Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Ines, Safra"'
Autor:
Asma Ounalli, Imen Moumni, Amal Mechaal, Aya Chakroun, Mbarka Barmat, Rim El Elj Rhim, Samia Menif, Ines Safra
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundGenetic variations in TP53 gene are known to be important in chronic lymphocytic leukemia (CLL) and may cause its inactivation which is associated with an aggressive form of the disease. Single nucleotide polymorphism (rs1042522:G>C) in TP5
Externí odkaz:
https://doaj.org/article/861ae5c3c4f14461a3a0488c10b6ac63
Publikováno v:
BMC Public Health, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background Given the increasing blood cancer incidence in Tunisia and recent discoveries proving the involvement of environmental factors, this study examined the environmental health literacy (EHL) of Tunisian secondary school students conc
Externí odkaz:
https://doaj.org/article/dabed703daa94351b63eebf72560ce51
Publikováno v:
HemaSphere, Vol 7, p e5685828 (2023)
Externí odkaz:
https://doaj.org/article/f6674a0db04a4012b117477abc4daa5e
Autor:
Mariem Chebbi, Khouloud Khalfaoui, Sihem Saidani, Ines Safra, Mbarka Barmate, Dorra Chaouechi, Monia Benkhaled, Monia Ouederni, Fethi Mellouli, Samia Menif, Imen Moumni
Publikováno v:
HemaSphere, Vol 7, p e0427349 (2023)
Externí odkaz:
https://doaj.org/article/6063017cd2164706a56ace3703ba4724
Autor:
Khouloud Zayoud, Asma Chikhaoui, Ichraf Kraoua, Anis Tebourbi, Dorra Najjar, Saker Ayari, Ines Safra, Imen Kraiem, Ilhem Turki, Samia Menif, Houda Yacoub-Youssef
Publikováno v:
Cells, Vol 13, Iss 5, p 402 (2024)
Cockayne syndrome (CS) is a rare autosomal recessive disorder that affects the DNA repair process. It is a progeroid syndrome predisposing patients to accelerated aging and to increased susceptibility to respiratory infections. Here, we studied the i
Externí odkaz:
https://doaj.org/article/b1269f6cfec544049e1cc507b336d0b9
Autor:
Arwa Tagoug, Ines Safra
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 39:245-257
Autor:
Asma Beldi-Ferchiou, Nour Skouri, Cyrine Ben Ali, Ines Safra, Abderrahman Abdelkefi, Saloua Ladeb, Karima Mrad, Tarek Ben Othman, Mélika Ben Ahmed
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0174835 (2017)
Sustained activation of JAK/STAT3 signaling pathway is classically described in Multiple Myeloma (MM). One explanation could be the silencing of the JAK/STAT suppressor genes, through the hypermethylation of SHP-1 and SOCS-1, previously demonstrated
Externí odkaz:
https://doaj.org/article/12c8c1aaea4341358b837b000ba59f80
Autor:
Khouloud, Marzouk, Nader, Slama, Ahlem, Bellalah, Ines, Safra, Montacer, Hafsi, Rayhan, Chabbeh
Publikováno v:
In Leukemia Research Reports 2024 21
Publikováno v:
Advances in Medical Sciences. 64:395-401
Acute myeloid leukemia (AML) is a heterogeneous disease. The discovery of novel discriminative biomarkers remains of utmost value for improving outcome predictions. Enhancer of zeste homolog 2 (EZH2) is a histone methyltransferase of H3K27me3. It is
Autor:
Melika Ben Ahmed, Raja Rekik, Saloua Ladeb, Neila Ben Romdhane, Oumayma Selmi, Imen Zamali, Ahlem Ben Hmid, Hajer Lamari, Ines Safra, Tarek Ben Othman
Publikováno v:
Cytokine
Cytokine, Elsevier, 2020, 134, pp.155210. ⟨10.1016/j.cyto.2020.155210⟩
Cytokine, Elsevier, 2020, 134, pp.155210. ⟨10.1016/j.cyto.2020.155210⟩
International audience; The role of the bone marrow microenvironment in supporting the proliferation and survival of the abnormal plasma cells in multiple myeloma (MM) is well established. Such microenvironment is rich of cytokines like IL-6, TGF-β,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c897d7a6c90211c54be389720425e000
https://hal-riip.archives-ouvertes.fr/pasteur-02942713
https://hal-riip.archives-ouvertes.fr/pasteur-02942713