-
2
-
-
13444250347
-
-
In Elsevier Saunders: Philadelphia, PA
-
Kumar V, Abbus AK, Fausto N, et al. Robbins & Cotran Pathologic Basis of Disease. In Elsevier Saunders: Philadelphia, PA, 2004; 1318.
-
(2004)
Robbins & Cotran Pathologic Basis of Disease
, pp. 1318
-
-
Kumar, V.1
Abbus, A.K.2
Fausto, N.3
-
3
-
-
0037370455
-
Cytogenetic findings in a case of nodular fasciitis of subclavicular region
-
DOI 10.1016/S0165-4608(02)00725-2, PII S0165460802007252
-
Velagaleti GV, Tapper JK, Panova NE, et al. Cytogenetic findings in a case of nodular fasciitis of subclavicular region. Cancer Genet Cytogenet 2003;141:160-163. (Pubitemid 36269218)
-
(2003)
Cancer Genetics and Cytogenetics
, vol.141
, Issue.2
, pp. 160-163
-
-
Velagaleti, G.V.N.1
Tapper, J.K.2
Panova, N.E.3
Miettinen, M.4
Gatalica, Z.5
-
6
-
-
77954407785
-
FNAC of nodular fasciitis mimicking a pleomorphic adenoma: Another diagnostic pitfall
-
Silvanto AM, Melly L, Hannan SA, et al. FNAC of nodular fasciitis mimicking a pleomorphic adenoma: another diagnostic pitfall. Cytopathology 2010;21:276-277.
-
(2010)
Cytopathology
, vol.21
, pp. 276-277
-
-
Silvanto, A.M.1
Melly, L.2
Hannan, S.A.3
-
7
-
-
0001253673
-
Subcutaneous pseudosarcomatous fibromatosis (fasciitis)
-
Konwaler B, Keasbey L, Kaplan L. Subcutaneous pseudosarcomatous fibromatosis (fasciitis). Am J Clin Pathol 1955;25:241-252.
-
(1955)
Am J Clin Pathol
, vol.25
, pp. 241-252
-
-
Konwaler, B.1
Keasbey, L.2
Kaplan, L.3
-
8
-
-
0028006838
-
Clonal chromosome aberrations in a case of nodular fasciitis
-
DOI 10.1016/0165-4608(94)90469-3
-
Sawyer JR, Sammartino G, Baker GF, et al. Clonal chromosome aberrations in a case of nodular fasciitis. Cancer Genet Cytogenet 1994;76:154-156. (Pubitemid 24317437)
-
(1994)
Cancer Genetics and Cytogenetics
, vol.76
, Issue.2
, pp. 154-156
-
-
Sawyer, J.R.1
Sammartino, G.2
Baker, G.F.3
Bell, J.M.4
-
9
-
-
0032189996
-
Involvement of 3q21 in nodular fasciitis
-
DOI 10.1016/S0165-4608(98)00066-1, PII S0165460898000661
-
Weibolt VM, Buresh CJ, Roberts CA, et al. Involvement of 3q21 in nodular fasciitis. Cancer Genet Cytogenet 1998;106:177-179. (Pubitemid 28476098)
-
(1998)
Cancer Genetics and Cytogenetics
, vol.106
, Issue.2
, pp. 177-179
-
-
Weibolt, V.M.1
Buresh, C.J.2
Roberts, C.A.3
Suijkerbuijk, R.F.4
Pickering, D.L.5
Neff, J.R.6
Bridge, J.A.7
-
10
-
-
0036965021
-
Clonal rearrangement of 15p11.2, 16p11.2, and 16p13.3 in a case of nodular fasciitis: Additional evidence favoring nodular fasciitis as a benign neoplasm and not a reactive tumefaction
-
DOI 10.1016/S0165-4608(02)00613-1, PII S0165460802006131
-
Donner LR, Silva T, Dobin SM. Clonal rearrangement of 15p11.2, 16p11.2, and 16p13.3 in a case of nodular fasciitis: additional evidence favoring nodular fasciitis as a benign neoplasm and not a reactive tumefaction. Cancer Genet Cytogenet 2002;139:138-140. (Pubitemid 36110654)
-
(2002)
Cancer Genetics and Cytogenetics
, vol.139
, Issue.2
, pp. 138-140
-
-
Donner, L.R.1
Silva, T.2
Dobin, S.M.3
-
12
-
-
7244239103
-
USP6 and CDH11 oncogenes identify the neoplastic cell in primary aneurysmal bone cysts and are absent in so-called secondary aneurysmal bone cysts
-
Oliveira AM, Perez-Atayde AR, Inwards CY, et al. USP6 and CDH11 oncogenes identify the neoplastic cell in primary aneurysmal bone cysts and are absent in so-called secondary aneurysmal bone cysts. Am J Pathol 2004;165:1773-1780. (Pubitemid 39435174)
-
(2004)
American Journal of Pathology
, vol.165
, Issue.5
, pp. 1773-1780
-
-
Oliveira, A.M.1
Perez-Atayde, A.R.2
Inwards, C.Y.3
Medeiros, F.4
Derr, V.5
Hsi, B.-L.6
Gebhardt, M.C.7
Rosenberg, A.E.8
Fletcher, J.A.9
-
13
-
-
19944423795
-
Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes
-
DOI 10.1038/sj.onc.1208506
-
Oliveira AM, Perez-Atayde AR, Dal Cin P, et al. Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes. Oncogene 2005;24:3419-3426. (Pubitemid 40756243)
-
(2005)
Oncogene
, vol.24
, Issue.21
, pp. 3419-3426
-
-
Oliveira, A.M.1
Perez-Atayde, A.R.2
Dal Cin, P.3
Gebhardt, M.C.4
Chen, C.-J.5
Neff, J.R.6
Demetri, G.D.7
Rosenberg, A.E.8
Bridge, J.A.9
Fletcher, J.A.10
-
14
-
-
33644837148
-
Aneurysmal bone cyst: A neoplasm driven by upregulation of the USP6 oncogene
-
Oliveira AM, Chou MM, Perez-Atayde AR, et al. Aneurysmal bone cyst: a neoplasm driven by upregulation of the USP6 oncogene. J Clin Oncol 2006;24:e1.
-
(2006)
J Clin Oncol
, vol.24
-
-
Oliveira, A.M.1
Chou, M.M.2
Perez-Atayde, A.R.3
-
15
-
-
1542615085
-
USP6 (Tre2) Fusion Oncogenes in Aneurysmal Bone Cyst
-
DOI 10.1158/0008-5472.CAN-03-2827
-
Oliveira AM, Hsi BL, Weremowicz S, et al. USP6 (Tre2) fusion oncogenes in aneurysmal bone cyst. Cancer Res 2004;64:1920-1923. (Pubitemid 38339434)
-
(2004)
Cancer Research
, vol.64
, Issue.6
, pp. 1920-1923
-
-
Oliveira, A.M.1
Hsi, B.-L.2
Weremowicz, S.3
Rosenberg, A.E.4
Dal Cin, P.5
Joseph, N.6
Bridge, J.A.7
Perez-Atayde, A.R.8
Fletcher, J.A.9
-
16
-
-
77954061516
-
TRE17/USP6 oncogene translocated in aneurysmal bone cyst induces matrix metalloproteinase production via activation of NF-kappaB
-
Ye Y, Pringle LM, Lau AW, et al. TRE17/USP6 oncogene translocated in aneurysmal bone cyst induces matrix metalloproteinase production via activation of NF-kappaB. Oncogene 2010;29: 3619-3629.
-
(2010)
Oncogene
, vol.29
, pp. 3619-3629
-
-
Ye, Y.1
Pringle, L.M.2
Lau, A.W.3
-
17
-
-
78449262528
-
Tre17/ubiquitin-specific protease 6 (USP6) oncogene translocated in aneurysmal bone cyst blocks osteoblastic maturation via an autocrine mechanism involving bone morphogenetic protein dysregulation
-
Lau AW, Pringle LM, Quick L, et al. Tre17/ubiquitin-specific protease 6 (USP6) oncogene translocated in aneurysmal bone cyst blocks osteoblastic maturation via an autocrine mechanism involving bone morphogenetic protein dysregulation. J Biol Chem 2010;285: 37111-37120.
-
(2010)
J Biol Chem
, vol.285
, pp. 37111-37120
-
-
Lau, A.W.1
Pringle, L.M.2
Quick, L.3
-
18
-
-
14144253827
-
Molecular diagnosis of Ewing's sarcoma/primitive neuroectodermal tumor in formalin-fixed paraffin-embedded tissues by RT-PCR and fluorescence in situ hybridization
-
DOI 10.1097/01.pdm.0000140192.27878.97
-
Qian X, Jin L, Shearer BM, et al. Molecular diagnosis of Ewing's sarcoma/primitive neuroectodermal tumor in formalin-fixed paraffinembedded tissues by RT-PCR and fluorescence in situ hybridization. Diagn Mol Pathol 2005;14:23-28. (Pubitemid 40283858)
-
(2005)
Diagnostic Molecular Pathology
, vol.14
, Issue.1
, pp. 23-28
-
-
Qian, X.1
Jin, L.2
Shearer, B.M.3
Ketterling, R.P.4
Jalal, S.M.5
Lloyd, R.V.6
-
19
-
-
71149096889
-
Carboxypeptidase M: A biomarker for the discrimination of well-differentiated liposarcoma from lipoma
-
Erickson-Johnson MR, Seys AR, Roth CW, et al. Carboxypeptidase M: a biomarker for the discrimination of well-differentiated liposarcoma from lipoma. Mod Pathol 2009;12:1541-1547.
-
(2009)
Mod Pathol
, vol.12
, pp. 1541-1547
-
-
Erickson-Johnson, M.R.1
Seys, A.R.2
Roth, C.W.3
-
20
-
-
33750701914
-
Generation of cells expressing improved doxycycline-regulated reverse transcriptional transactivator rtTA2S-M2
-
Welman A, Barraclough J, Dive C. Generation of cells expressing improved doxycycline-regulated reverse transcriptional transactivator rtTA2S-M2. Nat Protoc 2006;1:803-811.
-
(2006)
Nat Protoc
, vol.1
, pp. 803-811
-
-
Welman, A.1
Barraclough, J.2
Dive, C.3
-
21
-
-
0037139605
-
Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes
-
DOI 10.1016/S0378-1119(02)00455-9, PII S0378111902004559
-
D'Apolito M, Guarnieri V, Boncristiano M, et al. Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes. Gene 2005;286:215-222. (Pubitemid 34273877)
-
(2002)
Gene
, vol.286
, Issue.2
, pp. 215-222
-
-
D'Apolito, M.1
Guarnieri, V.2
Boncristiano, M.3
Zelante, L.4
Savoia, A.5
-
22
-
-
77952687450
-
Myosin II contributes to cellscale actin network treadmilling through network disassembly
-
Wilson CA, Tsuchida MA, Allen GM, et al. Myosin II contributes to cellscale actin network treadmilling through network disassembly. Nature 2010;465:373-377.
-
(2010)
Nature
, vol.465
, pp. 373-377
-
-
Wilson, C.A.1
Tsuchida, M.A.2
Allen, G.M.3
-
23
-
-
0037195954
-
Mutations in human nonmuscle myosin IIA found in patients with May-Hegglin anomaly and Fechtner syndrome result in impaired enzymatic function
-
DOI 10.1074/jbc.M208506200
-
Hu A, Wang F, Sellers JR. Mutations in human nonmuscle myosin IIA found in patients with May-Hegglin anomaly and Fechtner syndrome result in impaired enzymatic function. J Biol Chem 2002;277: 46512-46517. (Pubitemid 35417648)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.48
, pp. 46512-46517
-
-
Hu, A.1
Wang, F.2
Sellers, J.R.3
-
24
-
-
0038122781
-
Non-muscle myosin heavy chain (MYH9): A new partner fused to ALK in anaplastic large cell lymphoma
-
DOI 10.1002/gcc.10232
-
Lamant L, Gascoyne RD, Duplantier M, et al. Non-muscle myosin heavy chain (MYH9): a new partner fused to ALK in anaplastic large cell lymphoma. Genes Chromosomes Cancer 2003;37:427-432. (Pubitemid 36775787)
-
(2003)
Genes Chromosomes and Cancer
, vol.37
, Issue.4
, pp. 427-432
-
-
Lamant, L.1
Gascoyne, R.D.2
Duplantier, M.M.3
Armstrong, F.4
Raghab, A.5
Chhanabhai, M.6
Rajcan-Separovic, E.7
Raghab, J.8
Delsol, G.9
Espinos, E.10
-
25
-
-
16244412308
-
Plag1 and Plagl2 are oncogenes that induce acute myeloid leukemia in cooperation with Cbfb-MYH11
-
DOI 10.1182/blood-2004-09-3630
-
Landrette SF, Kuo YH, Hensen K, et al. Plag1 and Plag2 are oncogenes that induce acute myeloid leukemia in cooperation with Cbfb-MHY11. Blood 2005;105:2900-2907. (Pubitemid 40450321)
-
(2005)
Blood
, vol.105
, Issue.7
, pp. 2900-2907
-
-
Landrette, S.F.1
Kuo, Y.-H.2
Hensen, K.3
Van Doorn-Khosrovani, S.B.V.W.4
Perrat, P.N.5
Van De Ven, W.J.M.6
Delwel, R.7
Castilla, L.H.8
-
26
-
-
0034755959
-
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-hegglin anomaly and Fechtner, Sebastian, Epstein, and alport-like syndromes
-
DOI 10.1086/324267
-
Heath KE, Campos-Barros A, Toren A, et al. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Am J Hum Genet 2001; 69:1033-1045. (Pubitemid 33015818)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.5
, pp. 1033-1045
-
-
Heath, K.E.1
Campos-Barros, A.2
Toren, A.3
Rozenfeld-Granot, G.4
Carlsson, L.E.5
Savige, J.6
Denison, J.C.7
Gregory, M.C.8
White, J.G.9
Barker, D.F.10
Greinacher, A.11
Epstein, C.J.12
Glucksman, M.J.13
Martignetti, J.A.14
-
28
-
-
0031953233
-
A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma
-
DOI 10.1038/ng0298-184
-
Knezevich SR, McFadden DE, Tao W, et al. A novel ETV6-NTKR3 gene fusion in congenital fibrosarcoma. Nat Genet 1998;18: 184-187. (Pubitemid 28082471)
-
(1998)
Nature Genetics
, vol.18
, Issue.2
, pp. 184-187
-
-
Knezevich, S.R.1
McFadden, D.E.2
Tao, W.3
Lim, J.F.4
Sorensen, P.H.B.5
-
29
-
-
0031738824
-
Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: Cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma
-
Rubin BP, Chen CJ, Morgan TW, et al. Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTKR3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma. Am J Pathol 1998;153:1451-1458. (Pubitemid 28509901)
-
(1998)
American Journal of Pathology
, vol.153
, Issue.5
, pp. 1451-1458
-
-
Rubin, B.P.1
Chen, C.-J.2
Morgan, T.W.3
Xiao, S.4
Grier, H.E.5
Kozakewich, H.P.6
Perez-Atayde, A.R.7
Fletcher, J.A.8
-
30
-
-
0015253914
-
Nodular fasciitis
-
Allen PW. Nodular fasciitis. Pathology 1972;4:9-26.
-
(1972)
Pathology
, vol.4
, pp. 9-26
-
-
Allen, P.W.1
-
31
-
-
53249133197
-
Leukemia/lymphoma-associated gene fusions in normal individuals
-
Brassesco M. Leukemia/lymphoma-associated gene fusions in normal individuals. Genet Mol Res 2008;7:782-790.
-
(2008)
Genet Mol Res
, vol.7
, pp. 782-790
-
-
Brassesco, M.1
|