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- Q-Rt-PCR provides reliable measurements of BCR/abl fusion transcripts. It is potentially useful in assessing molecular residual disease after therapy.
People also ask
Can quantitative real-time PCR detect bcr/abl fusion transcripts?
Can BCR-ABL1 fusion transcripts be monitored by RT-PCR?
Is Q-RT-PCR useful in detecting bcr/abl fusion transcripts in chronic myelogenous Leuk?
How are BCR/ABL fusion transcripts normalized?
Can a next-generation sequencing based assay quantify BCR ABL1 and ABL1 transcript copy numbers?
Will Droplet digital RT-PCR be the preferred method for quantification of BCR-ABL1 fusion transcripts?
Jun 8, 2022 · Branford S, Hughes TP, Rudzki Z. Monitoring chronic myeloid leukaemia therapy by real-time quantitative PCR in blood is a reliable alternative to bone marrow cytogenetics.
- Matthew Salmon
Monitoring BCR-ABL1 fusion transcripts by real-time quantitative RT-PCR has become an important clinical test for the management of patients with chronic myeloid leukemia. However, it has some inherent limitations with regard to its lower limit of detection and limit of quantification.
- Lawrence J. Jennings, Lawrence J. Jennings, David George, Juliann Czech, Min Yu, Loren Joseph
- 2014
The reciprocal translocation t(9;22)(q34;q11) is associated with the BCR-ABL1 fusion that can be detected by fluorescence in situ hybridization (FISH) or reverse transcriptase polymerase chain reaction (RT-PCR) to establish the diagnosis .
May 29, 2023 · Real-time quantitative PCR (RQ-PCR) and droplet digital PCR (ddPCR) are used to quantify known fusion transcript types. RQ-PCR and ddPCR can detect major BCR::ABL1 transcripts. However, they did not differentiate between e13a2 and e14a2 types.
Mar 5, 2019 · In this study, we evaluated the ability of this in-house RQ-PCR method to detect low level BCR-ABL1 fusion transcripts using samples obtained in the ongoing Delightedly Overcome CML Expert Stop TKI (DOMEST) clinical trial to evaluate the rationale for cessation of imatinib .
Several studies have demonstrated the clinical utility of quantifying BCR-ABL1 fusion transcript levels in chronic myeloid leukemia (CML) patients. 1–7 Typically, this has been performed using real-time quantitative RT-PCR (RT-qPCR).
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