2011

• Al-Achkar W, Wafa A, Liehr T. Complex translocation involving four chromosomes in a novel Philadelphia-positive chronic myeloid leukemia case. Onc Lett 2011, 2:273-276.
• Al-Achkar W, Wafa A, Klein E, Aljapawe A. Biclonal myelodysplastic syndrome involving six chromosomes and monoallelic loss of RB1 - A rare case. Molecular Cytogenetics 2011, 4:16.
• Asim M, Hafeez BB, Siddiqui IA, Gerlach C, Patz M, Mukhtar H, Baniahmad A. Ligand-dependent corepressor acts as a novel androgen receptor corepressor, inhibits prostate cancer growth and is functionally inactivated by the Src kinase. J Biol Chem 2011, 286:37108-37117.
• Backsch C, Pauly B, Liesenfeld M, Scheungraber C, Gajda M, Mrasek K, Liehr T, Clad A, Schröck E, Runnebaum IB, Dürst M. Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma. Cancer Genetics 2011, 204:646-653.
• Baniahmad A. The corepressor Alien as a novel tumor suppressor? Horm Mol Biol Clin Invest 2011, 5:11-15.
• Braulke F, Schanz J, Steffens R, Liehr T, Manvelyan M, Chudoba I, Haase D. Two different del(5q) clones in a patient with myelodysplastic syndrome. Leuk Lymph 2011, 52:1811-1844.
• Bünger S, Haug U, Kelly FM, Klempt-Giessing K, Cartwright A, Posorski N, Dibbelt L, Fitzgerald SP, Bruch HP, Roblick UJ, von Eggeling F, Brenner H, Habermann JK. Toward standardized high-throughput serum diagnostics: multiplex-protein array identifies IL-8 and VEGF as serum markers for colon cancer. J Biomol Screen 2011, 16:10180.
• Cioffi MB, Sánchez A, Marchal JA, Kosyakova N, Liehr T, Trifonov V, Bertollo LAC. Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishes. BMC Evolutionary Biology 2011, 11:186.
• Cioffi MB, Sánchez A, Marchal JA, Kosyakova N, Liehr T, Trifonov V, Bertollo LAC. Correction to: Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species. Genetica 2018; 146:123
• de Bello Cioffi M, Sánchez A, Marchal JA, Kosyakova N, Liehr T, Trifonov V, Bertollo LA. Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species. Genetica 2011, 139:1065-1072.
• Delaney JT, Urbanek A, Wehder L, Perelaer J, Crecelius AC, von Eggeling F, Schubert US. Combinatorial optimization of multiple MALDI matrices on a single tissue sample using inkjet printing. ACS Comb Sci 2011, 13:218-222.
• de Souza MT, Mkrtchyan H, Hassan R, Ney-Garcia DR, de Azevedo AM, da Costa ES, de Figueiredo AF, Liehr T, Abdelhay E, Silva ML. Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis. Int J Hematol 2011; 93:232-236.
• Dobbernack G, Meinl W, Schade N, Florian S, Wend K, Voigt I, Himmelbauer H, Gross M, Liehr T, Glatt H. Altered tissue distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-DNA adducts in mice transgenic for human sulfotransferases 1A1 and 1A2. Carcinogenesis 2011, 32:1734-1740.
• Eladari D, Hübner CA. Novel mechanisms for NaCl reabsorption in the collecting duct. Curr Opin Nephrol Hypertens 2011 , 20:506-511.
• Elsing C, Voss A, Herrmann T, Kaiser I, Huebner CA, Schlenker T. Oxidative Stress Reduces Na+/H+ Exchange (NHE) Activity in a Biliary Epithelial Cancer Cell Line (Mz-Cha-1) Anticancer Res 2011, 31:459-456.
• Enkelmann A, Heinzelmann J, von Eggeling F, Walter M, Berndt A, Wunderlich H, Junker K. Specific protein and miRNA patterns characterise tumour-associated fibroblasts in bladder cancer. J Cancer Res Clin Oncol 2011, 137:751-759.
• Escher N, Kob R, Kaatz M, Melle C, Hipler C, von Eggeling F. Confirmation of the biological significance of transthyretin as a biomarker for cutaneous T-cell lymphoma by its protein interaction partners. Mol Med Report 2011, 4:157-161.
• Faria de Figueiredo A, Liehr T, Bhatt S, Binato R, Tavares de Souza M, Rodrigues Capela de Matos R, de Jesus Marques Salles T, Jordy FC, Ribeiro RC, Abdelhay E, Macedo Silva ML. A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia. Leuk Lymph 2011, 52:1593-1596.
• Garcia DRN, Bhatt S, Manvelyan M, de Souza MT, Binato R, Aguiar TF, Abdelhay E and Silva MLM. An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype. Mol Cytogenet 2011, 4:20. Gerlach C, Roell D, Baniahmad A. Analysis of Ligand-Specific Co-repressor Binding to the Androgen Receptor. Methods Mol Biol 2011; 776:199-223.
• Gerlach C, Roell D, Baniahmad A. Analysis of Ligand-Specific Co-repressor Binding to the Androgen Receptor. Methods Mol Biol 2011, 776:199-223
• Gläßer N, Zellner K, Kromeyer-Hauschild K. Validity of body mass index and waist circumference to detect excess fat mass in children aged 7-14 years. Eur J Clin Nutr 2011, 65:151-159.
• Hentschel J, Rubio I, Eberhart M, Hipler C, Schiefner J, Schubert K, Loncarevic IF, Wittig U, Baniahmad A, von Eggeling F. BCR-ABL- and Ras-independent activation of Raf as a novel mechanism of Imatinib resistance in CML. Int J Oncol 2011; 39:585-591.
• Holl RW, Kersting M, Kromeyer-Hauschild K, Reinehr T, Schäfer A, Tiedjen U, Widhalm K. [Certification of therapy institutions, obesity trainers, and obesity trainer academies by the German Working Group on Obesity in Children and Adolescents (AGA).] Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2011, 54:598-602. German.
• Hong W, Li J, Wang B, Chen L, Niu W, Yao Z, Baniahmad A. Epigenetic involvement of Alien/ESET complex in thyroid hormone-mediated repression of E2F1 gene expression and cell proliferation. Biochem Biophys Res Commun, 2011 415:650-655.
• Horsthemke B, Wawrzik M, Groß S, Lich C, Sauer B, Rost I, Krasemann E, Kosyakova N, Liehr T, Weise A, Dybowski JN, Hoffmann D, Wieczorek D. Parental origin and functional relevance of a de novo UBE3A variant. Eur J Med Genet 20111, 54:19-24.
• Huebner AK, Gandia M, Frommolt P, Maak A, Wicklein EM, Thiele H, Altmüller J, Wagner F, Viñuela A, Aguirre LA, Moreno F, Maier H, Rau I, Gießelmann S, Nürnberg G, Gal A, Nürnberg P, Hübner CA, Del Castillo I, Kurth I. Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss. Am J Hum Genet 2011, 88:621-627.
• Jain S, Kim HG, Lacbawan F, Meliciani I, Wenzel W, Kurth I, Sharma J, Schoeneman M, Ten S, Layman LC, Jacobson-Dickman E. Unique phenotype in a patient with CHARGE syndrome. Int J Pediatr Endocrinol 2011, 2011:11.
• Khalilov I, Chazal G, Chudotvorova I, Pellegrino C, Corby S, Ferrand N, Gubkina O, Nardou R, Tyzio R, Yamamoto S, Jentsch TJ, Hübner CA, Gaiarsa JL, Ben-Ari Y, Medina I. Enhanced Synaptic Activity and Epileptiform Events in the Embryonic KCC2 Deficient Hippocampus. Front Cell Neurosci 2011, 5:23.
• Klag T, Schnetzke U, Benz R, Zanow J, Glaser A, Pörner TC, Scholl S, Reiter A, Hochhaus A, La Rosée P. Leriche's syndrome and Löffler endocarditis in a 30-year-old patient presenting with hypereosinophilic syndrome. Ann Hematol. 2012, 91:139-141.
• Koch D, Spiwoks-Becker I, Sabanov V, Sinning A, Dugladze T, Stellmacher A, Ahuja R, Grimm J, Schüler S, Müller A, Angenstein F, Ahmed T, Diesler A, Moser M, Tom Dieck S, Spessert R, Boeckers TM, Fässler R, Hübner CA, Balschun D, Gloveli T, Kessels MM, Qualmann B. Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin I, EMBO J 2011, 30:4955-4969.
• Kraoua L, Chaabouni M, Ewers E, Chelly I, Ouertani I, Jemaa LB, Maazoul F, Liehr T, Chaabouni H. Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene in a patient with pigmentary dysplasia: case report. Europ J Med Genet 2011, 54:e446-450.
• Kromeyer-Hauschild K, Dortschy R, Stolzenberg H, Neuhauser H, Rosario AS. Nationally representative waist circumference percentiles in German adolescents aged 11.0-18.0 years. Int J Pediatr Obes 2011; 6:e129-137.
• Lausch E, Janecke A, Bros M, Trojandt S, Alanay Y, De Laet C, Hübner CA, Meinecke P, Nishimura G, Matsuo M, Hirano Y, Tenoutasse S, Kiss A, Rosa RF, Unger SL, Renella R, Bonafé L, Spranger J, Unger S, Zabel B, Superti-Furga A. Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity. Nat Genet 2011, 43:132-137.
• Liehr T. What is uniparental disomy (UPD)? [online] Oxford Gene Technology. Available at: http://www.ogt.co.uk/cytosure_whatisUPD.html
• Liehr T, Bartels I, Zoll B, Ewers E, Mrasek K, Kosyakova N, Merkas M, Hamid AB, von Eggeling F, Posorski N, Weise A. Is there a yet unreported unbalanced chromosomal abnormalities without phenotypic consequences in proximal 4p? Cytogenet Genome Res 2011, 132:121-123.
• Liehr T, Ewers E, Hamid AB, Kosyakova N, Voigt M, Weise A, Manvelyan M. Small supernumerary marker chromosomes and uniparental disomy have a story to tell. J Histochem Cytochem 2011; 59:842-848.
• Liehr T, Kosayakova N, Schröder J, Ziegler M, Kreskowski K, Pohle B, Bhatt S, Theuss L, Wilhelm K, Weise A, Mrasek K. Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Balk J Med Genet 2011, 14:13-16.
• Linke T, Scholten M, Baniahmad A. Detection of Ligand-Selective Interactions of the Human Androgen Receptor by SELDI-MS-TOF. Methods Mol Biol 2011; 776:225-251.
• Lorenz V, Hessenkemper W, Rödiger J, Kyrylenko S, Kraft F, Baniahmad A. Sodium butyrate induces cellular senescence in neuroblastoma and prostate cancer cells. Horm Mol Biol Clin Invest 2011, 7:265-272.
• Manolakos E, Vetro A, Kefalas K, Thomaidis L, Aperis G, Sotiriou S, Kitsos G, Merkas M, Sifakis S, Papoulidis I, Liehr T, Zuffardi O, Petersen MB. Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation. Am J Med Genet A. 2011,155:1476-1482.
• Manvelyan M, Cremer FW, Lancé J, Kläs R, Kelbova C, Ramel C, Reichenbach H, Schmidt C, Ewers E, Kreskowski K, Ziegler M, Kosyakova N, Liehr T. New cytogenetically visible copy number variant in region 8q21.2. Mol Cytogenet 2011, 4:1.
• Melo JB, Backx L, Vermeesch JR, Santos HG, Duarte AC, Kosyakova N, Weise A, von Eggeling F, Liehr T, Carreira IM. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances. J Appl Genet 2011, 52:193-200.
• Miene C, Weise A, Glei M. Impact of polyphenol metabolites produced by colonic microbiota on expression of COX-2 and GSTT2 in human colon cells (LT97). Nutr Cancer 2011, 63:653-662.
• Milenkovic T, Guc-Scekic M, Zdravkovic D, Topic V, Liehr T, Joksic G, Radivojevic D, Lakic N. Molecular analysis of ring Y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency. Balk J Med Genet 2011, 14:71-75.
• Pan D, Kalfa TA, Wang D, Risinger M, Crable S, Ottlinger A, Chandra S, Mount DB, Hübner CA, Franco RS, Joiner CH. K-Cl cotransporter gene expression during human and murine erythroid differentiation. J Biol Chem 2011 , 286:30492-30503.
• Pellestor F, Puechberty J, Weise A, Lefort G, Anahory T, Liehr T, Sarda P. Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. Fertil Steril 2011, 95:2433.e17-2433.e22.
• Pellestor F, Anahory T, Lefort G, Puechberty J, Liehr T, Hédon B, Sarda P. Complex chromosomal rearrangements: origin and meiotic behavior. Hum Reprod Update 2011, 17:476-494.
• Pilchowski R, Stöhr R, von Eggeling F, Hartmann A, Wunderlich H, Junker K. Specific protein patterns characterize metastatic potential of advanced bladder cancer. J Urol 2001; 186:713-720.
• Posorski N, Kaemmerer D, Ernst G, Grabowski P, Hoersch D, Hommann M, von Eggeling F. Localization of sporadic neuroendocrine tumors by gene expression analysis of their metastases. Clin Exp Metastasis 2011, 28:637-647.
• Reeb CA, Gerlach C, Heinssmann M, Prade I, Ceraline J, Roediger J, Roell D, Baniahmad A. A designed cell-permeable aptamer-based corepressor Peptide is highly specific for the androgen receptor and inhibits prostate cancer cell growth in a vector-free mode. Endocrinology 2011, 152:2174-2183.
• Roell D, Baniahmad A. The natural compounds atraric acid and N-butylbenzene-sulfonamide as antagonists of the human androgen receptor and inhibitors of prostate cancer cell growth. Mol Cell Endocrinol 2011, 332:1-8.
• Roell D, Rösler TW, Degen S, Matusch R, Baniahmad A. Antiandrogenic activity of anthranilic acid ester derivatives as novel lead structures to inhibit prostate cancer cell proliferation. Chem Biol Drug Des 2011, 77:450-459.
• Sheth F, Andrieux J, Ewers E, Kosyakova N, Weise A, Sheth H, Romana SP, Lelorc'h M, Delobel B, Theisen O, Liehr T, Nampoothiri S, Sheth J. Characterization of sSMC by FISH and molecular techniques Europ J Med Genet 2011, 54:247-255.
• Sinning A, Liebmann L, Kougioumtzes A, Westermann M, Bruehl C, Hübner CA. Synaptic glutamate release is modulated by the Na+-driven Cl-/HCO formula exchanger Slc4a8. J Neurosci 2011, 31:7300-7311.
• Soares-Ventura EM, Mkrtchyan H, de Jesus Marques-Salles T, Silva M, Santos N, de Araujo Silva Amaral B, Liehr T, Abdelhay E, Macedo Silva ML, Cartaxo Muniz MT. Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma. Leuk Res 2011, 35:e27-e29.
• Stuhrmann-Spangenberg M, Engels H, Fritz B, Gabriel H, Gläser D, Henn W, Liehr T, Miller K, Rieder H. S2-Leitlinie Humangenetische Diagnostik. medgen 2011 23:281-323
• Villa O, Mallo M, Kosyakova N, Salido M, Liehr T, Martínez-Avilés L, Pedro C, García-Aragonés M, Espinet B, Florensa L, Arenillas L, Cuscó I, Pérez Jurado LA, Solé F. Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array. Leuk Res 2011,35: e161- e163.
• Westrich V, Liehr T. Molecular cytogenetic approaches and array-diagnostics in prenatal medicine. MedGen 2011, 22:463-468.
• Woelfel C, Liehr T, Weise A, Langrehr J, Amin Kotb W, Pacyna-Gengelbach M, Katenkamp D, Petersen I. Molecular cytogenetic characterization of epithelioid hemangioendothelioma. Cancer Genetics 2011, 204:671-676.

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