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Fredrik Mertens
Fredrik Mertens
Department of Clinical Genetics, Lund University
Email verificata su med.lu.se
Titolo
Citata da
Citata da
Anno
WHO Classification of Tumours of Soft Tissue and Bone: WHO Classification of Tumours, vol. 5
C Fletcher, JA Bridge, PCW Hogendoorn, F Mertens
World Health Organization, 2013
5792*2013
World Health Organization classification of tumours. Pathology and genetics of tumours of soft tissue and bone
CDM Fletcher, K Unni, F Mertens
IARC press, 2002
35802002
The impact of translocations and gene fusions on cancer causation
F Mitelman, B Johansson, F Mertens
Nature Reviews Cancer 7 (4), 233-245, 2007
15352007
TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal
PJ Killela, ZJ Reitman, Y Jiao, C Bettegowda, N Agrawal, LA Diaz Jr, ...
Proceedings of the National Academy of Sciences 110 (15), 6021-6026, 2013
13232013
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
F Mitelman, F Mertens, B Johansson
Nature genetics 15 (4), 417-474, 1997
8491997
Mitelman database of chromosome aberration in cancer
F Mitelman
http://cgap. ncbi. nih. gov/chromo-somes/mitelman, 2005
6182005
Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics
LA Doyle, M Vivero, CDM Fletcher, F Mertens, JL Hornick
Modern Pathology 27 (3), 390-395, 2014
5772014
The der (17) t (X; 17)(p11; q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25
M Ladanyi, MY Lui, CR Antonescu, A Krause-Boehm, A Meindl, P Argani, ...
Oncogene 20 (1), 48-57, 2001
5732001
Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms
F Mertens, B Johansson, M H÷glund, F Mitelman
Cancer research 57 (13), 2765-2780, 1997
5481997
The emerging complexity of gene fusions in cancer
F Mertens, B Johansson, T Fioretos, F Mitelman
Nature Reviews Cancer 15 (6), 371-381, 2015
5352015
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
D Gisselsson, T Jonson, ┼ PetersÚn, B Str÷mbeck, P Dal Cin, M H÷glund, ...
Proceedings of the National Academy of Sciences 98 (22), 12683-12688, 2001
5002001
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
D Gisselsson, L Pettersson, M H÷glund, M Heidenblad, L Gorunova, ...
Proceedings of the National Academy of Sciences 97 (10), 5357-5362, 2000
4632000
Mitelman database of chromosome aberrations and gene fusions in cancer
F Mitelman
http://cgap. nci. nih. gov/Chromosomes/Mitelman, 2010
459*2010
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
CD Fletcher, M Akerman, P Dal Cin, I De Wever, N Mandahl, F Mertens, ...
The American journal of pathology 148 (2), 623, 1996
3871996
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
F Mitelman, B Johansson, F Mertens
Nature genetics 36 (4), 331-334, 2004
3842004
Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating AgentsImpact ofá…
EP Buddingh, ML Kuijjer, RAJ Duim, H BŘrger, K Agelopoulos, ...
Clinical Cancer Research 17 (8), 2110-2119, 2011
3522011
Fusion of the EWS and CHOP genes in myxoid liposarcoma.
I Panagopoulos, M H÷glund, F Mertens, N Mandahl, F Mitelman, P Aman
Oncogene 12 (3), 489-494, 1996
3431996
MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma
LA Doyle, E M÷ller, P Dal Cin, CDM Fletcher, F Mertens, JL Hornick
The American journal of surgical pathology 35 (5), 733-741, 2011
2972011
Amplification of cyclin D1 in squamous cell carcinoma of the head and neck and the prognostic value of chromosomal abnormalities and cyclin D1 overexpression
JA ┼kervall, RJAM Michalides, H Mineta, A Balm, ┼ Borg, MR Dictor, Y Jin, ...
Cancer 79 (2), 380-389, 1997
2891997
Identification of a novel, recurrent HEY1‐NCOA2 fusion in mesenchymal chondrosarcoma based on a genome‐wide screen of exon‐level expression data
L Wang, T Motoi, R Khanin, A Olshen, F Mertens, J Bridge, PD Cin, ...
Genes, Chromosomes and Cancer 51 (2), 127-139, 2012
2882012
Il sistema al momento non pu˛ eseguire l'operazione. Riprova pi¨ tardi.
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