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Results: 1-25/37
Authors:
Kinne, RW
Liehr, T
Beensen, V
Kunisch, E
Zimmermann, T
Holland, H
Pfeiffer, R
Stahl, HD
Lungershausen, W
Hein, G
Roth, A
Emmrich, F
Claussen, U
Froster, UG
Citation: Rw. Kinne et al., Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases, ARTHRITIS R, 3(5), 2001, pp. 319-330
Authors:
Liehr, T
Claussen, U
Gebhart, E
Citation: T. Liehr et al., Nucleus extraction from single mounted tissue sections (vol 15, pg 65, 1999), BIOMOL ENG, 18(2), 2001, pp. 67-67
Authors:
Von Eggeling, F
Gawriljuk, A
Fiedler, W
Ernst, G
Claussen, U
Klose, J
Romer, I
Citation: F. Von Eggeling et al., Fluorescent dual colour 2D-protein gel electrophoresis for rapid detectionof differences in protein pattern with standard image analysis software, INT J MOL M, 8(4), 2001, pp. 373-377
Authors:
Bleichert, A
Fiedler, W
Claussen, U
Ernst, G
Loncarevic, IF
Heller, A
Liehr, T
Kunert, C
Von Eggeling, F
Citation: A. Bleichert et al., A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients, INT J MOL M, 7(6), 2001, pp. 591-595
Authors:
Alves, G
Heller, A
Fiedler, W
Campos, MM
Claussen, U
Ornellas, AA
Liehr, T
Citation: G. Alves et al., Genetic imbalances in 26 cases of penile squamous cell carcinoma, GENE CHROM, 31(1), 2001, pp. 48-53
Authors:
Hohmann, H
Michel, S
Reiber, W
Gunther, M
Claussen, U
von Eggeling, F
Citation: H. Hohmann et al., Applicability of four new antibodies for the detection of fetal nucleated cells out of maternal blood by FISH analysis, FETAL DIAGN, 16(1), 2001, pp. 52
Authors:
Liehr, T
Reiter, LT
Lupski, JR
Murakami, T
Claussen, U
Rautenstrauss, B
Citation: T. Liehr et al., Regional localization of 10 mariner transposon-like ESTs by means of FISH - evidence for a correlation with fragile sites, MAMM GENOME, 12(4), 2001, pp. 326-328
Authors:
Lemke, J
Chudoba, I
Senger, G
Stumm, M
Loncarevic, IF
Henry, C
Zabel, B
Claussen, U
Citation: J. Lemke et al., Improved definition of chromosomal breakpoints using high-resolution multicolour banding, HUM GENET, 108(6), 2001, pp. 478-483
Authors:
Nietzel, A
Rocchi, M
Starke, H
Heller, A
Fiedler, W
Wlodarska, I
Loncarevic, IF
Beensen, V
Claussen, U
Liehr, T
Citation: A. Nietzel et al., A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH), HUM GENET, 108(3), 2001, pp. 199-204
Authors:
Mrasek, K
Heller, A
Rubtsov, N
Trifonov, V
Starke, H
Rocchi, M
Claussen, U
Liehr, T
Citation: K. Mrasek et al., Reconstruction of the female Gorilla gorilla karyotype using 25-color FISHand multicolor banding (MCB), CYTOG C GEN, 93(3-4), 2001, pp. 242-248
Authors:
Liehr, T
Beensen, V
Hauschild, R
Ziegler, M
Hartmann, I
Starke, H
Heller, A
Kahler, C
Schmidt, M
Reiber, W
Hesse, M
Claussen, U
Citation: T. Liehr et al., Pitfalls of rapid prenatal diagnosis using the interphase nucleus, PRENAT DIAG, 21(5), 2001, pp. 419-421
Authors:
Salafsky, IS
MacGregor, SN
Claussen, U
von Eggeling, F
Citation: Is. Salafsky et al., Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20, PRENAT DIAG, 21(10), 2001, pp. 860-863
Authors:
von Eggeling, F
Junker, K
Fiedler, W
Wollscheid, V
Durst, M
Claussen, U
Ernst, G
Citation: F. Von Eggeling et al., Mass spectrometry meets chip technology: A new proteomic tool in cancer research?, ELECTROPHOR, 22(14), 2001, pp. 2898-2902
Authors:
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
Citation: T. Liehr et al., Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21, CLIN GENET, 60(1), 2001, pp. 83-85
Authors:
Seidel, J
Schiller, S
Kelbova, C
Beensen, V
Orth, U
Vogt, S
Claussen, U
Zintl, F
Rappold, GA
Citation: J. Seidel et al., Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation, CLIN GENET, 59(2), 2001, pp. 115-121
Authors:
Starke, H
Raida, M
Trifonov, V
Clement, JH
Loncarevic, IF
Heller, A
Bleck, C
Nietzel, A
Rubtsov, N
Claussen, U
Liehr, T
Citation: H. Starke et al., Molecular cytogenetic characterization of an acquired minute supernumerarymarker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia, BR J HAEM, 113(2), 2001, pp. 435-438
Authors:
Ludecke, HJ
Schaper, J
Meinecke, P
Momeni, P
Gross, S
von Holtum, D
Hirche, H
Abramowicz, MJ
Albrecht, B
Apacik, C
Christen, HJ
Claussen, U
Devriendt, K
Fastnacht, E
Forderer, A
Friedrich, U
Goodship, THJ
Greiwe, M
Hamm, H
Hennekam, RCM
Hinkel, GK
Hoeltzenbein, M
Kayserili, H
Majewski, F
Mathieu, M
McLeod, R
Midro, AT
Moog, U
Nagai, T
Niikawa, N
Orstavik, KH
Plochl, E
Seitz, C
Schmidtke, J
Tranebjaerg, L
Tsukahara, M
Wittwer, B
Zabel, B
Gillessen-Kaesbach, G
Horsthemke, B
Citation: Hj. Ludecke et al., Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III, AM J HU GEN, 68(1), 2001, pp. 81-91
Authors:
Dahse, R
Utting, M
Werner, W
Schubert, J
Claussen, U
Junker, K
Citation: R. Dahse et al., Prognostic significance of mutations in the p53 gene in superficial bladder cancer, ONCOL REP, 7(5), 2000, pp. 931-936
Authors:
Heller, A
Chudoba, I
Bleck, C
Senger, G
Claussen, U
Liehr, T
Citation: A. Heller et al., Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias, INT J ONCOL, 16(3), 2000, pp. 461-468
Authors:
von Eggeling, F
Davies, H
Lomas, L
Fiedler, W
Junker, K
Claussen, U
Ernst, G
Citation: F. Von Eggeling et al., Tissue-specific microdissection coupled with ProteinChip (R) array technologies: Applications in cancer research, BIOTECHNIQU, 29(5), 2000, pp. 1066-1070
Authors:
Rubtsov, NB
Karamisheva, TV
Astakhova, NM
Liehr, T
Claussen, U
Zhdanova, NS
Citation: Nb. Rubtsov et al., Zoo-FISH with region-specific paints for mink chromosome 5q: delineation of inter- and intrachromosomal rearrangements in human, pig, and fox, CYTOG C GEN, 90(3-4), 2000, pp. 268-270
Authors:
Heller, A
Seidel, J
Hubler, A
Starke, H
Beensen, V
Senger, G
Rocchi, M
Wirth, J
Chudoba, I
Claussen, U
Liehr, T
Citation: A. Heller et al., Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review, J MED GENET, 37(7), 2000, pp. 529-532
Authors:
Dahse, R
Fieldler, W
Von Eggeling, F
Schimmel, B
Koscielny, S
Beleites, E
Claussen, U
Ernst, G
Citation: R. Dahse et al., P53 genotyping - An effective concept for molecular testing of head and neck cancer?, INT J MOL M, 4(3), 1999, pp. 279-283
Tumor suppressor gene p16 (CDKN2A) mutation status and promoter inactivation in head and neck cancer
Authors:
Riese, U
Dahse, R
Fiedler, W
Theuer, C
Koscielny, S
Ernst, G
Beleites, E
Claussen, U
von Eggeling, F
Citation: U. Riese et al., Tumor suppressor gene p16 (CDKN2A) mutation status and promoter inactivation in head and neck cancer, INT J MOL M, 4(1), 1999, pp. 61-65
Authors:
Liehr, T
Starke, H
Beensen, V
Kahler, C
Harbich, M
Brude, E
Ziegler, M
Claussen, U
Citation: T. Liehr et al., Translocation trisomy dup(21q) and free trisomy 21 can be distinguished byinterphase-FISH, INT J MOL M, 3(1), 1999, pp. 11-14