Characterization of a cryptic PML-RARA fusion by mate-pair sequencing in a case of acute promyelocytic leukemia with a normal karyotype and negative RARA FISH studies-Reference-Cited by-同舟云学术

Characterization of a cryptic PML-RARA fusion by mate-pair sequencing in a case of acute promyelocytic leukemia with a normal karyotype and negative RARA FISH studies

Published:2019-12-06 Issue:4 Volume:61 Page:975-978
ISSN:1042-8194
Container-title:Leukemia & Lymphoma
language:en
Short-container-title:Leukemia & Lymphoma

Author:

Schultz Matthew J.¹,Blackburn Patrick R.¹,Cogbill Christopher H.²,Pitel Beth A.¹,Smadbeck James B.³,Johnson Sarah H.³,Vasmatzis George³,Rech Karen L.⁴,Sukov William R.¹,Greipp Patricia T.¹,Hoppman Nicole L.¹,Baughn Linda B.¹,Ketterling Rhett P.¹⁴,Peterson Jess F.¹

Affiliation:

1. Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA;

2. Department of Pathology, Gunderson Lutheran Medical Center, La Crosse, WI, USA;

3. Center for Individualized Medicine-Biomarker Discovery, Mayo Clinic, Rochester, MN, USA;

4. Division of Hematopathology, Department of Laboratory Medicine and Genomics, Mayo Clinic, Rochester, MN, USA

Publisher

Informa UK Limited

Subject

Cancer Research,Oncology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10428194.2019.1699081

Reference15 articles.

1. Retinoic Acid and Arsenic Trioxide for Acute Promyelocytic Leukemia

2. Acute Promyelocytic Leukemia: A Review and Discussion of Variant Translocations

3. BIMA V3: an aligner customized for mate pair library sequencing

4. SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq)

5. Copy number variant analysis using genome-wide mate-pair sequencing

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1. Cytogenetically Cryptic Acute Promyelocytic Leukemia: A Diagnostic Challenge;International Journal of Molecular Sciences;2023-08-22

2. Clinical and genomic characterization of an ATRA‐insensitive acute promyelocytic leukemia variant with a FNDC3B::RARB fusion;Genes, Chromosomes and Cancer;2023-06-07

3. Mate Pair Sequencing: Next-Generation Sequencing for Structural Variant Detection;Methods in Molecular Biology;2023

4. Typical, atypical and cryptic t(15;17)(q24;q21) ( PML::RARA ) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual‐color dual‐fusion FISH studies;Genes, Chromosomes and Cancer;2022-06-10

5. Cytogenetically cryptic PML::RARA fusion in acute promyelocytic leukemia: Testing strategies in the modern era;Leukemia Research Reports;2022