Zobrazeno 1 - 10
of 66
pro vyhledávání: '"J. M. Woodruff"'
Publikováno v:
Sarcoma, Vol 4, Iss 4, Pp 173-177 (2000)
Purpose. Angiosarcoma is a rare tumor with endothelial cell differentiation that may arise in any anatomic location.The purpose of this report was to identify prognostic factors on outcome in a group of prospectively followed patients with confirm
Externí odkaz:
https://doaj.org/article/c8890bd0f06a48f4be002f758fc79d15
Publikováno v:
Cancer. 77:467-473
Autor:
J M Woodruff, R T Senie
Publikováno v:
ORL. 53:194-209
To better characterize the clinical and pathological features of the laryngeal atypical carcinoid (LAC), 127 of the published cases were analyzed. The LAC had a predilection for males (3 m:1 f), with a peak incidence in the 6th and 7th decades of lif
Publikováno v:
Sarcoma
Purpose. Angiosarcoma is a rare tumor with endothelial cell differentiation that may arise in any anatomic location.The purpose of this report was to identify prognostic factors on outcome in a group of prospectively followed patients with confirmed
Autor:
D, Polsky, S, Mastorides, D, Kim, M, Dudas, L, Leon, D, Leung, J M, Woodruff, M F, Brennan, I, Osman, C, Cordon-Cardo
Publikováno v:
Histology and histopathology. 21(7)
Function of the retinoblastoma tumor suppressor protein (pRB) may be compromised at a genetic level by gene loss or mutation or at a post-translational level by hyperphosphorylation. In this study, we examined adult soft tissue sarcomas (ASTS) to det
Publikováno v:
Histology and histopathology. 18(3)
In terms of their morphology, clinical associations and behavior, peripheral nerve sheath tumors are among the most varied of human neoplasm. Not surprisingly, such tumors are subject to frequent misdiagnosis. This is particularly true of the spectru
Autor:
C R, Antonescu, S J, Tschernyavsky, R, Decuseara, D H, Leung, J M, Woodruff, M F, Brennan, J A, Bridge, J R, Neff, J R, Goldblum, M, Ladanyi
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(12)
A specific TLS-CHOP fusion gene resulting from the t(12;16) is present in at least 95% of myxoid liposarcomas (MLS). Three common forms of the TLS-CHOP fusion have been described, differing by the presence or absence of TLS exons 6-8 in the fusion pr
Autor:
A, Hoos, J J, Lewis, C R, Antonescu, M E, Dudas, L, Leon, J M, Woodruff, M F, Brennan, C, Cordon-Cardo
Publikováno v:
Cancer research. 61(7)
Desmoid tumors and fibrosarcomas (FS) are part of a wide spectrum of disordered fibroblastic growth that display striking clinical and phenotypic differences. This study was designed to characterize molecular abnormalities that are associated with th
Autor:
W G, Hawkins, A, Hoos, C R, Antonescu, M J, Urist, D H, Leung, J S, Gold, J M, Woodruff, J J, Lewis, M F, Brennan
Publikováno v:
Cancer. 91(4)
Rhabdomyosarcoma (RMS) in adults (ageor = 16 years) is rare, accounting for less than 3% of adult soft tissue sarcomas. There is little information describing the disease biology or clinicopathologic factors that influence survival in adults with RMS
Autor:
C R, Antonescu, A, Elahi, M, Humphrey, M Y, Lui, J H, Healey, M F, Brennan, J M, Woodruff, S C, Jhanwar, M, Ladanyi
Publikováno v:
The Journal of molecular diagnostics : JMD. 2(3)
Myxoid liposarcoma (LS), the most common subtype of LS, is known to be characterized by the specific t(12;16) resulting in a TLS-CHOP fusion in almost all cases. We wished to address the following questions: (i) Is this genetic hallmark also present