Assil Fahs
Overview
Explore the profile of Assil Fahs including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
95
Followers
0
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Recent Articles
1.
Rammal G, Fahs A, Kobeissy F, Mechref Y, Zhao J, Zhu R, et al.
J Proteome Res
. 2023 Sep;
22(11):3660-3661.
PMID: 37769164
No abstract available.
2.
Fahs A, Hussein N, Zalzali H, Ramadan F, Ghamloush F, Tamim H, et al.
Cells
. 2022 Jul;
11(15).
PMID: 35892564
Rhabdomyosarcoma (RMS) is an aggressive childhood soft-tissue tumor, with propensity for local invasion and distant metastasis. Exosomes are secreted vesicles that mediate paracrine signaling by delivering functional proteins and miRNA...
3.
Fahs A, Ramadan F, Ghamloush F, Ayoub A, Ali Ahmad F, Kobeissy F, et al.
Front Oncol
. 2020 Oct;
10:1784.
PMID: 33117671
Rhabdomyosarcoma (RMS) is a highly malignant soft tissue sarcoma classified into two major histologic subtypes: embryonal (ERMS) and alveolar (ARMS). ARMS subtype is clinically more aggressive, and characterized by an...
4.
Ramadan F, Fahs A, Ghayad S, Saab R
Cancer Metastasis Rev
. 2020 Jan;
39(1):287-301.
PMID: 31989508
Rhabdomyosarcoma (RMS) is an aggressive childhood mesenchymal tumor with two major molecular and histopathologic subtypes: fusion-positive (FP)RMS, characterized by the PAX3-FOXO1 fusion protein and largely of alveolar histology, and fusion-negative...
5.
Ghamloush F, Ghayad S, Rammal G, Fahs A, Ayoub A, Merabi Z, et al.
Sci Rep
. 2019 Oct;
9(1):14242.
PMID: 31578374
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children. The alveolar subtype (ARMS) is clinically more aggressive, and characterized by an oncogenic fusion protein PAX3-FOXO1 that drives oncogenic...
6.
Rammal G, Fahs A, Kobeissy F, Mechref Y, Zhao J, Zhu R, et al.
J Proteome Res
. 2019 Aug;
18(10):3567-3579.
PMID: 31448612
Exosomes are important intercellular communication vehicles, secreted into body fluids by multiple cell types, including tumor cells. They have been demonstrated to contribute to the metastatic progression of tumor cells...
7.
Ghayad S, Rammal G, Sarkis O, Basma H, Ghamloush F, Fahs A, et al.
Cancer Biol Ther
. 2018 Oct;
20(3):272-283.
PMID: 30307360
Rhabdomyosarcoma (RMS) is an aggressive childhood sarcoma with two distinct subtypes, embryonal (ERMS) and alveolar (ARMS) histologies. More effective treatment is needed to improve outcomes, beyond conventional cytotoxic chemotherapy. The...