Detalhe da pesquisa
1.
The H3F3 K36M mutant antibody is a sensitive and specific marker for the diagnosis of chondroblastoma.
Histopathology
; 69(1): 121-7, 2016 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-26844533
2.
GNAS mutations are not detected in parosteal and low-grade central osteosarcomas.
Mod Pathol
; 28(10): 1336-42, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26248895
3.
Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma: characterization of five cases.
Skeletal Radiol
; 42(7): 947-57, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23381465
4.
IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours.
J Pathol
; 224(3): 334-43, 2011 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-21598255
5.
Undifferentiated Sarcomas Develop through Distinct Evolutionary Pathways.
Cancer Cell
; 35(3): 441-456.e8, 2019 03 18.
Artigo
Inglês
| MEDLINE | ID: mdl-30889380
6.
Assessment of MUC4 expression in primary bone tumours.
Histopathology
; 63(1): 142-3, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23668430
7.
IDH1 mutations are not found in cartilaginous tumours other than central and periosteal chondrosarcomas and enchondromas.
Histopathology
; 60(2): 363-5, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22074484
8.
The driver landscape of sporadic chordoma.
Nat Commun
; 8(1): 890, 2017 10 12.
Artigo
Inglês
| MEDLINE | ID: mdl-29026114
9.
Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma.
Nat Commun
; 8: 15936, 2017 06 23.
Artigo
Inglês
| MEDLINE | ID: mdl-28643781
10.
Gout-mimicking sarcoma recurrence at a prosthesis bone interface remote from any joint.
J Med Imaging Radiat Oncol
; 59(5): 605-7, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25677047
11.
Isocitrate dehydrogenase 1 mutations (IDH1) and p16/CDKN2A copy number change in conventional chondrosarcomas.
Virchows Arch
; 466(2): 217-22, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25432631
12.
Next-generation sequencing is highly sensitive for the detection of beta-catenin mutations in desmoid-type fibromatoses.
Virchows Arch
; 467(2): 203-10, 2015 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-25838078
13.
Clinical outcome in patients with peripherally-sited atypical lipomatous tumours and dedifferentiated liposarcoma.
J Pathol Clin Res
; 1(2): 106-12, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-27499897
14.
Diagnostic value of H3F3A mutations in giant cell tumour of bone compared to osteoclast-rich mimics.
J Pathol Clin Res
; 1(2): 113-23, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-27499898
15.
Recurrent PTPRB and PLCG1 mutations in angiosarcoma.
Nat Genet
; 46(4): 376-379, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24633157
16.
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.
Nat Genet
; 45(12): 1479-82, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24162739
17.
A common single-nucleotide variant in T is strongly associated with chordoma.
Nat Genet
; 44(11): 1185-7, 2012 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-23064415
18.
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
Nat Genet
; 43(12): 1262-5, 2011 Nov 06.
Artigo
Inglês
| MEDLINE | ID: mdl-22057236
19.
Detection of USP6 gene rearrangement in nodular fasciitis: an important diagnostic tool.
Virchows Arch
; 463(1): 97-8, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23748914