نتایج جستجو برای: extension workers ews

تعداد نتایج: 262547  

Journal: :International journal of oncology 2010
K Minobe R Ono A Matsumine F Shibata-Minoshima K Izawa T Oki J Kitaura T Iino J Takita S Iwamoto H Hori Y Komada A Uchida Y Hayashi T Kitamura T Nosaka

Ewing's sarcoma (EWS) is a malignant bone tumor that frequently occurs in teenagers. Genetic mutations which cause EWS have been investigated, and the most frequent one proved to be a fusion gene between EWS gene of chromosome 22 and the FLI1 gene of chromosome 11. However, a limited numbers of useful biological markers for diagnosis of EWS are available. In this study, we identified ADAMTS4 (a...

2006
Oscar M. Tirado Silvia Mateo-Lozano Joaquín Villar Luis E. Dettin Anna Llort Soledad Gallego Jozef Ban Heinrich Kovar

Tumors of the Ewing’s sarcoma family (ESFT), such as Ewing’s sarcoma (EWS) and primitive neuroectodermal tumors (PNET), are highly aggressive malignancies predominantly affecting children and young adults. ESFT express chimeric transcription factors encoded by hybrid genes fusing the EWS gene with several ETS genes, most commonly FLI-1 . EWS/FLI1 proteins are responsible for the malignant pheno...

2014
David J. Elzi Meihua Song Kevin Hakala Susan T. Weintraub Yuzuru Shiio

Ewing sarcoma is a cancer of bone and soft tissue in children that is characterized by a chromosomal translocation involving EWS and an Ets family transcription factor, most commonly Fli-1. EWS-Fli-1 fusion accounts for 85% of cases. The growth and survival of Ewing sarcoma cells are critically dependent on EWS-Fli-1. A large body of evidence has established that EWS-Fli-1 functions as a DNA-bi...

2017
Tsion Zewdu Minas Didier Surdez Tahereh Javaheri Miwa Tanaka Michelle Howarth Hong-Jun Kang Jenny Han Zhi-Yan Han Barbara Sax Barbara E. Kream Sung-Hyeok Hong Haydar Çelik Franck Tirode Jan Tuckermann Jeffrey A. Toretsky Lukas Kenner Heinrich Kovar Sean Lee E. Alejandro Sweet-Cordero Takuro Nakamura Richard Moriggl Olivier Delattre Aykut Üren

Ewing sarcoma (ES) involves a tumor-specific chromosomal translocation that produces the EWS-FLI1 protein, which is required for the growth of ES cells both in vitro and in vivo. However, an EWS-FLI1-driven transgenic mouse model is not currently available. Here, we present data from six independent laboratories seeking an alternative approach to express EWS-FLI1 in different murine tissues. We...

2011
Kurt R. Weiss David J. Biau Rej Bhumbra Anthony M. Griffin Martin E. Blackstein Peter Chung Charles Catton Brian O'Sullivan Peter C. Ferguson Jay S. Wunder

Introduction. Ewing's sarcomas (EWSs) of bone and soft tissue are neuroectodermal tumors that affect both axial and appendicular locations. We hypothesized that axial location predicted poor outcome in EWS patients. Materials and Methods. Sixty-seven patients (57 with bone EWS and 10 with soft tissue EWS) were identified from our database. Thirty-four (51%) had axial EWS and 33 (49%) had append...

2008
M. A. Jafarizadeh

Two kinds of Bell-states diagonal (BSD) entanglement witnesses (EW) are constructed by using the algebra of Dirac γ matrices in the space-time of arbitrary dimension d, where the first kind can detect some BSD relativistic and non-relativistic m-partite multispinor bound entangled states in Hilbert space of dimension 2m⌊d/2⌋, including the bipartite Bell-type and iso-concurrence type states in ...

Journal: :Cancer research 2006
Oscar M Tirado Silvia Mateo-Lozano Joaquín Villar Luis E Dettin Anna Llort Soledad Gallego Jozef Ban Heinrich Kovar Vicente Notario

Tumors of the Ewing's sarcoma family (ESFT), such as Ewing's sarcoma (EWS) and primitive neuroectodermal tumors (PNET), are highly aggressive malignancies predominantly affecting children and young adults. ESFT express chimeric transcription factors encoded by hybrid genes fusing the EWS gene with several ETS genes, most commonly FLI-1. EWS/FLI-1 proteins are responsible for the malignant pheno...

Journal: :Cancer research 2010
Ophélie Meynet Katia Scotlandi Emmanuelle Pradelli Maria C Manara Mario P Colombo Heidy Schmid-Antomarchi Piero Picci Alain Bernard Ghislaine Bernard

Ewing's sarcoma (EWS) is an aggressive tumor of children and young adults that requires intensive treatment. The search for new prognostic factors is very important to choose the most appropriate therapy and to better understand the biology of the disease for the development of new therapeutic tools. We found that Xg, a thus far poorly described molecule and member of the CD99 family, is expres...

Journal: :Molecular and cellular biology 1993
W A May S L Lessnick B S Braun M Klemsz B C Lewis L B Lunsford R Hromas C T Denny

EWS/FLI-1 is a chimeric protein formed by a tumor-specific 11;22 translocation found in both Ewing's sarcoma and primitive neuroectodermal tumor of childhood. EWS/FLI-1 has been shown to be a potent transforming gene, suggesting that it plays an important role in the genesis of these human tumors. We now demonstrate that EWS/FLI-1 has the characteristics of an aberrant transcription factor. Sub...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2010
Hayriye V Erkizan Vladimir N Uversky Jeffrey A Toretsky

Targeted therapy for cancer, which is specifically directed toward the cancer without any potential for effects outside of controlling the tumor, is a gold standard for treatment. Ewing's sarcoma contains the potential target EWS-FLI1, as a result of a pathognomonic chromosomal translocation. The EWS-FLI1 fusion protein includes the EWS domain, a potent transcriptional activator alongside the h...

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