Based on current findings, the presence of NPM1 mutations in acute myeloid leukemia (AML) patients is associated with an increased probability of complete remission (CR) and better overall survival (OS). We determined the incidence and prognostic relevance of NPM1 mutations, their association with FLT3 and IDH mutations, and other clinical characteristics in Serbian adult AML patients. Samples from 111 adult de novo AML patients, including 73 AML cases with a normal karyotype (NK-AML), were studied. NPM1, FLT3, and IDH mutations were detected by PCR and direct sequencing. NPM1 mutations were detected in 22.5% of patients. The presence of NPM1 mutations predicted a low CR rate and shorter OS. NPM1 mutations showed an association with both FL...
Mutations in the NPM1 gene represent the most frequent genetic alterations in patients with acute my...
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML)....
NPM1 mutations represent frequent genetic alterations in patients with acute myeloid leukemia (AML) ...
Based on current findings, the presence of NPM1 mutations in acute myeloid leukemia (AML) patients i...
Based on current findings, the presence of NPM1 mutations in acute myeloid leukemia (AML) patients i...
Mutations in the nucleophosmin (NPM1) and fms-like tyrosine kinase-3 (FLT3) genes are the most commo...
Fms-like tyrosine kinase 3 (FLT3) and Nucleophosmin1 (NPM1) mutations are the most common molecular ...
Item does not contain fulltextNucleophosmin (NPM1) mutations occur frequently in adult cytogenetical...
Nucleophosmin (NPM1) mutations occur frequently in adult cytogenetically normal acute myeloid leukem...
PURPOSE Nucleophosmin 1 (NPM1) mutations are associated with a favorable prognosis in acute myeloid ...
OBJECTIVE: Mutations of the nucleophosmin (NPM1) gene are considered as the most frequent acute myel...
Background. Mutations in NPM1 and FLT3 genes represent the most frequent genetic alterations and imp...
Acute myeloid leukemia (AML) is a malignancy of proliferative, clonal, abnormally differentiated cel...
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML)....
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML)....
Mutations in the NPM1 gene represent the most frequent genetic alterations in patients with acute my...
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML)....
NPM1 mutations represent frequent genetic alterations in patients with acute myeloid leukemia (AML) ...
Based on current findings, the presence of NPM1 mutations in acute myeloid leukemia (AML) patients i...
Based on current findings, the presence of NPM1 mutations in acute myeloid leukemia (AML) patients i...
Mutations in the nucleophosmin (NPM1) and fms-like tyrosine kinase-3 (FLT3) genes are the most commo...
Fms-like tyrosine kinase 3 (FLT3) and Nucleophosmin1 (NPM1) mutations are the most common molecular ...
Item does not contain fulltextNucleophosmin (NPM1) mutations occur frequently in adult cytogenetical...
Nucleophosmin (NPM1) mutations occur frequently in adult cytogenetically normal acute myeloid leukem...
PURPOSE Nucleophosmin 1 (NPM1) mutations are associated with a favorable prognosis in acute myeloid ...
OBJECTIVE: Mutations of the nucleophosmin (NPM1) gene are considered as the most frequent acute myel...
Background. Mutations in NPM1 and FLT3 genes represent the most frequent genetic alterations and imp...
Acute myeloid leukemia (AML) is a malignancy of proliferative, clonal, abnormally differentiated cel...
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML)....
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML)....
Mutations in the NPM1 gene represent the most frequent genetic alterations in patients with acute my...
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML)....
NPM1 mutations represent frequent genetic alterations in patients with acute myeloid leukemia (AML) ...