-
1
-
-
0027378164
-
Cytogenetic deletion maps of hematologic neoplasms: Circumstantial evidence for tumor suppressor loci
-
Johansson B, Mertens F, Mitelman F: Cytogenetic deletion maps of hematologic neoplasms: Circumstantial evidence for tumor suppressor loci. Genes Chromosom Cancer 8:205, 1993
-
(1993)
Genes Chromosom Cancer
, vol.8
, pp. 205
-
-
Johansson, B.1
Mertens, F.2
Mitelman, F.3
-
3
-
-
0019190556
-
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14
-
Sparkes RS, Sparkes MC, Wilson MG, Towner JW, Benedict W, Murphree AL, Yunis JJ: Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14. Science 208:1042, 1980
-
(1980)
Science
, vol.208
, pp. 1042
-
-
Sparkes, R.S.1
Sparkes, M.C.2
Wilson, M.G.3
Towner, J.W.4
Benedict, W.5
Murphree, A.L.6
Yunis, J.J.7
-
4
-
-
0026342232
-
Abnormalities of the retinoblastoma gene in the pathogenesis of acute leukemia
-
Ahuja HG, Jat PS, Foti A, Bar-Eli M, Cline MJ: Abnormalities of the retinoblastoma gene in the pathogenesis of acute leukemia. Blood 78:3259, 1991
-
(1991)
Blood
, vol.78
, pp. 3259
-
-
Ahuja, H.G.1
Jat, P.S.2
Foti, A.3
Bar-Eli, M.4
Cline, M.J.5
-
5
-
-
0025201977
-
Deletion of the human retinoblastoma gene in primary leukemias
-
Chen Y-C, Chen P-J, Yeh S-H, Tien H-F, Wang C-H, Tang J-L, Hong R-L: Deletion of the human retinoblastoma gene in primary leukemias. Blood 76:2060, 1990
-
(1990)
Blood
, vol.76
, pp. 2060
-
-
Chen, Y.-C.1
Chen, P.-J.2
Yeh, S.-H.3
Tien, H.-F.4
Wang, C.-H.5
Tang, J.-L.6
Hong, R.-L.7
-
6
-
-
84984562874
-
Inactivation of the retinoblastoma gene in acute myelogenous leukemia
-
Tang J-L, Yeh S-H, Chen P-J, Lin M-T, Tien H-F, Chen Y-C: Inactivation of the retinoblastoma gene in acute myelogenous leukemia. Br J Haematol 82:502, 1992
-
(1992)
Br J Haematol
, vol.82
, pp. 502
-
-
Tang, J.-L.1
Yeh, S.-H.2
Chen, P.-J.3
Lin, M.-T.4
Tien, H.-F.5
Chen, Y.-C.6
-
7
-
-
0029886284
-
The retinoblastoma gene (rb1) in acute myeloid leukemia: Analysis of gene rearrangements, protein expression and comparison of disease outcome
-
Jamal R, Gale RE, Thomas N Shaun B, Wheatley K, Linch DC: The retinoblastoma gene (rb1) in acute myeloid leukemia: Analysis of gene rearrangements, protein expression and comparison of disease outcome. Br J Haematol 94:342, 1996
-
(1996)
Br J Haematol
, vol.94
, pp. 342
-
-
Jamal, R.1
Gale, R.E.2
Thomas, N.3
Shaun, B.4
Wheatley, K.5
Linch, D.C.6
-
8
-
-
0028237103
-
Inactivation of the retinoblastoma gene appears to be very uncommon in myelodysplastic syndromes
-
Preudhomme C, Vachee A, Lepelley P, Vanrumbeke M, Zandecki M, Quesnel B, Cosson A, Fenaux P: Inactivation of the retinoblastoma gene appears to be very uncommon in myelodysplastic syndromes. Br J Haematol 87:61, 1994
-
(1994)
Br J Haematol
, vol.87
, pp. 61
-
-
Preudhomme, C.1
Vachee, A.2
Lepelley, P.3
Vanrumbeke, M.4
Zandecki, M.5
Quesnel, B.6
Cosson, A.7
Fenaux, P.8
-
9
-
-
0026354581
-
Molecular definition of interstitial deletions of chromosome 13 in leukemic cells
-
Morris CM, Cochrane JM, Benjes SM, Crossen PE, Fitzgerald PH: Molecular definition of interstitial deletions of chromosome 13 in leukemic cells. Genes Chromosom Cancer 3:455, 1991
-
(1991)
Genes Chromosom Cancer
, vol.3
, pp. 455
-
-
Morris, C.M.1
Cochrane, J.M.2
Benjes, S.M.3
Crossen, P.E.4
Fitzgerald, P.H.5
-
10
-
-
0029417029
-
Cytogenetic analysis of B cell chronic lymphoid leukemias classified according to morphologic and immunophenotypic (FAB) criteria
-
Hernandez JM, Mecucci C, Criel A, Meeus P, Michaux L, Van Hoot A, Verhoef G, Louwagie A, Scheiff J-M, Michaux J-L, Boogaerts M, Van den Berghe H: Cytogenetic analysis of B cell chronic lymphoid leukemias classified according to morphologic and immunophenotypic (FAB) criteria. Leukemia 9:2140, 1995
-
(1995)
Leukemia
, vol.9
, pp. 2140
-
-
Hernandez, J.M.1
Mecucci, C.2
Criel, A.3
Meeus, P.4
Michaux, L.5
Van Hoot, A.6
Verhoef, G.7
Louwagie, A.8
Scheiff, J.-M.9
Michaux, J.-L.10
Boogaerts, M.11
Van Den Berghe, H.12
-
11
-
-
0028589109
-
Molecular cytogenetic analysis of RB-1 deletions in chronic B-cell leukemias
-
Dönner H, Pilz T, Fischer K, Cabot G, Diehl D, Fink T, Stilgenbauer S, Bentz M, Lichter P: Molecular cytogenetic analysis of RB-1 deletions in chronic B-cell leukemias. Leuk Lymphoma 16:97, 1994
-
(1994)
Leuk Lymphoma
, vol.16
, pp. 97
-
-
Dönner, H.1
Pilz, T.2
Fischer, K.3
Cabot, G.4
Diehl, D.5
Fink, T.6
Stilgenbauer, S.7
Bentz, M.8
Lichter, P.9
-
12
-
-
0026514343
-
Retinoblastoma gene deletions in B-cell chronic lymphocytic leukemia
-
Liu Y, Grandér D, Söderhäll S, Juliusson G, Gahrton G, Einhorn S: Retinoblastoma gene deletions in B-cell chronic lymphocytic leukemia. Genes Chromosom Cancer 4:250, 1992
-
(1992)
Genes Chromosom Cancer
, vol.4
, pp. 250
-
-
Liu, Y.1
Grandér, D.2
Söderhäll, S.3
Juliusson, G.4
Gahrton, G.5
Einhorn, S.6
-
13
-
-
0027396831
-
Evidence for a tumour suppressor locus (DBM) in human B-cell neoplasia telomeric to the retinoblastoma gene
-
Brown AG, Ross FM, Dunne EM, Steel CM, Weir-Thompson EM: Evidence for a tumour suppressor locus (DBM) in human B-cell neoplasia telomeric to the retinoblastoma gene. Nat Genet 3:67, 1993
-
(1993)
Nat Genet
, vol.3
, pp. 67
-
-
Brown, A.G.1
Ross, F.M.2
Dunne, E.M.3
Steel, C.M.4
Weir-Thompson, E.M.5
-
14
-
-
0028997488
-
Frequent homozygous deletions of D13S218 on 13q14 in B-cell chronic lymphocytic leukemia independent of disease stage and retinoblastoma gene inactivation
-
Newcomb EW, Thomas A, Selkirk A, Lee SY, Potmesil M: Frequent homozygous deletions of D13S218 on 13q14 in B-cell chronic lymphocytic leukemia independent of disease stage and retinoblastoma gene inactivation. Cancer Res 55:2044, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 2044
-
-
Newcomb, E.W.1
Thomas, A.2
Selkirk, A.3
Lee, S.Y.4
Potmesil, M.5
-
15
-
-
0028929990
-
Deletion cartography around the D13S25 locus in B cell chronic lymphocytic leukemia and accurate mapping of the involved tumor suppressor gene
-
Devilder MC, François S, Bosic C, Moreau A, Mellerin MP, Le Paslier D, Bataille R, Moisan JP: Deletion cartography around the D13S25 locus in B cell chronic lymphocytic leukemia and accurate mapping of the involved tumor suppressor gene. Cancer Res 55:1355, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 1355
-
-
Devilder, M.C.1
François, S.2
Bosic, C.3
Moreau, A.4
Mellerin, M.P.5
Le Paslier, D.6
Bataille, R.7
Moisan, J.P.8
-
16
-
-
0029130021
-
13q deletions in lymphoid malignancies
-
Liu Y, Hermanson M, Grandér D, Merup M, Wu X, Heyman M, Rasool O, Juliusson G, Gahrton G, Detlofsson R, Nikiforova N, Buys C, Söderhäll S, Yankovsky N, Zabarovsky E, Einhorn S: 13q deletions in lymphoid malignancies. Blood 86:1911, 1995
-
(1995)
Blood
, vol.86
, pp. 1911
-
-
Liu, Y.1
Hermanson, M.2
Grandér, D.3
Merup, M.4
Wu, X.5
Heyman, M.6
Rasool, O.7
Juliusson, G.8
Gahrton, G.9
Detlofsson, R.10
Nikiforova, N.11
Buys, C.12
Söderhäll, S.13
Yankovsky, N.14
Zabarovsky, E.15
Einhorn, S.16
-
17
-
-
0029099360
-
Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization
-
Stilgenbauer S, Leupolt E, Ohl S, Wei G, Schröder M, Fischer K, Bentz M, Lichter P, Döhner H: Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization. Cancer Res 55:3475, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 3475
-
-
Stilgenbauer, S.1
Leupolt, E.2
Ohl, S.3
Wei, G.4
Schröder, M.5
Fischer, K.6
Bentz, M.7
Lichter, P.8
Döhner, H.9
-
18
-
-
0029859483
-
Minimal region of loss at 13q14 in B-cell chronic lymphocytic leukemia
-
Bullrich F, Veronese ML, Kitada S, Jurlander J, Caligiuri MA, Reed JC, Croce CM: Minimal region of loss at 13q14 in B-cell chronic lymphocytic leukemia. Blood 88:3109, 1996
-
(1996)
Blood
, vol.88
, pp. 3109
-
-
Bullrich, F.1
Veronese, M.L.2
Kitada, S.3
Jurlander, J.4
Caligiuri, M.A.5
Reed, J.C.6
Croce, C.M.7
-
19
-
-
0029759197
-
Successful use of the same slide for consecutive fluorescence in situ hybridization experiments
-
Dierlamm J, Wlodarska I, Michaux L, La Starza R, Zeller W, Mecucci C, Van den Berghe H: Successful use of the same slide for consecutive fluorescence in situ hybridization experiments. Genes Chromosom Cancer 16:261, 1996
-
(1996)
Genes Chromosom Cancer
, vol.16
, pp. 261
-
-
Dierlamm, J.1
Wlodarska, I.2
Michaux, L.3
La Starza, R.4
Zeller, W.5
Mecucci, C.6
Van Den Berghe, H.7
-
20
-
-
0029653653
-
A YAC contig map of the human genome
-
Chumakov IM, Rigault P, Le Gall I, Bellanné-Chantelot C, Billault A, Guillou S, Soularue P, Guasconi G, Poullier E, Gros I, Belova M, Sambucy J-L, Susini L, Gervy P, Glibert 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 E, 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, Gyapay 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
Bellanné-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
Glibert, 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.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
Gyapay, 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..
-
21
-
-
2642672157
-
-
Whitehead Institute for Biomedical Research/MIT Center for Genome Research
-
GDB: Human Genome Database [database online]. Whitehead Institute for Biomedical Research/MIT Center for Genome Research, available from Internet: http://www-genome.wi.mit.edu/
-
GDB: Human Genome Database [Database Online]
-
-
-
22
-
-
0027336301
-
The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene
-
Hawthorn LA, Chapman R, Oscier D, Cowell JK: The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene. Oncogene 8:1415, 1993
-
(1993)
Oncogene
, vol.8
, pp. 1415
-
-
Hawthorn, L.A.1
Chapman, R.2
Oscier, D.3
Cowell, J.K.4
-
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
-
-
0029794418
-
Frequent somatic deletion of the 13q12.3 locus encompassing BRCA2 in chronic lymphocytic leukemia
-
Garcia-Marco JA, Caldas C, Price CM, Wiedemann LM, Ashworth A, Catovsky D: Frequent somatic deletion of the 13q12.3 locus encompassing BRCA2 in chronic lymphocytic leukemia. Blood 88: 1568, 1996
-
(1996)
Blood
, vol.88
, pp. 1568
-
-
Garcia-Marco, J.A.1
Caldas, C.2
Price, C.M.3
Wiedemann, L.M.4
Ashworth, A.5
Catovsky, D.6
-
25
-
-
0031015872
-
Deletion of 13q14.3 and not 13q12 is the most common genetic abnormality detected in chronic lymphocytic leukemia cells
-
Panayiotidis P, Ganeshaguru K, Hoffbrand AV, Rowntree C, Jabbar SAB, Foroni L: Deletion of 13q14.3 and not 13q12 is the most common genetic abnormality detected in chronic lymphocytic leukemia cells. Blood 89:734,1997
-
(1997)
Blood
, vol.89
, pp. 734
-
-
Panayiotidis, P.1
Ganeshaguru, K.2
Hoffbrand, A.V.3
Rowntree, C.4
Jabbar, S.A.B.5
Foroni, L.6
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