[HTML][HTML] Chronic myeloid leukemia-from the Philadelphia chromosome to specific target drugs: A literature review
MM Sampaio, MLC Santos, HS Marques… - World journal of …, 2021 - ncbi.nlm.nih.gov
Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm and was the first
neoplastic disease associated with a well-defined genotypic anomaly―the presence of the …
neoplastic disease associated with a well-defined genotypic anomaly―the presence of the …
CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate …
A Pardanani, RP Ketterling, SR Brockman, HC Flynn… - Blood, 2003 - ashpublications.org
Imatinib mesylate is effective in the treatment of hematologic malignancies that are
characterized by either abl-or PDGFR β-activating mutations. The drug is also active in a …
characterized by either abl-or PDGFR β-activating mutations. The drug is also active in a …
Chromosome anomalies detected by interphase fluorescence in situ hybridization: correlation with significant biological features of B‐cell chronic lymphocytic …
GW Dewald, SR Brockman… - British journal of …, 2003 - Wiley Online Library
Fluorescence in situ hybridization (FISH) was used to detect 6q–, 11q–,+ 12, 13q–, 17p–and
translocations involving 14q32 in interphase nuclei from blood and/or bone marrow from …
translocations involving 14q32 in interphase nuclei from blood and/or bone marrow from …
Preclinical validation of fluorescence in situ hybridization assays for clinical practice
AE Wiktor, DL Van Dyke, PJ Stupca, RP Ketterling… - Genetics in …, 2006 - nature.com
Purpose: Validation of fluorescence in situ hybridization assays is required before using
them in clinical practice. Yet, there are few published examples that describe the validation …
them in clinical practice. Yet, there are few published examples that describe the validation …
[HTML][HTML] Cytogenetics: past, present and future
TP Kannan, BA Zilfalil - The Malaysian journal of medical sciences …, 2009 - ncbi.nlm.nih.gov
Fifty years have elapsed since the discovery of the number of human chromosomes in 1956.
Newer techniques have been developed since then, ranging from the initial conventional …
Newer techniques have been developed since then, ranging from the initial conventional …
A review of the challenge in measuring and standardizing BCR-ABL1
S Yu, M Cui, X He, R Jing, H Wang - Clinical Chemistry and …, 2017 - degruyter.com
Breakpoint cluster region-Abelson (BCR-ABL1) translocation is the characteristic sign of
chronic myeloid leukemia (CML). The quantitation of BCR-ABL1 messenger RNA is …
chronic myeloid leukemia (CML). The quantitation of BCR-ABL1 messenger RNA is …
Molecular, cytogenetic, and hematological analysis of chronic myeloid leukemia patients and discovery of two novel translocations
Chronic myeloid leukemia (CML) is a disease of hematopoietic stem cells and is caused by
the balanced translocations among the long arms of chromosomes 9 and 22, which are …
the balanced translocations among the long arms of chromosomes 9 and 22, which are …
Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia
GS Nowakowski, GW Dewald, JD Hoyer… - British journal of …, 2005 - Wiley Online Library
Translocations involving IGH are common in some lymphoid malignancies but are believed
to be rare in chronic lymphocytic leukaemia (CLL). To study the clinical utility of fluorescence …
to be rare in chronic lymphocytic leukaemia (CLL). To study the clinical utility of fluorescence …
Fluorescent-labeled DNA probes applied to novel biological aspects of B-cell chronic lymphocytic leukemia
SR Fink, SF Paternoster, SA Smoley, HC Flynn… - Leukemia research, 2005 - Elsevier
Fluorescent-labeled DNA probes were used to study 52 chronic lymphocytic leukemia (B-
CLL) patients for (1) disease progression,(2) angiogenesis genes,(3) T-cell leukemia 1 gene …
CLL) patients for (1) disease progression,(2) angiogenesis genes,(3) T-cell leukemia 1 gene …
A novel tricolor, dual-fusion fluorescence in situ hybridization method to detect BCR/ABL fusion in cells with t (9; 22)(q34; q11. 2) associated with deletion of DNA on …
SA Smoley, SR Brockman, SF Paternoster… - Cancer genetics and …, 2004 - Elsevier
Dual-color, dual-fusion fluorescence in situ hybridization (D-FISH) can accurately detect and
quantify cells with BCR/ABL fusion in< 1% of 500 nuclei in 80% of patients with chronic …
quantify cells with BCR/ABL fusion in< 1% of 500 nuclei in 80% of patients with chronic …