-
1
-
-
0027478524
-
t(5; 12)(q31;p12). A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia
-
Wessels JW, Fibbe WE, van der Keur D, Landegent JE, van der Plas DC, den Ottolander GJ, Roozendaal KJ, Beverstock GC: t(5; 12)(q31;p12). A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia. Cancer Genet Cytogenet 65:7, 1993
-
(1993)
Cancer Genet Cytogenet
, vol.65
, pp. 7
-
-
Wessels, J.W.1
Fibbe, W.E.2
Van Der Keur, D.3
Landegent, J.E.4
Van Der Plas, D.C.5
Den Ottolander, G.J.6
Roozendaal, K.J.7
Beverstock, G.C.8
-
2
-
-
0028224348
-
Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5; 12) chromosomal translocation
-
Golub TR, Barker GF, Lovett M, Gilliland D: Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5; 12) chromosomal translocation. Cell 77:307, 1994
-
(1994)
Cell
, vol.77
, pp. 307
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.4
-
3
-
-
0030464979
-
ETV6 gene rearrangements in hematopoietic malignant disorders
-
Wlodarska I, Mecucci C, Baens M, Marynen P, Van den Berghe H: ETV6 gene rearrangements in hematopoietic malignant disorders. Leuk Lymphoma 23:287, 1996
-
(1996)
Leuk Lymphoma
, vol.23
, pp. 287
-
-
Wlodarska, I.1
Mecucci, C.2
Baens, M.3
Marynen, P.4
Van Den Berghe, H.5
-
4
-
-
0028911281
-
Recurrent chromosomal translocations and fusion genes in leukemia-lymphoma cell lines
-
Drexler HG, MacLeod RAF, Borkhardt A, Janssen JWG: Recurrent chromosomal translocations and fusion genes in leukemia-lymphoma cell lines. Leukemia 9:480, 1995
-
(1995)
Leukemia
, vol.9
, pp. 480
-
-
Drexler, H.G.1
MacLeod, R.A.F.2
Borkhardt, A.3
Janssen, J.W.G.4
-
5
-
-
0011144513
-
Human leukemia cell lines. Evidence for differentiation toward T- and B-cell axis within a leukemia
-
Minowada J, Oshimura M, Abe S, Greaves MF, Janossy G, Sandberg AA: Human leukemia cell lines. Evidence for differentiation toward T- and B-cell axis within a leukemia. Proc Am Assoc Cancer Res 19:109, 1978
-
(1978)
Proc Am Assoc Cancer Res
, vol.19
, pp. 109
-
-
Minowada, J.1
Oshimura, M.2
Abe, S.3
Greaves, M.F.4
Janossy, G.5
Sandberg, A.A.6
-
6
-
-
0018408021
-
Characterization of a leukemic cell line of the pre-B phenotype
-
Hurwitz R, Hozier J, LeBien T, Minowada J, Gajl-Peczalska K, Kubonishi I, Kersey J: Characterization of a leukemic cell line of the pre-B phenotype. Int J Cancer 23:174, 1979
-
(1979)
Int J Cancer
, vol.23
, pp. 174
-
-
Hurwitz, R.1
Hozier, J.2
LeBien, T.3
Minowada, J.4
Gajl-Peczalska, K.5
Kubonishi, I.6
Kersey, J.7
-
7
-
-
0013414605
-
PBEI: A pre B acute lymphoblastic leukemia cell line derived from long term bone marrow culture
-
abstr 148
-
Pirrucello SJ, Lang MS, Sanger WG: PBEI: A pre B acute lymphoblastic leukemia cell line derived from long term bone marrow culture. Blood 78:39a, 1991 (abstr 148, suppl 1)
-
(1991)
Blood
, vol.78
, Issue.1 SUPPL.
-
-
Pirrucello, S.J.1
Lang, M.S.2
Sanger, W.G.3
-
8
-
-
0026668426
-
Dup(12) (q13qter) in two t(14; 18)-Negative Follicular B-non-Hodgkin's Lymphomas
-
Wlodarska I, Mecucci C, Vandenberghe E, De Wolf-Peeters C, Thomas J, Hilliker C, Schoenmakers E, Stul M, Marynen P, Cassiman JJ, Van den Berghe H: Dup(12) (q13qter) in two t(14; 18)-Negative Follicular B-non-Hodgkin's Lymphomas. Genes Chromosomes Cancer 4:302, 1992
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 302
-
-
Wlodarska, I.1
Mecucci, C.2
Vandenberghe, E.3
De Wolf-Peeters, C.4
Thomas, J.5
Hilliker, C.6
Schoenmakers, E.7
Stul, M.8
Marynen, P.9
Cassiman, J.J.10
Van Den Berghe, H.11
-
9
-
-
0029889231
-
Genomic organisation of TEL: The human ETS-variant gene 6 (ETV6)
-
Baens M, Peeters P, Guo C, Aerssens J, Marynen P: Genomic organisation of TEL: The human ETS-variant gene 6 (ETV6). Genome Res 6:404, 1996
-
(1996)
Genome Res
, vol.6
, pp. 404
-
-
Baens, M.1
Peeters, P.2
Guo, C.3
Aerssens, J.4
Marynen, P.5
-
10
-
-
0027329049
-
Characterisation of two chromosome 12 cosmid libraries and development of STSs from cosmids mapped by FISH
-
Montgomery KT, LeBlanc JM, Tsai P, McNinch JS, Ward DC, de Jong PJ, Kucherlapati R, Krauter KS: Characterisation of two chromosome 12 cosmid libraries and development of STSs from cosmids mapped by FISH. Genomics 17:682, 1993
-
(1993)
Genomics
, vol.17
, pp. 682
-
-
Montgomery, K.T.1
LeBlanc, J.M.2
Tsai, P.3
McNinch, J.S.4
Ward, D.C.5
De Jong, P.J.6
Kucherlapati, R.7
Krauter, K.S.8
-
11
-
-
0029416826
-
An STS-based map of the human genome
-
Hudson TJ, Stein LD, Gerety SS, Ma J, Castle AB, Silva J, Slonim DK, Baptista R, Kruglyak L, Xu SH, Colbert AME, Rosenberg C, Reeve-Daly MP, Rozen S, Hui L, Wu X, Vestergaard C, Wilson KM, Bae JS, Maitra S, Ganiatsas S, Evans, CA, DeAngelis MM, Ingalls KA, Nahf RW, Horton LT, Anderson MO, Collymore AJ, Ye W, Kouyoumjian V, Zemsteva IS, Tam J, Devine R, Courtney DF, Renauld MT, Nguyen HT, Fizames C, Fauré S, Gyapay G, Dib C, Morissette J, Orlin JB, Birren BW, Goodman N, Weissenbach J, Hawkins TL, Foote S, Page DC, Lander ES: An STS-based map of the human genome. Science 270:1945, 1995
-
(1995)
Science
, vol.270
, pp. 1945
-
-
Hudson, T.J.1
Stein, L.D.2
Gerety, S.S.3
Ma, J.4
Castle, A.B.5
Silva, J.6
Slonim, D.K.7
Baptista, R.8
Kruglyak, L.9
Xu, S.H.10
Colbert, A.M.E.11
Rosenberg, C.12
Reeve-Daly, M.P.13
Rozen, S.14
Hui, L.15
Wu, X.16
Vestergaard, C.17
Wilson, K.M.18
Bae, J.S.19
Maitra, S.20
Ganiatsas, S.21
Evans, C.A.22
DeAngelis, M.M.23
Ingalls, K.A.24
Nahf, R.W.25
Horton, L.T.26
Anderson, M.O.27
Collymore, A.J.28
Ye, W.29
Kouyoumjian, V.30
Zemsteva, I.S.31
Tam, J.32
Devine, R.33
Courtney, D.F.34
Renauld, M.T.35
Nguyen, H.T.36
Fizames, C.37
Fauré, S.38
Gyapay, G.39
Dib, C.40
Morissette, J.41
Orlin, J.B.42
Birren, B.W.43
Goodman, N.44
Weissenbach, J.45
Hawkins, T.L.46
Foote, S.47
Page, D.C.48
Lander, E.S.49
more..
-
12
-
-
0029096009
-
A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12
-
Raeymaekers P, Van Zand K, Lin J, Cassiman JJ, Marynen P: A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12. Genomics 29:170, 1996
-
(1996)
Genomics
, vol.29
, pp. 170
-
-
Raeymaekers, P.1
Van Zand, K.2
Lin, J.3
Cassiman, J.J.4
Marynen, P.5
-
13
-
-
0029653616
-
A second-generation YAC contig map of human chromosome 12
-
Krauter K, Montgomery K, Yoon S-J, LeBlanc-Straceski J, Renault B, Marondel I, Herdman V, Cupelli L, Banks A, Lieman J, Menninger J, Bray-Ward P, Nadkarni Prakash, Weisenbach J, Le Paslier D, Rigault P, Chumakov I, Cohen D, Miller P, Ward D, Kucherlapati R: A second-generation YAC contig map of human chromosome 12. Nature 377:321, 1995 (suppl)
-
(1995)
Nature
, vol.377
, Issue.SUPPL.
, pp. 321
-
-
Krauter, K.1
Montgomery, K.2
Yoon, S.-J.3
LeBlanc-Straceski, J.4
Renault, B.5
Marondel, I.6
Herdman, V.7
Cupelli, L.8
Banks, A.9
Lieman, J.10
Menninger, J.11
Bray-Ward, P.12
Prakash, N.13
Weisenbach, J.14
Le Paslier, D.15
Rigault, P.16
Chumakov, I.17
Cohen, D.18
Miller, P.19
Ward, D.20
Kucherlapati, R.21
more..
-
14
-
-
0029653653
-
A YAC contig map of the human genome
-
Chumakov IM, Rigault P, Le Gall I, Bellanne-Chantelot C, Billault A, Guillou S, Soularue P, Guasconi G, Poullier E, Gros I, Belova M, Sambucy J-L, Susini L, Gervy P, Gilbert F, Beaufils S, Bui H, Massart C, De Tand M-F, Dukasz F, Lecoulant S, Ougen P, Perrot V, Saumier M, Soravito C, Bahouayila R, Cohen-Akenine A, Barillot EM, Bertrand S, Codani J-J, Caterina D, Georges I, Lacroix B, Lucotte G, Sahbatou M, Schmit C, Sangouard M, Tubacher E, Dib C, Fauré S, Fizames C, Guapay G, Millasseau P, Nguyen S, Muselet D, Vignal A, Morissette J, Menninger J, Lieman J, Desai T, Banks A, Bray-Ward P, Ward D, Hudson T, Gerety S, Foote S, Stein L, Page DC, Lander ES, Weissenbach J, Le Paslier D, Cohen D: A YAC contig map of the human genome. Nature 377:175, 1995
-
(1995)
Nature
, vol.377
, pp. 175
-
-
Chumakov, I.M.1
Rigault, P.2
Le Gall, I.3
Bellanne-Chantelot, C.4
Billault, A.5
Guillou, S.6
Soularue, P.7
Guasconi, G.8
Poullier, E.9
Gros, I.10
Belova, M.11
Sambucy, J.-L.12
Susini, L.13
Gervy, P.14
Gilbert, F.15
Beaufils, S.16
Bui, H.17
Massart, C.18
De Tand, M.-F.19
Dukasz, F.20
Lecoulant, S.21
Ougen, P.22
Perrot, V.23
Saumier, M.24
Soravito, C.25
Bahouayila, R.26
Cohen-Akenine, A.27
Barillot, E.M.28
Bertrand, S.29
Codani, J.-J.30
Caterina, D.31
Georges, I.32
Lacroix, B.33
Lucotte, G.34
Sahbatou, M.35
Schmit, C.36
Sangouard, M.37
Tubacher, E.38
Dib, C.39
Fauré, S.40
Fizames, C.41
Guapay, G.42
Millasseau, P.43
Nguyen, S.44
Muselet, D.45
Vignal, A.46
Morissette, J.47
Menninger, J.48
Lieman, J.49
Desai, T.50
Banks, A.51
Bray-Ward, P.52
Ward, D.53
Hudson, T.54
Gerety, S.55
Foote, S.56
Stein, L.57
Page, D.C.58
Lander, E.S.59
Weissenbach, J.60
Le Paslier, D.61
Cohen, D.62
more..
-
15
-
-
0027211748
-
A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridization
-
Saltman DL, Dolganov GM, Warrington JA, Wasmuth JJ, Lovett M: A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridization. Genomics 16:726, 1993
-
(1993)
Genomics
, vol.16
, pp. 726
-
-
Saltman, D.L.1
Dolganov, G.M.2
Warrington, J.A.3
Wasmuth, J.J.4
Lovett, M.5
-
16
-
-
0027320808
-
A high-resolution cytogenetic map of human chromosome 5: Localization of 206 new cosmid markers by direct R-banding fluorescence in situ hybridization
-
Takahashi E, Hitomi A, Nakamura Y: A high-resolution cytogenetic map of human chromosome 5: Localization of 206 new cosmid markers by direct R-banding fluorescence in situ hybridization. Genomics 17:234, 1993
-
(1993)
Genomics
, vol.17
, pp. 234
-
-
Takahashi, E.1
Hitomi, A.2
Nakamura, Y.3
-
17
-
-
0023133299
-
Human-fms gene is retained in acute lymphoblastic leukemia cells with del(5)(q32)
-
Ohyashiki JH, Ohyashiki K, Sandberg AA, Minowada J, Kinniburgh AJ: Human-fms gene is retained in acute lymphoblastic leukemia cells with del(5)(q32). Cytogenet Cell Genet 25:341, 1987
-
(1987)
Cytogenet Cell Genet
, vol.25
, pp. 341
-
-
Ohyashiki, J.H.1
Ohyashiki, K.2
Sandberg, A.A.3
Minowada, J.4
Kinniburgh, A.J.5
-
18
-
-
0021944206
-
Human c-fms proto-oncogene: Comparative analysis with an abnormal allele
-
Verbeek JS, Roebroek AJM, van den Ouweland AMW, Bloemers HPJ, Van de Ven WJM: Human c-fms proto-oncogene: Comparative analysis with an abnormal allele. Mol Cell Biol 5:422, 1985
-
(1985)
Mol Cell Biol
, vol.5
, pp. 422
-
-
Verbeek, J.S.1
Roebroek, A.J.M.2
Van Den Ouweland, A.M.W.3
Bloemers, H.P.J.4
Van De Ven, W.J.M.5
-
19
-
-
0027970838
-
Chromosomal translocations in human cancer
-
Rabbitts TH: Chromosomal translocations in human cancer. Nature 372:143, 1994
-
(1994)
Nature
, vol.372
, pp. 143
-
-
Rabbitts, T.H.1
-
20
-
-
0028805405
-
High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia
-
Romana SP, Poirel H, Leconiat M, Flexor M-A, Mauchauffé M, Jonveaux P, Macintyre EA, Berger R, Bernard OA: High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood 86:4263, 1995
-
(1995)
Blood
, vol.86
, pp. 4263
-
-
Romana, S.P.1
Poirel, H.2
Leconiat, M.3
Flexor, M.-A.4
Mauchauffé, M.5
Jonveaux, P.6
Macintyre, E.A.7
Berger, R.8
Bernard, O.A.9
-
21
-
-
0025361918
-
Activation of the interleukin-3 gene by chromosome translocations in acute lymphocytic leukemia with eosinophilia
-
Meeker TC, Hardy D, Willman C, Hogan T, Abrams J: Activation of the interleukin-3 gene by chromosome translocations in acute lymphocytic leukemia with eosinophilia. Blood 76:285, 1990
-
(1990)
Blood
, vol.76
, pp. 285
-
-
Meeker, T.C.1
Hardy, D.2
Willman, C.3
Hogan, T.4
Abrams, J.5
-
22
-
-
0028096970
-
Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases
-
Kobayashi H, Montgomery KT, Bohlander SK, Adra CN, Lim BL, Kucherlapati RS, Donis-Keller H, Holt MS, Le Beau MM, Rowley JD: Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases. Blood 10:3473, 1994
-
(1994)
Blood
, vol.10
, pp. 3473
-
-
Kobayashi, H.1
Montgomery, K.T.2
Bohlander, S.K.3
Adra, C.N.4
Lim, B.L.5
Kucherlapati, R.S.6
Donis-Keller, H.7
Holt, M.S.8
Le Beau, M.M.9
Rowley, J.D.10
-
23
-
-
0029921262
-
The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies
-
Wlodarska I, Marynen P, La Starza R, Mecucci C, Van Den Berghe H: The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies. Cytogenet Cell Genet 72:229, 1996
-
(1996)
Cytogenet Cell Genet
, vol.72
, pp. 229
-
-
Wlodarska, I.1
Marynen, P.2
La Starza, R.3
Mecucci, C.4
Van Den Berghe, H.5
-
24
-
-
0030034007
-
Molecular characterization of 12p abnormalities in hematologic malignancies: Deletion of KIP1, rearrangement of TEL, and amplification of CCND2
-
Höglund M, Johansson B, Pedersen-Bjergaard J, Marynen P, Mitelman F: Molecular characterization of 12p abnormalities in hematologic malignancies: Deletion of KIP1, rearrangement of TEL, and amplification of CCND2, Blood 87:324, 1996
-
(1996)
Blood
, vol.87
, pp. 324
-
-
Höglund, M.1
Johansson, B.2
Pedersen-Bjergaard, J.3
Marynen, P.4
Mitelman, F.5
-
25
-
-
0021856563
-
The 5q- anomaly
-
Van den Berghe H, Vermaelen K, Mecucci C, Barbieri D, Tricot G: The 5q-anomaly. Cancer Genet Cytogenet 17:189, 1985
-
(1985)
Cancer Genet Cytogenet
, vol.17
, pp. 189
-
-
Van Den Berghe, H.1
Vermaelen, K.2
Mecucci, C.3
Barbieri, D.4
Tricot, G.5
-
26
-
-
0026668359
-
Cytogenetics
-
Koeffler HP (ed): Philadelphia, PA, Saunders
-
Mecucci C, Van Den Berghe H: Cytogenetics, in Koeffler HP (ed): Myelodyplastic syndromes. Philadelphia, PA, Saunders, 1992, p 523
-
(1992)
Myelodyplastic Syndromes
, pp. 523
-
-
Mecucci, C.1
Van Den Berghe, H.2
-
27
-
-
0027315865
-
Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid disease
-
Le Beau MM, Esponosa R III, Neuman WL, Stock W, Roulston D, Larson RA, Keinanen M, Westbrook CA: Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid disease. Proc Natl Acad Sci USA 90:5484, 1993
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 5484
-
-
Le Beau, M.M.1
Esponosa III, R.2
Neuman, W.L.3
Stock, W.4
Roulston, D.5
Larson, R.A.6
Keinanen, M.7
Westbrook, C.A.8
-
28
-
-
0028014297
-
Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in patients with 5q- Chromosome
-
Nagarajan L, Zavadel J, Claxton D, Lu X, Fariman J, Warrington JA, Wasmuth JJ, Chinault AC, Sever CE, Slovak ML, Willman CL, Deisseroth AB: Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in patients with 5q-chromosome. Blood 83:199, 1994
-
(1994)
Blood
, vol.83
, pp. 199
-
-
Nagarajan, L.1
Zavadel, J.2
Claxton, D.3
Lu, X.4
Fariman, J.5
Warrington, J.A.6
Wasmuth, J.J.7
Chinault, A.C.8
Sever, C.E.9
Slovak, M.L.10
Willman, C.L.11
Deisseroth, A.B.12
-
29
-
-
0029142818
-
Physical mapping of the critical 5q31 locus
-
Fairman J, Chumakov I, Chinault C, Nowell PC, Nagarajan L: Physical mapping of the critical 5q31 locus. Proc Natl Acad Sci USA 92:7406, 1995
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 7406
-
-
Fairman, J.1
Chumakov, I.2
Chinault, C.3
Nowell, P.C.4
Nagarajan, L.5
-
30
-
-
0028214564
-
Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: Delineation of the critical region on 5q and identification of a 5q- breakpoint
-
Boultwood J, Fidler C, Lewis S, Kelly S, Sheridan H, Littlewood TJ, Buckle VJ, Wainscoat JS: Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: Delineation of the critical region on 5q and identification of a 5q-breakpoint. Genomics 19:425, 1994
-
(1994)
Genomics
, vol.19
, pp. 425
-
-
Boultwood, J.1
Fidler, C.2
Lewis, S.3
Kelly, S.4
Sheridan, H.5
Littlewood, T.J.6
Buckle, V.J.7
Wainscoat, J.S.8
-
31
-
-
4244130868
-
Anomalies of chromosome 5q in myelodysplasia and acute myelogenous leukemia: Evidence for multiple critical loci
-
abstr
-
Fairman J, Zhao L, Liang H, Claxton D, Chumakov I, Liang JC, Nowell PC, Nagarajan L: Anomalies of chromosome 5q in myelodysplasia and acute myelogenous leukemia: Evidence for multiple critical loci. Blood 86:164a, 1995 (abstr, suppl 1)
-
(1995)
Blood
, vol.86
, Issue.1 SUPPL.
-
-
Fairman, J.1
Zhao, L.2
Liang, H.3
Claxton, D.4
Chumakov, I.5
Liang, J.C.6
Nowell, P.C.7
Nagarajan, L.8
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