about
Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisationPeters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferaseRapid detection of genomic imbalances using micro-arrays consisting of pooled BACs covering all human chromosome arms.The second European interdisciplinary Ewing sarcoma research summit--A joint effort to deconstructing the multiple layers of a complex diseaseSequencing Overview of Ewing Sarcoma: A Journey across Genomic, Epigenomic and Transcriptomic LandscapesThe NFATc2 gene is involved in a novel cloned translocation in a Ewing sarcoma variant that couples its function in immunology to oncologySecondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXTLoss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppressionCentriole movements in mammalian epithelial cells during cytokinesisA short-term in vivo model for giant cell tumor of bone.p120-catenin prevents multinucleation through control of MKLP1-dependent RhoA activity during cytokinesis.Fluorescent CXCR4 targeting peptide as alternative for antibody staining in Ewing sarcomaHigh-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays.Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study.Establishment and detailed functional and molecular genetic characterisation of a novel sacral chordoma cell line, MUG-Chor1.Molecular pathology and its diagnostic use in bone tumors.'The chicken or the egg?' dilemma strikes back for the controlling mechanism in chordoma(#).A common single-nucleotide variant in T is strongly associated with chordoma.Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.COBRA: combined binary ratio labeling of nucleic-acid probes for multi-color fluorescence in situ hybridization karyotyping.A balanced t(5;17) (p15;q22-23) in chondroblastoma: frequency of the re-arrangement and analysis of the candidate genes.Evaluation of high-resolution microarray platforms for genomic profiling of bone tumours.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 samplesBreakpoint characterization of large deletions in EXT1 or EXT2 in 10 multiple osteochondromas familiesFamilial adenomatous polyposis-associated desmoids display significantly more genetic changes than sporadic desmoids.Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.No haploinsufficiency but loss of heterozygosity for EXT in multiple osteochondromasA novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B gene.Three new chondrosarcoma cell lines: one grade III conventional central chondrosarcoma and two dedifferentiated chondrosarcomas of bone.GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.Non-random mtDNA segregation patterns indicate a metastable heteroplasmic segregation unit in m.3243A>G cybrid cells.A 17q21.31 microdeletion encompassing the MAPT gene in a mentally impaired patient.Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2.Guidelines for molecular karyotyping in constitutional genetic diagnosis.Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15-activated allogeneic and autologous NK cells.Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the Wnt/beta-catenin signaling pathway.Cathepsin K is the principal protease in giant cell tumor of bone.Expression of the immune regulation antigen CD70 in osteosarcoma.A novel strategy for human papillomavirus detection and genotyping with SybrGreen and molecular beacon polymerase chain reactionCellular/intramuscular myxoma and grade I myxofibrosarcoma are characterized by distinct genetic alterations and specific composition of their extracellular matrix
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Karoly Szuhai
@ast
Karoly Szuhai
@en
Karoly Szuhai
@es
Karoly Szuhai
@nl
Karoly Szuhai
@sl
type
label
Karoly Szuhai
@ast
Karoly Szuhai
@en
Karoly Szuhai
@es
Karoly Szuhai
@nl
Karoly Szuhai
@sl
prefLabel
Karoly Szuhai
@ast
Karoly Szuhai
@en
Karoly Szuhai
@es
Karoly Szuhai
@nl
Karoly Szuhai
@sl
P108
P106
P21
P31
P496
0000-0002-1228-4245