Access the full text.
Sign up today, get DeepDyve free for 14 days.
C. Marshall (1991)
Tumor suppressor genesCell, 64
M. Gessler, A. Poustka, W. Cavenee, R. Neve, S. Orkin, G. Bruns (1990)
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumpingNature, 343
E. Fearon, Kathleen Cho, J. Nigro, S. Kern, J. Simons, J. Ruppert, S. Hamilton, Antonette Preisinger, Giles Thomas, K. Kinzler, B. Vogelstein (1990)
Identification of a chromosome 18q gene that is altered in colorectal cancers.Science, 247 4938
S. Poel, N. McCabe, H. Gill, R. Espinosa, Yogesh Patel, A. Harden, Peter Rubinelli, Stephen Smith, Michelle LeBeau, Janet Rowley (1991)
Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.Proceedings of the National Academy of Sciences of the United States of America, 88 23
Martin Dyer, P. Fischer, Elisabeth Nacheva, W. Labastide, A. Karpas (1990)
A new human B-cell non-Hodgkin's lymphoma cell line (Karpas 422) exhibiting both t (14;18) and t(4;11) chromosomal translocations.Blood, 75 3
(1991)
Cytogenetic analysis of hematological malignant diseases
Y. Akao, M. Seto, T. Takahashi, I. Kubonishi, I. Miyoshi, S. Nakazawa, Y. Tsujimoto, C. Croce, R. Ueda (1991)
Molecular cloning of the chromosomal breakpoint of a B-cell lymphoma with the t(11;14)(q23;q32) translocation.Cancer research, 51 5
(1993)
Variability of l lq23
Il) and t(11;19) translocations
S. Stilgenbauer, H. Döhner, M. Bulgay-Mörschel, S. Weitz, M. Bentz, P. Lichter (1993)
High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics.Blood, 81 8
Alison Brown, Rossi Fm, Dunne Em, Steel Cm, Weir-Thompson Em (1993)
Evidence for a new tumour suppressor locus (DBM) in human B–cell neoplasia telomeric to the retinoblastoma geneNature Genetics, 3
D. Tkachuk, S. Kohler, M. Cleary (1992)
Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemiasCell, 71
Toshiya Inaba, H. Matsushime, M. Valentine, M. Roussel, M. Roussel, C. Sherr, C. Sherr, A. Look, A. Look (1992)
Genomic organization, chromosomal localization, and independent expression of human cyclin D genes.Genomics, 13 3
J. Yunis, N. Ramsay (1978)
Retinoblastoma and subband deletion of chromosome 13.American journal of diseases of children, 132 2
Y. Kaneko, J. Rowley, D. Variakojis, J. Haren, Y. Ueshima, K. Daly, L. Kluskens (1983)
Prognostic implications of karyotype and morphology in patients with non‐Hodgkin's lymphomaInternational Journal of Cancer, 32
M. Djabali, L. Selleri, P. Parry, M. Bower, B. Young, G. Evans (1992)
A trithorax–like gene is interrupted by chromosome 11q23 translocations in acute leukaemiasNature Genetics, 2
E. Solomon, J. Borrow, A. Goddard (1991)
Chromosome aberrations and cancer.Science, 254 5035
P. Thompson (1989)
Cancer CytogeneticsJournal of Medical Genetics, 26
(1991)
Mitelman F (ed): Guideline for Cancer Cytogenrrics
G. Cimino, T. Nakamura, Y. Gu, O. Canaani, R. Prasad, W. Crist, A. Carroll, M. Baer, C. Bloomfield, P. Nowell (1992)
An altered 11-kilobase transcript in leukemic cell lines with the t(4;11)(q21;q23) chromosome translocation.Cancer research, 52 13
Z. Kelman, M. Prokocimer, S. Peller, Y. Kahn, G. Rechavi, Y. Manor, A. Cohen, V. Rotter (1989)
Rearrangements in the p53 gene in Philadelphia chromosome positive chronic myelogenous leukemia.Blood, 74 7
N. McCabe, Robert BURNETTt, Heidi GILLt, Michael THIRMANt, David MBANGKOLLOt, M. Kipiniak, Elizabeth MELLEt, Sheryl Der, POELtt, Janet ROWLEYtI (1992)
Cloning of cDNAs of the MLL gene that detect DNA rearrangements and altered RNA transcripts in human leukemic cells with 11q23 translocations.Proceedings of the National Academy of Sciences of the United States of America, 89 24
Janet Rowley, Manuel Diaz, Rafael Espinosa, Yogesh Patel, Elizabeth Melle, S. Ziemin, Patricia Taillon-Miller, Peter Lichter, Glen Evans, J.H. Kersey, David Ward, Peter Domer, M. Beau (1990)
Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome.Proceedings of the National Academy of Sciences of the United States of America, 87
Gerald Edelman (1988)
Morphoregulatory molecules.Biochemistry, 27 10
J. Yunis (1978)
Trisomy for the distal end of the short arm of chromosome 3: a syndrome.American journal of diseases of children, 132 1
Yutaka Kobayashi, J. Yang, E. Shindo, A. Tojo, K. Tani, K. Ozawa, S. Asano (1993)
HRX gene rearrangement in acute lymphoblastic leukemia after adjuvant chemotherapy of breast cancer [letter; comment]Blood, 82
(1991)
Jhl(1991) Human gene mapping
(1990)
Mapping chromosome band llq23 in human acute leukemia with biorinylated
R. Mashal, M. Shtalrid, M. Talpaz, H. Kantarjian, Larry Smith, M. Beran, A. Cork, J. Trujillo, J. Gutterman, A. Deisseroth (1990)
Rearrangement and expression of p53 in the chronic phase and blast crisis of chronic myelogenous leukemia.Blood, 75 1
S. Baker, E. Fearon, J. Nigro, S. Hamilton, A. Preisinger, J. Jessup, P. Vantuinen, D. Ledbetter, D. Barker, Y. Nakamura, Raymond White, B. Vogelstein (1989)
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.Science, 244 4901
Hirofumi Kobayashi, R. Espinosa, M. Thirman, Elizabeth Davis, M. Diaz, M. Beau, Janet Rowley (1993)
Variability of 11q23 rearrangements in hematopoietic cell lines identified with fluorescence in situ hybridization.Blood, 81 11
F. Mitelman, Y. Kaneko, J. Trent (1990)
Report of the committee on chromosome changes in neoplasiaCytogenetic and Genome Research, 55
Y. Gu, Tomonori Nakamura, H. Alder, R. Prasad, O. Canaani, G. Cimino, C. Croce, E. Canaani (1992)
The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 geneCell, 71
Yukihiro Akao, Masao Seto, Kazuhito Yamamoto, S. Iida, Shinpei Nakazawa, Johji Inazawa, Tatsuo Abe, Toshitada Takahashi, R. Ueda (1992)
The RCK gene associated with t(11;14) translocation is distinct from the MLL/ALL-1 gene with t(4;11) and t(11;19) translocations.Cancer research, 52 21
(1993)
A cDNA probe deteccs all rearrangements of the MLL gene in leukemia with common and rare l lq 23 translocations
H. Kobayashi, R. Espinosa, M. Thirman, H. Gill, A. Fernald, M. Diaz, M. Beau, J. Rowley (1993)
Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization.Blood, 82 2
Yen-Ju Chen, P.-J. Chen, Shiou-Hwei Yeh, H. Tien, Wang Ch, Jih-Luh Tang, Ruey-Long Hong (1990)
Deletion of the human retinoblastoma gene in primary leukemias.Blood, 76 10
Hirofumi Kobayashi, R. Espinosa, M. Thirman, A. Fernald, K. Shannon, M. Diaz, M. Beau, J. Rowley (1993)
Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridizationGenes, 7
W. Lee, R. Bookstein, F. Hong, L. Young, J. Shew, E. Lee (1987)
Human retinoblastoma susceptibility gene: cloning, identification, and sequenceScience, 235
K. Call, T. Glaser, C. Ito, A. Buckler, J. Pelletier, D. Haber, E. Rose, A. Kral, H. Yeger, W. Lewis, Carol Jones, D. Housman (1990)
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locusCell, 60
H. Ahuja, M. Bar‐eli, S. Advani, S. Benchimol, M. Cline (1989)
Alterations in the p53 gene and the clonal evolution of the blast crisis of chronic myelocytic leukemia.Proceedings of the National Academy of Sciences of the United States of America, 86 17
U. Francke, L. Holmes, L. Atkins, V. Riccardi (1979)
Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.Cytogenetics and cell genetics, 24 3
Zhu Chen, N. Brand, A. Chen, -. Sai, Juan Chen, J. Tong, Zhen-yi Wang, S. Waxman, A. Zelent (1993)
Fusion between a novel Krüppel‐like zinc finger gene and the retinoic acid receptor‐alpha locus due to a variant t(11;17) translocation associated with acute promyelocytic leukaemia.The EMBO Journal, 12
J. Cheng, P. Scully, J. Shew, W. Lee, V. Vila, M. Haas (1990)
Homozygous deletion of the retinoblastoma gene in an acute lymphoblastic leukemia (T) cell line.Blood, 75 3
Y. Kaneko, J. Rowley, H. Maurer, D. Variakojis, J. Moohr (1982)
Chromosome pattern in childhood acute nonlymphocytic leukemia (ANLL).Blood, 60 2
Christine Harrison (1992)
Catalog of Chromosome Aberrations in CancerJournal of Medical Genetics, 29
A. Levine (1990)
Tumor suppressor genesBioEssays, 12
We studied samples containing deletions of the long arm of chromosome 11 (11 q) from patients with hematologic malignancies by using cytogenetic and fluorescence in situ hybridization (FISH) techniques. Cytogenetic analysis of 28 patients and of a cell line showed that all deletions included band 11q23. FISH analysis demonstrated that the proximal part of 11q23, including NCAM, was deleted in 13 of 15 patients and the cell line. Recurring chromosomal losses in human tumors have been regarded as evidence that the affected regions contain tumor‐suppressor genes. These results suggest that the putative tumor‐suppressor gene is proximal to the MLL gene which is also located in 11q23. © 1993 Wiley‐Liss, Inc.
Genes, Chromosomes and Cancer – Wiley
Published: Dec 1, 1993
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.