Karoly Szuhai

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Publications in SciGraph latest 50 shown

  • 2017-12 Fluorescent CXCR4 targeting peptide as alternative for antibody staining in Ewing sarcoma in BMC CANCER
  • 2017-12 DNA methylation and transcriptional trajectories during human development and reprogramming of isogenic pluripotent stem cells in NATURE COMMUNICATIONS
  • 2017-09-06 Corrigendum: p120-catenin prevents multinucleation through control of MKLP1-dependent RhoA activity during cytokinesis in NATURE COMMUNICATIONS
  • 2017-07-24 Actomyosin drives cancer cell nuclear dysmorphia and threatens genome stability in NATURE COMMUNICATIONS
  • 2016-12-22 p120-catenin prevents multinucleation through control of MKLP1-dependent RhoA activity during cytokinesis in NATURE COMMUNICATIONS
  • 2016-10 Inhibition of Bcl-2 family members sensitizes mesenchymal chondrosarcoma to conventional chemotherapy: report on a novel mesenchymal chondrosarcoma cell line in LABORATORY INVESTIGATION
  • 2016-08 Expression of CCL21 in Ewing sarcoma shows an inverse correlation with metastases and is a candidate target for immunotherapy in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 2016-08 Establishment and characterization of a new human myxoid liposarcoma cell line (DL-221) with the FUS-DDIT3 translocation in LABORATORY INVESTIGATION
  • 2016-07 Activation of the vitamin D receptor selectively interferes with calcineurin-mediated inflammation: a clinical evaluation in the abdominal aortic aneurysm in LABORATORY INVESTIGATION
  • 2015-12 Mesenchymal stromal cells of osteosarcoma patients do not show evidence of neoplastic changes during long-term culture in CLINICAL SARCOMA RESEARCH
  • 2015-12 Expression of the immune regulation antigen CD70 in osteosarcoma in CANCER CELL INTERNATIONAL
  • 2015-10 Microarray Techniques to Analyze Copy-Number Alterations in Genomic DNA: Array Comparative Genomic Hybridization and Single-Nucleotide Polymorphism Array in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2014-05 GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma in NATURE GENETICS
  • 2013 Array-CGH Analysis of Cutaneous Anaplastic Large Cell Lymphoma in ARRAY COMPARATIVE GENOMIC HYBRIDIZATION
  • 2012-12 Paratesticular desmoplastic small round cell tumour: an unusual tumour with an unusual fusion; cytogenetic and molecular genetic analysis combining RT-PCR and COBRA-FISH in CLINICAL SARCOMA RESEARCH
  • 2012-12 Three new chondrosarcoma cell lines: one grade III conventional central chondrosarcoma and two dedifferentiated chondrosarcomas of bone in BMC CANCER
  • 2012-11 A common single-nucleotide variant in T is strongly associated with chordoma in NATURE GENETICS
  • 2012-11 Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches in VIRCHOWS ARCHIV
  • 2012-10 Characterization of a New Human Cell Line (CH-3573) Derived from a Grade II Chondrosarcoma with Matrix Production in PATHOLOGY & ONCOLOGY RESEARCH
  • 2012-04 Angiomatoid Fibrous Histiocytoma: Pleomorphic Variant Associated with Multiplication of EWSR1-CREB1 Fusion Gene in PATHOLOGY & ONCOLOGY RESEARCH
  • 2012-03 Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT in ONCOGENE
  • 2012-03 1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma in ONCOGENE
  • 2012-01 Analysis of stromal cells in osteofibrous dysplasia and adamantinoma of long bones in MODERN PATHOLOGY
  • 2011-12 Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome in NATURE GENETICS
  • 2011-12 Oncogenic functions of hMDMX in in vitro transformation of primary human fibroblasts and embryonic retinoblasts in MOLECULAR CANCER
  • 2011-12 A short-term in vivo model for giant cell tumor of bone in BMC CANCER
  • 2011-12 Opening the archives for state of the art tumour genetic research: sample processing for array-CGH using decalcified, formalin-fixed, paraffin-embedded tissue-derived DNA samples in BMC RESEARCH NOTES
  • 2011-12 Genome-wide analysis of Ollier disease: Is it all in the genes? in ORPHANET JOURNAL OF RARE DISEASES
  • 2011-12 Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 Multiple Osteochondromas families in BMC MEDICAL GENETICS
  • 2011-04 Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15-activated allogeneic and autologous NK cells in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 2010-12 Kinome profiling of myxoid liposarcoma reveals NF-kappaB-pathway kinase activity and Casein Kinase II inhibition as a potential treatment option in MOLECULAR CANCER
  • 2010-12 Evaluation of high-resolution microarray platforms for genomic profiling of bone tumours in BMC RESEARCH NOTES
  • 2010-12 Centriole movements in mammalian epithelial cells during cytokinesis in BMC CELL BIOLOGY
  • 2010-02 Cutaneous Anaplastic Large Cell Lymphoma and Peripheral T-Cell Lymphoma NOS Show Distinct Chromosomal Alterations and Differential Expression of Chemokine Receptors and Apoptosis Regulators in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2009-12 A balanced t(5;17) (p15;q22-23) in chondroblastoma: frequency of the re-arrangement and analysis of the candidate genes in BMC CANCER
  • 2008-01 Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation in BRITISH JOURNAL OF CANCER
  • 2007-12 Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer in BMC GENOMICS
  • 2007-11 Guidelines for molecular karyotyping in constitutional genetic diagnosis in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-05 Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2006-12 Clonal T- and natural killer-cell large granular lymphocyte proliferations in a single patient established by array-based comparative genomic hybridization analysis in LEUKEMIA
  • 2006-08 A complex rearrangement on chromosome 22 affecting both homologues; haplo-insufficiency of the Cat eye syndrome region may have no clinical relevance in HUMAN GENETICS
  • 2006-06 COBRA: combined binary ratio labeling of nucleic-acid probes for multi-color fluorescence in situ hybridization karyotyping in NATURE PROTOCOLS
  • 2006-03 Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model in MODERN PATHOLOGY
  • 2006-02 Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2005-12 Expression analysis of candidate breast tumour suppressor genes on chromosome 16q in BREAST CANCER RESEARCH
  • 2005-04 Array CGH detection of a cryptic deletion in a complex chromosome rearrangement in HUMAN GENETICS
  • 2004-11 Primary synovial sarcoma of the heart: a cytogenetic and molecular genetic analysis combining RT-PCR and COBRA-FISH of a case with a complex karyotype in MODERN PATHOLOGY
  • 2002-07 Connexin 26 mutations in cases of sensorineural deafness in eastern Austria in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-03 A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease in EUROPEAN JOURNAL OF HUMAN GENETICS
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