2008

Asim M, Siddiqui IA, Hafeez BB, Baniahmad A, Mukhtar H. Src kinase potentiates androgen receptor transactivation function and invasion of androgen-independent prostate cancer C4-2 cells. Oncogene 2008, 27:3596-3604.
Balikova I, Martens K, Melotte C, Amyere M, Van Vooren S, Moreau Y, Vetrie D, Fiegler H, Carter NP, Liehr T, Vikkula M, Matthijs G, Fryns JP, Casteels I, Devriendt K, Vermeesch JR. Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16. Am J Hum Genet 2008, 82:181-187.
Ebert B, Melle C, Lieckfeldt E, Zöller D, von Eggeling F, Fisahn J. Protein profiling of single epidermal cell types from Arabidopsis thaliana using surface-enhanced laser desorption and ionization technology. J Plant Physiol 2008, 165:1227-1237.
Garwe F, Bauerschäfer U, Csaki A, Steinbrück A, Ritter K, Bochmann A, Bergmann J, Weise A, Akimov D, Maubach G, König K, Hüttmann G, Paa W, Popp J, Fritzsche W. Optically controlled thermal management on the nanometer length scale. Nanotechnology 2008, 19: 055207 (12pp)
Goeman F, Otto K, Kyrylenko S, Schmidt O, Baniahmad A. ING2 recruits histone methyltransferase activity with methylation site specificity distinct from histone H3 lysines 4 and 9. Biochim Biophys Acta 2008, 1783:1673-1680.
Hermanussen M, Tutkuviene J, Cesnys G, Lindeberg S, Kromeyer-Hauschild K, Stanley G, Godina E, Bogin B, Varela-Silva MI, Finlayson G, Rühli F, Woitek U, Tresguerres JA, Lieberman LS, Detel W. The role of taste and appetite regulation in the understanding of overweight and obesity. Georgian Med News 2008, 159:34-39.
Hong W, Baniahmad A, Liu Y, Li H. Bag-1M is a component of the in vivo DNA-glucocorticoid receptor complex at hormone-regulated promoter. J Mol Biol 2008, 384:22-30.
Hovhannisyan GG, Mkrtchyan H, Liehr T, Aroutiounian R. Distribution of the chromosomes X, 7 and 18 in mitomycin C induced micronuclei. Balk J Med Gen 2008:45-49.
Iourov IY, Vorsanova SG, Liehr T, Monakhov VV, Soloviev IV, Yurov YB Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Cytogenet Genome Res 2008, 121:302-306.
Karadeniz N, Mrasek K, Weise A. Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding. Mol Cytogenet 2008, 7;1:17.
Kilian O, Dahse R, Alt V, Zardi L, Hentschel J, Schnettler R, Kosmehl H. mRNA Expression and Protein Distribution of Fibronectin Splice Variants and High-Molecular Weight Tenascin-C in Different Phases of Human Fracture Healing. Calcif Tissue Int. 2008 Jul 29. [Epub ahead of print]
Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18. Eur J Pediatr 2008, 167:655-659.
Korsten-Reck U, Kromeyer-Hauschild K, Korsten K, Baumstark MW, Dickhuth HH, Berg A. Frequency of secondary dyslipidemia in obese children. Vasc Health Risk Manag 2008; 4:1089-1094.
Kromeyer-Hauschild K, Gläßer N, Zellner K. Perzentile für den Taillenumfang von Jenaer Kindern im Alter von 6 bis 18 Jahren. Aktuelle Ernährungsmedizin 2008, 33:116-122.
Lian J, Yin Y, Oliver-Bonet M, Liehr T, Ko E, Turek P, Sun F, Martin RH. Variation in crossover interference levels on individual chromosomes from human males. Hum Mol Genet 2008, 17:2583-2594.
Liehr T. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics. Methods Mol Biol 2008, 444:27-38.
Liehr T. The multicolor fluorescence in situ hybridization (mFISH) homepage. Balk J Med Gen 2008; 11:27-31.
Liehr T. Multicolor-fluorescence in situ hybridization - Molecular cytogenetics in nowadays diagnostics and research. Med Gen 2008, 20:374-378 (German)
Liehr T, Mrasek K, Kosyakova N, Ogilvie CM, Vermeesch J, Trifonov V, Rubtsov N. Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them. Mol Cytogenet 2008, 4;1:12.
Liehr T, Wegner R-D, Stumm M, Joksi G, Polityko A, Kosyakova N, Ewers E, Reich D, Wagner R, Weise A. Pallister-Killian syndrome. Rare phenotypic features and variable karyotypes. Balk J Med Gen 2009:65-67
Loncarevic IF, Hering A, Posorski N, Linden T, Hoyer H, Bucsky P. Number of genomic imbalances correlates with the overall survival for adrenocortical cancer in childhood. Pediatr Blood Cancer 2008, 51:356-362.
Macedo Silva ML, Raimondi SC, Abdelhay E, Gross M, Mkrtchyan H, de Figueiredo AF, Ribeiro RC, de Jesus Marques-Salles T, Sobral ES, Gerardin Land MP, Liehr T. Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo. Cancer Genet Cytogenet 2008, 182:56-60.
Manolakos E, Kosyakova N, Thomaidis L, Neroutsou R, Weise A, Mihalatos M, Orru S, Kokotas H, Kitsos G, Liehr T, Petersen M. Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH. Mol Cytogenet 2008 1:24.
Manvelyan M, Riegel M, Santos M, Fuster C, Pellestor F, Mazauric ML, Schulze B, Polityko A, Tittelbach H, Reising-Ackermann G, Belitz B, Hehr U, Kelbova C, Volleth M, Gödde E, Anderson J, Küpferling P, Köhler S, Duba HC, Dufke A, Aktas D, Martin T, Schreyer I, Ewers E, Reich D, Mrasek K, Weise A, Liehr T. 32 new cases with small supernumerary marker chromosomes (sSMC) detected in connection with fertility problems - detailed molecular cytogenetic characterization and review of the literature. Int J Mol Med 2008, 21:705-714.
Manvelyan M, Hunstig F, Mrasek K, Bhatt S, Pellestor F, Weise A, Liehr T. Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Mol Cytogenet 2008, 1:9.
Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T. Chromosome distribution in human sperm - a 3D multicolor banding-study. Mol Cytogenet. 2008, 1:25.
Meigen C, Keller A, Gausche R, Kromeyer-Hauschild K, Blüher S, Kiess W, Keller E. Secular trends in body mass index in German children and adolescents: a cross-sectional data analysis via CrescNet between 1999 and 2006. Metabolism 2008, 57:934-993.
Melle C, Ernst G, Schimmel B, Bleul A, von Eggeling F. Colon-Derived Liver Metastasis, Colorectal Carcinoma, and Hepatocellular Carcinoma Can Be Discriminated by the Ca2+-Binding Proteins S100A6 and S100A11. PLoS ONE 2008; 3:e3767.
Mkrtchyan H, Ghazaryan S, Avetisyan G, Hovhannisyan H, Muradyan L, Daghbashyan S, Karst C, Gross M, Hinreiner S, Aroutiounian R, Liehr T. Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosome. Oncol Reports 2008, 20:99-104.
Moehren U, Papaioannou M, Reeb CA, Grasselli A, Nanni S, Asim M, Roell D, Prade I, Farsetti A, Baniahmad A. Wild-type but not mutant androgen receptor inhibits expression of the hTERT telomerase subunit: a novel role of AR mutation for prostate cancer development. FASEB J 2008, 22:1258-67.
Moehren U, Papaioannou M, Reeb CA, Grasselli A, Nanni S, Asim M, Roell D, Prade I, Farsetti A, Baniahmad A,Dehm SM. Wild-type but not mutant androgen receptor inhibits expression of the hTERT telomerase subunit: A novel role of AR mutation for prostate cancer development. Urol Oncol 2008, 26:690-691.
Mothes H, Melle C, Ernst G, Kaufmann R, von Eggeling F, Settmacher U. Human Neutrophil Peptides 1-3--early markers in development of colorectal adenomas and carcinomas. Dis Markers 2008; 25:123-129.
Mrasek K, Krüger G, Bauer I, Müller-Navia J, Liehr T, Weise A. A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences. Cytogenet Genome Res 2008, 121:286-287.
Murzik U, Hemmerich P, Weidtkamp-Peters S, Ulbricht T, Bussen W, Hentschel J, von Eggeling F, Melle C. Rad54B Targeting to DNA Double-Strand Break Repair Sites Requires Complex Formation with S100A11. Mol Biol Cell 2008, 1:2926-2935.
Papaioannou M, Reeb CA, Grasselli A, Nanni S, Asim M, Roell D, Prade I, Farsetti A, Baniahmad A, Moehren U Dehm SM. Wild-type but not mutant androgen receptor inhibits expression of the hTERT telomerase subunit: A novel role of AR mutation for prostate cancer development. Urol Oncol 2008, 26:690-691.
Polityko AD, Lazjuk GI, Liehr T. High resolution molecular cytogenetic approaches and study of marker chromsomes. Medica Genetics 2008, 7:34-40. (in Russian)
Pramparo T, de Gregori M, Gimelli S, Ciccone R, Frondizi D, Liehr T, Pellacani S, Masi G, Brovedani P, Zuffardi O, Guerrini R. A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation. Am J Med Genet A. 2008, 146A:1754-1760.
Rodriguez L, Liehr T, Martinez-Fernandez ML, Lara A, Torres A, Martinez-Frias ML. A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man. Molecular Cytogenetics 2008, 1:4
Scholl S, Theuer C, Scheble V, Kunert C, Heller A, Mügge LO, Fricke HJ, Höffken K, Wedding U. Clinical impact of nucleophosmin mutations and Flt3 internal tandem duplications in patients older than 60 yr with acute myeloid leukaemia. Eur J Haematol 2008, 80:208-215.
Shoukier M, Teske U, Weise A, Engel W, Argyriou L. Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasia. Clin Genet 2008, 73:320-330.
Söderholm AA, Viiliäinen J, Lehtovuori PT, Eskelinen H, Roell D, Baniahmad A, Nyrönen TH. Computationally identified novel diphenyl- and phenylpyridine androgen receptor antagonist structures. J Chem Inf Model 2008, 48:1882-1890.
Trifonov V, Fluri S, Binkert F, Nandini A, Anderson J, Rodriguez L, Gross M, Kosyakova N, Mkrtchyan H, Ewers E, Reich D, Weise A, Liehr T. Three new cases of complex rearranged small supernumerary marker chromosomes. Evidence for an underestimated entity? Mol Cytogenet 2008, 1:6.
Von Eggeling F, Bleul A, Loncarevic IF, Michel S, Heller A, Melle C. Tapping an unexploited repository: Carnoy's fixed cell pellets for proteomic biomarker research in leukemia Mol Medicine Rep 2008, 1:585-558.
Vorsanova SG, Iourov IY, Voinova-Ulas VY, Weise A, Monakhov VV, Kolotii AD, Soloviev IV, Novikov PV, Liehr T, Yurov YB. Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature. Mol Cytogenet 2008, 1:13
Weise A, Liehr T. Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies. Expert Rev Mol Diagn 2008, 8:355-357.
Weise A, Liehr T. Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH). Methods Mol Biol 2008, 444:39-48.
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 FISH (pod-FISH) distinguishes homologues human chromosomes on a single cell level. Int J Mol Med 2008, 21:189-200.
Weise A, Mrasek K, Fickelscher I, Claussen U, Cheung SW, Cai WW, Liehr T, Kosyakova N. Molecular Definition of High-resolution Multicolor Banding Probes: First Within the Human DNA Sequence Anchored FISH Banding Probe Set. J Histochem Cytochem 2008, 56:487-493.
Yurov YB, Iourov IY, Vorsanova SG, Demidova IA, Kravetz VS, Beresheva AK, Kolotii AD, Monakhov VV, Uranova NA, Vostrikov VM, Soloviev IV, Liehr T. The schizophrenia brain exhibits low-level mosaic aneuploidy involving chromosome 1. Schizophr Res 2008, 98:139-147.
Yurov YB, Liehr T, Shaffer LG , Iourov IY, Vorsanova SG. A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics. Mol Cytogenet 2008, 1:1