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Volumn 126, Issue 1, 2001, Pages 20-25

Co-existence of alternative forms of 8q gain in cytogenetic clones of three patients with acute myeloid leukemia, pointing to 8q22∼8qter as a region of biologic significance

(4) Batanian, Jacqueline R a,b Ma, En b Huang, Yufeng b Gadre, Bharti b

a SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE (United States)

b Cardinal Glennon Hospital (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; BONE MARROW CELL; CASE REPORT; CHROMOSOME 8Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CLINICAL FEATURE; CLONE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DOSAGE; HUMAN; HUMAN CELL; MALE; PARTIAL TRISOMY; PRIORITY JOURNAL; TRISOMY 8;

ACUTE DISEASE; AGED; AGED, 80 AND OVER; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOID; MALE; MIDDLE AGED;

EID: 0035305437 PISSN: 01654608 EISSN: None Source Type: Journal
DOI: 10.1016/S0165-4608(00)00385-X Document Type: Article

Times cited : (7)

References (18)

1
- 0004958683
- Cancer Cytogenetics, 2nd ed, New York: Willey-Liss
- (1995)
- Heim, S.¹ Mitelman, F.²

2
- 0026728034
- Quantitative acute leukemia cytogenetics
- (1992) Genes Chromosom Cancer , vol.5 , pp. 57-66
- Mitelman, F.¹ Heim, S.²

3
- 0004935714
- Mitelman F. Tumor etiology and chromosome pattern-evidence from human and experimental neoplasms. In: Arrighi FE, Rao PN, Stubblefield E, editors. Genes, chromosomes and neoplasia. New York: Raven, 1981, 335-50.

4
- 0004960764
- ISCN. An international system for human cytogenetic nomenclature. F Mitelman, ed. Basel: S. Karger, 1995.

5
- 0032423289
- Molecular abnormalities in myeloid leukemias and myelodysplastic syndromes
- (1998) Leuk Res , vol.22 , Issue.12 , pp. 1113-1122
- Sawyers, C.¹

6
- 0028124528
- p53 and human cancers
- (1994) Brit Med Bull , vol.50 , pp. 582-599
- Lane, D.P.¹

7
- 0345368042
- Pentasomy 8q in myelodysplasia
- (1998) Cancer Genet Cytogenet , vol.100 , pp. 179-181
- Kwong, Y.¹ Chan, T.²

8
- 0033991184
- Tetrasomy 8 evolving into a segmental triplication 8q in a case of acute monocytic leukemia
- 9.
- (2000) Cancer Genet Cytogenet , vol.116 , pp. 74-76
- Qumsiyeh, M.¹ Cheng, C.² Eyre, J.³ Mann, K.⁴ Zhang, X.⁵

9
- 0029371867
- The pathogenetic significance of acquired trisomy 8 is not reducible to amplification of a single chromosome band
- (1995) Cancer Genet Cytogenet , vol.83 , pp. 176-177
- Mertens, F.¹ Johansson, M.²

10
- 0030978165
- Genetic abnormalities in chronic lymphocytic leukemia and their clinical and prognostic implications
- (1997) Cancer Genet Cytogenet , vol.94 , pp. 27-35
- Dierlamm, J.¹ Michauz, L.² Criel, A.³ Wlodarska, I.⁴ Van Den Berghe, H.⁵ Hossfeld, D.K.⁶

11
- 0028341345
- ALL-1 partial duplication in acute leukemia
- (1994) Proc Natl Acad Sci USA , vol.91 , pp. 6236-6239
- Schichman, S.¹ Caligiuri, M.² Gu, Y.³ Strout, M.⁴ Canaani, E.⁵ Bloomfield, C.⁶ Croce, C.⁷

12
- 0028326283
- The balanced and the unbalanced chromosome aberrations of acute myeloid leukemia may develop in different ways and may contribute differently to malignant transformation
- (1994) Blood , vol.83 , pp. 2780-2786
- Pedersen-Bjergaard, J.¹ Rowley, J.²

13
- 0031811713
- A study to determine whether trisomy 8, deleted 9q and trisomy 22 are markers of cryptic rearrangements of PML/RARalpha, AML1/ETO and CBFB/MYH11 respectively in acute myeloid leukemia
- (1998) Br J Haem , vol.101 , pp. 338-340
- Langabeer, S.E.¹ Grimwade, D.² Walker, H.³ Robers, J.R.⁴ Burnett, A.K.⁵ Goldstone, A.H.⁶ Lynch, D.C.⁷

14
- 0033022836
- Association between structural and numerical chromosomal aberrations in acute myeloblastic leukemia; a study by RT-PCR and FISH in 447 patients with de-novo AML
- (1999) Ann Hematol , vol.78 , pp. 265-269
- Krauter, J.¹ Ganser, A.² Bergmann, L.³ Raghavachar, A.⁴ Hoelzer, D.⁵ Lubbert, M.⁶ Schlimok, G.⁷ Arnold, R.⁸ Kirchner, H.⁹ Port, M.¹⁰ Heil, G.¹¹

15
- 0033993884
- Uneven frequencies of secondary chromosomal abnormalities in acute myeloid leukemias with t(3;21), t(15;17), and inv(16)
- (2000) Cancer Genet Cytogenet , vol.117 , pp. 159-162
- Berger, R.¹ Busson-Le Coniat, M.²

16
- 0032822953
- The AML1-ETO Chimaeric transcription factor in acute myeloid leukaemia; biology and clinical significance
- (1999) Br J Haem , vol.106 , pp. 296-308
- Downing, J.¹

17
- 0029900407
- Co-expression of two FAB-specific chromosome changes, t(15;17) and t(8;21), in a case of acute promyelocytic leukemia
- (1996) Ann Hematol , vol.72 , pp. 375-377
- Movafagh, A.¹ Varma, N.² Varma, S.³

18
- 0004936489
- Golub TR. The genetics of AML: an update. In: Hematology 1999: American Society of Hematology Education program book, 1999. pp. 102-11.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.