AML with gain of chromosome 8 as the sole chromosomal abnormality (+8sole) is associated with a specific molecular mutation pattern including ASXL1 mutations in 46.8% of the patients

التفاصيل البيبلوغرافية
العنوان: AML with gain of chromosome 8 as the sole chromosomal abnormality (+8sole) is associated with a specific molecular mutation pattern including ASXL1 mutations in 46.8% of the patients
المؤلفون: Christiane Eder, Tamara Alpermann, Manja Meggendorfer, Susanne Schnittger, Torsten Haferlach, Claudia Haferlach, Niroshan Nadarajah, Wolfgang Kern
المصدر: Leukemia research. 39(3)
سنة النشر: 2014
مصطلحات موضوعية: Adult, Male, Cancer Research, NPM1, Adolescent, Genetic stability, Trisomy, Biology, Trisomy 8, medicine.disease_cause, Cohort Studies, chemistry.chemical_compound, Young Adult, hemic and lymphatic diseases, CEBPA, medicine, Humans, In Situ Hybridization, Fluorescence, Aged, Neoplasm Staging, Aged, 80 and over, Mutation, Chromosome, Karyotype, Hematology, Middle Aged, medicine.disease, Prognosis, Molecular biology, Repressor Proteins, Survival Rate, Leukemia, Myeloid, Acute, Oncology, RUNX1, chemistry, fms-Like Tyrosine Kinase 3, Case-Control Studies, Karyotyping, Core Binding Factor Alpha 2 Subunit, Female, Nucleophosmin, Chromosomes, Human, Pair 8, Follow-Up Studies
الوصف: Trisomy 8 is the most frequent cytogenetically gained aberration in AML. We compared 79 adult de novo AML with trisomy 8 as the sole cytogenetic abnormality (+8sole) to 511 normal karyotype AML patients (NK). +8sole patients were older (p=0.013), presented lower WBC counts (p=0.010), harbored more often ASXL1 mutations (p
تدمد: 1873-5835
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::151a286912c4863d8560e9a9c9afdf29Test
https://pubmed.ncbi.nlm.nih.gov/25592059Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....151a286912c4863d8560e9a9c9afdf29
قاعدة البيانات: OpenAIRE