Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Karolin Hansén Nord"'
Autor:
David Gisselsson, Jenny Nilsson, Natalie Andersson, Jenny Karlsson, Karolin Hansén Nord, Karim Saba, Linda Magnusson
Publikováno v:
Genes, Chromosomes and Cancer. 62:93-100
Autor:
Karim H. Saba, Judith V.M.G. Bovée, Suk Wai Lam, Michal Kovac, Johan Staaf, Diana C.J. Spierings, Vaiyapuri Sumathi, Jakob Hofvander, Louise Cornmark, Karoly Szuhai, Karolin Hansén Nord, Linda Magnusson, Daniel Baumhoer, Hilda van den Bos, Emelie Styring, Otte Brosjö, Floris Foijer, Jenny Nilsson
Publikováno v:
The Journal of Pathology: Clinical Research
The Journal of Pathology: Clinical Research, Vol 6, Iss 4, Pp 231-237 (2020)
Journal of pathology clinical research, 6(4), 231-237. Wiley
Journal of Pathology: Clinical Research, 6(4), 231-237. WILEY
The Journal of Pathology: Clinical Research, Vol 6, Iss 4, Pp 231-237 (2020)
Journal of pathology clinical research, 6(4), 231-237. Wiley
Journal of Pathology: Clinical Research, 6(4), 231-237. WILEY
Osteoblastoma is a locally aggressive tumour of bone. Until recently, its underlying genetic features were largely unknown. During the past two years, reports have demonstrated that acquired structural variations affect the transcription factor FOS i
Autor:
Lucia Carbone, Clelia Tiziana Storlazzi, Christopher W. Whelan, Pietro D'Addabbo, Gemma Macchia, Karolin Hansén Nord, Mariano Rocchi, Monica Zoli, Stefania Purgato, Fredrik Mertens, Giovanni Perini
Publikováno v:
Genes, Chromosomes and Cancer. 54:156-167
Gene amplification is relatively common in tumors. In certain subtypes of sarcoma, it often occurs in the form of ring and/or giant rod-shaped marker (RGM) chromosomes whose mitotic stability is frequently rescued by ectopic novel centromeres (neocen
Autor:
Fredrik Mertens, Fredrik Vult von Steyern, Henrik Lilljebjörn, Christopher D.M. Fletcher, Ingrid Øra, Jenny Nilsson, Charles Walther, Linda Magnusson, Johnbosco Tayebwa, Karolin Hansén Nord, Henryk A. Domanski, Thoas Fioretos
Publikováno v:
The Journal of Pathology. 232:534-540
Pseudomyogenic haemangioendothelioma (PHE) is an intermediate malignant vascular soft tissue tumour primarily affecting children and young adults. The molecular basis of this neoplasm is unknown. We here used chromosome banding analysis, fluorescence
Autor:
Michal Kovac, Karolin Hansén Nord, Daniel Baumhoer, Michaela Nathrath, Maxim Barenboim, Baptiste Ameline, Karim H. Saba
Publikováno v:
Cancer Research. 79:3654-3654
Background: Osteosarcoma, the most common primary tumor of bone, generally harbors complex structural rearrangements. In this study, we identified frequent mono- and bi-allelic deletions of the two long non-coding RNAs TUSC7 and LINC00901, both locat
Autor:
Thomas Wiebe, Fredrik Mertens, Fredrik Vult von Steyern, Charles Walther, Henrik C. F. Bauer, Henryk A. Domanski, Karolin Hansén Nord, David Gisselsson, Nils Mandahl, Jenny Nilsson
Publikováno v:
Cancer Genetics. 206:299-303
Soft tissue tumors in children under one year of age (infants) are rare. The etiology is usually unknown, with external factors or congenital birth defects and hereditary syndromes being recognized in only a small proportion of the cases. We ascertai
Autor:
Karolin Hansén Nord, Arezoo Mohajeri, Jason L. Hornick, Anna Collin, Nils Mandahl, Johnbosco Tayebwa, Linda Magnusson, Fredrik Mertens, Jenny Nilsson, Raf Sciot, Henryk A. Domanski, Olle Larsson, Maria Debiec-Rychter, Fredrik Vult von Steyern, Otte Brosjö
Publikováno v:
Genes, Chromosomes and Cancer. 52:873-886
Solitary fibrous tumor (SFT) is a mesenchymal neoplasm displaying variable morphologic and clinical features. To identify pathogenetically important genetic rearrangements, 44 SFTs were analyzed using a variety of techniques. Chromosome banding and f
Autor:
Andrew L. Folpe, Fredrik Mertens, Johan Wejde, Elsa Arbajian, Linda Magnusson, Otte Brosjö, Karolin Hansén Nord
Publikováno v:
American Journal of Surgical Pathology. 37:613-616
The EWSR1 gene in chromosome band 22q12 is a promiscuous fusion partner involved in a vast array of tumors characterized by gene fusions. In this study, we report the finding of a new fusion gene, EWSR1-NFATC1, in a hemangioma of the bone; genetic re
Publikováno v:
Cancer Genetics. 205:470-473
The transcriptional enhancer region in intron 1 of the proto-oncogene MDM2 contains a polymorphic site (SNP309) that may harbor a G or a T nucleotide. Previous studies have shown that the G allele confers a higher affinity for the Sp1 transcription f
Autor:
Raf Sciot, Emely Möller, Karolin Hansén Nord, Jenny Nilsson, Linda Magnusson, Fredrik Mertens, Samuel Gebre-Medhin, Olle Larsson, Nils Mandahl, Maria Debiec-Rychter, Otte Brosjö, Fredrik Vult von Steyern, Henryk A. Domanski, Vickie Y. Jo, Christopher D.M. Fletcher
Publikováno v:
The American Journal of Pathology. 181:1069-1077
Ossifying fibromyxoid tumor (OFMT) is a soft tissue tumor of unknown lineage. Although most cases are histologically and clinically benign, some show malignant morphological features and local recurrences are not uncommon; a few may even metastasize.