MRÁZ, Marek and Šárka POSPÍŠILOVÁ. Detection of a deletion at 22q11 locus involving ZNF280A/ZNF280B/PRAME/GGTLC2 in B-cell malignancies: simply a consequence of an immunoglobulin lambda light chain rearrangement. British journal of haematology. England: Wiley-Blackwell, 2019, vol. 186, No 4, p. "E91"-"E94", 4 pp. ISSN 0007-1048. Available from: https://dx.doi.org/10.1111/bjh.15922.
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Basic information
Original name Detection of a deletion at 22q11 locus involving ZNF280A/ZNF280B/PRAME/GGTLC2 in B-cell malignancies: simply a consequence of an immunoglobulin lambda light chain rearrangement
Authors MRÁZ, Marek (203 Czech Republic, guarantor, belonging to the institution) and Šárka POSPÍŠILOVÁ (203 Czech Republic, belonging to the institution).
Edition British journal of haematology, England, Wiley-Blackwell, 2019, 0007-1048.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30205 Hematology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 5.518
RIV identification code RIV/00216224:14740/19:00108506
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1111/bjh.15922
UT WoS 000478608100010
Keywords in English array CGH; chronic lymphocytic leukaemia; loss of 22q11; lambda light chain; deletion
Tags 14110212, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 26/2/2020 15:29.
Abstract
In this journal, Mestichelli et al (2018) recently reported that a submicroscopic 22q11 deletion is a potentially significant genomic aberration in chronic lymphocytic leukaemia (CLL), and that this alteration is missed by current routine techniques. This was based on the analysis of 23 CLL cases by oligonucleotide-based array comparative genomic hybridisation (aCGH; CytoChipCancer 4x180K, Illumina). The authors found 4 CLL cases with a deletion located at 22q11 that ranged in size from 0.68 Mb–0.49 Mb. The authors claimed that the minimally deleted region included the ZNF280A, ZNF280B, GGTLC2 and PRAME genes. The deletion in the 22q11 region was originally described by Gunn et al (2009) using aCGH and detected in 28 out of 187 analysed CLL cases.
Links
NV18-03-00054, research and development projectName: ÚLOHA MICRORNA A JEJICH CÍLOVÝCH MOLEKUL V TRANSFORMACI FOLIKULÁRNÍHO LYMFOMU A AGRESIVITĚ CHRONICKÉ LYMFOCYTÁRNÍ LEUKÉMIE
Investor: Ministry of Health of the CR
PrintDisplayed: 10/7/2024 06:06