Research Topics
Species | Aurelia M Meloni-EhrigSummaryAffiliation: Quest Diagnostics Country: USA Publications
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Detail Information
Publications
Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemiaAurelia M Meloni-Ehrig
Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
Cancer Genet Cytogenet 161:82-5. 2005..Fluorescence in situ hybridization performed using the probes TEL/AML1 and immunoglobulin heavy chain (IGH) showed no fusion involving the TEL and AML1 genes and only a single IGH signal in 20% of the interphase cells analyzed...
Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcomaAurelia Meloni-Ehrig
Department of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
Cancer Genet Cytogenet 191:43-5. 2009..We postulate that the t(2;8)(q35;q13) is a specific abnormality in congenital ERMS, and that it involves the PAX3 gene at 2q35 and a non-yet identified gene at 8q13...
Cytogenetics and genetics of human cancer: methods and accomplishmentsAvery A Sandberg
Cancer Genet Cytogenet 203:102-26. 2010..We also look at a few of the more recent genomic developments in cancer and offer an opinion as to what all these findings add up to...
Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusionCarlos A Tirado
Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
Cancer Genet Cytogenet 161:70-3. 2005....
Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignanciesCarlos A Tirado
Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
Cancer Genet Cytogenet 170:61-4. 2006..The key mechanism might be the loss of TP53 as well as other tumor suppressor genes in 20q that may have a critical role in tumor genesis...
Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemiaJoann C Kelly
Cytogenetics Department, Quest Diagnostics Nichols Institute, Chantilly, VA 20151, USA
Cancer Genet Cytogenet 192:36-9. 2009..CML patients with an ABL1/ETV6 fusion historically have demonstrated a variable and sometimes transient response to treatment with imatinib mesylate, which was also the case in the present patient...
Exon scanning by reverse transcriptase-polymerase chain reaction for detection of known and novel EML4-ALK fusion variants in non-small cell lung cancerHeather R Sanders
Department of Hematology and Oncology, Quest Diagnostics Nichols Institute, San Juan Capistrano, CA, USA
Cancer Genet 204:45-52. 2011..This RT-PCR-based exon scanning approach avoids the limitations of screening only for previously identified EML4-ALK fusions and provides a simple molecular assay for fusion detection in a clinical diagnostics setting...
Commentary on ISCN 2005Aurelia M Meloni-Ehrig
Cancer Genet Cytogenet 175:89-90. 2007
