Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: ANEUPLOIDY - , . Treffer: 33

2019

Mann, K; Petek, E; Pertl, B Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence PCR.
Methods Mol Biol. 2019; 1885: 139-160.
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2018

Schenk, M; Groselj-Strele, A; Eberhard, K; Feldmeier, E; Kastelic, D; Cerk, S; Weiss, G Impact of polar body biopsy on embryo morphokinetics-back to the roots in preimplantation genetic testing?
J Assist Reprod Genet. 2018; 35(8):1521-1528 [OPEN ACCESS]
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2017

Holland, O; Kroneis, T; El-Heliebi, A; McDowell-Hook, M; Stone, P; Sedlmayr, P; Chamley, L Detection of Fetal Sex, Aneuploidy and a Microdeletion from Single Placental Syncytial Nuclear Aggregates.
Fetal Diagn Ther. 2017; 41(1):32-40
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2016

Belic, J; Koch, M; Ulz, P; Auer, M; Gerhalter, T; Mohan, S; Fischereder, K; Petru, E; Bauernhofer, T; Geigl, JB; Speicher, MR; Heitzer, E mFast-SeqS as a Monitoring and Pre-screening Tool for Tumor-Specific Aneuploidy in Plasma DNA.
Adv Exp Med Biol. 2016; 924:147-155
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Bogen, D; Brunner, C; Walder, D; Ziegler, A; Abbasi, R; Ladenstein, RL; Noguera, R; Martinsson, T; Amann, G; Schilling, FH; Ussowicz, M; Benesch, M; Ambros, PF; Ambros, IM The genetic tumor background is an important determinant for heterogeneous MYCN-amplified neuroblastoma.
Int J Cancer. 2016; 139(1):153-163 [OPEN ACCESS]
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2015

Belic, J; Koch, M; Ulz, P; Auer, M; Gerhalter, T; Mohan, S; Fischereder, K; Petru, E; Bauernhofer, T; Geigl, JB; Speicher, MR; Heitzer, E Rapid Identification of Plasma DNA Samples with Increased ctDNA Levels by a Modified FAST-SeqS Approach.
Clin Chem. 2015; 61(6):838-849 [OPEN ACCESS]
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Meena, JK; Cerutti, A; Beichler, C; Morita, Y; Bruhn, C; Kumar, M; Kraus, JM; Speicher, MR; Wang, ZQ; Kestler, HA; d'Adda di Fagagna, F; Günes, C; Rudolph, KL Telomerase abrogates aneuploidy-induced telomere replication stress, senescence and cell depletion.
EMBO J. 2015; 34(10):1371-1384 [OPEN ACCESS]
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2013

Gottschalk, B; Klein, A Restoration of wild-type p53 in drug-resistant mouse breast cancer cells leads to differential gene expression, but is not sufficient to overcome the malignant phenotype.
Mol Cell Biochem. 2013; 379(1-2): 213-227.
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Seiringer, M; Maurer, M; Shebl, O; Dreier, K; Tews, G; Ziehr, S; Schappacher-Tilp, G; Petek, E; Ebner, T Efficacy of a sperm-selection chamber in terms of morphology, aneuploidy and DNA packaging.
Reprod Biomed Online. 2013; 27(1):81-88 [OPEN ACCESS]
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2011

Mann, K; Petek, E; Pertl, B Prenatal detection of chromosome aneuploidy by quantitative-fluorescence PCR.
Methods Mol Biol. 2011; 688:207-226
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2009

Ladika-Davidovic, B; Coric, M; Bura, M; Brcic, L; Kusic, Z; Seiwerth, S Heterogeneity of DNA content in laryngeal squamous cell carcinoma in relation to histopathological variables.
Acta Otolaryngol. 2009; 129(7): 768-773.
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2008

Bink, K; Haralambieva, E; Kremer, M; Ott, G; Beham-Schmid, C; de Leval, L; Peh, SC; Laeng, HR; Jütting, U; Hutzler, P; Quintanilla-Martinez, L; Fend, F Primary extramedullary plasmacytoma: similarities with and differences from multiple myeloma revealed by interphase cytogenetics.
Haematologica. 2008; 93(4): 623-626. [OPEN ACCESS]
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Geigl, JB; Obenauf, AC; Schwarzbraun, T; Speicher, MR Defining 'chromosomal instability'.
Trends Genet. 2008; 24(2): 64-69.
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Mann, K; Petek, E; Pertl, B Prenatal detection of chromosome aneuploidy by quantitative fluorescence PCR.
Methods Mol Biol. 2008; 444(4):71-94
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2007

Majer, S; Bauer, M; Magnet, E; Strele, A; Giegerl, E; Eder, M; Lang, U; Pertl, B Maternal urine for prenatal diagnosis--an analysis of cell-free fetal DNA in maternal urine and plasma in the third trimester.
Prenat Diagn. 2007; 27(13):1219-1223
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2006

Bauer, M; Hutterer, G; Eder, M; Majer, S; Leshane, E; Johnson, KL; Peter, I; Bianchi, DW; Pertl, B A prospective analysis of cell-free fetal DNA concentration in maternal plasma as an indicator for adverse pregnancy outcome.
Prenat Diagn. 2006; 26(9):831-836
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2004

Auner, HW; Zebisch, A; Schimek, MG; Bodner, C; Hiden, K; Linkesch, W; Haas, OA; Beham-Schmid, C; Sill, H High expression of the sister-chromatid separation regulator and proto-oncogene hSecurin occurs in a subset of myeloid leukaemias but is not implicated in the pathogenesis of aneuploidy.
Leukemia. 2004; 18(2):303-308 [OPEN ACCESS]
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2003

Petek, E; Pertl, B; Tschernigg, M; Bauer, M; Mayr, J; Wagner, K; Kroisel, PM Characterisation of a 19-year-old long-term survivor with Edwards syndrome.
Genet Couns. 2003; 14(2):239-244 (- Case Report)
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2002

Bunz, F; Fauth, C; Speicher, MR; Dutriaux, A; Sedivy, JM; Kinzler, KW; Vogelstein, B; Lengauer, C Targeted inactivation of p53 in human cells does not result in aneuploidy.
Cancer Res. 2002; 62(4):1129-1133 [OPEN ACCESS]
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Kroisel, PM; Wagner, K; Zierler, H; Petek, E Pitfalls in prenatal and postnatal detection of partial trisomy and tetrasomy 13 by rapid aneuploidy detection.
Prenat Diagn. 2002; 22(3):267-269 (- Case Report)
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2001

Grote, HJ; Friedrichs, N; Pomjanski, N; Guhde, HF; Reich, O; Böcking, A Prognostic significance of DNA cytometry in carcinoma of the uterine cervix FIGO stage IB and II.
Anal Cell Pathol. 2001; 23(3-4):97-105 [OPEN ACCESS]
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Ladenstein, R; Ambros, IM; Pötschger, U; Amann, G; Urban, C; Fink, FM; Schmitt, K; Jones, R; Slociak, M; Schilling, F; Ritter, J; Berthold, F; Gadner, H; Ambros, PF Prognostic significance of DNA di-tetraploidy in neuroblastoma.
Med Pediatr Oncol. 2001; 36(1):83-92
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Samura, O; Sohda, S; Johnson, KL; Pertl, B; Ralston, S; Delli-Bovi, LC; Bianchi, DW Diagnosis of trisomy 21 in fetal nucleated erythrocytes from maternal blood by use of short tandem repeat sequences.
Clin Chem. 2001; 47(9):1622-1626 [OPEN ACCESS]
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1999

Pertl, B; Kopp, S; Kroisel, PM; Tului, L; Brambati, B; Adinolfi, M Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samples.
J Med Genet. 1999; 36(4):300-303 [OPEN ACCESS]
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Pertl, B; Pieber, D; Lercher-Hartlieb, A; Orescovic, I; Haeusler, M; Winter, R; Kroisel, P; Adinolfi, M Rapid prenatal diagnosis of aneuploidy by quantitative fluorescent PCR on fetal samples from mothers at high risk for chromosome disorders.
Mol Hum Reprod. 1999; 5(12):1176-1179 [OPEN ACCESS]
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1998

Pertl, B; Sherlock, J; Adinolfi, M Rapid prenatal detection of aneuploidies by fluorescent polymerase chain reaction - Reply.
AM J OBSTET GYNECOL . 1998; 178(5): 1101-1102.
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1997

Adinolfi, M; Pertl, B; Sherlock, J Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction.
Prenat Diagn. 1997; 17(13):1299-1311
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1996

Pertl, B; Weitgasser, U; Kopp, S; Kroisel, PM; Sherlock, J; Adinolfi, M Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCR.
Hum Genet. 1996; 98(1):55-59
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1995

Adinolfi, M; Sherlock, J; Pertl, B Rapid detection of selected aneuploidies by quantitative fluorescent PCR.
Bioessays. 1995; 17(7): 661-664.
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Ried, T; Just, KE; Holtgreve-Grez, H; du Manoir, S; Speicher, MR; Schröck, E; Latham, C; Blegen, H; Zetterberg, A; Cremer, T Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and aneuploid carcinomas.
Cancer Res. 1995; 55(22):5415-5423 [OPEN ACCESS]
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Rosanelli, GP; Steindorfer, P; Wirnsberger, GH; Klimpfinger, M; Ratschek, M; Puerstner, P; Auner, H; Berhold, A Mutant p53 expression and DNA analysis in human breast cancer comparison with conventional clinicopathological parameters.
Anticancer Res. 1995; 15(2):581-586
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1993

du Manoir, S; Speicher, MR; Joos, S; Schröck, E; Popp, S; Döhner, H; Kovacs, G; Robert-Nicoud, M; Lichter, P; Cremer, T Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.
Hum Genet. 1993; 90(6):590-610
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1990

Feichtinger, H; Tötsch, M; Schmid, KW; Weger, AR; Mikuz, G Co-existence of two aneuploid stemlines in benign adenomas.
Virchows Arch A Pathol Anat Histopathol. 1990; 416(3): 277-279.
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