2005

Baniahmad A. Nuclear hormone receptor co-repressors. J Steroid Biochem Mol Biol 2005, 93:89-97.
Barber JCK, Thomas NS, Collinson MN, Dennis NR, Liehr T, Weise A, Belitz B, Pfeiffer L, Kirchhoff M, Krag-Olsen B, Lundsteen C. Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences. Europ J Hum Gen 2005, 13:283-291.
Barber JC, Maloney V, Hollox EJ, Stuke-Sontheimer A, du Bois G, Daumiller E, Klein-Vogler U, Dufke A, Armour JA, Liehr T. Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet 2005, 13:1131-1136.
Busch A, Michel S, Hoppe C, Driesch D, Claussen U, von Eggeling F. Proteome Analysis of Maternal Serum Samples for Trisomy 21 Pregnancies Using ProteinChip Arrays and Bioinformatics. J Histochem Cytochem 2005, 53:341-343.
Diegmann J, Junker K, Gerstmayer B, Bosio A, Hindermann W, Rosenhahn J, von Eggeling F.,Identification of CD70 as a diagnostic biomarker for clear cell renal cell carcinoma by gene expression profiling, real-time RT-PCR and immunohistochemistry. Eur J Cancer 2005, 41:1794-801.
Finke L, Nöther S. A palato-nasal cyst assiciated with mesiodens and possible fibro-osseous dysplasia in a male of the migrations period. Paleopathology Newsletter 2005, 131:19-24
Gessner G, Schonherr K, Soom M, Hansel A, Asim M, Baniahmad A, Derst C, Hoshi T, Heinemann SH. BKCa channels activating at resting potential without calcium in LNCaP prostate cancer cells. J Membr Biol 2005, 208:229-240.
Glaser M, Karst C, Gross M, Mkrtchyan H, Liehr T. Chromosome torsions in cytogenetic preparations of bone-marrow - artifacts or leukemia-specific? Balk J Med Gen 2005, 8:27-31.
Goeman F, Thormeyer D, Abad M, Serrano M, Schmidt O, Palmero I, Baniahmad A. Growth inhibition by the tumor suppressor p33ING1 in immortalized and primary cells: involvement of two silencing domains and effect of Ras. Mol Cell Biol 2005, 25:422-431.
Gutiérrez-Mateo C, Benet J, Starke H, Oliver-Bonet M, Munné S, Liehr T, Navarro J. Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique. Hum Reprod 2005, 20:3395-3401.
Herbert Z, Gothe S, Caldwell JD, Bernstein HG, Melle C, von Eggeling F, Lewis J, Jirikowski GF. Identification of sex hormone-binding globulin in the human hypothalamus. Neuroendocrinology 2005, 81:287-293.
Junker K, Gneist J, Melle C, Driesch D, Schubert J, Claussen U, Von Eggeling F. Identification of protein pattern in kidney cancer using ProteinChip arrays and bioinformatics. Int J Mol Med 2005, 15:285-90.
Junker K, Hindermann W, von Eggeling F, Diegmann J, Haessler K, Schubert J.CD70: a new tumor specific biomarker for renal cell carcinoma. J Urol 2005, 173:2150-2153.
Karst C, Heller A, Claussen U, Gebhart E, Liehr T. Abstract Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia. Int J Oncol 2005, 27:355-359.
Keller U, Grabenbauer G, Kuechler A, Sprung CN, Müller E, Sauer R, Distel L. Cytogenetic instability in young patients with multiple primary cancers. Cancer Genet Cytogenet 2005, 157:25-32.
Korsten-Reck U, Kromeyer-Hauschild K, Wolfarth B, Dickhuth HH, Berg A. Freiburg Intervention Trial for Obese Children (FITOC): results of a clinical observation study. Int J Obes Relat Metab Disord 2005, 29:356-361.
Kuechler A, Ziegler M, Blank C, Rommel B, Bullerdiek J, Ahrens J, Claussen U, Liehr T. A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for ICSI. J Histochem Cytochem 2005, 53:355-357.
Kautenburger T, Beyer-Sehlmeyer G, Festag G, Haag N, Kuhler S, Kuchler A, Weise A, Marian B, Peters WH, Liehr T, Claussen U, Pool-Zobel BL: 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. J Cancer Res Clin Oncol 2005, 131:692-700
Lehmann R, Melle C, Escher N, von Eggeling F. Detection and identification of protein interactions of S100 proteins by ProteinChip technology. J Proteome Res 2005, 4:1717-1721.
Liehr T. Eine erste Genotyp-Phänotyp-Korrelation bei kleinen überzähligen Marker-Chromosomen (small supernumerary marker chromosomes = sSMC) des Menschen. Medgen 2005, 17:454-456.
Liehr T, Weier H-UG. 14th Workshop on Fetal Cells and Fetal DNA. J Histochem Cytochem 2005, 53:253-254.
Liehr T, Ziegler M. Rapid prenatal diagnostics in the interphase nucleus - procedure and cut-off rates. J Histochem Cytochem 2005; 53:289-291.
Liehr T, Brude E, Gillessen-Kaesbach G, König R, Mrasek K, von Eggeling F, Starke H. Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15 - case report plus review of similar cases. Europ J Gen 2005, 48:175-181.
Liehr T, Mrasek K, Starke H, Claussen U, Schreiber G. Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient. Cytogenet Genome Res 2005, 111:179-181.
Melle C, Ernst G, Schimmel B, Bleul A, Kaufmann R, Hommann M, Richter KK, Daffner W, Settmacher U, Claussen U, von Eggeling F. Characterization of pepsinogen C as a potential biomarker for gastric cancer using a histo-proteomic approach. J Proteome Res 2005, 4:1799-1804.
Melle C, Ernst G, Schimmel B, Bleul A, Thieme H, Kaufmann R, Mothes H, Settmacher U, Claussen U, Halbhuber KJ, Von Eggeling F. Discovery and identification of alpha-defensins as low abundant, tumor-derived serum markers in colorectal cancer. Gastroenterology 2005 Jul;129:66-73.
Melle C, Osterloh D, Ernst G, Schimmel B, Bleul A, von Eggeling F. Identification of proteins from colorectal cancer tissue by two-dimensional gel electrophoresis and SELDI mass spectrometry. Int J Mol Med 2005, 16:11-17.
Macedo Silva ML, Land M, Heller A, Abdelhay E, do Socorro Pombo-de-Oliveira M, Ribeiro R, Alves G, Lerner D, Liehr T. New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome. Oncol Rep 2005, 14:663-666.
Mrasek K, Starke H, Liehr t. Another small supernumerary marker chromosome (sSMC) derived from chromosome 2 - towards a genotype/ phenotype correlation. J Histochem Cytochem 2005, 53:367-370.
Mueller J, von Eggeling F, Driesch D, Schubert J, Melle C, Junker K. ProteinChip technology reveals distinctive protein expression profiles in the urine of bladder cancer patients. Eur Urol 2005, 47:885-893
Oliver-Bonet M, Benet J, Sun F, Navarro J, Abad C, Liehr T, Starke H, Greene C, Ko E, Martin RH. Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure. Human Reproduction 2005, 20:683-688.
Papaioannou M, Reeb C, Asim M, Dotzlaw H, Baniahmad A. Co-activator and co-repressor interplay on the human androgen receptor. Andrologia 2005, 37:211-212.
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. Cytogenet Genome Res 2005, 111:171-174.
Pramparo T, Mattina T, Gimelli S, Liehr T, Zuffardi O. Narrowing the deleted region associated with the 15q21 syndrome. Eur J Med Genet 2005, 48:346-352.
Rodriguez L, Starke H, Guardia NM, Tonnies H, Neitzel H, Kozlowski P, Mazauric ML, Heller A, Grondona FL, Mansilla E, Santos Munoz MJ, Liehr T, Martinez-Frias ML. Three new cases with a supernumerary ring chromosome 1. Clin Dysmorphol 2005, 14:169-175.
Schierl T, Häckel M, Bruchhaus H: Anthropologischer Befund zu den Körpergräbern der jüngeren Römischen Kaiser- und der Völkerwanderungszeit. In:Liebersee - Ein polykultureller Bestattungsplatz an der sächsischen Elbe von Jan Bemman und Esther M.Wesely-Arents Band 5, Veröffentlichungen des Landesamtes für Archäologie mit Landesmuseum für Vorgeschichte. 2005, 48:264-270
Schmidt S, Claussen U, Liehr T, Weise A. Evolution versus constitution: differences in chromosomal inversion. Hum Genet 2005, 117:213-219.
Scholl S, Loncarevic IF, Krause C, Clement JH, Hoffken K, Sayer HG. Analyses of minimal residual disease based on Flt3 mutations in allogeneic peripheral blood stem cell transplantation. J Cancer Res Clin Oncol 2005, 131:279-283.
Scholl S, Krause C, Loncarevic IF, Muller R, Kunert C, Wedding U, Sayer HG, Clement JH, Hoffken K. Specific detection of Flt3 point mutations by highly sensitive real-time polymerase chain reaction in acute myeloid leukemia. J Lab Clin Med 2005, 145:295-304.
Scholl S, Loncarevic IF, Krause C, Kunert C, Clement JH, Hoffken K. Minimal residual disease based on patient specific Flt3-ITD and -ITT mutations in acute myeloid leukemia. Leuk Res 2005, 29:849-853.
Schreyer I, Neumann A, Beensen V, Eichhorn K-H, Heller A, Claussen U, Liehr T. dup(13)(q14.2-q14.3) - yet another new differential diagnostic aspect for short stature like phenotype. J Histochem Cytochem 2005, 53 :365-366.
Starke H, Mrasek K, Liehr T. 3 cases with enlarged acrocentric p-arms - 2 cases with cryptic partial trisomies. J Histochem Cytochem 2005, 53:359-360.
Sun F, Oliver-Bonet M, Liehr T, Starke H, Trpkov K, Ko E, Rademaker A, Martin RH. Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males. Hum Mol Gen 2005, 14:3013-3018
Trifonov V, Karst C, Claussen U, Mrasek K, Michel S, Avner P, Liehr T. Microdissection-derived Murine Mcb Probes from Somatic Cell Hybrids. J Histochem Cytochem 2005, 53:791-792.
Trimborn M, Liehr T, Belitz b, Pfeiffer L, Varon R, Neitzel H, Tönnies H. Prenatal diagnosis and molecular cytogenetic characterisation of a complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI). J Histochem Cytochem 2005, 53:351-354.
Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype. Eur J Med Genet 2005, 48:319-327.
von Beust G, Sauter SM, Liehr T, Burfeind P, Bartels I, Starke H, von Eggeling F, Zoll B. Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay. Am J Med Genet A 2005, 137:59-64.
Weise A, Starke H, Mrasek K, Claussen U, Liehr T. New insights into the evolution of chromosome 1. Cytogenet Genome Res 2005, 108:217-222.
Weise A, Liehr T, Claussen U, Halbhuber K-J. Increased efficiency of fluorescence in situ hybridization (FISH) using the microwave. J Histochem Cytochem 2005, 53:1301-1303.
Xiao F, Mirwald A, Papaioannou M, Baniahmad A, Klug J. Secretoglobin 2A1 is under selective androgen control mediated by a peculiar binding site for Sp family transcription factors.Mol Endocrinol 2005, 19:2964-2978.