204 related articles for article (PubMed ID: 31456164)
21. Cytogenetic Variation of B-Lymphoblastic Leukemia With Intrachromosomal Amplification of Chromosome 21 (iAMP21): A Multi-Institutional Series Review.
Johnson RC; Weinberg OK; Cascio MJ; Dahl GV; Mitton BA; Silverman LB; Cherry AM; Arber DA; Ohgami RS
Am J Clin Pathol; 2015 Jul; 144(1):103-12. PubMed ID: 26071468
[TBL] [Abstract][Full Text] [Related]
22. Coexistence of ETV6/RUNX1 and MLL aberrations in B-cell precursor acute lymphoblastic leukemia discloses a small subclass of BCP-ALL.
Amare Kadam PS; Raje GC; Pais AP; Banavali S
Cancer Genet Cytogenet; 2008 Apr; 182(1):27-32. PubMed ID: 18328947
[TBL] [Abstract][Full Text] [Related]
23. An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome.
Harrison CJ; Moorman AV; Schwab C; Carroll AJ; Raetz EA; Devidas M; Strehl S; Nebral K; Harbott J; Teigler-Schlegel A; Zimmerman M; Dastuge N; Baruchel A; Soulier J; Auclerc MF; Attarbaschi A; Mann G; Stark B; Cazzaniga G; Chilton L; Vandenberghe P; Forestier E; Haltrich I; Raimondi SC; Parihar M; Bourquin JP; Tchinda J; Haferlach C; Vora A; Hunger SP; Heerema NA; Haas OA;
Leukemia; 2014 May; 28(5):1015-21. PubMed ID: 24166298
[TBL] [Abstract][Full Text] [Related]
24. High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.
Karrman K; Forestier E; Andersen MK; Autio K; Borgström G; Heim S; Heinonen K; Hovland R; Kerndrup G; Johansson B;
Br J Haematol; 2006 Nov; 135(3):352-4. PubMed ID: 16965388
[TBL] [Abstract][Full Text] [Related]
25. Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: experience at a single institution.
Pérez-Vera P; Montero-Ruiz O; Frías S; Ulloa-Avilés V; Cárdenas-Cardós R; Paredes-Aguilera R; Rivera-Luna R; Carnevale A
Cancer Genet Cytogenet; 2005 Oct; 162(2):140-5. PubMed ID: 16213362
[TBL] [Abstract][Full Text] [Related]
26. [Prognostic significance of TEL/AML1 rearrangement and its additional genetic changes in Korean childhood precursor B-acute lymphoblastic leukemia].
Chung HY; Kim KH; Jun KR; Jang S; Park CJ; Chi HS; Im HJ; Seo JJ; Seo EJ
Korean J Lab Med; 2010 Feb; 30(1):1-8. PubMed ID: 20197715
[TBL] [Abstract][Full Text] [Related]
27. Interphase FISH on TEL/AML1 positive acute lymphoblastic leukemia relapses--analysis of clinical relevance of additional TEL and AML1 copy number changes.
Peter A; Heiden T; Taube T; Körner G; Seeger K
Eur J Haematol; 2009 Nov; 83(5):420-32. PubMed ID: 19594616
[TBL] [Abstract][Full Text] [Related]
28. Diagnostic utility of multiprobe fluorescence in situ hybridization assay for detecting cytogenetic aberrations in acute leukemia.
Kim BR; Choi JL; Kim JE; Woo KS; Kim KH; Kim JM; Kim SH; Han JY
Ann Lab Med; 2014 May; 34(3):198-202. PubMed ID: 24790906
[TBL] [Abstract][Full Text] [Related]
29. Coexistence of iAMP21 and
Gu J; Reynolds A; Fang L; DeGraffenreid C; Sterns K; Patel KP; Medeiros LJ; Lin P; Lu X
Mol Cytogenet; 2016; 9():84. PubMed ID: 27895713
[TBL] [Abstract][Full Text] [Related]
30. ETV6/RUNX1 fusion at diagnosis and relapse: some prognostic indications.
Martineau M; Jalali GR; Barber KE; Broadfield ZJ; Cheung KL; Lilleyman J; Moorman AV; Richards S; Robinson HM; Ross F; Harrison CJ
Genes Chromosomes Cancer; 2005 May; 43(1):54-71. PubMed ID: 15704129
[TBL] [Abstract][Full Text] [Related]
31. [Copy number variations in pediatric ETV6/RUNX1 positive acute lymphoblastic leukemia].
Zou Y; Zhang L; Liu X; Guo Y; Yang W; Zhang J; Liu F; Liu T; Wang S; Chen X; Ruan M; Qi B; Chang L; Chen Y; Zhu X
Zhonghua Er Ke Za Zhi; 2016 Mar; 54(3):209-13. PubMed ID: 26957068
[TBL] [Abstract][Full Text] [Related]
32. Evaluation of multiplex ligation-dependent probe amplification as a method for the detection of copy number abnormalities in B-cell precursor acute lymphoblastic leukemia.
Schwab CJ; Jones LR; Morrison H; Ryan SL; Yigittop H; Schouten JP; Harrison CJ
Genes Chromosomes Cancer; 2010 Dec; 49(12):1104-13. PubMed ID: 20815030
[TBL] [Abstract][Full Text] [Related]
33. Minimal residual disease monitoring in childhood B lymphoblastic leukemia with t(12;21)(p13;q22); ETV6-RUNX1: concordant results using quantitation of fusion transcript and flow cytometry.
Alm SJ; Engvall C; Asp J; Palmqvist L; Abrahamsson J; Fogelstrand L
Int J Lab Hematol; 2017 Apr; 39(2):121-128. PubMed ID: 28004528
[TBL] [Abstract][Full Text] [Related]
34. Characterization of unusual iAMP21 B-lymphoblastic leukemia (iAMP21-ALL) from the Mayo Clinic and Children's Oncology Group.
Koleilat A; Smadbeck JB; Zepeda-Mendoza CJ; Williamson CM; Pitel BA; Golden CL; Xu X; Greipp PT; Ketterling RP; Hoppman NL; Peterson JF; Harrison CJ; Akkari YMN; Tsuchiya KD; Shago M; Baughn LB
Genes Chromosomes Cancer; 2022 Dec; 61(12):710-719. PubMed ID: 35771717
[TBL] [Abstract][Full Text] [Related]
35. iAMP21 screening by MLPA assay: Need for identification of characteristic pattern of amplification in addition to mean probe ratios to avoid false positivity.
Vijayan A; Singh M; Bansal D; Sreedharanunni S; Varma N; Sachdeva MUS; Bhatia P
Int J Lab Hematol; 2020 Feb; 42(1):e30-e34. PubMed ID: 31364804
[No Abstract] [Full Text] [Related]
36. ETV6/RUNX1-positive childhood acute lymphoblastic leukemia (ALL): The spectrum of clonal heterogeneity and its impact on prognosis.
Ampatzidou M; Papadhimitriou SI; Paterakis G; Pavlidis D; Tsitsikas Κ; Kostopoulos IV; Papadakis V; Vassilopoulos G; Polychronopoulou S
Cancer Genet; 2018 Aug; 224-225():1-11. PubMed ID: 29778230
[TBL] [Abstract][Full Text] [Related]
37. Heterogeneity of Abnormal RUNX1 Leading to Clinicopathologic Variations in Childhood B-Lymphoblastic Leukemia.
Knez VM; Carstens BJ; Swisshelm KL; McGranahan AN; Liang X
Am J Clin Pathol; 2015 Aug; 144(2):305-14. PubMed ID: 26185316
[TBL] [Abstract][Full Text] [Related]
38. Prospective gene expression analysis accurately subtypes acute leukaemia in children and establishes a commonality between hyperdiploidy and t(12;21) in acute lymphoblastic leukaemia.
van Delft FW; Bellotti T; Luo Z; Jones LK; Patel N; Yiannikouris O; Hill AS; Hubank M; Kempski H; Fletcher D; Chaplin T; Foot N; Young BD; Hann IM; Gammerman A; Saha V
Br J Haematol; 2005 Jul; 130(1):26-35. PubMed ID: 15982341
[TBL] [Abstract][Full Text] [Related]
39. CpG island methylator phenotype redefines the prognostic effect of t(12;21) in childhood acute lymphoblastic leukemia.
Roman-Gomez J; Jimenez-Velasco A; Agirre X; Castillejo JA; Navarro G; Calasanz MJ; Garate L; San Jose-Eneriz E; Cordeu L; Prosper F; Heiniger A; Torres A
Clin Cancer Res; 2006 Aug; 12(16):4845-50. PubMed ID: 16914570
[TBL] [Abstract][Full Text] [Related]
40. ETV6-ABL1 fusion combined with monosomy 7 in childhood B-precursor acute lymphoblastic leukemia.
Uemura S; Nishimura N; Hasegawa D; Shono A; Sakaguchi K; Matsumoto H; Nakamachi Y; Saegusa J; Yokoi T; Tahara T; Tamura A; Yamamoto N; Saito A; Kozaki A; Kishimoto K; Ishida T; Nino N; Takafuji S; Mori T; Iijima K; Kosaka Y
Int J Hematol; 2018 May; 107(5):604-609. PubMed ID: 29177615
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
