【摘 要】
：
Chronic myeloid leukemia (CML) is a clonal disease from hematopoietic stem cells.Surviving leukemia stem cells (LSCs) and progenitor cells are a potential source for CML relapse and progression.Recent
【机 构】
：
Department of Hematology,The Affiliated Hospital of Xuzhou Medical College
【出 处】
：
The 35th World Congress of the International Society of Hema
论文部分内容阅读
Chronic myeloid leukemia (CML) is a clonal disease from hematopoietic stem cells.Surviving leukemia stem cells (LSCs) and progenitor cells are a potential source for CML relapse and progression.Recent data reported that IL-1 receptor accessory protein (IL1RAP) gene was differentially expressed in CML versus normal stem and progenitor cells.However,whether the level of IL1RAP is associated with clinical phases of CML,and correlations between IL1RAP expression and detections of diagnosis is still unclear.
其他文献
Objective Previously we have shown that miR-663 was increased in bone marrow derived mesenchymal stem cells (BMSCs) from SLE patients and involved in the functional deficiency of BMSCs through inhibit
Objective Previously we have shown that miR-663 was increased in bone marrow derived mesenchymal stem cells (BMSCs) from SLE patients and involved in the functional deficiency of BMSCs through inhibit
Thalassemia is a group of hereditary hemolytic anemia,which has high incidence in south China,especially inGuangdong,Guangxi and other province.Hematopoietic stem cell transplantation is the most effe
The aim of this study to evaluate granulocyte colony stimulating factor (G-CSF) level in chronic renal failure patients,and to investigate its impact on neutrophil activation,endothelial dysfunction a
Background And Aims Progressive iron overload is the most important and fatal complication in beta-thalassemia.However,little is known about the relationship among ineffective erythropoiesis,the role
The Arkray Adams A1c HA-8180T analyzer is relatively new HPLC based hemoglobin (Hb) analyzer designated for both Hb A1c testing and Hb typing using reverse-phase cation exchange chromatography.We exam
Introduction Thalassemias are a heterogeneous group of autosomal recessive disorders that are characterized by hypochromic microcytic anemia caused by disturbed synthesis of one or more hemoglobin cha
Although thalassemia intermedia patients have mild anemia and do not require regular blood transfusion,they may still suffer from a number of serious clinical complications.We have characterized the m
Background Behcets disease (BD) is a disease of unknown cause which is clinically characterized by recurrent oral and genital ulcers,uveitis,polyarthritis,gastrointestinal involvement,and vasculitis.T
Aim We report a single-center experience in treating 12 patients with severe aplastic anemia (SAA) who received immunosuppressive treatment combined with unrelated cord blood infusion.Methods The medi