Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Abdel-Aziz Zidan"'
Autor:
Medhat M. El Amawy, Seham Gouda Ameen, Hind A. Hegazy, Magda Abdel Aziz Zidan, Dalia M. Abd El-Hassib
Publikováno v:
Meta Gene. 29:100915
Objectives Evaluation of the frequency of X-ray Cross Complementing group 1 (XRCC1) Arg399Gln polymorphism among patients with end-stage renal disease (ESRD) patients and to determine if a possible association was present. Subjects & methods Blood sa
Publikováno v:
Hematology (Amsterdam, Netherlands). 19(5)
The Wilms' tumor (WT1) gene mutations were detected in patients with most forms of acute leukemia. However, the biological significance and the prognostic impact of WT1 mutation in Egyptian patients with acute myeloid leukemia with normal karyotype (
Autor:
MOHAMED LABIB SALEM, Said Abdou, Mohamed El-Shanshory, Mohamed Attia, Abdel-Aziz Zidan, Shymaa Sobhy, Mona Zidan
Publikováno v:
The Journal of Immunology. 196:211.11-211.11
Background Acute lymphoblastic leukemia (ALL) is the most common cancer diagnosed in children. The precise mechanisms behind the relapse in this disease are not clearly known. One possible mechanism could be the accumulation of regulatory cells inclu
Autor:
Tadeu Ambros, Abdel-Aziz Zidan, Maria Pallin, Alberto Montero, Mathias Lichtenheld, Marcela Díaz-Montero
Publikováno v:
The Journal of Immunology. 188:126.28-126.28
The impact of T cell receptor (TCR) affinity during homeostatic proliferation has been demonstrated using naive CD8+ T cells with high and low affinity TCR derived from different precursors. In this study, we investigated the impact of TCR affinity u
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::11177611e7219714fef8054ea245ee7d
http://www.scopus.com/inward/record.url?eid=2-s2.0-84903225774&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84903225774&partnerID=MN8TOARS