scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1024463273 |
P356 | DOI | 10.1186/GM191 |
P932 | PMC publication ID | 3092121 |
P698 | PubMed publication ID | 20860819 |
P5875 | ResearchGate publication ID | 46402863 |
P50 | author | Anindya Dutta | Q37369581 |
Ankit Malhotra | Q57431318 | ||
P2093 | author name string | Yoshiyuki Shibata | |
P2860 | cites work | Mfold web server for nucleic acid folding and hybridization prediction | Q24498105 |
Complex landscapes of somatic rearrangement in human breast cancer genomes | Q24631412 | ||
Replication stalling at unstable inverted repeats: interplay between DNA hairpins and fork stabilizing proteins | Q24655285 | ||
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing | Q29614576 | ||
Yeast genome analysis identifies chromosomal translocation, gene conversion events and several sites of Ty element insertion | Q30438104 | ||
Polymerase chain reaction-based suppression of repetitive sequences in whole chromosome painting probes for FISH. | Q33213247 | ||
Paired-end diTagging for transcriptome and genome analysis | Q33319230 | ||
Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing | Q34329023 | ||
Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses | Q34973377 | ||
The BCR-ABL story: bench to bedside and back | Q35698382 | ||
Monitoring CML patients responding to treatment with tyrosine kinase inhibitors: review and recommendations for harmonizing current methodology for detecting BCR-ABL transcripts and kinase domain mutations and for expressing results | Q35849776 | ||
Conventional cytogenetics and FISH in the detection of BCR/ABL fusion in chronic myeloid leukemia (CML). | Q36490622 | ||
Chronic myeloid leukemia in 2007. | Q37023335 | ||
BCR-ABL in chronic myelogenous leukemia--how does it work? | Q37195693 | ||
Chimeric transcript discovery by paired-end transcriptome sequencing | Q37257656 | ||
Molecular biology of bcr-abl1-positive chronic myeloid leukemia | Q37283128 | ||
Translation of the Philadelphia chromosome into therapy for CML. | Q37344094 | ||
Technical aspects and clinical applications of measuring BCR-ABL1 transcripts number in chronic myeloid leukemia. | Q37526747 | ||
FISH mapping of Philadelphia negative BCR/ABL1 positive CML. | Q39959667 | ||
Long DNA palindromes, cruciform structures, genetic instability and secondary structure repair | Q40582078 | ||
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis | Q41768874 | ||
Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans. | Q42150838 | ||
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia. | Q43997460 | ||
Masked Philadelphia chromosome due to atypical BCR/ABL localization on the 9q34 band and duplication of the der(9) in a case of chronic myelogenous leukemia | Q46842771 | ||
Genomic translocation breakpoint sequences are conserved in BCR-ABL1 cell lines despite the presence of amplification. | Q51822793 | ||
Rapid isolation of translocation breakpoints in chronic myeloid and acute promyelocytic leukaemia. | Q53483254 | ||
Chimeric BCR/ABL gene detected by fluorescence in situ hybridization in three new cases of Philadelphia chromosome-negative chronic myelocytic leukemia. | Q54787431 | ||
Comparison of genomic DNA and cDNA for detection of residual disease after treatment of chronic myeloid leukemia with allogeneic bone marrow transplantation | Q71078516 | ||
Philadelphia-negative chronic myeloid leukaemia: detection by FISH of BCR-ABL fusion gene localized either to chromosome 9 or chromosome 22 | Q72772407 | ||
Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia | Q73386657 | ||
P433 | issue | 9 | |
P304 | page(s) | 70 | |
P577 | publication date | 2010-09-22 | |
P1433 | published in | Genome Medicine | Q15816848 |
P1476 | title | Detection of DNA fusion junctions for BCR-ABL translocations by Anchored ChromPET | |
P478 | volume | 2 |
Q39961918 | Characterization of 46 patient-specific BCR-ABL1 fusions and detection of SNPs upstream and downstream the breakpoints in chronic myeloid leukemia using next generation sequencing. |
Q38787015 | Current trends in molecular diagnostics of chronic myeloid leukemia |
Q37070022 | Extracellular vesicle-mediated transfer of donor genomic DNA to recipient cells is a novel mechanism for genetic influence between cells |
Q24603102 | Extrachromosomal microDNAs and chromosomal microdeletions in normal tissues |
Q33905061 | FusionMap: detecting fusion genes from next-generation sequencing data at base-pair resolution |
Q34557870 | Genome Fusion Detection: a novel method to detect fusion genes from SNP-array data |
Q34781322 | Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia |
Q35904266 | Imatinib mesylate therapy in patients of chronic myeloid leukemia with Philadelphia chromosome positive: an experience from eastern India |
Q92417685 | Insights into the prenatal origin of childhood acute lymphoblastic leukemia |
Q34338922 | Paired-end sequencing of Fosmid libraries by Illumina |
Q38762631 | Present and future of molecular monitoring in chronic myeloid leukaemia |
Q54309446 | TKI dasatinib monotherapy for a patient with Ph-like ALL bearing ATF7IP/PDGFRB translocation. |
Q35227216 | Transferred BCR/ABL DNA from K562 extracellular vesicles causes chronic myeloid leukemia in immunodeficient mice |
Search more.