Introduction. Translocation t(12;21)(p13;q22) is one of the most common structural genetic abnormalities in childhood acute lymphoblastic leukemia (ALL). It cannot be detected by conventional G-banding, so a reverse-transcriptase polymerase chain reaction (RT-PCR) or fluorescent in situ hybridization are used for this purpose.The aim of the study was to evaluate the prognostic significance of qualitative and quantitative detection of ETV6-RUNX1 fusion gene transcript at various time points in childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL) patients.Materials and methods. ETV6-RUNX1 fusion gene transcript was revealed by both reverse-transcriptase PCR and quantitative real-time PCR (RQ-PCR) in 34 out of 166 (20.5 %) childre...
The molecular approach for the analysis of leukemia associated chromosomal translocations has led to...
Background Acute lymphoblastic leukemia (ALL) in children is a heterogeneous disease with different ...
Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL The genomic fusi...
The prognostic impact of t(12;21)(p13;q22) [ETV6/RUNX1 fusion] in paediatric acute lymphoblastic leu...
Background: t(12;21) (p12;q22) and t(9;22) (q34;q11) translocations have prognostic significance in...
Abstract Background In childhood B-precursor acute lymphoblastic leukemia (B-ALL), the ETV6/RUNX1 fu...
Ostra białaczka limfoblastyczna (ALL) to najczęściej występująca choroba nowotworowa w populacji ped...
BACKGROUND: Assessment of minimal residual disease (MRD) is an integral component for response monit...
The t(12;21) translocation generates the ETV6/RUNX1 fusion gene, present in 25% of childhood acute l...
The t(12;21)(p13;q22) fusion gene is the most frequent genetic lesion described in precursor B cell ...
Although the Philadelphia chromosome (Ph') has been iden-tified as an adverse prognostic factor...
Background: Variations in disease presentation and outcome of leukemia treatment has been associated...
um.edu.my In childhood acute lymphoblastic leukaemia (ALL), cytogenetics play an important role in d...
In childhood acute lymphoblastic leukaemia (ALL), cytogenetics play an important role in diagnosis, ...
Contemporary protocols ensure high-remission rate and long-term free survival in children with acute...
The molecular approach for the analysis of leukemia associated chromosomal translocations has led to...
Background Acute lymphoblastic leukemia (ALL) in children is a heterogeneous disease with different ...
Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL The genomic fusi...
The prognostic impact of t(12;21)(p13;q22) [ETV6/RUNX1 fusion] in paediatric acute lymphoblastic leu...
Background: t(12;21) (p12;q22) and t(9;22) (q34;q11) translocations have prognostic significance in...
Abstract Background In childhood B-precursor acute lymphoblastic leukemia (B-ALL), the ETV6/RUNX1 fu...
Ostra białaczka limfoblastyczna (ALL) to najczęściej występująca choroba nowotworowa w populacji ped...
BACKGROUND: Assessment of minimal residual disease (MRD) is an integral component for response monit...
The t(12;21) translocation generates the ETV6/RUNX1 fusion gene, present in 25% of childhood acute l...
The t(12;21)(p13;q22) fusion gene is the most frequent genetic lesion described in precursor B cell ...
Although the Philadelphia chromosome (Ph') has been iden-tified as an adverse prognostic factor...
Background: Variations in disease presentation and outcome of leukemia treatment has been associated...
um.edu.my In childhood acute lymphoblastic leukaemia (ALL), cytogenetics play an important role in d...
In childhood acute lymphoblastic leukaemia (ALL), cytogenetics play an important role in diagnosis, ...
Contemporary protocols ensure high-remission rate and long-term free survival in children with acute...
The molecular approach for the analysis of leukemia associated chromosomal translocations has led to...
Background Acute lymphoblastic leukemia (ALL) in children is a heterogeneous disease with different ...
Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL The genomic fusi...