Search Results - "Mourad, Zeinab I"

Prevalence of iron deficiency anemia and beta thalassemia carriers among relatives of beta thalassemia patients in Nile Delta region, Egypt: a multicenter study by El-Shanshory, Mohamed R, Sherief, Laila M, Hassab, Hoda M, Ragab, Seham M, Yahia Sohier, Mansour, Ahmed K, Ahmed, Adel S, Abdou, Said H, Helmy, Amal M, Watany, Mona M, Gad ALllah Ahmed M, Guindy, Myriam A, Mourad, Zeinab I, Soliman, Mohamed A, El-Farahaty, Reham M, El-Dahtory Faeza, Darwish, Ahmad, Elmabood, Suzy Abd, Kabbash, Ibrahim A, Saied, Shimaa M

“…BackgroundScreening of β thalassemia among close relatives is more feasible in highly prevalent countries with limited resources. The purpose of this study is…”
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The prognostic impact of loss of chromosome 7 material detected by fluorescence in situ hybridization (FISH) in myeloid malignancies by El-Menoufy, Mohamed Amr M., Mourad, Zeinab I., Farahat, Nahla M.

“…Monosomy 7 (−7) or deletion in its long arm [del(7q)] is among the most common chromosomal abnormalities in myeloid malignancies. There are prognostic…”
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A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia by Mikhail, Fady M., Coignet, Lionel, Hatem, Nadia, Mourad, Zeinab I., Farawela, Hala M., Kaffash, Dalal M. El, Farahat, Nahla, Nucifora, Giuseppina

“…AML1 is among the most frequent targets of chromosomal rearrangements in human leukemias. We report here the molecular analysis of a t(4;21)(q28;q22) that has…”
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Telomerase activity in Philadelphia positive chronic myeloid leukaemia by Rasoul, Naglaa Abdel, Elhalawani, Nabil, Nafae, Mohammed Hassan A, Elkaffash, Dalal M, Mourad, Zeinab I

“…Telomerase is a specialized type of reverse transcriptase that catalyzes the synthesis and extension of telomeric DNA. Activation of telomerase and…”
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A new translocation that rearranges the AML1 gene in a patient with T-cell acute lymphoblastic leukemia by Mikhail, Fady M, Serry, Kadreya A, Hatem, Nadia, Mourad, Zeinab I, Farawela, Hala M, El Kaffash, Dalal M, Coignet, Lionel, Nucifora, Giuseppina

“…The AML1 gene (also known as RUNX1 or CBFA2), located in chromosome band 21q22, encodes a transcription factor which heterodimerizes with the CBFβ protein…”
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Surface expression of transferrin receptors (CD71) on peripheral blood T-lymphocytes in patients with chronic hepatitis C: Relation to serum iron status and disease activity by El Aggan, Hoda A., Mourad, Zeinab I., Abdel^Moeti, Amr A.

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