2009
- Al Achkar W, Wafa A, Mkrtchyan H, Moassass F, Liehr T. Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report. Mol Cytogenet 2009, 2:21
- Aktas D, Weise A, Utine E, Alehan D, Mrasek K, Eggeling FV, Thieme H, Tuncbilek E, Liehr T. Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report. Mol Cytogenet 2009, 2:14.
- Auber B, Bruemmer V, Zoll B, Burfeind P, Boehm D, Liehr T, Brockmann K, Willichowski E, Argyriou L, Bartels I. Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation. Mol Cytogenet 2009, 2:10.
- Aurich H, Sgodda M, Kaltwaßer P, Vetter M, Weise A, Liehr T, Brulport M, Hengstler JG, Dollinger MM, Fleig WE, Christ B. Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo. Gut 2009; 58:570-581.
- Barros Cordeiro AP, da Silva FPE, Pieczarka JC, Nagamachi CY, Anselmo NP, Brito JR, Vasconcelos DS, Liehr T, Weise A, de Oliveira EHC. Comparative analysis of proliferative and genetic alterations in a primary chordoid meningioma and its recurrent case using locus-specific probes and AgNOR. Mol Med Rep 2009, 2:449-454.
- Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Manvelyan M, Hunstig F, Lefort G, Weise A, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. Eur J Hum Genet 2009, 17:44-50.
- Bindl R, Bruchhaus H. Untersuchungen zur histologischen Sterbealterschätzung. Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2009, VII:107-12.
- Carreira IM, Melo JB, Rodrigues C, Backx L, Vermeesch J, Weise A, Kosyakova N, Oliveira G, Matoso E. Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31->qter) detected in an autistic boy. Molecular Cytogenetics 2009, 2:16.
- Dahse R, Driemel O, Schwarz S, Dahse J, Kromeyer-Hauschild K, Berndt A, Kosmehl H. Epidermal growth factor receptor kinase domain mutations are rare in salivary gland carcinomas. Br J Cancer 2009, 100:623-625.
- Dahse R, Driemel O, Schwarz S, Kromeyer-Hauschild K, Berndt A, Kosmehl H. KRAS status and epidermal growth factor receptor expression as determinants for anti-EGFR therapies in salivary gland carcinomas. Oral Oncol. 2009;45:826-829.
- Dahse R, Kromeyer-Hauschild K, Berndt A, Kosmehl H. No incidence of BRAF mutations in salivary gland carcinomas--implications for anti-EGFR therapies. J Biomed Biotechnol. 2009, 2009:501736.
- de Figueiredo AF, Mkrtchyan H, Liehr T, Soares Ventura EM, de Jesus Marques-Salles T, Santos N, Ribeiro RC, Abdelhay E, Macedo Silva ML. A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21. Cancer Genet Cytogenet 2009, 193:123-126.
- de Jesus Marques-Salles T, Liehr T, Mkrtchyan H, Raimondi SC, Tavares de Souza M, Faria de Figueiredo A, Rouxinol S, Jordy Macedo FC, Abdelhay E, Santos N, Macedo Silva ML. A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia. Cancer Genet Cytogenet. 2009, 189:59-62.
- Eisold M, Asim M, Eskelinen H, Linke T, Baniahmad A. Inhibition of MAPK-signaling pathway promotes the interaction of the corepressor SMRT with the human androgen receptor and mediates repression of prostate cancer cell growth in the presence of antiandrogens. J Mol Endocrinol 2009, 42:429-435.
- Ergul E, Liehr T, Mrasek K, Sazci A. A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male. Fertil Steril 2009, 92:391.e9-391.e12.
- Erlecke J, Hartmann I, Hoffmann M, Kroll T, Starke H, Heller A, Gloria A, Sayer HG, Johannes T, Claussen U, Liehr T, Loncarevic IF. Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells. Mol Cytogenet 2009, 2:12.
- Gallagher A, Gunther MM, Bruchhaus H. Population continuity, demic diffusion and Neolithic origins in central-southern Germany: the evidence from body proportions. Homo. 2009;60:95-126.
- Gross M, Mkrtchyan H, Glaser M, Fricke HJ, Höffken K, Heller A, Weise A, Liehr T. Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. Int J Oncol 2009, 34:417-423.
- Hong W, Baniahmad A, Li J, Chang C, Gao W, Liu Y. Bag-1M inhibits the transactivation of the glucocorticoid receptor via recruitment of corepressors. FEBS Lett. 2009,583:2451-2456.
- Iourov IY, Vorsanova SG, Liehr T, Yurov YB. Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning. Neurobiol Dis 2009, 34:212-220.
- Iourov IY, Vorsanova SG, Liehr T, Kolotii AD, Yurov YB. Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain. Hum Mol Genet. 2009;18:2656-2669.
- Kitsiou-Tzeli S, Manolakos E, Lagou M, Anagnostopoulou K, Kontodiou M, Kosyakova N, Ewers E, Weise A, Garas A, Orru S, Liehr T, Metaxotou A. Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Mol Cytogenet 2009, 2:1/ 2:8.
- Kob R, Kelm J, Posorski N, Baniahmad A, von Eggeling F, Melle C. Regulation of the anaphase-promoting complex by the COP9 signalosome. Cell Cycle 2009; 8:2041-2049.
- Korsten-Reck U, Korsten K, Kreuser F, Wölker U, Etzold D, Berg A, Dickhuth HH, Kromeyer-Hauschild K. Das Freiburger Interventionsprogramm FITOC. Adipositas 2009, 3:11-16.
- Korsten-Reck U, Korsten K, Haeberle K, Kromeyer-Hauschild K, Dickhuth HH, Schulz E. The psychosocial situation of obese children: Psychological factors and quality of life. Psychology Research and Behavior Managment 2009, 2:23-29.
- Kosyakova N, Weise A, Mrasek K, Claussen U, Liehr T, Nelle H. The hierarchically organized splitting of chromosomal bands for all human chromosomes. Mol Cytogenet 2009, 2:4.
- Korsten-Reck U, Korsten K, Haeberle K, Kromeyer-Hauschild K, Dickhuth HH, Schulz E. The psychosocial situation of obese children: Psychological factors and quality of life. Psychology Research and Behavior Managment 2009, 2:23-29.
- Liehr T. The internet page on small supernumerary marker chromosomes (sSMC). ECA Newsletter 2009, 23:10-14.
- Liehr T. Small supernumerary marker chromosomes (sSMC) - a spotlight on some nomenclature problems. J Histochem Cytochem 2009, 57:991-993.
- Liehr T, Stumm M, Wegner R-D, Bhatt S, Hickmann P, Patsalis PC, Meins M, Morlot S, Klaschka V, Ewers E, Hinreiner S, Mrasek K, Kosyakova N, Cai WW, Cheung SW, Weise A. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenet Genome Res 2009, 24:102-105.
- Liehr T, Ewers E, Kosyakova N, Klaschka V, Rietz F, Wagner R, Weise A. Handling small supernumerary marker chromosomes in prenatal diagnostics. Expert Rev Mol Diagn. 2009, 9:317-324.
- Macedo Silva ML, do Socorro Pombo-de-Oliveira M, Raimondi SC, Liehr T, Abdelhay E, Faria de Figueiredo A, Tavares de Souza M, Ribeiro Ney Garcia D, Maria Soares de Ventura E, Martins de Sousa A, Mkrtchyan H. Unbalanced chromosome 1 abnormalities in four infants with Down syndrome and acute megakaryocytic leukemia. Mol Cytogenet 2009, 2:7.
- Manolakos E, Vetro A, Kitmirides S, Papoulidis I, Kosyakova N, Mrasek K, Weise A, Agapitos E, Orru S, Peitsidis P, Liehr T, Petersen MB. Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH. Prenat Diagn. 2009, 29:884-888.
- Manvelyan M, Kempf P, Weise A, Mrasek K, Heller A, Lier A, Höffken K, Fricke H-J, Sayer HG, Liehr T, Mkrtchyan H. Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics. Int J Mol Med 2009, 24:335-341.
- Melle C, Ernst G, Winkler R, Schimmel B, Klussmann JP, Wittekindt C, Guntinas-Lichius O, von Eggeling F. Proteomic analysis of human papillomavirus-related oral squamous cell carcinoma: Identification of thioredoxin and epidermal-fatty acid binding protein as upregulated protein markers in microdissected tumor tissue. Proteomics 2009, 9:2193-2201.
- Melle C, Ernst G, Grosheva M, Angelov DN, Irintchev A, Guntinas-Lichius O, von Eggeling F. Proteomic analysis of microdissected facial nuclei of the rat following facial nerve injury. J Neurosc Meth 2009, 185:23-28.
- Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation. Cytogenet Genome Res 2009, 125:109-114.
- Mkrtchyan H, Scheler S, Klein I, Fahr A, Couraud P-O, Romero IA, Weksler B, Liehr T. Molecular cytogenetic characterization of the human cerebral microvessel endothelial cell line hCMEC/D3. Cytogenet Genome Res 2009; 126:313-317.
- Polityko AD, Khurs OM, Kulpanovich AI, Mosse KA, Solntsava AV, Rumyantseva NV, Naumchik IV, Liehr T, Weise, Mkrtchyan H. Paternally derived der(7)t(Y;7)(p11.1~11.2;p22.3)dn in a mosaic case with Turner syndrome. Europ J Med Gen 2009,52:207-210.
- Polityko A, Khurs O, Liehr T. Human genomic disorders. Analysis of 22q11. Proceedings of the Institute of Genetics and Cytology of National Academy of Sciences Belarus, Minsk, Special issue "Molecular and applied genetics" 2009; 10:80-88 (Russian).
- Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Patil S, Ziegler M, Liehr T. A neocentric isochromosome Yp present as additional small supernumerary marker chromosome--evidence against U-type exchange mechanism? Cytogenet Genome Res. 2009, 125:115-116.
- Schreyer I, Hampel P. [ADHD among boys in childhood: quality of life and parenting behavior] Z Kinder Jugendpsychiatr Psychother. 2009, 37:69-75.
- Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Desai M, Andrieux J, Vermeesch J, Hamid AB, Ziegler M, Liehr T. A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome. Mol Cytogenet 2009, 2:22.
- Soysal Y, Balci S, Hekimler K, Liehr T, Ewers E, Schoumans J, Bui TH, Içduygu FM, Kosyakova N, Imirzalıoğlu N. Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. Am J Med Gen A 2009, 149A:2782-2787.
- Tzschach A, Ramel C, Kron A, Seipel B, Wüster C, Cordes U, Liehr T, Hoeltzenbein M, Menzel C, Ropers HH, Ullmann R, Kalscheuer V, Decker J, Steinberger D. Hypergonadotropic hypogonadism in a patient with inv ins (2;4). Int J Androl 2009, 32:226-230.
- Uroz L, Liehr T, Mrasek K, Templado C. CenM-FISH on human spermatocyte I and II metaphases. Hum Reprod 2009, 24:2029-2033.
- Wehder L, Arndt S, Murzik U, Bosserhoff AK, Kob R, von Eggeling F, Melle C. Annexin A5 is involved in migration and invasion of oral carcinoma. Cell Cycle 2009, 8:1-7.
- Weise A, Mrasek K, Ewers E, Mkrtchyan H, Kosyakova N, Liehr T. Diagnostic applications of fluorescence in situ hybridization. Expert Opin Med Diagn 2009, 3:453-460.
- Winklmeier A, Contreras-Shannon V, Arndt S, Melle C, Bosserhoff AK. Cadherin-7 interacts with melanoma inhibitory activity protein and negatively modulates melanoma cell migration. Cancer Sci 2009, 100:261-268.
- Würbach A, Zellner K, Kromeyer-Hauschild K. Meal patterns among children and adolescents and their associations with weight status and parental characteristics. Public Health Nutr 2009, 26:1-7.
- Zellner K, Ulbricht G, Kromeyer-Hauschild K. Langzeittendenzen des Body Mass Index und der Energieaufnahme bei Jenaer Schulkindern. Ernährungsumschau 2009; 56: 667ff.
Bücher/ Books
note added in June 2013
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