SCOPUS 정보 검색 플랫폼

Leukemia

Volumn 15, Issue 3, 2001, Pages 468-472

Multicolor spectral karyotyping identifies novel translocations in childhood acute lymphoblastic leukemia

(5) Mathew, S a Rao, P H b Dalton, J a Downing, J R a Raimondi, S C a

a ST JUDE CHILDREN S RESEARCH HOSPITAL (United States)

b BAYLOR COLLEGE OF MEDICINE (United States)

Author keywords

Childhood ALL; Novel translocations; Spectral karyotyping

Indexed keywords

AML 1 PROTEIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ARTICLE; BLAST CELL; CHILD; CHILDHOOD CANCER; CHROMOSOME 13Q; CHROMOSOME 17Q; CHROMOSOME 19P; CHROMOSOME 21Q; CHROMOSOME 7Q; CHROMOSOME 8Q; CHROMOSOME 9P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CHROMOSOME G BAND; CHROMOSOME MARKER; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 17; CHROMOSOME TRANSLOCATION 19; CHROMOSOME TRANSLOCATION 7; CHROMOSOME TRANSLOCATION 8; CHROMOSOME TRANSLOCATION 9; CHROMOSOME TRANSLOCATION X; CHROMOSOME XP; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE LOCUS; HUMAN; HUMAN CELL; KARYOTYPE; KARYOTYPING; METAPHASE CHROMOSOME; MOLECULAR PROBE; MULTICOLOR SPECTRAL KARYOTYPING; PRIORITY JOURNAL; TELOMERE;

EID: 0035077452 PISSN: 08876924 EISSN: None Source Type: Journal
DOI: 10.1038/sj.leu.2401989 Document Type: Article

Times cited : (34)

References (22)

1
- 0005528601
- Cancer Cytogenetics, 2nd edn. Wiley Liss: New York
- (1995)
- Heim, S.¹ Mitelman, F.²

2
- 0029004541
- Fusion of the TEL gene on 12p13 to the AML1 on 21q22 in acute lymphoblastic leukemia
- (1995) Proc Natl Acad Sci USA , vol.92 , pp. 4917-4921
- Golub, T.R.¹ Barker, G.F.² Bohlander, S.K.³ Hiebert, S.W.⁴ Ward, D.C.⁵ Bray-Ward, P.⁶ Morgan, E.⁷ Raimondi, S.C.⁸ Rowley, J.D.⁹ Gilliland, D.G.¹⁰

3
- 0029045087
- The t(12;21) of acute lymphoblastic leukemia results in a TEL-AML1 gene fusion
- (1995) Blood , vol.85 , pp. 3662-3670
- Romana, S.P.¹ Mauchauffe, M.² Le Coniat, M.³ Chumakov, I.⁴ Le Paslier, D.⁵ Berger, R.⁶ Bernard, O.A.⁷

4
- 0028805405
- High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia
- (1995) Blood , vol.86 , pp. 4263-4269
- Romana, S.P.¹ Poirel, H.² Le Coniat, M.³ Flexor, M.A.⁴ Mauchauffe, M.⁵ Jonveaux, P.⁶ Macintyre, E.A.⁷ Berger, R.⁸ Bernard, O.A.⁹

5
- 13344282725
- TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis
- (1995) Leukemia , vol.9 , pp. 1985-1989
- Shurtleff, S.A.¹ Buijs, A.² Behm, F.G.³ Rubnitz, J.E.⁴ Raimondi, S.C.⁵ Hancock, M.L.⁶ Chan, G.C.-F.⁷ Pui, C.-H.⁸ Grosveld, G.⁹ Downing, J.R.¹⁰

6
- 0038214755
- Multicolor spectral karyotyping of human chromosomes
- (1996) Science , vol.273 , pp. 494-497
- Schrock, E.¹ du Manoir, S.² Veldman, T.³ Schoell, B.⁴ Wienberg, J.⁵ Ferguson-Smith, M.A.⁶ Ning, Y.⁷ Ledbetter, D.H.⁸ Bar-Am, I.⁹ Soenksen, D.¹⁰ Garini, Y.¹¹ Ried, T.¹²

7
- 0030909689
- Hidden chromosomes abnormalities in hematological malignancies detected by multicolor spectral karyotyping
- (1997) Nat Genet , vol.15 , pp. 406-410
- Veldman, T.¹ Vignon, C.² Schrock, E.³ Rowley, J.D.⁴ Ried, T.⁵

8
- 0032170964
- Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma
- (1998) Blood , vol.92 , pp. 1743-1748
- Rao, P.H.¹ Cigudosa, J.C.² Ning, Y.³ Calasanz, M.J.⁴ Iida, S.⁵ Tagawa, S.⁶ Michaeli, J.⁷ Klein, B.⁸ Dalla-Favera, R.⁹ Jhanwar, S.C.¹⁰ Ried, T.¹¹ Chaganti, R.S.K.¹²

9
- 0032402134
- Identification of new nonrandom translocations in multiple myeloma with multicolor spectral karyotyping
- (1998) Blood , vol.92 , pp. 4269-4278
- Sawyer, J.R.¹ Lukacs, J.L.² Munshi, N.³ Desikan, K.R.⁴ Singhal, S.⁵ Mehta, J.⁶ Siegel, D.⁷ Shaughnessy, J.⁸ Barlogie, B.⁹

10
- 0032746867
- Combined spectral karyotyping and DAPl banding analysis of chromosome abnormalities in myelodysplastic syndrome
- (1999) Genes Chromosom Cancer , vol.26 , pp. 336-345
- Kakazu, N.¹ Taniwaki, M.² Horiike, S.³ Nishida, K.⁴ Tatekawa, T.⁵ Nagai, M.⁶ Takahashi, T.⁷ Akaogi, T.⁸ Inazawa, J.⁹ Ohki, M.¹⁰ Abe, T.¹¹

11
- 0000622646
- Cytogenetics as a diagnostic aid for childhood hematological disorders. Conventional cytogenetic techniques, Fluorescence in situ hybridization and comparative genomic hybridization
- Hanausek M, Walaszek Z, (eds). Methods in Molecular Medicine, Tumor Marker Protocols. Humana Press: Totowa
- (1998) , vol.14 , pp. 209-227
- Raimondi, S.C.¹ Mathew, S.² Pui, C.H.³

12
- 0005609138
- An International System for Human Cytogenetic Nomenclature. Karger: Basel
- (1995)
- Mitelman, F.¹

13
- 4243937033
- Cryptic translocations in myelodysplastic syndrome karyotypes are revealed by spectral karyotyping
- (1998) Am J Hum Genet , vol.63
- Griffin, C.A.¹ Hawkins, A.L.² Henkle, C.T.³ Boone, L.B.⁴ Thomas, G.H.⁵ Stamberg, J.⁶ Dvoark, C.⁷ Heffner, A.⁸

14
- 0033559758
- Spectral karyotype analysis of T-cell acute leukemia
- (1999) Blood , vol.93 , pp. 2038-2042
- Rowley, J.D.¹ Reshmi, S.² Carlson, K.³ Roulston, D.⁴

15
- 0005566931
- Catalog of Chromosome Aberrations in Cancer. Wiley-Liss: New York
- (1998)
- Mitelman, F.¹

16
- 0025579569
- Trisomy 21 in neoplastic cells
- (1990) Am J Med Genet Suppl , vol.7 , pp. 62-66
- Mitelman, F.¹ Heim, S.² Mandahl, N.³

17
- 0025188811
- Biology and clinical significance of cytogenetic abnormalities in childhood acute lymphoblastic leukemia
- (1990) Blood , vol.76 , pp. 1449-1463
- Pui, C.H.¹ Crist, W.M.² Look, A.T.³

18
- 0026537436
- Trisomy 21 as the sole acquired abnormality in children with acute lymphoblastic leukemia
- (1992) Leukemia , vol.6 , pp. 171-175
- Raimondi, S.C.¹ Pui, C.-H.² Head, D.³ Behm, F.⁴ Privitera, E.⁵ Roberson, P.K.⁶ Gaston, K.R.⁷ Williams, D.L.⁸

19
- 0028117159
- Multiple genetic events involving RB1 gene deletion and amplification of chromosome 21 in a case of acute lymphoblastic leukemia
- (1994) Genes Chromosom Cancer , vol.9 , pp. 72-75
- Liu, Y.¹ Soderhall, S.² Heyman, M.³ Grander, D.⁴ Brondum-Nielsen, K.⁵ Einhorn, S.⁶

20
- 0034090392
- AML1 gene amplification: A novel finding in childhood acute lymphoblastic leukemia
- (2000) Hematologica , vol.85 , pp. 362-366
- Niini, T.¹ Kanerva, J.² Vettenranta, K.³ Saarinen-Pihkala, U.M.⁴ Knuutila, S.⁵

21
- 2642683176
- Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities
- (1997) Hum Genet , vol.101 , pp. 255-262
- Schrock, E.¹ Veldman, T.² Padilla-Nash, H.³ Ning, Y.⁴ Spurbeck, J.⁵ Jalal, S.⁶ Shaffer, L.G.⁷ Papenhausen, P.⁸ Kozma, C.⁹ Phelan, M.C.¹⁰ Kjeldsen, E.¹¹ Schonberg, S.A.¹² O'Brien, P.¹³ Biesecker, L.¹⁴ du Manoir, S.¹⁵ Reid, T.¹⁶

22
- 16044371402
- A complete set of human telomeric probes and their clinical application
- (Group 1), (Group 2) National Institutes of Health and Institute of Molecular Medicine collaboration.
- (1996) Nat Genet , vol.14 , pp. 86-89
- Ning, Y.¹ Roschke, A.² Smith, A.C.M.³ Macha, M.⁴ Prescht, K.⁵ Riethman, H.⁶ Ledbetter, D.⁷ Flint, J.⁸ Horseley, S.⁹ Regan, R.¹⁰ Kearney, L.¹¹ Knight, S.¹² Svaloy, K.¹³ Brown, W.R.A.¹⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.