{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,6]],"date-time":"2025-08-06T13:25:58Z","timestamp":1754486758542},"reference-count":34,"publisher":"Spandidos Publications","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2016,3]]},"DOI":"10.3892\/ol.2016.4169","type":"journal-article","created":{"date-parts":[[2016,1,29]],"date-time":"2016-01-29T13:53:03Z","timestamp":1454075583000},"page":"2117-2122","source":"Crossref","is-referenced-by-count":6,"title":["A novel IGH@ gene rearrangement associated with CDKN2A\/B deletion in young adult B-cell acute lymphoblastic leukemia"],"prefix":"10.3892","volume":"11","author":[{"given":"MONEEB A.K.","family":"OTHMAN","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"BEATA","family":"GRYGALEWICZ","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"BARBARA","family":"PIENKOWSKA-GRELA","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"JOLANTA","family":"RYGIER","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"ANNA","family":"EJDUK","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"MARTINA","family":"RINCIC","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"JOANA B.","family":"MELO","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"ISABEL M.","family":"CARREIRA","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"BRITTA","family":"MEYER","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"THOMAS","family":"LIEHR","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2249","published-online":{"date-parts":[[2016,1,29]]},"reference":[{"key":"key20180108094258_b1-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1347","DOI":"10.1016\/j.humpath.2012.02.004","article-title":"Advances in the molecular pathobiology of B-lymphoblastic leukemia","volume":"43","author":"Zhou","year":"2012","journal-title":"Hum Pathol"},{"key":"key20180108094258_b2-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"59","DOI":"10.12703\/P6-59","article-title":"Pathogenesis and prognostication in acute lymphoblastic leukemia","volume":"6","author":"Zuckerman","year":"2014","journal-title":"F1000Prime Rep"},{"key":"key20180108094258_b3-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1186\/2162-3619-3-16","article-title":"Childhood B-acute lymphoblastic leukemia: A genetic update","volume":"3","author":"Woo","year":"2014","journal-title":"Exp Hematol Oncol"},{"key":"key20180108094258_b4-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1362","DOI":"10.1038\/leu.2010.93","article-title":"A new recurrent translocation t(11;14)(q24;q32) involving IGH@ and miR-125b-1 in B-cell progenitor acute lymphoblastic leukemia","volume":"24","author":"Chapiro","year":"2010","journal-title":"Leukemia"},{"key":"key20180108094258_b5-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1453","DOI":"10.1200\/JCO.2013.51.3242","article-title":"IGH@ translocations are prevalent in teenagers and young adults with acute lymphoblastic leukemia and are associated with a poor outcome","volume":"32","author":"Russell","year":"2014","journal-title":"J Clin Oncol"},{"key":"key20180108094258_b6-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"3560","DOI":"10.1182\/blood-2006-03-010835","article-title":"Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia","volume":"108","author":"Chapiro","year":"2006","journal-title":"Blood"},{"key":"key20180108094258_b7-ol-0-0-4169","first-page":"183","article-title":"A new case of t(5;14)(q31;q32) in a pediatric acute lymphoblastic leukemia presenting with hypereosinophilia","volume":"16","author":"Gallego","year":"2012","journal-title":"Atlas Genet Cytogenet Oncol Haematol"},{"key":"key20180108094258_b8-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"614","DOI":"10.1038\/leu.2008.250","article-title":"A novel translocation, t(14;19)(q32;p13), involving IGH@ and the cytokine receptor for erythropoietin","volume":"23","author":"Russell","year":"2009","journal-title":"Leukemia"},{"key":"key20180108094258_b9-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"3100","DOI":"10.1200\/JCO.2011.40.3907","article-title":"IGH@ translocations, CRLF2 deregulation and microdeletions in adolescents and adults with acute lymphoblastic leukemia","volume":"30","author":"Moorman","year":"2012","journal-title":"J Clin Oncol"},{"key":"key20180108094258_b10-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1490","DOI":"10.1182\/blood-2009-09-235986","article-title":"Immunoglobulin heavy chain locus chromosomal translocations in B-cell precursor acute lymphoblastic leukemia: Rare clinical curios or potent genetic drivers?","volume":"115","author":"Dyer","year":"2010","journal-title":"Blood"},{"key":"key20180108094258_b11-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"387","DOI":"10.1182\/blood-2007-07-092015","article-title":"t(6;14)(p22;q32): A new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)","volume":"111","author":"Russell","year":"2008","journal-title":"Blood"},{"key":"key20180108094258_b12-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1016\/j.cancergencyto.2009.06.013","article-title":"Homozygous deletion of CDKN2A (p16, p14) and CDKN2B (p15) genes is a poor prognostic factor in adult but not in childhood B-lineage acute lymphoblastic leukemia: A comparative deletion and hypermethylation study","volume":"195","author":"Kim","year":"2009","journal-title":"Cancer Genet Cytogenet"},{"key":"key20180108094258_b13-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1182\/asheducation.V2012.1.389.3798360","article-title":"The molecular genetic makeup of acute lymphoblastic leukemia","volume":"2012","author":"Mullighan","year":"2012","journal-title":"Hematology Am Soc Hematol Educ Program"},{"key":"key20180108094258_b14-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1228","DOI":"10.1016\/j.leukres.2008.01.014","article-title":"CDKN2A deletions in acute lymphoblastic leukemia of adolescents and young adults: An array CGH study","volume":"32","author":"Usvasalo","year":"2008","journal-title":"Leuk Res"},{"key":"key20180108094258_b15-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1007\/s00277-003-0808-9","article-title":"Acute lymphoblastic leukemia in elderly: The Polish Adult Leukemia Group (PALG) experience","volume":"83","author":"Robak","year":"2004","journal-title":"Ann Hematol"},{"key":"key20180108094258_b16-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1159\/000069817","article-title":"Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosis","volume":"98","author":"Claussen","year":"2002","journal-title":"Cytogenet Genome Res"},{"key":"key20180108094258_b17-ol-0-0-4169","author":"Shaffer","year":"2013","journal-title":"An International System for Human Cytogenetic Nomenclature (2013)"},{"key":"key20180108094258_b18-ol-0-0-4169","doi-asserted-by":"crossref","DOI":"10.1007\/978-3-540-70581-9","author":"Liehr","year":"2009","journal-title":"Fluorescence In Situ Hybridization (FISH) - Application Guide"},{"key":"key20180108094258_b19-ol-0-0-4169","first-page":"335","article-title":"Microdissection based high resolution multicolor banding for all 24 human chromosomes","volume":"9","author":"Liehr","year":"2002","journal-title":"Int J Mol Med"},{"key":"key20180108094258_b20-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1159\/000076286","article-title":"Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method","volume":"103","author":"Weise","year":"2003","journal-title":"Cytogenet Genome Res"},{"key":"key20180108094258_b21-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1369\/jhc.2008.950550","article-title":"Molecular definition of high-resolution multicolor banding probes: First within the human DNA sequence anchored FISH banding probe set","volume":"56","author":"Weise","year":"2008","journal-title":"J Histochem Cytochem"},{"key":"key20180108094258_b22-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"625","DOI":"10.3892\/or.2014.3624","article-title":"MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report","volume":"33","author":"Othman","year":"2015","journal-title":"Oncol Rep"},{"key":"key20180108094258_b23-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1016\/j.cancergencyto.2008.08.008","article-title":"Translocation (14;14)(q11;q32) with simultaneous involvement of the IGH and CEBPE genes in B-lineage acute lymphoblastic leukemia","volume":"187","author":"Han","year":"2008","journal-title":"Cancer Genet Cytogenet"},{"key":"key20180108094258_b24-ol-0-0-4169","author":"Mitelman","journal-title":"Mitelman Database of Chromosome Aberrations and Gene Fusions in Cancer (2014)"},{"key":"key20180108094258_b25-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1159\/000227835","article-title":"A neocentric isochromosome Yp present as additional small supernumerary marker chromosome - evidence against U-type exchange mechanism?","volume":"125","author":"Sheth","year":"2009","journal-title":"Cytogenet Genome Res"},{"key":"key20180108094258_b26-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"4245","DOI":"10.1158\/1078-0432.CCR-11-0395","article-title":"Primary central nervous system lymphomas: A validation study of array-based comparative genomic hybridization in formalin-fixed paraffin-embedded tumor specimens","volume":"17","author":"Braggio","year":"2011","journal-title":"Clin Cancer Res"},{"key":"key20180108094258_b27-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1118","DOI":"10.1002\/gcc.20613","article-title":"The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1","volume":"47","author":"Parker","year":"2008","journal-title":"Genes Chromosomes Cancer"},{"key":"key20180108094258_b28-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"832","DOI":"10.1136\/gutjnl-2012-304037","article-title":"A disrupted RNA editing balance mediated by ADARs (Adenosine DeAminases that act on RNA) in human hepatocellular carcinoma","volume":"63","author":"Chan","year":"2014","journal-title":"Gut"},{"key":"key20180108094258_b29-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1586","DOI":"10.1101\/gr.6493107","article-title":"Altered adenosine-to-inosine RNA editing in human cancer","volume":"17","author":"Paz","year":"2007","journal-title":"Genome Res"},{"key":"key20180108094258_b30-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1038\/leu.2013.277","article-title":"An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions","volume":"28","author":"Clappier","year":"2014","journal-title":"Leukemia"},{"key":"key20180108094258_b31-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"9234","DOI":"10.1200\/JCO.2005.03.6137","article-title":"Overexpression of the ETS-related gene, ERG, predicts a worse outcome in acute myeloid leukemia with normal karyotype: A Cancer and Leukemia Group B study","volume":"23","author":"Marcucci","year":"2005","journal-title":"J Clin Oncol"},{"key":"key20180108094258_b32-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1016\/j.ajhg.2013.06.003","article-title":"Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosa","volume":"93","author":"Davidson","year":"2013","journal-title":"Am J Hum Genet"},{"key":"key20180108094258_b33-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"849","DOI":"10.1158\/1078-0432.CCR-0607-3","article-title":"Gene expression profiles predict survival and progression of pleural mesothelioma","volume":"10","author":"Pass","year":"2004","journal-title":"Clin Cancer Res"},{"key":"key20180108094258_b34-ol-0-0-4169","doi-asserted-by":"crossref","first-page":"1341","DOI":"10.1086\/380309","article-title":"Mutations in the ZNF41 gene are associated with cognitive deficits: Identification of a new candidate for X-linked mental retardation","volume":"73","author":"Shoichet","year":"2003","journal-title":"Am J Hum Genet"}],"container-title":["Oncology Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/spandidos-publications.com\/10.3892\/ol.2016.4169\/download","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,14]],"date-time":"2020-09-14T16:11:47Z","timestamp":1600099907000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.spandidos-publications.com\/10.3892\/ol.2016.4169"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,1,29]]},"references-count":34,"journal-issue":{"issue":"3","published-online":{"date-parts":[[2016,1,29]]},"published-print":{"date-parts":[[2016,3]]}},"alternative-id":["10.3892\/ol.2016.4169"],"URL":"https:\/\/doi.org\/10.3892\/ol.2016.4169","relation":{},"ISSN":["1792-1074","1792-1082"],"issn-type":[{"value":"1792-1074","type":"print"},{"value":"1792-1082","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,1,29]]}}}