A somatic EZH2 mutation in childhood acute myeloid leukemia

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The Relationship between Mutation in HOXB1 Gene and Acute Myeloid Leukemia

Background: HOX genes are an exceedingly preserved family of homeodomain-involving transcription factors. They are related to a number of malignancies, comprising acute myeloid leukemia (AML). This study aimed to evaluate the effect of HOXB1 7bp deletion mutation on HOXB1gene expression in 36 individuals. Materials and Methods: The present cross-sectional study was done on a large Iranian fami...

متن کامل

A Case Report: Acute Myeloid Leukemia (FAB M7)

Acute myeloid leukemia (AML-M7) is a type of pediatric AML accounting for 3–10% of primary childhood AML and children may present with a broad variety of symptoms including low-grade fever, diarrhea, easy bruising, failure to gain weight and life-threatening conditions. We report a rare case of AML .A 26-month-old boy who presented with weakness and fatigue. He was diagnosed as a case of AMLM-7...

متن کامل

features of childhood acute myeloid leukemia in iran: a report from double center study

acute myeloblastic leukemia is one of the important malignancies in children. for better managing the prognosis of this disease, there should be enough information about common features of this malignancy. the aim of this study was to evaluate these common features in children with acute myeloblastic leukemia. a total of 104 eligible children less than 15-year-old have been referred from 2007-2...

متن کامل

MYELOID NEOPLASIA Ezh2 augments leukemogenicity by reinforcing differentiation blockage in acute myeloid leukemia

Departments of 1Cellular and Molecular Medicine and 2Clinical Cell Biology and Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan; 3Japan Science and Technology Corporation, Core Research for Evolutional Science and Technology, Tokyo, Japan; 4Department of Medicine and Clinical Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan; 5Laboratory of Functional Ge...

متن کامل

Detection of R882 Mutations in DNMT3A Gene in Acute Myeloid Leukemia: A Method Comparison Study

Background: Somatic mutations in the hotspot region of the DNA-methyltransferase 3A (DNMT3A) gene were recurrently identified in acute myeloid leukemia (AML). It is believed that DNMT3A mutations confer an adverse prognosis for AML patients. These lines of evidence support the need for a rapid and cost-efficient method for the detection of these mutations. The present study aimed to establish h...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Leukemia

سال: 2012

ISSN: 0887-6924,1476-5551

DOI: 10.1038/leu.2012.16