DOI: 10.1038/sj.leu.2403846. Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia

Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia

10.1038/sj.leu.2403846

Crossref journal-article

Springer Science and Business Media LLC

Leukemia (297)

Bibliography

Noguera, N. I., Ammatuna, E., Zangrilli, D., Lavorgna, S., Divona, M., Buccisano, F., Amadori, S., Mecucci, C., Falini, B., & Lo-Coco, F. (2005). Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia. Leukemia, 19(8), 1479â1482.

Authors 10

N I Noguera (first)
E Ammatuna (additional)
D Zangrilli (additional)
S Lavorgna (additional)
M Divona (additional)
F Buccisano (additional)
S Amadori (additional)
C Mecucci (additional)
B Falini (additional)
F Lo-Coco (additional)

References 12 Referenced 104

Cheson BD, Bennett JM, Kopecky KJ, Buchner T, Willman CL, Estey EH et al. International working group for diagnosis, standardization of response criteria, treatment outcomes, and reporting standards for the rapeutic trials in acute myeloid leukemia. Revised recommendations of the international working group for diagnosis, standardization of response criteria, treatment outcomes, and reporting standards for therapeutic trials in acute myeloid leukemia. J Clin Oncol 2003; 15: 4642–4649. (10.1200/JCO.2003.04.036) / J Clin Oncol by BD Cheson (2003)
Falini B, Mecucci C, Tiacci E, Alcalay M, Rosati R, Pasqualucci L, et al, GIMEMA Acute Leukemia Working Party. Cytoplasmic nucleophosmin (NPM) identifies a subtype of acute myelogenous leukemia with a normal karyotype and NPM1 gene mutations. N Engl J Med 2005; 352: 254–266. (10.1056/NEJMoa041974) / N Engl J Med by B Falini (2005)
Thiede C, Steudel C, Mohr B, Schaich M, Schakel U, Platzbecker U et al. Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis. Blood 2002; 99: 4326–4335. (10.1182/blood.V99.12.4326) / Blood by C Thiede (2002)
Gilliland DG, Griffin JD . The roles of FLT3 in hematopoiesis and leukemia. Blood 2002; 100: 1532–1542. (10.1182/blood-2002-02-0492) / Blood by DG Gilliland (2002)
Abu-Duhier FM, Goodeve AC, Wilson GA, Gari MA, Peake IR, Rees DC et al. FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group. Br J Haematol 2000; 111: 190–195. (10.1046/j.1365-2141.2000.02317.x) / Br J Haematol by FM Abu-Duhier (2000)
Rombouts WJ, Lowenberg B, van Putten WL, Ploemacher RE . Improved prognostic significance of cytokine-induced proliferation in vitro in patients with de novo acute myeloid leukemia of intermediate risk: impact of internal tandem duplications in the Flt3 gene. Leukemia 2001; 15: 1046–1053. (10.1038/sj.leu.2402157) / Leukemia by WJ Rombouts (2001)
Martinelli G, Piccaluga PP, LoCoco F . FLT3 inhibition as tailored therapy for acute myeloid leukemia. Haematologica 2003; 88: 4–8. / Haematologica by G Martinelli (2003)
Noguera NI, Breccia M, Divona M, Diverio D, Costa V, De Santis S et al. Alterations of the FLT3 gene in acute promyelocytic leukemia: association with diagnostic characteristics and analysis of clinical outcome in patients treated with the Italian AIDA protocol. Leukemia 2002; 16: 2185–2189. (10.1038/sj.leu.2402723) / Leukemia by NI Noguera (2002)
Nishimura Y, Ohkubo T, Furuichi Y, Umekawa H . Tryptophans 286 and 288 in the C-terminal region of protein B231 are important for its nucleolar localization. Biosci. Biotechnol Biochem 2002; 66: 2239–2242. (10.1271/bbb.66.2239) / Biosci. Biotechnol Biochem by Y Nishimura (2002)
Chomczynsky P, Sacchi N . Single step method of RNA isolation by acid guanidium thiocyanate – phenol chloroform extraction. Anal Biochem 1987; 162: 156–159. / Anal Biochem by P Chomczynsky (1987)
van Dongen JJ, Macintyre EA, Gabert JA, Delabesse E, Rossi V, Saglio G et al. Standardized RT-PCR analysis of fusion gene transcripts from chromosome aberrations in acute leukemia for detection of minimal residual disease. Report of the BIOMED-1 Concerted Action: investigation of minimal residual disease in acute leukemia. Leukemia 1999; 13: 1901–1928. (10.1038/sj.leu.2401592) / Leukemia by JJ van Dongen (1999)
Liu QR, Chan PK . Characterization of seven processed pseudogenes of nucleophosmin/B23 in the human genome. DNA Cell Biol 1993; 12: 149–156. (10.1089/dna.1993.12.149) / DNA Cell Biol by QR Liu (1993)

Dates

Type	When
Created	20 years, 2 months ago (June 23, 2005, 6:43 a.m.)
Deposited	3 years, 5 months ago (March 31, 2022, 9:25 p.m.)
Indexed	5 days, 15 hours ago (Aug. 30, 2025, 1:07 p.m.)
Issued	20 years, 2 months ago (June 23, 2005)
Published	20 years, 2 months ago (June 23, 2005)
Published Online	20 years, 2 months ago (June 23, 2005)
Published Print	20 years, 1 month ago (Aug. 1, 2005)

Funders 0

None

BibTeX

@article{Noguera_2005, title={Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia}, volume={19}, ISSN={1476-5551}, url={http://dx.doi.org/10.1038/sj.leu.2403846}, DOI={10.1038/sj.leu.2403846}, number={8}, journal={Leukemia}, publisher={Springer Science and Business Media LLC}, author={Noguera, N I and Ammatuna, E and Zangrilli, D and Lavorgna, S and Divona, M and Buccisano, F and Amadori, S and Mecucci, C and Falini, B and Lo-Coco, F}, year={2005}, month=jun, pages={1479–1482} }

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