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AbdElmontalab FY, Fadl IE, Abushama HM, Kreskowski K, Liehr T. Molecular cytogenetic study of the NF2 gene deletion in meningioma in Sudanese patients. Balk J Med Genet 2013, 16:29-32
Abo-Zeid MA, Liehr T, El-Daly SM, Gamal-Eldeen AM, Glei M, Shabaka A, Bhatt S, Hamid A. Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by Indocyanine Green in breast adenocarcinoma MCF-7 cells. Photodiagn Photodynam Therapy 2013, 10:194-202.
Al-Achkar W, Aljapawe A, Almedani S, Liehr T, Wafa A. A novel cytogenetic abnormality t(7;8)(p11.2:q11.2) and a four-way Philadelphia translocation in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 617-620.
Al-Achkar W, Wafa A, Liehr T. A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case. Oncol Lett 2013, 5: 605-608.
Al-Achkar W, Wafa A, Moassass F, Klein E, Liehr T. Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 1579-1582.
Al-Achkar W, Wafa A, Ikhtiar A, Liehr T. Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 1656-1658.
Al-Achkar W, Wafa A, Assaad M, Ehlers C, Liehr T. A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7. Mol Med Rep 2013, 7: 1545-1548.
Al Achkar W, Wafa A, Aljapawe A, Liehr T. A de novo del(9)(p22.3) in a primary plasma cell leukemia case. Mol Cytogenet 2013, 6:33.
Al-achkar W, Aljapawe A, Othman MA, Wafa A. A de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints. Molecular Cytogenetics 2013, 6:18.
Al-Achkar W, Moassass F, Ikhtiar A, Othman MAK, Liehr T, Wafa A. Cytogenetic evolution in a patient with chronic developing a secondary acute myelogenous leukemia subtype M5 resistant to Imatinib mesylate therapy. J Leuk 2013, 1: 118.
Al Achkar W, Wafa A, Aljapawe A, Othman MAK, Liehr T. A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case. Case Rep Clin Med 2013, 2: 517-520.
Al-Achkar , Wafa A, Al-Ablog A, Moassas F, Liehr T. Molecular cytogenetic characterization on an inv(Y)(p11.2q11.221q11.222) in a Syrian family. Balk J Med Genet 2013, 16:73-76
Alexandrov T, Becker M, Guntinas-Lichius O, Ernst G, von Eggeling F. MALDI-imaging segmentation is a powerful tool for spatial functional proteomic analysis of human larynx carcinoma. J Cancer Res Clin Oncol 2013, 139:85-95.
Alves G, Pereira DA, Sandim V, Ornellas AA, Escher N, Melle C, von Eggeling F. Urine screening by Seldi-Tof, followed by biomarker identification, in a Brazilian cohort of patients with Renal Cell Carcinoma (RCC). Int Braz J Urol 2013, 39:228-239.
Antoine MW, Hübner CA, Arezzo JC, Hébert JM. A causative link between inner ear defects and long-term striatal dysfunction. Science 2013, 341:1120-1123.
Aust N, Schüle S, Altendorf-Hofmann AK, Chen Y, Knösel T, Dirsch O, Settmacher U, Weise A, Mrasek K, Liehr T. Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases. J Cancer Res Clin Oncol 2013, 139:1861-1867.
Baniahmad A. Why do we need to age? Horm Mol Biol Clin Invest 2013, 16:3-5
Baniahmad A, Tresguerres JA, Zouboulis CC. Special issue on hormones and ageing. Horm Mol Biol Clin Investig 2013, 16:1-2.
Barber JC, Hall V, Maloney VK, Huang S, Roberts AM, Brady AF, Foulds N, Bewes B, Volleth M, Liehr T, Mehnert K, Bateman M, White H. 16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. Eur J Hum Genet 2013, 21:182-189.
Beetz C, Koch N, Khundadze M, Zimmer G, Nietzsche S, Hertel N, Huebner AK, Mumtaz R, Schweizer M, Dirren E, Karle KN, Irintchev A, Alvarez V, Redies C, Westermann M, Kurth I, Deufel T, Kessels MM, Qualmann B, Hübner CA. A spastic paraplegia mouse model reveals REEP1-dependent ER shaping. J Clin Invest 2013, 123:4273-4282 - see also J Clin Invest 2014,124:2809.
Bhatt AD, Liehr T, Bakshi SR. Phenotypic spectrum in uniparental disomy: low incidence or lack of study? Indian J Hum Genet 2013, 19: 311-314.
Bocklitz TW, Crecelius AC, Matthäus C, Tarcea N, von Eggeling F, Schmitt M, Schubert US, Popp J. Deeper understanding of biological tissue: quantitative correlation of maldi-tof and Raman imaging. Anal Chem 2013; 85:10829-10834.
Cavdarli B, Ozgen G, Kaymak AO, Göker B, Liehr T, Ergun MA, Percin EF. A case with double translocation and Sjögren syndrome. Turkiye Klinikleri J Med Sci 2013, 33:263-236.
Chambrey R, Kurth I, Peti-Peterdi J, Houillier P, Purkerson JM, Leviel F, Hentschke M, Zdebik AA, Schwartz GJ, Hübner CA, Eladari D. Renal intercalated cells are rather energized by a proton than a sodium pump. Proc Natl Acad Sci U S A 2013, 110:7928-7933.
Cioffi MB, Liehr T, Trifonov V, Molina WF, Bertollo LAC. Independent sex chromosome evolution in lower vertebrates: A molecular cytogenetic overview in the Erythrinidae fish family. Cytogenet Genome Res 2013, 141:186-194.
Eckey M, Kraft F, Kob R, Escher N, Asim M, Fischer H, Fritsche MK, Melle C, Baniahmad A. The corepressor activity of Alien is controlled by CREB-binding protein/p300. FEBS J 2013, 280:1861-1868.
Fan X, Pinthong K, Mkrtchyan H, Siripiyasing P, Kosyakova N, Supiwong W, Tanomtong A, Chaveerach A, Liehr T, de Bello Cioffi M, Weise A. First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae). Mol Cytogenet 2013, 6:58.
Foertsch F, Teichmann N, Kob R, Hentschel J, Laubscher U, Melle C. S100A11 is involved in the regulation of the stability of cell cycle regulator p21(CIP1/WAF1) in human keratinocyte HaCaT cells. FEBS J 2013, 280:3840-3853.
Guilherme RS, Dutra ARN, Perez AB, Takeno SS, Oliveira MM, Kulikowski D, Klein E, Hamid AB, Liehr T, Melaragno MI. First report of a small supernumerary der(8;14) marker chromosome. Cytogenet Genome Res 2013, 139:284-288.
Guilherme RS, Klein E, Hamid AB, Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen MB, Manolakos E, Kosyakova N, Liehr T. Human ring chromosomes - new insights for their clinical significance. Balk J Med Genet 2013, 16:13-19.
Guilherme RS, Cernach MC, Sfakianakis TE, Takeno SS, Nardozza LM, Rossi C, Bhatt SS, Liehr T, Melaragno MI. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification. Cytogenet Genome Res 2013, 141:317-323.
Heinrich-Weltzien R, Monse B, Benzian H, Heinrich J, Kromeyer-Hauschild K. Association of dental caries and weight status in 6- to 7-year-old Filipino children. Clin Oral Investig 2013, 17:1515-1523.
Heinrich-Weltzien R, Zorn C, Monse B, Kromeyer-Hauschild K. Relationship between malnutrition and the number of permanent teeth in Filipino 10- to 13-year-olds. Biomed Res Int 2013, 2013:205950.
Hessenkemper W, Baniahmad A. Targeting heat shock proteins in prostate cancer. Curr Med Chem 2013, 20:2731-2740.
Hoelscher M, Richter N, Melle C, von Eggeling F, Schaenzer A, Nestler U. SELDI-TOF analysis of glioblastoma cyst fluid is an approach for assessing cellular protein expression. Neurol Res 2013, 35:993-1001.
Huebner AK, Hübner CA. Ionentransport und Taubheit. Medgen. 2013, 25:475-479.
Hübner CA, Holthoff K. Anion transport and GABA signaling.Front Cell Neurosci 2013, 7:177.
Hunstig F, Hammersen J, Kunert C, Petersen I, Merz H, Glaser A, Teichgräber U, Hochhaus A, Rosée PL. Complete remission after treatment with single-agent ofatumumab in a patient with high-risk leukemic mantle-cell lymphoma. J Clin Oncol 2013, 31:e312-315.
Jacques T, Picard N, Miller RL, Riemondy KA, Houillier P, Sohet F, Ramakrishnan SK, Büsst CJ, Jayat M, Cornière N, Hassan H, Aronson PS, Hennings JC, Hübner CA, Nelson RD, Chambrey R, Eladari D. Overexpression of pendrin in intercalated cells produces chloride-sensitive hypertension. J Am Soc Nephrol 2013, 24:1104-1113.
Jancuskova T, Plachy R, Stika J, Zemankova L, Hardekopf DW, Liehr T, Kosyakova N, Cmejla R, Zejskova L, Kozak T, Zak P, Zavrelova A, Havlikova P, Karas M, Junge A, Ramel C, Pekova S. A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients. Leuk Res 2013, 37:1363-1373.
Jančušková T, Plachý R, Štika J, Krutílková L, Hardekopf DW, Liehr T, Kosyakova N, Čmejla R, Žejšková L, Kozák T, Žák P, Karas M, Peková S. Identifikace novych molekularnich “marker pro sledovani minimalni rezidualni nemoci u akutnich leumkemii. Transfuze a Hematologie Dnes 2013, 19:8-21.
Kalkunte SS, Neubeck S, Norris WE, Cheng SB, Kostadinov S, Vu Hoang D, Ahmed A, von Eggeling F, Shaikh Z, Padbury J, Berg G, Olofsson A, Markert UR, Sharma S. Transthyretin is dysregulated in preeclampsia, and its native form prevents the onset of disease in a preclinical mouse model. Am J Pathol 2013, 183:1425-1436.
Karadeniz N, Liehr T, Mrasek K, Aşık I, Aşık Z, Kosyakova N, Mkrtchyan H. C-type lectins and human epithelial membrane protein1: Are they new proteins in keratin disorders? Open J Genet 2013, 3:262-269
Karamysheva TV, Prokhorovich MA, Lagarkova MA, Kiselev SL, Liehr T, Rubtsov NB. Chromosome rearrangements in sublines of human embryonic stem cell lines hESM01 and hESM03. BioDiscovery 2013, 7:1.
Koehler K, Malik M, Mahmood S, Gießelmann S, Beetz C, Hennings JC, Huebner AK, Grahn A, Reunert J, Nürnberg G, Thiele H, Altmüller J, Nürnberg P, Mumtaz R, Babovic-Vuksanovic D, Basel-Vanagaite L, Borck G, Brämswig J, Mühlenberg R, Sarda P, Sikiric A, Anyane-Yeboa K, Zeharia A, Ahmad A, Coubes C, Wada Y, Marquardt T, Vanderschaeghe D, Van Schaftingen E, Kurth I, Huebner A, Hübner CA. Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction. Am J Hum Genet 2013, 93:727-734.
Kosyakova N, Hamid AB, Chaveerach A, Pinthong K, Siripiyasing P, Supiwong W, Romanenko S, Trifonov V, Fan X. Generation of multicolor banding probes for chromosomes of different species. Molecular Cytogenetics 2013, 6:6.
Kosyakova N, Trifonov V, Romanenko S, Mkrtchyan H, Graphodatsky A, Liehr T. Murine multicolor banding. Tsitologiya 2013, 55:259-260.
Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD, Kulpanovich AI, Egorova T, Jaroshevich E, Frolova A, Shorokh N, Naumchik IV, Volleth M, Schreyer I, Nelle H, Stumm M, Wegner R, Reising-Ackermann G, Merkas M, Brecevic L, Martin T, Rodríguez L, Bhatt S, Ziegler M, Kreskowski K, Weise A, Sazci A, Vorsanova S, Cioffi Md, Ergul E. Heteromorphic variants of chromosome 9. Molecular Cytogenetics 2013, 6:14.
Kreuser F, Kromeyer-Hauschild K, Gollhofer A, Korsten-Reck U, Röttger K. "Obese equals lazy?" analysis of the association between weight status and physical activity in children. J Obes 2013, 2013:437017.
Kromeyer-Hauschild K, Neuhauser H, Schaffrath Rosario A, Schienkiewitz A. Abdominal obesity in German adolescents defined by waist-to-height ratio and its association to elevated blood pressure: The KiGGS study. Obes Facts. 2013, 6:165-175.
Khundadze M, Kollmann K, Koch N, Biskup C, Nietzsche S, Zimmer G, Hennings JC, Huebner AK, Symmank J, Jahic A, Ilina EI, Karle K, Schöls L, Kessels M, Braulke T, Qualmann B, Kurth I, Beetz C, Hübner CA. A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system. PLoS Genet 2013, 9:e1003988.
Leibiger C, Kosyakova N, Mkrtchyan H, Glei M, Trifonov V, Liehr T. First molecular cytogenetic high resolution characterization of the NIH 3T3 cell line by murine multicolor banding. J Histochem Cytochem 2013, 61: 306-312.
Leipold E, Liebmann L, Korenke GC, Heinrich T, Gießelmann S, Baets J, Ebbinghaus M, Goral RO, Stödberg T, Hennings JC, Bergmann M, Altmüller J, Thiele H, Wetzel A, Nürnberg P, Timmerman V, De Jonghe P, Blum R, Schaible HG, Weis J, Heinemann SH, Hübner CA, Kurth I. A de novo gain-of-function mutation in SCN11A causes loss of pain perception. Nat Genet 2013, 45:1399-1404.
Liehr T. Copy number variations - is there a biological difference between submicroscopic and microscopically visible ones? OA Genetics 2013, 1:2.
Liehr T, Kosyakova N. Small supernumerary marker chromosomes (sSMC) - what about the genotype-phenotype correlation? Tsitologiya 2013, 55: 165-166.
Liehr T, Weise A, Hamid AB, Fan X, Klein E, Aust N, Othman MA, Mrasek K, Kosyakova N. Multicolor fluorescence in situ hybridization methods in nowadays clinical diagnostics. Exp Rev Mol Diag 2013, 13: 251-255.
Liehr T, Klein E, Mrasek K, Kosyakova N, Guilherme RS, Aust N, Venner C, Weise A, Hamid AB. Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes. Cytogenet Genome Res 2013, 139: 158-163.
Liehr T, Heng H, Yurov Y, Meloni-Ehrig A, Iourov I. Molecular Cytogenetics: the first impact factor (2.36) journal: Molecular Cytogenetics. Mol Cytogenet 2013, 6:28.
Liehr T, Cirkovic S, Lalic T, Guc-Scekic M, de Almeida C, Weimer J, Iourov I, Melaragno MI, Guilherme RS, Stefanou EG, Aktas D, Kreskowski K, Klein E, Ziegler M, Kosyakova N, Volleth M, Hamid AB. Complex small supernumerary marker chromosomes - an update. Mol Cytogenet 2013, 6:46.
Manolakos M, Vetro A, Papadopoulou E, Kefalas K, Lagou M, Thomaidis L, Peitsidis P, Sifakis S, Divane A, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four break rearrangement. Cytogenet Genome Res 2013, 140: 12-20.
Matos RRC, Mkrchyan H, Amaral BA, Liehr T, de Souza MT, Ney-Garcia DR, Santos N, Marques-Salles TJ, Ribeiro RC, Figueiredo AF, Silva MLM. An unusual cytogenetic rearrangement originating from two different abnormalities in chromosome 6 in a child with acute promyelocytic leukemia. Acta Hematologica 2013, 130:23-26.
Matoso E, Melo JB, Ferreira SI, Jardim A, Castelo TM, Weise A, Carreira IM. Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder. Am J Med Genet A 2013, 161A:1923-1928.
Meyer T, Guntinas-Lichius O, von Eggeling F, Ernst G, Akimov D, Schmitt M, Dietzek B, Popp J. Multimodal nonlinear microscopic investigations on head and neck squamous cell carcinoma: toward intraoperative imaging. Head Neck 2013; 35:E280-E287.
Ney-Garcia DR, Vieira TP, Liehr T, Bhatt S, de Souza MT, de Figueiredo AF, Ribeiro RC, Silva MLM. A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone. Blood Cells Mol Dis 2013, 50:131-133.
Ney Garcia DR, Vieira TP, Liehr T, Abdelhay E, Binato R, Neves F, de Souza MT, Ribeiro RC, Silva MLM . Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia. Atlas Genet Cytogenet Oncol Haematol. July 2013. URL : http://AtlasGeneticsOncology.org/Reports/t1919p13q13NeyGarciaID100072.html
Nolan LS, Maier H, Hermans-Borgmeyer I, Girotto G, Ecob R, Pirastu N, Cadge BA, Hübner C, Gasparini P, Strachan DP, Davis A, Dawson SJ. Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice. Neurobiol Aging 2013, 34:2077.e1-9.
Ou J, Wang W, Liehr T, Klein E, Hamid AB, Wang F, Duan C, Li H. Characterization of three small supernumerary marker chromosomes (sSMC) in humans. J Matern Fetal Neonatal Med 2013, 26:106-108.
Papaioannou M, Söderholm AA, Hong W, Dai Y, Roediger J, Roell D, Thiele M, Nyrönen TH, Baniahmad A. Computational and functional analysis of the androgen receptor antagonist atraric acid and its derivatives. Anticancer Agents Med Chem. 2013, 13:801-810.
Plachta-Danielzik S, Bosy-Westphal A, Kehden B, Gehrke MI, Kromeyer-Hauschild K, Grillenberger M, Willhöft C, Heymsfield SB, Müller MJ. Adiposity rebound is misclassified by BMI rebound. Eur J Clin Nutr 2013, 67:984-989.
Roos A, von Kaisenberg CS, Eggermann T, Schwanitz G, Löffler C, Weise A, Mrasek K, Junge A, Caliebe A, Belitz B, Kautza M, Schüler H, Zerres K, Heidemann S. Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies. Arch Gynecol Obstet 2013, 288:1153-1158.
Ruusuvuori E, Huebner AK, Kirilkin I, Yukin AY, Blaesse P, Helmy M, Kang HJ, El Muayed M, Hennings JC, Voipio J, Sestan N, Hübner CA, Kaila K. Neuronal carbonic anhydrase VII provides GABAergic excitatory drive to exacerbate febrile seizures. EMBO J 2013 ,32:2275-2286.
Schmidt T, Bartels I, Liehr T, Burfeind P, Zoll B, Shoukiera M. A family with an inverted tandem duplication 5q22.1-q23.2. Cytogenet Genome Res 2013,139:65-70.
Sheth FJ, Liehr T, Kumari P, Akinde R, Sheth HJ, Sheth JJ. Chromosomal abnormalities in couples with repeated fetal loss: an Indian retrospective study. Indian J Hum Genet 2013, 19: 415-422.
Shmukler BE, Hsu A, Alves J, Trudel M, Rust MB, Hubner CA, Rivera A, Alper SL. N-ethylmaleimide activates a Cl(-)-independent component of K(+) flux in mouse erythrocytes. Blood Cells Mol Dis 2013, 51:9-16.
Sinning A, Hübner CA. Minireview: pH and synaptic transmission. FEBS Lett 2013, 587:1923-1928.
Supiwong W, Liehr T, Cioffi MB, Chaveerach A, Kosyakova N, Pinthong K, Tanee T and Tanomtong A. Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae). Mol Cytogenet 2013, 6:51.
Vasconcelos DS, da Silva FPE, Quintana LG, Anselmo NP, Othman MAK, Liehr T, de Oliveira EHC. Numerical aberrations of chromosome 17 and TP53 in brain metastases derived from breast cancer. Genet Mol Res 2013, 12:2594-2600.
Vičić A, Zudenigo D, Korać P, Liehr T, Stipoljev F. Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygroma. Gene 2013, 531: 90-91.
Yomade O, Spies-Weisshart B, Glaser A, Schnetzke U, Hochhaus A, Scholl S. Impact of NOD2 polymorphisms on infectious complications following chemotherapy in patients with acute myeloid leukaemia. Ann Hematol 2013, 92:1071-1077.
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