2007

Arndt S, Melle C, Mondal K, Klein G, von Eggeling F, Bosserhoff AK. Interactions of TANGO and leukocyte integrin CD11c/CD18 regulate the migration of human monocytes. J Leukoc Biol 2007, 82:1466-1472.
Backx L, Van Esch H, Melotte C, Kosyakova N, Starke H, Frijns JP, Liehr T, Vermeesch JR.Array painting using microdissected chromosomes to map chromosomal breakpoints. Cytogenet Genome Res 2007, 11:158-166.
Balci S, Unal A, Engiz O, Aktas D, Liehr T, Gross M, Mrasek K, Saygi S. Bilateral periventricular nodular heterotopia (PNH), severe mental retardation and epilepsy in a male patient with 46,XY,der(19) t(X;19)(q11.1-11.2;p13.3) due to maternal balanced translocation) Develop Med Child Neurol 2007, 49:219-224.
Bartels I, Starke H, Argyriou L, Sauter SM, Zoll B, Liehr T. An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. Eur J Med Genet Gen 2007,50:133-138.
Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Mol Hum Reprod. 2007, 13:751-756.
Bindl R, Braun S, Bruchhaus H. Altersschätzung anhand des Os coxae - ein Beitrag zur Individualanalyse. Beiträge zur Archäozoologie und Prä-historischen Anthropologie, 2007, VI:157-165
Bindl R, Herrmann E, Bruchhaus H. "Individualanalyse anhand des Os sacrum - ein Beitrag zur Altersschätzung". Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:166-173
Bochkov NP, Voronina ES, Kosyakova NV, Liehr T, Rzhaninova AA, Katosova LD, Platonova VI, Gol'dshtein DV. Chromosome variability of human multipotent mesenchymal stromal cells. Bull Exp Biol Med 2007, 143:122-126.
Bornhöft B, Gottschaldt U, Bindl R, Bruchhaus H: "Untersuchungen zur Geschlechtsbestimmung anhand der Mandibula". Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:189-181
Carreira IM, Mascarenhas A, Matoso E, Couceiro AB, Ramos L, Dufke A, Mazauric M, Stressig R, Kosyakova N, Melo JB, Liehr T. Three Unusual but Cytogenetically Similar Cases With up to Five Different Cell Lines Involving Structural and Numerical Abnormalities of Chromosome 18. J Histochem Cytochem 2007, 55:1123-1128.
Csaki A, Garwe F, Steinbruck A, Maubach G, Festag G, Weise A, Riemann I, Konig K, Fritzsche W. A parallel approach for subwavelength molecular surgery using gene-specific positioned metal nanoparticles as laser light antennas. Nano Lett 2007, 7:247-253.
Driemel O, Kosmehl H, Rosenhahn J, Berndt A, Reichert TE, Zardi L, Dahse R. Expression analysis of extracellular matrix components in brush biopsies of oral lesions. Anticancer Res 2007, 27:1565-1570.
Driemel O, Murzik U, Escher N, Melle C, Bleul A, Dahse R, Reichert TE, Ernst G, von Eggeling F. Protein profiling of oral brush biopsies: S100A8 and S100A9 can differentiate between normal, premalignant and tumor cells., Proteomics - Clinical Applications 2007, 1:486-493
Escher N, Kob R, Tenbaum SP, Eisold M, Baniahmad A, von Eggeling F, Melle C.Various members of the E2F transcription factor family interact in vivo with the corepressor alien. J Proteome Res 2007, 6:1158-1164.
Escher N, Kaatz M, Melle C, Hipler C, Ziemer M, Driesch D, Wollina U, von Eggeling F. Posttranslational modifications of transthyretin are serum markers in patients with mycosis fungoides. Neoplasia 2007, 9:254-259.
Eckey M, Hong W, Papaioannou M, Baniahmad A. The nucleosome assembly activity of NAP1 is enhanced by Alien. Mol Cell Biol 2007, 27:3557-3568.
Fegers I, Kob R, Eckey M, Schmidt O, Goeman F, Papaioannou M, Escher N, von Eggeling F, Melle C, Baniahmad A. The tumor suppressors p33ING1 and p33ING2 interact with alien in vivo and enhance alien-mediated gene silencing. J Proteome Res 2007, 6:4182-4188.
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. Cytogenet Genome Res 2007, 119:2-8.
Fickelscher I, Starke H, Schulze E, Ernst G, Kosyakova N, Mkrtchyan H, Mac Dermont K, Sebire N, Liehr T. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1-evidence for high variability in mosaicism in different tissues of sSMC carriers. Prenat Diagn 2007, 27:783-785.
Fickelscher I, Liehr T, Watts K, Bryant V, Barber JCK, Siebert R, Heidemann S, Hertz JM, Tumer Z, Thomas NS. The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity, Am J Hum Gen 2007, 81:847-856.
Glei M, Schaeferhenrich A, Claussen U, Kuechler A, Liehr T, Weise A, Marian B, Sendt W, Pool-Zobel BL. Comet Fluorescence in situ Hybridization Analysis for Oxidative Stress-Induced DNA Damage in Colon Cancer Relevant Genes. Toxicol Sci 2007, 96:279-284.
Häckel M, Uerlings H, Bruchhaus H. "Geschlechtsbestimmung am Pars petrosa - eine universell anwendbare Methode ?", Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:181-188
Hullmann M, Reichert TE, Dahse R, von Eggeling F, Pistner H, Kosmehl H, Driemel O. [Oral cytology : Historical development, current status, and perspectives.] Mund Kiefer Gesichtschir 2007, 11:1-9.
Iourov IY, Liehr T, Vorsanova SG, Yurov YB. Interphase chromosome-specific multicolor banding (ICS-MCB): A new tool for analysis of interphase chromosomes in their integrity. Biomol Eng 2007; 24: 415-417.
Kaiser M, Volkmann A, Bruchhaus H: "Eine neue Methode zur Berechnung des Erhaltungszustandes subadulter Gebissindividuen am Beispiel der Gräberfelder Melchendorf (Bronzezeit) und Briesnitz (Mittelalter)", Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007, VI:151-156
Knöbel Y, Weise A, Glei M, Sendt W, Claussen U, Pool-Zobel BL. Ferric iron is genotoxic in non-transformed and preneoplastic human colon cells. Food Chem Toxicol 2007,45:804-811.
Kob R, Baniahmad A, Escher N, von Eggeling F, Melle C. Detection and identification of transcription factors as interaction partners of alien in vivo. Cell Cycle 2007, 6:993-996.
Koppe T, Schöbel S, Bärenklau M., Bruchhaus H., Jankauskas R., Kaduk W: Factors affecting the variation in the adult tempopromandibular joint of archaeological human populations Annals of anatomy, 2007, 189, p 320-325.
Korsten-Reck U, Kaspar T, Korsten K, Kromeyer-Hauschild K, Bös K, Berg A, Dickhuth H-H. Motor abilities and aerobic fitness of obese children Int J Sports Med 2007, 28:762-767.
Koscielny S, Dahse R, Ernst G, von Eggeling F. The Prognostic Relevance of p16 Inactivation in Head and Neck Cancer. ORL J Otorhinolaryngol Relat Spec 2007, 69:30-36.
Kromeyer-Hauschild K, Zellner K. Trends in overweight and obesity and changes in the distribution of body mass index in schoolchildren of Jena, East Germany. Eur J Clin Nutr 2007, 61:404-411.
Krumbholz A, Seidel J, Mentzel H-J, Kauf E, Kromeyer-Hauschild K. Diagnostik der Neurofibromatose Typ 1 im Kindesalter - Anthropometrische Merkmale als zusätzliche Kriterien. Monatsschr Kinderheilkd 2007 (DOI 10.1007/s00112-007-1639-x)
Liehr T, Weise A. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med 2007, 19:719-731.
Liehr T, Trifonov V, Polityko A, Brecevic A, Mrasek K, Weise A, Ewers E, Reich D, Iourov I, Mkrtchyan H, Manvelyan M, Kosyakova N. Characterization of small supernumerary marker chromosomes (sSMC) by a simple molecular and molecular cytogenetics approach. Balkan J Med Gen 2007, 10:33-37.
Liehr T, Utine GE, Trautmann U, Rauch A, Kuechler A, Pietracz J, Bocian E, Kosyakova N, Mrasek K, Boduroglu K, Weise A, Aktas D. Neocentric small supernumerary marker chromosomes (sSMC) - three more cases plus review of the literature. Cytogenet Genome Res 2007, 118:31-37.
Manvelyan M, Schreyer I, Hols-Herpertz I, Kahler S, Niemann R, Hehr U, Belitz B, Bartels I, Gotz J, Huhle D, Kossakiewicz M, Tittelbach H, Neubauer S, Polityko A, Mazauric M-L, Wegner R, Stumm M, Kupferling P, Suss F, Kunze H, Weise A, Liehr T, Mrasek K. 48 new cases with infertility due to balanced chromosomal rearrangements - detailed molecular cytogenetic analysis of the 90 involved breakpoints. Int J Mol Med 2007, 19:855-864.
Marx FP, Soehn AS, Berg D, Melle C, Schiesling C, Lang M, Kautzmann S, Strauss KM, Franck T, Engelender S, Pahnke J, Dawson S, von Eggeling F, Schulz JB, Riess O, Krüger R. The proteasomal subunit S6 ATPase is a novel synphilin-1 interacting protein--implications for Parkinson's disease. FASEB J 2007, 21:1759-1767.
Mattes J, Whitehead B, Liehr T, Wilkinson I, Bear J, Fagan K, Craven P, Bennett B, Edwards M. Paternal uniparental isodisomy for chromosome 14 with a mosaicism for a supernumerary marker chromosome 14. Am J Med Gen A, 2007, 143A:2165-2171.
Melle C, Ernst G, Scheibner O, Kaufmann R, Schimmel B, Bleul A, Settmacher U, Hommann M, Claussen U, von Eggeling F. Identification of specific protein markers in microdissected hepatocellular carcinoma. J Proteome Res 2007, 6:306-315.
Melle C, Ernst G, Escher N, Hartmann D, Schimmel B, Bleul A, Thieme H, Kaufmann R, Felix K, Friess HM, Settmacher U, Hommann M, Richter KK, Daffner W, Taubig H, Manger T, Claussen U, von Eggeling F. Protein profiling of microdissected pancreas carcinoma and identification of HSP27 as a potential serum marker. Clin Chem 2007, 53:629-635.
Moehren U, Papaioannou M, Reeb CA, Hong W, Baniahmad A. Alien interacts with the human androgen receptor and inhibits prostate cancer cell growth. Mol Endocrinol 2007, 21:1039-4108.
Moss A, M. Wabitsch, K. Kromeyer-Hauschild, T. Reinehr, B.M. Kurth: Prävalenz von Übergewicht und Adipositas bei deutschen Einschulkindern
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2007, 50: 1424-1431
Müller C, Bauer A, Bindl R Bruchhaus H."Beitrag der Wirbelsäule für die Individualanalyse", Beiträge zur Archäozoologie und Prähistorischen Anthropologie, 2007; Band VI, S.174 - 180
Müller C, Wiederanders B, Fuhrmann R, Venbrocks RA, Mollenhauer J, Claussen U, Ruttger A. [Intra-articular pain during gonarthrosis: a case report about an extremely increased cathepsin expression in chondrocytes] Z Orthop Unfall 2007, 145:313-316. (German)
Neubert A, Bruchhaus H. "Mehrfachbestattungen des Spätneolithikums und der Frühbronzezeit in Mitteldeutschland - komplexer Gegenstand archäoanthro-pologischer Forschung". Beiträge zur Archäozoologie und Prähistorischen Anthropologie 2007, VI:16-20
Papaioannou M, Melle C, Baniahmad A. The coregulator Alien. Nucl Recept Signal 2007, 5:e008.
Pietrzak J, Mrasek K, Obersztyn E, Stankiewicz P, Kosyakova N, Weise A, Cheung S Wai, Cai W Wen, Eggeling F von, Mazurczak T, Bocian E, Liehr T. Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients. J Appl Genet 2007, 48:167-175.
Rodriguez L, Liehr T, Mrasek K, Mansilla E, Martinez-Fernandez ML, Garcia A, Martinez-Frias ML. Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review. Am J Med Genet A 2007, 143A:2727-2732
Rosenhahn J, Weise A, Michel S, Hennig K, Hartmann I, Schiefner J, Schubert K, Liehr T, Von Eggeling F, Loncarevic IF. Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R. Int J Oncol 2007, 31:121-128.
Santos M, Mrasek K, Rigola MA, Starke H, Liehr T, Fuster C. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success. Fertil Steril 2007, 88:969.e11-969-e17.
Sauter SM, Bohm D, Bartels I, Burfeind P, Laccone FA, Neesen J, Wilken B, Liehr T, Zoll B. Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay. Am J Med Genet A 2007, 143:1091-1099.
Schmidt K, Bindl R, Bruchhaus H. "Möglichkeiten der Körperhöhenschätzung am Beispiel ausgewählter schnurkeramischer Skelette". Beiträge zur Archäozoologie und Prähistorischen Anthropologie 2007, VI:194-204
Schmidt K, Bindl R, Bruchhaus H. "Möglichkeiten der Körperhöhenschätzung an ausgewählten neolethischen und bronzezeitlichen Skeletten". Archäologische Informationen 2007, 30:51-69 und Bulletin der Schweizerischen Gesellschaft für Anthropologie 13:51-69
Scholl S, Melle C, Bleul A, Spies-Weisshart B, Kunert C, Höffken K, von Eggeling F. Specific pattern of protein expression in acute myeloid leukemia harboring FLT3-ITD mutations. Leuk Lymphoma 2007, 48:2418-2423.
Schröder S, Kromeyer-Hauschild K. Bedeutung der Eltern-Kind-Beziehung bei adipösen Kindern und Jugendlichen Ernährungs-Umschau. 2007; 54:64-69
Seidel J, Hübler A, Schlenvoigt D, Hilliges P, Harbich M, Kuechler A, Liehr T, Claussen U, Kauf E. Schwere Wachstumsretardierung bei Deletion des IGF1-Rezeptor-Gens. Praktische Pädiatrische 2007, 13: 1-5.
Serra A, Schackert HK, Mohr B, Weise A, Liehr T, Fitze G. t(11;19)(q21;p12 approximately p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma. J Pediatr Surg 2007, 42:e23-29.
Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Martin RH. Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males. Cytogenet Genome Res 2007, 119:27-32
Tenbaum SP, Papaioannou M, Reeb CA, Goeman F, Escher N, Kob R, von Eggeling F, Melle C, Baniahmad A. Alien inhibits E2F1 gene expression and cell proliferation. Biochim Biophys Acta 2007, 1773:1447-1454.
Thiele K, Uerlings H, Lessig R, Edelmann J, Braun S, Bindl R, Bornhöft B, Neubert A, Bruchhaus H. "Morphologische und molekulargenetische Untersuchungen zur Identifizierung einer skelettierten Leiche", Beiträge zur Archäozoologie und Prähistorischen Anthropologie 2007, VI:205-210
Tönnies H, Pietrzak J, Bocian E, Macdermont K, Kuechler A, Belitz B, Trautmann U, Schmidt A, Schulze B, Rodriguez L, Binkert F, Yardin C, Kosyakova N, Volleth M, Mkrtchyan H, Schreyer I, von Eggeling F, Weise A, Mrasek K, Liehr T. New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank. J Histochem Cytochem. 2007, 55:651-660.
Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T. Distal partial trisomy 1q: report of two cases and a review of the literature. Prenat Diagn 2007, 27:865-871.
Uyanik G, Morris-Rosendahl DJ, Stiegler J, Klapecki J, Gross C, Berman Y, Martin P, Dey L, Spranger S, Korenke GC, Schreyer I, Hertzberg C, Neumann TE, Burkart P, Spaich C, Meng M, Holthausen H, Adčs L, Seidel J, Mangold E, Buyse G, Meinecke P, Schara U, Zeschnigk C, Muller D, Helland G, Schulze B, Wright ML, Kortge-Jung S, Hehr A, Bogdahn U, Schuierer G, Kohlhase J, Aigner L, Wolff G, Hehr U, Winkler J. Location and type of mutation in the LIS1 gene do not predict phenotypic severity. Neurology 2007, 69:442-447.
von Eggeling F, Melle C, Ernst G. Microdissecting the proteome. Proteomics. 2007, 7:2729-2737.
von Eggeling F, Ernst G. Microdissected tissue: an underestimated source for biomarker discovery? Biomark Med. 2007, 1:217-219.
Weise A, Gross M, Schmidt S, Claussen U, Liehr T. New aspects of chromosomal evolution in the gorilla and the orangutan. Int J Mol Med. 2007, 19:437-443.
Zellner K, Ulbricht U, Kromeyer-Hauschild K. Long-term trends in body mass index of children in Jena, East Germany. Econ Hum Biol 2007, 5:426-434.
Zoll B, Böhm D, Sauter SM, Liehr T, Funke R, Auber B, Bartels I, Burfeind P. Subtelomere Rerrangements. Eine Ursache für geistige Behinderung? Kinder und Jugendarzt 2007, 38:236-243.