beensen Volkmar; Schulze Eberhart; Starke Heike; Claussen Uwe; Schreyer Isolde
Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).
Prenatal diagnosis 2004;24(12):1022-4.
2004: Polityko Anna; Maltseva Olga; Rumyantseva Natalia; Khurs Olga; Seidel Jörg; Claussen Uwe; Weise Anja; Liehr Thomas; Starke Heike
Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.
International journal of molecular medicine 2004;14(6):977-9.
2004: Liehr T; Starke H; Weise A; Lehrer H; Claussen U
Multicolor FISH probe sets and their applications.
Histology and histopathology 2004;19(1):229-37.
2004: Heller Anita; Loncarevic Ivan F; Glaser Melanie; Gebhart Erich; Trautmann Udo; Claussen Uwe; Liehr Thomas
Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints.
International journal of oncology 2004;24(1):127-36.
2004: Heller Anita; Fricke Hans-Joerg; Starke Heike; Loncarevic Ivan F; Claussen Uwe; Liehr Thomas
Characterization of a highly aberrant plasma cell leukemia karyotype: a case report.
Oncology reports 2004;11(1):89-92.
2004: Liehr T; Claussen U; Starke H
Small supernumerary marker chromosomes (sSMC) in humans.
Cytogenetic and genome research 2004;107(1-2):55-67.
2004: Lehrer H; Weise A; Michel S; Starke H; Mrasek K; Heller A; Kuechler A; Claussen U; Liehr T
The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB).
Cytogenetic and genome research 2004;105(1):25-8.
2004: Liehr T; Hickmann G; Kozlowski P; Claussen U; Starke H
Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2004;12(3):239-44.
2003: Starke Heike; Nietzel Angela; Weise Anja; Heller Anita; Mrasek Kristin; Belitz Britta; Kelbova Christine; Volleth Marianne; Albrecht Beate; Mitulla Beate; Trappe Ralf; Bartels Iris; Adolph Sabine; Dufke Andreas; Singer Sylke; Stumm Markus; Wegner Rolf-Dieter; Seidel Jörg; Schmidt Angela; Kuechler Alma; Schreyer Isolde; Claussen Uwe; von Eggeling Ferdinand; Liehr Thomas
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Human genetics 2003;114(1):51-67.
2003: Oliver-Bonet Maria; Liehr Thomas; Nietzel Angela; Heller Anita; Starke Heike; Claussen Uwe; Codina-Pascual Montserrat; Pujol Aïda; Abad Carlos; Egozcue Josep; Navarro Joaquima; Benet Jordi
Karyotyping of human synaptonemal complexes by cenM-FISH.
European journal of human genetics : EJHG 2003;11(11):879-83.
2003: Heller Anita; Trifonov Vladimir; Rubtsov Nikolai; Sauerbrey Axel; Starke Heike; Loncarevic Ivan F; Claussen Uwe; Liehr Thomas
Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS.
Oncology reports 2003;10(6):1789-92.
2003: Heller Anita; Brecevic Lukrecija; Glaser Melanie; Loncarevic Ivan; Gebhart Erich; Claussen Uwe; Liehr Thomas
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations.
Cancer genetics and cytogenetics 2003;146(1):81-3.
2003: Starke Heike; Mitulla Beate; Beensen Volkmar; Trifonov Vladimir; Rubtsov Nikolai; Heller Anita; Ziegler Monika; Neumann Annett; Claussen Uwe; Liehr Thomas
First postnatal case of mosaic del(22)/r(22).
Prenatal diagnosis 2003;23(9):765-7.
2003: Kinne Raimund W; Kunisch Elke; Beensen Volkmar; Zimmermann Thomas; Emmrich Frank; Petrow Peter; Lungershausen Wolfgang; Hein Gert; Braun Rudolf K; Foerster Martin; Kroegel Claus; Winter Rando; Liesaus Eckehard; Fuhrmann Renée A; Roth Andreas; Claussen Uwe; Liehr Thomas
Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations.
Genes, chromosomes & cancer 2003;38(1):53-67.
2003: Seidel Jörg; Heller Anita; Senger Gabriele; Starke Heike; Chudoba Ilse; Kelbova Christina; Tönnies Holger; Neitzel Heidemarie; Haase Claudia; Beensen Volkmar; Zintl Felix; Claussen Uwe; Liehr Thomas
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.
European journal of pediatrics 2003;162(9):582-8.
2003: Liehr T; Ziegler M; Starke H; Heller A; Kuechler A; Kittner G; Beensen V; Seidel J; Hässler H; Müsebeck J; Claussen U
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism.
Clinical genetics 2003;64(2):166-7.
2003: Mrasek Kristin; Heller Anita; Rubtsov Nikolai; Trifonov Vladimir; Starke Heike; Claussen Uwe; Liehr Thomas
Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding.
International journal of molecular medicine 2003;12(2):139-46.
2003: Kuechler Alma; Dreidax Mareike; Pigorsch Steffi U; Liehr Thomas; Claussen Uwe; Wendt Thomas G; Dunst Jürgen
Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISH.
Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2003;179(7):493-8.
2003: Heller Anita; Rubtsov Nikolai; Kytölä Soili; Karamysheva Tatyana V; Sablina Olga V; Degtyareva Marina M; Starke Heike; Metzke Hermann; Claussen Uwe; Liehr Thomas
Highly complex karyotypic changes in acute myelogenous leukemia: a case report.
International journal of oncology 2003;23(1):139-43.
2003: Trifonov Vladimir; Seidel Jörg; Starke Heike; Martina Prechtel; Beensen Volkmar; Ziegler Monika; Hartmann Isabell; Heller Anita; Nietzel Angela; Claussen Uwe; Liehr Thomas
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter.
Prenatal diagnosis 2003;23(5):427-30.
2003: Schaeferhenrich Anja; Beyer-Sehlmeyer Gabriele; Festag Grit; Kuechler Alma; Haag Natja; Weise Anja; Liehr Thomas; Claussen Uwe; Marian Brigitte; Sendt Wolfgang; Scheele Johannes; Pool-Zobel Beatrice Louise
Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal.
Mutation research 2003;526(1-2):19-32.
2003: Liehr T; Starke H; Heller A; Weise A; Beensen V; Senger G; Kittner G; Prechtel M; Claussen U; Seidel J
Evidence for a new microdeletion syndrome in 15q21.
International journal of molecular medicine 2003;11(5):575-7.
2003: Schaeferhenrich A; Sendt W; Scheele J; Kuechler A; Liehr T; Claussen U; Rapp A; Greulich K-O; Pool-Zobel B L
Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 2003;41(5):655-64.
2003: Weise Anja; Harbarth Peter; Claussen Uwe; Liehr Thomas
Fluorescence in situ hybridization (FISH) on human chromosomes using photoprobe biotin-labeled probes.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2003;51(4):549-51.
2003: Nietzel A; Albrecht B; Starke H; Heller A; Gillessen-Kaesbach G; Claussen U; Liehr T
Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report.
Journal of medical genetics 2003;40(3):e28.
2003: Kuechler Alma; Weise Anja; Michel Susanne; Schaeferhenrich Anja; Pool-Zobel Beatrice L; Claussen Uwe; Liehr Thomas
Precise breakpoint characterization of the colon adenocarcinoma cell line HT-29 clone 19A by means of 24-color fluorescence in situ hybridization and multicolor banding.
Genes, chromosomes & cancer 2003;36(2):207-10.
2003: Starke Heike; Mitulla Beate; Nietzel Angela; Heller Anita; Beensen Volkmar; Grosswendt Gisela; Claussen Uwe; von Eggeling Ferdinand; Liehr Thomas
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16.
American journal of medical genetics. Part A 2003;116A(1):26-30.
2003: Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Pool-Zobel B L; Claussen U; Liehr T
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method.
Cytogenetic and genome research 2003;103(1-2):34-9.
2003: Weise A; Rittinger O; Starke H; Ziegler M; Claussen U; Liehr T
De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature.
Cytogenetic and genome research 2003;103(1-2):14-6.
2002: Steinhaeuser Ulf; Starke Heike; Nietzel Angela; Lindenau Joerg; Ullmann Peter; Claussen Uwe; Liehr Thomas
Suspension (S)-FISH, a new technique for interphase nuclei.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2002;50(12):1697-8.
2002: Starke Heike; Seidel Jörg; Henn Wolfram; Reichardt Sylvia; Volleth Marianne; Stumm Markus; Behrend Christine; Sandig Klaus R; Kelbova Christine; Senger Gabriele; Albrecht Beate; Hansmann Ingo; Heller Anita; Claussen Uwe; Liehr Thomas
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements.
European journal of human genetics : EJHG 2002;10(12):790-800.
2002: Lemke Johannes; Claussen Jan; Michel Susanne; Chudoba Ilse; Mühlig Peter; Westermann Martin; Sperling Karl; Rubtsov Nikolai; Grummt Ulrich-Walter; Ullmann Peter; Kromeyer-Hauschild Katrin; Liehr Thomas; Claussen Uwe
The DNA-based structure of human chromosome 5 in interphase.
American journal of human genetics 2002;71(5):1051-9.
2002: Hohmann Harald; Michel Susanne; Reiber Wolfgang; Kähler Christiane; Claussen Uwe; Von Eggeling Ferdinand
Cultivation of fetal erythroid precursors from maternal blood: isolation and characterization by PCR and FISH.
International journal of molecular medicine 2002;10(3):257-61.
2002: Liehr Thomas; Schreyer Isolde; Neumann Annett; Beensen Volkmar; Ziegler Monika; Hartmann Isabell; Starke Heike; Heller Anita; Nietzel Angela; Claussen Uwe
Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei.
Prenatal diagnosis 2002;22(6):497-9.
2002: Weise A; Starke H; Heller A; Tönnies H; Volleth M; Stumm M; Gabriele S; Nietzel A; Claussen U; Liehr T
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.
Journal of medical genetics 2002;39(6):434-9.
2002: Heller Anita; Starke Heike; Trifonov Vladimir; Rubtsov Nikolai; Wedding Ulrich; Loncarevic Ivan; Bleck Cordula; Claussen Uwe; Liehr Thomas
A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding.
International journal of oncology 2002;20(6):1179-81.
2002: Loncarevic Ivan F; Römer Jennifer; Starke Heike; Heller Anita; Bleck Cordula; Ziegler Monika; Fiedler Wolfgang; Liehr Thomas; Clement Joachim H; Claussen Uwe
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia.
Genes, chromosomes & cancer 2002;34(2):193-200.
2002: Liehr Thomas; Heller Anita; Starke Heike; Claussen Uwe
FISH banding methods: applications in research and diagnostics.
Expert review of molecular diagnostics 2002;2(3):217-25.
2002: Liehr Thomas; Claussen Uwe
Current developments in human molecular cytogenetic techniques.
Current molecular medicine 2002;2(3):283-97.
2002: Liehr Thomas; Schmidt Matthias; Starke Heike; Ziegler Monika; Kittner Gabriele; Heller Anita; Rubtsov Nikolai; Trifonov Vladimir; Claussen Uwe
First case of trisomy 13 plus mosaic trisomy 1q.
Fetal diagnosis and therapy 2002;17(3):133-6.
2002: Kuechler Alma; Neubauer Susann; Grabenbauer Gerhard G; Claussen Uwe; Liehr Thomas; Sauer Rolf; Wendt Thomas G
Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity?
Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2002;178(4):209-15.
2002: Fiedler Wolfgang; Hoppe Constance; Schimmel Bettina; Koscielny Sven; Dahse Regine; Bereczki Zsuzsa; Claussen Uwe; Ernst Günther; von Eggeling Ferdinand
Molecular characterization of head and neck tumors by analysis of telomerase activity and a panel of microsatellite markers.
International journal of molecular medicine 2002;9(4):417-23.
2002: Liehr Thomas; Heller Anita; Starke Heike; Rubtsov Nikolai; Trifonov Vladimir; Mrasek Kristin; Weise Anja; Kuechler Alma; Claussen Uwe
Microdissection based high resolution multicolor banding for all 24 human chromosomes.
International journal of molecular medicine 2002;9(4):335-9.
2002: Mueller Claudia; Riese Ulrike; Kosmehl Hartwig; Dahse Regine; Claussen Uwe; Ernst Guenther
Telomerase activity in microdissected human breast cancer tissues: association with p53, p21 and outcome.
International journal of oncology 2002;20(2):385-90.
2002: Dahse Regine; Utting Michael; Werner Wolfram; Schimmel Bettina; Claussen Uwe; Junker Kerstin
TP53 alterations as a potential diagnostic marker in superficial bladder carcinoma and in patients serum, plasma and urine samples.
International journal of oncology 2002;20(1):107-15.
2002: Claussen U; Michel S; Mühlig P; Westermann M; Grummt U-W; Kromeyer-Hauschild K; Liehr T
Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosis.
Cytogenetic and genome research 2002;98(2-3):136-46.
2002: Liehr T; Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Weier H-U G; Claussen U
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.
Cytogenetic and genome research 2002;97(1-2):43-50.
2001: Starke H; Senger G; Kossakiewicz M; Tittelbach H; Rau D; Rubtsov N; Trifonov V; Heller A; Hartmann I; Claussen U; Liehr T
Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).
Prenatal diagnosis 2001;21(12):1049-52.
2001: Von Eggeling F; Gawriljuk A; Fiedler W; Ernst G; Claussen U; Klose J; Römer I
Fluorescent dual colour 2D-protein gel electrophoresis for rapid detection of differences in protein pattern with standard image analysis software.
International journal of molecular medicine 2001;8(4):373-7.
2001: Liehr T; Beensen V; Starke H; Hauschild R; Hempell E; Fritsche V; Hoppe C; Grosswendt G; Prechtel M; Ziegler M; Claussen U; von Eggeling F
Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21.
Clinical genetics 2001;60(1):83-5.
2001: Lemke J; Chudoba I; Senger G; Stumm M; Loncarevic I F; Henry C; Zabel B; Claussen U
Improved definition of chromosomal breakpoints using high-resolution multicolour banding.
Human genetics 2001;108(6):478-83.
2001: Bleichert A; Fiedler W; Claussen U; Ernst G; Loncarevic I F; Heller A; Liehr T; Kunert C; von Eggeling F
A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients.
International journal of molecular medicine 2001;7(6):591-5.
2001: Starke H; Raida M; Trifonov V; Clement J H; Loncarevic I F; Heller A; Bleck C; Nietzel A; Rubtsov N; Claussen U; Liehr T
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia.
British journal of haematology 2001;113(2):435-8.
2001: Liehr T; Beensen V; Hauschild R; Ziegler M; Hartmann I; Starke H; Heller A; Kähler C; Schmidt M; Reiber W; Hesse M; Claussen U
Pitfalls of rapid prenatal diagnosis using the interphase nucleus.
Prenatal diagnosis 2001;21(5):419-21.
2001: Nietzel A; Rocchi M; Starke H; Heller A; Fiedler W; Wlodarska I; Loncarevic I F; Beensen V; Claussen U; Liehr T
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).
Human genetics 2001;108(3):199-204.
2001: Seidel J; Schiller S; Kelbova C; Beensen V; Orth U; Vogt S; Claussen U; Zintl F; Rappold G A
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation.
Clinical genetics 2001;59(2):115-21.
2001: Hohmann H; Michel S; Reiber W; Günther M; Claussen U; von Eggeling F
Applicability of four new antibodies for the detection of fetal nucleated cells out of maternal blood by FISH analysis.
Fetal diagnosis and therapy 2001;16(1):52-6.
2001: Kuechler A; Mueller C R; Liehr T; Claussen U
Detection of microdeletions in the short arm of the X chromosome by chromosome stretching.
Cytogenetics and cell genetics 2001;95(1-2):12-6.
2001: Kinne R W; Liehr T; Beensen V; Kunisch E; Zimmermann T; Holland H; Pfeiffer R; Stahl H D; Lungershausen W; Hein G; Roth A; Emmrich F; Claussen U; Froster U G
Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases.
Arthritis research 2001;3(5):319-30.
2001: Mrasek K; Heller A; Rubtsov N; Trifonov V; Starke H; Rocchi M; Claussen U; Liehr T
Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB).
Cytogenetics and cell genetics 2001;93(3-4):242-8.
2000: von Eggeling F; Davies H; Lomas L; Fiedler W; Junker K; Claussen U; Ernst G
Tissue-specific microdissection coupled with ProteinChip array technologies: applications in cancer research.
BioTechniques 2000;29(5):1066-70.
2000: Dahse R; Utting M; Werner W; Schubert J; Claussen U; Junker K
Prognostic significance of mutations in the p53 gene in superficial bladder cancer.
Oncology reports 2000;7(5):931-6.
2000: Heller A; Seidel J; Hübler A; Starke H; Beensen V; Senger G; Rocchi M; Wirth J; Chudoba I; Claussen U; Liehr T
Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.
Journal of medical genetics 2000;37(7):529-32.
2000: Heller A; Chudoba I; Bleck C; Senger G; Claussen U; Liehr T
Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.
International journal of oncology 2000;16(3):461-8.
2000: Koscielny S; Dahse R; Sonntag J; Riese U; Theuer C; Hofmann M E; von Eggeling F; Claussen U; Beleites E; Ernst G; Fiedler W
Clinical implications of telomerase activity and inactivation of the tumor suppressor gene p16 (CDKN2A) in head and neck cancer.
Otolaryngologia polska. The Polish otolaryngology 2000;54(3):291-5.
1999: Starke H; Schreyer I; Kähler C; Fiedler W; Beensen V; Heller A; Nietzel A; Claussen U; Liehr T
Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.
Prenatal diagnosis 1999;19(12):1169-74.
1999: Dahse R; Fiedler W; Junker K; Schlichter A; Schubert J; Claussen U
Telomerase activity and telomere lengths: alterations in renal cell carcinomas.
Kidney international 1999;56(4):1289-90.
1999: Fiedler W; Junker K; Schlichter A; Schubert J; Ernst G; Dahse R; Claussen U
Determination of telomerase activity for differential analysis of multifocal renal cell carcinomas.
Kidney international 1999;56(4):1286-8.
1999: Schlichter A; Fiedler W; Junker K; Dahse R; Claussen U; Schubert J
Determination of telomerase activity in multifocal renal cell carcinoma.
International journal of oncology 1999;15(3):577-81.
1999: Dahse R; Fiedler W; von Eggeling F; Schimmel B; Koscielny S; Beleites E; Claussen U; Ernst G
P53 genotyping - an effective concept for molecular testing of head and neck cancer?
International journal of molecular medicine 1999;4(3):279-83.
1999: Reichenbach H; Holland H; Dalitz E; Demandt C; Meiner A; Chudoba I; Lemke J; Claussen U; Froster U G
De novo complete trisomy 5p: clinical report and FISH studies.
American journal of medical genetics 1999;85(5):447-51.
1999: von Eggeling F; Werner G; Theuer C; Riese U; Dahse R; Fiedler W; Schimmel B; Ernst G; Karte K; Claussen U; Wollina U
Analysis of the tumor suppressor gene p16(INK4A) in microdissected melanoma metastases by sequencing, and microsatellite and methylation screening.
Archives of dermatological research 1999;291(7-8):474-7.
1999: Chudoba I; Franke Y; Senger G; Sauerbrei G; Demuth S; Beensen V; Neumann A; Hansmann I; Claussen U
Maternal UPD 20 in a hyperactive child with severe growth retardation.
European journal of human genetics : EJHG 1999;7(5):533-40.
1999: Riese U; Dahse R; Fiedler W; Theuer C; Koscielny S; Ernst G; Beleites E; Claussen U; von Eggeling F
Tumor suppressor gene p16 (CDKN2A) mutation status and promoter inactivation in head and neck cancer.
International journal of molecular medicine 1999;4(1):61-5.
1999: Junker K; Werner W; Mueller C; Ebert W; Schubert J; Claussen U
Interphase cytogenetic diagnosis of bladder cancer on cells from urine and bladder washing.
International journal of oncology 1999;14(2):309-13.
1999: Liehr T; Starke H; Beensen V; Kähler C; Harbich M; Brude E; Ziegler M; Claussen U
Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.
International journal of molecular medicine 1999;3(1):11-4.
1999: Chudoba I; Plesch A; Lörch T; Lemke J; Claussen U; Senger G
High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes.
Cytogenetics and cell genetics 1999;84(3-4):156-60.
1997: Senger G; Chudoba I; Friedrich U; Tommerup N; Claussen U; Brøndum-Nielsen K
Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
Prenatal diagnosis 1997;17(4):369-74.
1997: Junker K; Schlichter A; Junker U; Knöfel B; Kosmehl H; Schubert J; Claussen U
Cytogenetic, histopathologic, and immunologic studies of multifocal renal cell carcinoma.
Cancer 1997;79(5):975-81.
1997: von Eggeling F; Michel S; Günther M; Schimmel B; Claussen U
Determination of the origin of single nucleated cells in maternal circulation by means of random PCR and a set of length polymorphisms.
Human genetics 1997;99(2):266-70.
1997: Hliscs R; Mühlig P; Claussen U
The nature of G-bands analyzed by chromosome stretching.
Cytogenetics and cell genetics 1997;79(1-2):162-6.
1997: Hliscs R; Mühlig P; Claussen U
The spreading of metaphases is a slow process which leads to a stretching of chromosomes.
Cytogenetics and cell genetics 1997;76(3-4):167-71.
1996: Schlichter A; Junker K; Kosmehl H; Katenkamp D; Claussen U; Schubert J
[Cyto- and molecular genetic studies of renal cell carcinoma with special reference to multifocal carcinoma lesions]
Der Urologe. Ausg. A 1996;35(4):305-9.
1996: Dahse R; Fiedler W; Ernst G; Kosmehl H; Schlichter A; Schubert J; Claussen U
Changes in telomere lengths in renal cell carcinomas.
Cellular and molecular biology (Noisy-le-Grand, France) 1996;42(4):477-85.
1996: Rubtsov N; Senger G; Kuzcera H; Neumann A; Kelbova C; Junker K; Beensen V; Claussen U
Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.
Human genetics 1996;97(6):705-9.
1995: Klink A; Schiebel K; Winkelmann M; Rao E; Horsthemke B; Lüdecke H J; Claussen U; Scherer G; Rappold G
The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability.
Human molecular genetics 1995;4(5):869-78.
1995: Claussen U; Voigt H J; Ulmer R; Beinder E
[Rapid karyotyping in the 2nd and 3rd trimester: results and experiences]
Geburtshilfe und Frauenheilkunde 1995;55(1):41-8.
1994: Wienberg J; Jauch A; Lüdecke H J; Senger G; Horsthemke B; Claussen U; Cremer T; Arnold N; Lengauer C
The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1994;2(5):405-10.
1994: Voigt H J; Beinder E; Claussen U
[Ultrasound detection of suspected chromosome abnormalities in the 1st and 2nd trimester. Results of a prospective study]
Geburtshilfe und Frauenheilkunde 1994;54(8):460-7.
1994: Stosiek N; Ulmer R; von den Driesch P; Claussen U; Hornstein O P; Rott H D
Chromosomal mosaicism in two patients with epidermal verrucous nevus. Demonstration of chromosomal breakpoint.
Journal of the American Academy of Dermatology 1994;30(4):622-5.
1994: Claussen U; Ulmer R; Beinder E; Voigt H J
Six years' experience with rapid karyotyping in prenatal diagnosis: correlations between phenotype detected by ultrasound and fetal karyotype.
Prenatal diagnosis 1994;14(2):113-21.
1994: Bardenheuer W; Szymanski S; Lux A; Lüdecke H J; Horsthemke B; Claussen U; Senger G; Smith D I; Wang N D; LePaslier D
Characterization of a microdissection library from human chromosome region 3p14.
Genomics 1994;19(2):291-7.
1994: Claussen U; Mazur A; Rubtsov N
Chromosomes are highly elastic and can be stretched.
Cytogenetics and cell genetics 1994;66(2):120-5.
1993: Claussen U; Ulmer R; Beinder E; Voigt H J
Rapid karyotyping in prenatal diagnosis: a comparative study of the 'pipette method' and the 'in situ' technique for chromosome harvesting.
Prenatal diagnosis 1993;13(12):1085-93.
1993: von Eggeling F; Freytag M; Fahsold R; Horsthemke B; Claussen U
Rapid detection of trisomy 21 by quantitative PCR.
Human genetics 1993;91(6):567-70.
1993: Slim R; Levilliers J; Lüdecke H J; Claussen U; Nguyen V C; Gough N M; Horsthemke B; Petit C
A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivation.
Genomics 1993;16(1):26-33.
1992: Puech A; Ahnine L; Lüdecke H J; Senger G; Ivens A; Jeanpierre C; Little P; Horsthemke B; Claussen U; Jones C
11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.
Genomics 1992;13(4):1274-80.
1992: Horsthemke B; Claussen U; Hesse S; Lüdecke H J
PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.
PCR methods and applications 1992;1(4):229-33.
1992: Claussen U; Kleider W; Müller H G; Wille N; Baumann H A
Quality control in routine chromosome analysis: prediction of total number of bands for the individual case analyzed.
Clinical genetics 1992;41(2):100-4.
1992: Carey A H; Claussen U; Lüdecke H J; Horsthemke B; Ellis D; Oakey H; Wilson D; Burn J; Williamson R; Scambler P J
Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(2):101-5.
1991: Fahsold R; Rott H D; Claussen U; Schmalenberger B
Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3).
Clinical genetics 1991;40(4):326-8.
1991: Hampton G; Leuteritz G; Lüdecke H J; Senger G; Trautmann U; Thomas H; Solomon E; Bodmer W F; Horsthemke B; Claussen U
Characterization and mapping of microdissected genomic clones from the adenomatous polyposis coli (APC) region.
Genomics 1991;11(2):247-51.
1991: Trautmann U; Leuteritz G; Senger G; Claussen U; Ballhausen W G
Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probe.
Human genetics 1991;87(4):495-7.
1991: Fiedler W; Claussen U; Lüdecke H J; Senger G; Horsthemke B; Geurts Van Kessel A; Goertzen W; Fahsold R
New markers for the neurofibromatosis-2 region generated by microdissection of chromosome 22.
Genomics 1991;10(3):786-91.
1991: Davis L M; Zabel B; Senger G; Lüdecke H J; Metzroth B; Call K; Housman D; Claussen U; Horsthemke B; Shows T B
A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus.
Genomics 1991;10(3):588-92.
1991: Claussen U; Ludecke H J; Senger G; Horsthemke B
Construction of band-specific DNA-libraries by microdissection of GTG-banded human chromosomes and universal enzymatic DNA amplification.
Bulletin de l'Association des anatomistes 1991;75(229):133-6.
1991: Newsham I; Claussen U; Lüdecke H J; Mason M; Senger G; Horsthemke B; Cavenee W
Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.
Genes, chromosomes & cancer 1991;3(2):108-16.
1990: Davis L M; Senger G; Lüdecke H J; Claussen U; Horsthemke B; Zhang S S; Metzroth B; Hohenfellner K; Zabel B; Shows T B
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clones.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(18):7005-9.
1990: MacKinnon R N; Hirst M C; Bell M V; Watson J E; Claussen U; Ludecke H J; Senger G; Horsthemke B; Davies K E
Microdissection of the fragile X region.
American journal of human genetics 1990;47(2):181-6.
1990: Senger G; Lüdecke H J; Horsthemke B; Claussen U
Microdissection of banded human chromosomes.
Human genetics 1990;84(6):507-11.
1990: Lüdecke H J; Senger G; Claussen U; Horsthemke B
Construction and characterization of band-specific DNA libraries.
Human genetics 1990;84(6):512-6.
1990: Buiting K; Neumann M; Lüdecke H J; Senger G; Claussen U; Antich J; Passarge E; Horsthemke B
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.
Genomics 1990;6(3):521-7.
1989: Lüdecke H J; Burdiek R; Senger G; Claussen U; Passarge E; Horsthemke B
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome.
Human genetics 1989;82(4):327-9.
1989: Lüdecke H J; Senger G; Claussen U; Horsthemke B
Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification.
Nature 1989;338(6213):348-50.
1986: Voigt H J; Claussen U; Ulmer R
[Fetal neck edema--early sonographic indications of a chromosome abnormality]
Geburtshilfe und Frauenheilkunde 1986;46(12):879-82.

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