Search Results - "Tobal, K"
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549 RAF Fusion Transcripts Detected in Medulloblastoma but not Ependymoma Using RT-RQPCR Assays on RNA Isolated From FFPE Tissues
Published in European journal of cancer (1990) (01-07-2012)Get full text
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Development of standardized approaches to reporting of minimal residual disease data using a reporting software package designed within the European LeukemiaNet
Published in Leukemia (01-07-2011)“…Quantitative PCR (qPCR) for detection of fusion transcripts and overexpressed genes is a promising tool for following minimal residual disease (MRD) in…”
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Molecular quantitation of minimal residual disease in acute myeloid leukemia with t(8;21) can identify patients in durable remission and predict clinical relapse
Published in Blood (01-02-2000)“…One of the most common translocations in acute myeloid leukemia (AML) is the t(8;21), which produces the fusion gene AML1-MTG8. We have developed a sensitive…”
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Elevated levels of WT1 transcripts in bone marrow harvests are associated with a high relapse risk in patients autografted for acute myeloid leukaemia
Published in Bone marrow transplantation (Basingstoke) (01-07-2005)“…Relapse postautograft in acute myeloid leukaemia (AML), may in part arise from leukaemia cells present in the bone marrow (BM) inoculum, and the level of…”
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RT-PCR method with increased sensitivity shows persistence of PML-RARA fusion transcripts in patients in long-term remission of APL
Published in Leukemia (01-09-1998)“…RT-PCR methods have been developed, to date, by various groups to amplify the PML-RARA fusion gene produced by the t(15;17) in APL patients. However, these…”
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Monitoring minimal residual disease and predicting relapse in APL by quantitating PML-RARα transcripts with a sensitive competitive RT-PCR method
Published in Leukemia (01-07-2001)“…Qualitative RT-PCR methods used for monitoring minimal residual disease (MRD) in APL patients fail to predict relapse in up to 25% of patients in remission. We…”
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Quantitation of PML-RARα transcripts in APL patients
Published in Leukemia (01-08-2000)Get full text
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The diagnosis of delayed post-operative endophthalmitis by polymerase chain reaction of bacterial DNA in vitreous samples
Published in Journal of medical microbiology (01-06-1994)“…1 Departments of Clinical Science, Institute of Ophthalmology, Bath Street, London EC1V 9EL * Department of Medical Microbiology. University College London…”
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Detection of CBFB/MYH11 transcripts in patients with inversion and other abnormalities of chromosome 16 at presentation and remission
Published in British journal of haematology (01-09-1995)“…The pericentric inversion of chromosome 16 [inv(16)(p13q22)] and t(16;16)(p13;q22) are chromosomal rearrangements frequently associated with AML FAB type M4Eo…”
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Detection and quantitation of the CBFβ/MYH11 transcripts associated with the inv(16) in presentation and follow-up samples from patients with AML
Published in Leukemia (01-03-1997)“…We have developed a competitor-based RT-PCR technique which will detect and quantitate the CBFβ/MYH11 transcripts associated with inv(16)(q22;p13) and have…”
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Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM0902) study
Published in Leukemia (01-10-2013)“…Reliable detection of JAK2 -V617F is critical for accurate diagnosis of myeloproliferative neoplasms (MPNs); in addition, sensitive mutation-specific assays…”
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Increased expression and mutation of p53 in choroidal melanoma
Published in British journal of cancer (01-11-1992)“…Using CM-1 antibody directed against the human p53 protein, high levels of mutant p53 protein expression were found in 12 out of 18 malignant choroidal…”
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Detection of melanocytes from uveal melanoma in peripheral blood using the polymerase chain reaction
Published in Investigative ophthalmology & visual science (01-08-1993)“…Uveal melanoma is the most common intraocular malignancy in adults and can cause loss of vision in the affected eye and death from metastasis, usually to the…”
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Mutation of the human FMS gene (M-CSF receptor) in myelodysplastic syndromes and acute myeloid leukemia
Published in Leukemia (01-07-1990)“…We studied 41 patients with myelodysplastic syndromes or acute myeloid leukemia to assess the presence of point mutations in the human FMS gene (M-CSF…”
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