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of 3
pro vyhledávání: '"Mahjoobeh Jafari Vesiehsari"'
Autor:
Abbas Azadmehr, Mahjoobeh Jafari Vesiehsari, Mahmoud Hajiahmadi, Morteza Oladnabi, Shaghayegh Askarian-Amiri, Farzane Ordoni Aval
Publikováno v:
International Journal of Cancer Management.
Background: T-lineage acute lymphoblastic leukemia (T-ALL) is a malignant hyperplastic disease of the hematopoietic system. This tumor is the most common tumor in children and adolescents. Myeloid cell leukemia-1 (Mcl-1) is described as a prosurvival
Autor:
Masoud Karimlou, Koorosh Kamali, Elham Darabi, Maryam Neishabury, Mahjoobeh Jafari Vesiehsari, Fahimeh Zamani, Elaheh Keyhani, Setareh Talebi Kakroodi
Publikováno v:
Hemoglobin. 40:198-201
The impact of Hb F on severity of sickle cell disease and β-thalassemia (β-thal) is well documented. The XmnI-HBG2, BCL11A and HBS1L-MYB single nucleotide polymorphisms (SNPs) have been introduced as the most important factors causing variation in
Autor:
Mahjoobeh Jafari Vesiehsari, Maryam Neishabury, Azita Azarkeivan, Hossein Najmabadi, Elahe Keyhani, Fahimeh Zamani, Seyedeh Sedigheh Abedini, Setareh Talebi Kakroodi, Masumeh Sadat Eslami
Publikováno v:
Blood cells, moleculesdiseases. 51(2)
article i nfo To study the influence of the β globin locus control region (LCR) genotypic background on the phenotype modifying role of BCL11A polymorphisms, 100 cases of thalassemia, 48 homozygous for the A allele and 52 homozygous for the G allele