151 related articles for article (PubMed ID: 27374714)
1. Frequency and Clinical Characteristics of Intrachromosomal Amplification of Chromosome 21 in Korean Childhood B-lineage Acute Lymphoblastic Leukemia.
Kim J; Lyu CJ; Shin S; Lee ST; Choi JR
Ann Lab Med; 2016 Sep; 36(5):475-80. PubMed ID: 27374714
[TBL] [Abstract][Full Text] [Related]
2. MLPA as a complementary tool for diagnosis of chromosome 21 aberrations in childhood BCP-ALL.
Wrona E; Braun M; Pastorczak A; Taha J; Lejman M; Kowalczyk J; Fendler W; Młynarski W
J Appl Genet; 2019 Nov; 60(3-4):347-355. PubMed ID: 31456164
[TBL] [Abstract][Full Text] [Related]
3. Evaluation of multiplex ligation dependent probe amplification (MLPA) for identification of acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21 (iAMP21) in a Brazilian population.
Fuka G; Farias-Vieira TM; Hummel L; Blunck CB; Santoro JC; Terra-Granado E; Barbosa TC; Emerenciano M; Pombo-de-Oliveira MS
Mol Cytogenet; 2015; 8():35. PubMed ID: 26060508
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [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]
6. Minimal residual disease-based treatment is adequate for relapse-prone childhood acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21: the experience of the ALL-BFM 2000 trial.
Attarbaschi A; Panzer-Grümayer R; Mann G; Möricke A; König M; Mecklenbräuker A; Teigler-Schlegel A; Bradtke J; Harbott J; Göhring G; Stanulla M; Schrappe M; Zimmermann M; Haas OA;
Klin Padiatr; 2014 Nov; 226(6-7):338-43. PubMed ID: 25431866
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. [Detection of copy number variations in pediatric ETV6/RUNX1-positive acute lymphoblastic leukemia with multiplex ligation-dependent probe amplification].
Zhang L; Liu XM; Guo Y; Yang WY; Zhang JY; Liu F; Liu TF; Wang SC; Chen XJ; Ruan M; Qi BQ; Chang LX; Zou Y; Chen YM; Zhu XF
Zhongguo Dang Dai Er Ke Za Zhi; 2016 Jan; 18(1):34-8. PubMed ID: 26781410
[TBL] [Abstract][Full Text] [Related]
10. Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21.
Capela de Matos RR; Othman M; Ferreira GM; Monteso K; de Souza MT; Rouxinol M; Melo JB; Carreira IM; Abdelhay E; Liehr T; Ribeiro RC; Silva M
Cancer Genet; 2022 Apr; 262-263():16-22. PubMed ID: 34974289
[TBL] [Abstract][Full Text] [Related]
11. Is intrachromosomal amplification of chromosome 21 (iAMP21) always intrachromosomal?
Tsuchiya KD; Davis B; Gardner RA
Cancer Genet; 2017 Dec; 218-219():10-14. PubMed ID: 29153092
[TBL] [Abstract][Full Text] [Related]
12. Intrachromosomal amplification of chromosome 21 is associated with inferior outcomes in children with acute lymphoblastic leukemia treated in contemporary standard-risk children's oncology group studies: a report from the children's oncology group.
Heerema NA; Carroll AJ; Devidas M; Loh ML; Borowitz MJ; Gastier-Foster JM; Larsen EC; Mattano LA; Maloney KW; Willman CL; Wood BL; Winick NJ; Carroll WL; Hunger SP; Raetz EA
J Clin Oncol; 2013 Sep; 31(27):3397-402. PubMed ID: 23940221
[TBL] [Abstract][Full Text] [Related]
13. [A case report of childhood acute lymphoblastic leukemia with intrachromosomal amplification of AML1 gene in chromosome 21 and TEL deletion].
Yang W; Xiong F; Huang H; Wu Y; Lin Y; Fan X; Liu Z; Zhang X; Xu H; Zeng H; Zeng S
Zhonghua Xue Ye Xue Za Zhi; 2015 Jul; 36(7):569. PubMed ID: 26304079
[No Abstract] [Full Text] [Related]
14. Genomic characterization implicates iAMP21 as a likely primary genetic event in childhood B-cell precursor acute lymphoblastic leukemia.
Rand V; Parker H; Russell LJ; Schwab C; Ensor H; Irving J; Jones L; Masic D; Minto L; Morrison H; Ryan S; Robinson H; Sinclair P; Moorman AV; Strefford JC; Harrison CJ
Blood; 2011 Jun; 117(25):6848-55. PubMed ID: 21527530
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prevalence of ETV6-RUNX1 fusion gene in children with acute lymphoblastic leukemia in China.
Gao YJ; Zhu XH; Yang Y; Wu Y; Lu FJ; Zhai XW; Wang HS
Cancer Genet Cytogenet; 2007 Oct; 178(1):57-60. PubMed ID: 17889709
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia.
Al-Shehhi H; Konn ZJ; Schwab CJ; Erhorn A; Barber KE; Wright SL; Gabriel AS; Harrison CJ; Moorman AV
Genes Chromosomes Cancer; 2013 Feb; 52(2):202-13. PubMed ID: 23077088
[TBL] [Abstract][Full Text] [Related]
19. Risk-directed treatment intensification significantly reduces the risk of relapse among children and adolescents with acute lymphoblastic leukemia and intrachromosomal amplification of chromosome 21: a comparison of the MRC ALL97/99 and UKALL2003 trials.
Moorman AV; Robinson H; Schwab C; Richards SM; Hancock J; Mitchell CD; Goulden N; Vora A; Harrison CJ
J Clin Oncol; 2013 Sep; 31(27):3389-96. PubMed ID: 23940220
[TBL] [Abstract][Full Text] [Related]
20. Siblings with ETV6/RUNX1-positive B-lymphoblastic leukemia: A single site experience and review of the literature.
Martig DS; Williamson CM; Xu X; Sukov WR; Greipp PT; Hoppman NL; Baughn LB; Ketterling RP; Peterson JF
Ann Diagn Pathol; 2020 Oct; 48():151588. PubMed ID: 32836179
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]