-
1
-
-
0028789523
-
Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres
-
Sullivan BA, Schwartz S. Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres. Hum Mol Genet 1995; 4: 2189-2197.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2189-2197
-
-
Sullivan, B.A.1
Schwartz, S.2
-
2
-
-
0031944422
-
Localization of motor-related proteins and associated complexes to active, but not inactive, centromeres
-
Faulkner NE, Vig B, Echeverri J, Wodeman L, Vallee RB. Localization of motor-related proteins and associated complexes to active, but not inactive, centromeres. Hum Mol Genet 1998; 7: 671-677.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 671-677
-
-
Faulkner, N.E.1
Vig, B.2
Echeverri, J.3
Wodeman, L.4
Vallee, R.B.5
-
3
-
-
0024521583
-
Alphoid satellite DNA is tightly associated with centromere antigens in human chromosomes throughout the cell cycle
-
Masumoto H, Sugimoto K, Okazaki T. Alphoid satellite DNA is tightly associated with centromere antigens in human chromosomes throughout the cell cycle. Exp Cell Res 1989; 181: 181-196.
-
(1989)
Exp Cell Res
, vol.181
, pp. 181-196
-
-
Masumoto, H.1
Sugimoto, K.2
Okazaki, T.3
-
4
-
-
0027527478
-
Localization of DNA sequences required from human centromere function through an analysis of rearranged Y chromosomes
-
Tyler-Smith C, Oakey RJ, Larin Z, Fisher RB, Crocker M, Affara NA, Ferguson-Smith MA, Muenke M, Zuffardi O, Jobling MA. Localization of DNA sequences required from human centromere function through an analysis of rearranged Y chromosomes. Nat Genet 1993; 5: 368-375.
-
(1993)
Nat Genet
, vol.5
, pp. 368-375
-
-
Tyler-Smith, C.1
Oakey, R.J.2
Larin, Z.3
Fisher, R.B.4
Crocker, M.5
Affara, N.A.6
Ferguson-Smith, M.A.7
Muenke, M.8
Zuffardi, O.9
Jobling, M.A.10
-
5
-
-
0030884929
-
Human centromeric DNAs
-
Lee C, Wevrick R, Fosher RB, Ferguson-Smith MA, Lin CC. Human centromeric DNAs. Hum Genet 1997; 100: 291-304.
-
(1997)
Hum Genet
, vol.100
, pp. 291-304
-
-
Lee, C.1
Wevrick, R.2
Fosher, R.B.3
Ferguson-Smith, M.A.4
Lin, C.C.5
-
6
-
-
0026625878
-
The non-random dic(9;12) translocation in acute lymphoblastic leukemia is associated with B-progenitor phenotype and an excellent prognosis
-
Mahmoud H, Carroll AJ, Behm F, Raimondi SC, Schuster J, Borowitz M, Land V, Pullen DJ, Vietti TJ, Crist W. The non-random dic(9;12) translocation in acute lymphoblastic leukemia is associated with B-progenitor phenotype and an excellent prognosis. Leukemia 1992; 6: 703-707.
-
(1992)
Leukemia
, vol.6
, pp. 703-707
-
-
Mahmoud, H.1
Carroll, A.J.2
Behm, F.3
Raimondi, S.C.4
Schuster, J.5
Borowitz, M.6
Land, V.7
Pullen, D.J.8
Vietti, T.J.9
Crist, W.10
-
7
-
-
0028897672
-
Dicentric (9;12) in acute lymphocytic leukemia and other hematological malignancies: Report from a dic(9;12) study group
-
Behrendt H, Charrin C, Gibbons B, Harrison CJ, Hawkins JM, Heerema NA, Horschler-Botel B, Huret JL, Lai JL, Lampert F, Nelken B, Perot C, Ritterbach J, Schlegelberger B, Secker-Walker L, Slater R, Slovak ML, Tanzer J, Van Den Akker J. Dicentric (9;12) in acute lymphocytic leukemia and other hematological malignancies: report from a dic(9;12) study group. Leukemia 1995; 9: 102-106.
-
(1995)
Leukemia
, vol.9
, pp. 102-106
-
-
Behrendt, H.1
Charrin, C.2
Gibbons, B.3
Harrison, C.J.4
Hawkins, J.M.5
Heerema, N.A.6
Horschler-Botel, B.7
Huret, J.L.8
Lai, J.L.9
Lampert, F.10
Nelken, B.11
Perot, C.12
Ritterbach, J.13
Schlegelberger, B.14
Secker-Walker, L.15
Slater, R.16
Slovak, M.L.17
Tanzer, J.18
Van Den Akker, J.19
-
8
-
-
0029076862
-
dic(9;20): A new recurrent chromosome abnormality in adult acute lymphoblastic leukemia
-
Rieder H, Schnittger S, Bodenstein H, Schwonzen M, Wormann B, Berkovic D, Ludwig WD, Hoelzer D, Fonatsch C. dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemia. Genes Chromos Cancer 1995; 13: 54-61.
-
(1995)
Genes Chromos Cancer
, vol.13
, pp. 54-61
-
-
Rieder, H.1
Schnittger, S.2
Bodenstein, H.3
Schwonzen, M.4
Wormann, B.5
Berkovic, D.6
Ludwig, W.D.7
Hoelzer, D.8
Fonatsch, C.9
-
9
-
-
0028860943
-
A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11)
-
Slater R, Smit E, Kroes W, Bellomo MJ, Muhlematter D, Harbott J, Behrendt H, Hahlen K, Veerman AJ, Hagemeijer A. A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11). Leukemia 1995; 9: 1613-1619.
-
(1995)
Leukemia
, vol.9
, pp. 1613-1619
-
-
Slater, R.1
Smit, E.2
Kroes, W.3
Bellomo, M.J.4
Muhlematter, D.5
Harbott, J.6
Behrendt, H.7
Hahlen, K.8
Veerman, A.J.9
Hagemeijer, A.10
-
10
-
-
0030465498
-
Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients
-
Heerema NA, Maben KD, Bernstein J, Breitfeld PP, Neiman RS, Vance GH. Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients. Cancer Genet Cytogenet 1996; 92: 111-115.
-
(1996)
Cancer Genet Cytogenet
, vol.92
, pp. 111-115
-
-
Heerema, N.A.1
Maben, K.D.2
Bernstein, J.3
Breitfeld, P.P.4
Neiman, R.S.5
Vance, G.H.6
-
13
-
-
85038168020
-
Cytogenetics of Burkitt's lymphoma-leukaemia: A review
-
Lenoir G, O'Connor G, Olwendy CLM (eds). International Agency for Research on Cancer: Lyon
-
Berger R, Bernheim A. Cytogenetics of Burkitt's lymphoma-leukaemia: a review. In: Lenoir G, O'Connor G, Olwendy CLM (eds). Burkitt's Lymphoma: a Human Cancer Model. International Agency for Research on Cancer: Lyon, 1995, pp 65-80.
-
(1995)
Burkitt's Lymphoma: A Human Cancer Model
, pp. 65-80
-
-
Berger, R.1
Bernheim, A.2
-
14
-
-
0028330771
-
t(12;21): A new recurrent translocation in acute lymphoblastic leukemia
-
Romana SP, Le Coniat M, Berger R. t(12;21): a new recurrent translocation in acute lymphoblastic leukemia. Genes Chromos Cancer 1994; 9: 186-191.
-
(1994)
Genes Chromos Cancer
, vol.9
, pp. 186-191
-
-
Romana, S.P.1
Le Coniat, M.2
Berger, R.3
-
15
-
-
0032520975
-
Molecular cloning of translocation t(1:14)(q21;q32) defines a novel gene (bcl9) at chromosome 1q21
-
Willis TG, Zalcberg IR, Coignet LJA, Wlodarska I, Stul M, Jadayel DM, Bastard C, Treleaven JG, Catovsky D, Silva MLM, Dyer MJS. Molecular cloning of translocation t(1:14)(q21;q32) defines a novel gene (BCL9) at chromosome 1q21. Blood 1991; 91: 1873-1881.
-
(1991)
Blood
, vol.91
, pp. 1873-1881
-
-
Willis, T.G.1
Zalcberg, I.R.2
Coignet, L.J.A.3
Wlodarska, I.4
Stul, M.5
Jadayel, D.M.6
Bastard, C.7
Treleaven, J.G.8
Catovsky, D.9
Silva, M.L.M.10
Dyer, M.J.S.11
-
16
-
-
0030853615
-
Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: A report including three novel translocations involving the TEL/ETV6 gene
-
Berger R, Le Coniat M, Lacronique V, Daniel M-T, Lessard M, Berthou C, Marynen P, Bernard OA. Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: a report including three novel translocations involving the TEL/ETV6 gene. Leukemia 1997; 11: 1400-1403.
-
(1997)
Leukemia
, vol.11
, pp. 1400-1403
-
-
Berger, R.1
Le Coniat, M.2
Lacronique, V.3
Daniel, M.-T.4
Lessard, M.5
Berthou, C.6
Marynen, P.7
Bernard, O.A.8
-
17
-
-
0030999555
-
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
-
Mitelman F, Mertens F, Johansson B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet 1997; 15: 417-474.
-
(1997)
Nat Genet
, vol.15
, pp. 417-474
-
-
Mitelman, F.1
Mertens, F.2
Johansson, B.3
-
18
-
-
0030065735
-
Centromeric breakage as major cause of cytogenetic abnormalities in oral squamous cell carcinoma
-
Hermsen MAJA, Joenje H, Arwert F, Welters MJP, Braakhuis BJM, Bagnay M, Westerveld A, Slater R. Centromeric breakage as major cause of cytogenetic abnormalities in oral squamous cell carcinoma. Genes Chromos Cancer 1994; 15: 1-9.
-
(1994)
Genes Chromos Cancer
, vol.15
, pp. 1-9
-
-
Hermsen, M.A.J.A.1
Joenje, H.2
Arwert, F.3
Welters, M.J.P.4
Braakhuis, B.J.M.5
Bagnay, M.6
Westerveld, A.7
Slater, R.8
-
19
-
-
0025924612
-
Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization
-
Speleman F, Mangelschots K, Vercruyssen M, Dal Cin P, Aventin A, Offner F, Laureys G, Van den Berghe H, Leroy J. Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization. Cytogenet Cell Genet 1991; 56: 14-17.
-
(1991)
Cytogenet Cell Genet
, vol.56
, pp. 14-17
-
-
Speleman, F.1
Mangelschots, K.2
Vercruyssen, M.3
Dal Cin, P.4
Aventin, A.5
Offner, F.6
Laureys, G.7
Van Den Berghe, H.8
Leroy, J.9
-
20
-
-
0029873238
-
Breakpoints in a, b, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions
-
Ramesh KH, Verma RS. Breakpoints in a, b, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions. J Med Genet 1996; 33: 395-398.
-
(1996)
J Med Genet
, vol.33
, pp. 395-398
-
-
Ramesh, K.H.1
Verma, R.S.2
-
21
-
-
0027097635
-
Breakpoints in Robertsonian translocations are localised to satellite III DNA by fluorescence in situ hybridization
-
Gravholt CH, Friedrich U, Caprani M, Jorgensen AL. Breakpoints in Robertsonian translocations are localised to satellite III DNA by fluorescence in situ hybridization. Genomics 1992; 14: 924-930.
-
(1992)
Genomics
, vol.14
, pp. 924-930
-
-
Gravholt, C.H.1
Friedrich, U.2
Caprani, M.3
Jorgensen, A.L.4
-
22
-
-
0017327251
-
Chromosome 1 heteromorphism in patients with malignant disease: A constitutional marker for a high risk group?
-
Atkin NB. Chromosome 1 heteromorphism in patients with malignant disease: a constitutional marker for a high risk group? Br Med J 1977; 1: 358.
-
(1977)
Br Med J
, vol.1
, pp. 358
-
-
Atkin, N.B.1
-
23
-
-
0017589707
-
Abnormal chromosomes and number 1 heterochromatin variants revealed in C-band preparations from 13 bladder carcinomas
-
Atkin NB, Baker MC. Abnormal chromosomes and number 1 heterochromatin variants revealed in C-band preparations from 13 bladder carcinomas. Cytobios 1977; 18: 101-109.
-
(1977)
Cytobios
, vol.18
, pp. 101-109
-
-
Atkin, N.B.1
Baker, M.C.2
-
24
-
-
0017724718
-
Pericentric inversion of chromosome 1: Frequency and possible association with cancer
-
Atkin NB, Baker MC. Pericentric inversion of chromosome 1: frequency and possible association with cancer. Cytogenet Cell Genet 1977; 19: 180-184.
-
(1977)
Cytogenet Cell Genet
, vol.19
, pp. 180-184
-
-
Atkin, N.B.1
Baker, M.C.2
-
25
-
-
0017769415
-
Anomalies de fréquence du chromosome 1qh + dans la leucémie myéloïde chronique
-
Berger R, Bernheim A. Anomalies de fréquence du chromosome 1qh + dans la leucémie myéloïde chronique. CR Acad Sci Paris, Série D 1977; 285: 1183-1185.
-
(1977)
CR Acad Sci Paris, Série D
, vol.285
, pp. 1183-1185
-
-
Berger, R.1
Bernheim, A.2
-
28
-
-
0018377965
-
Risk of malignancy and chromosomal polymorphism: A possible mechanism of association
-
Shabtai F, Halbrecht I. Risk of malignancy and chromosomal polymorphism: a possible mechanism of association. Clin Genet 1979; 15: 73-77.
-
(1979)
Clin Genet
, vol.15
, pp. 73-77
-
-
Shabtai, F.1
Halbrecht, I.2
-
30
-
-
0022403644
-
Chromosome 1 heterochromatin variants and cancer: A reassessment
-
Atkin NB, Brito-Babapulle V. Chromosome 1 heterochromatin variants and cancer: a reassessment. Cancer Genet Cytogenet 1985; 8: 325-331.
-
(1985)
Cancer Genet Cytogenet
, vol.8
, pp. 325-331
-
-
Atkin, N.B.1
Brito-Babapulle, V.2
-
31
-
-
0029586756
-
The centromere: Hub of chromosomal activities
-
Pluta AF, Mackay AM, Ainsztein AM, Goldberg IG, Earnshaw WC. The centromere: hub of chromosomal activities. Science 1995; 270: 1591-1594.
-
(1995)
Science
, vol.270
, pp. 1591-1594
-
-
Pluta, A.F.1
Mackay, A.M.2
Ainsztein, A.M.3
Goldberg, I.G.4
Earnshaw, W.C.5
-
32
-
-
0031000436
-
Centromeres, checkpoints and chromatid cohesion
-
Allshire RC. Centromeres, checkpoints and chromatid cohesion. Curr Opin Genet Dev 1997; 7: 264-273.
-
(1997)
Curr Opin Genet Dev
, vol.7
, pp. 264-273
-
-
Allshire, R.C.1
-
33
-
-
0022378301
-
The organization of two related sunfamilies of a human tandemly repeated DNA is chromosome specific
-
Jeanpierre M, Weil D, Gallano P, Creau-Goldberg N, Junien C. The organization of two related sunfamilies of a human tandemly repeated DNA is chromosome specific. Hum Genet 1985; 70: 302-310.
-
(1985)
Hum Genet
, vol.70
, pp. 302-310
-
-
Jeanpierre, M.1
Weil, D.2
Gallano, P.3
Creau-Goldberg, N.4
Junien, C.5
-
34
-
-
0023414542
-
Chromosome-specific alpha satellite DNA from human chromosome 1 : Hierarchical structure and genomic organization of a polymorphic doamin spanning several hundred kilo-base pairs of centromeric DNA
-
Waye JS, Durfy SJ, Pinkel D, Kenwrick S, Patterson M, Davies KE, Willard HF. Chromosome-specific alpha satellite DNA from human chromosome 1 : hierarchical structure and genomic organization of a polymorphic doamin spanning several hundred kilo-base pairs of centromeric DNA. Genomics 1987; 1: 43-51.
-
(1987)
Genomics
, vol.1
, pp. 43-51
-
-
Waye, J.S.1
Durfy, S.J.2
Pinkel, D.3
Kenwrick, S.4
Patterson, M.5
Davies, K.E.6
Willard, H.F.7
-
35
-
-
0025980674
-
A survey of genomic distribution of alpha satellite DNA on all human chromosomes, and derivation of a new consensus sequence
-
Choo KH, Vissel B, Nagy A, Earle E, Kalitsis P. A survey of genomic distribution of alpha satellite DNA on all human chromosomes, and derivation of a new consensus sequence. Nucleic Acids Res 1991; 19: 1179-1182.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 1179-1182
-
-
Choo, K.H.1
Vissel, B.2
Nagy, A.3
Earle, E.4
Kalitsis, P.5
-
36
-
-
0026070467
-
A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization
-
Rocchi M, Archidiacono N, Ward DC, Baldini A. A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization. Genomics 1991; 9: 517-523.
-
(1991)
Genomics
, vol.9
, pp. 517-523
-
-
Rocchi, M.1
Archidiacono, N.2
Ward, D.C.3
Baldini, A.4
-
37
-
-
0028650742
-
Human satellites 2 and 3
-
Jeanpierre M. Human satellites 2 and 3. Ann Génét 1994; 37: 163-171.
-
(1994)
Ann Génét
, vol.37
, pp. 163-171
-
-
Jeanpierre, M.1
-
38
-
-
0030589716
-
Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18 and 19
-
Finelli P, Antonacci R, Marzella R, Lonoce A, Archidiacono N, Rocchi M. Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18 and 19. Genomics 1996; 38: 325-330.
-
(1996)
Genomics
, vol.38
, pp. 325-330
-
-
Finelli, P.1
Antonacci, R.2
Marzella, R.3
Lonoce, A.4
Archidiacono, N.5
Rocchi, M.6
-
39
-
-
0032076941
-
Centromeres take flight: Alpha satellite and the quest for the human centromere
-
Murphy TD, Karpen GH. Centromeres take flight: alpha satellite and the quest for the human centromere. Cell 1998; 93: 317-320.
-
(1998)
Cell
, vol.93
, pp. 317-320
-
-
Murphy, T.D.1
Karpen, G.H.2
-
40
-
-
0031473740
-
Centromere DNA dynamics: Latent centromeres and neocentromere formation
-
Choo KHA. Centromere DNA dynamics: latent centromeres and neocentromere formation. Am J Hum Genet 1997; 61: 1225-1233.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1225-1233
-
-
Choo, K.H.A.1
-
41
-
-
0031985323
-
Turning on centromere
-
Choo KHA. Turning on centromere. Nat Genet 1998; 18: 3-4.
-
(1998)
Nat Genet
, vol.18
, pp. 3-4
-
-
Choo, K.H.A.1
-
42
-
-
8544263835
-
Characterization of neocentromeres in marker chromosomes lacking detectable alpha-satellite DNA
-
Depinet TW, Zackowski JL, Earnshaw WC, Kaffe S, Sekhon GS, Stallard R, Characterization of neocentromeres in marker chromosomes lacking detectable alpha-satellite DNA. Hum Mol Genet 1997; 6: 1195-1204.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1195-1204
-
-
Depinet, T.W.1
Zackowski, J.L.2
Earnshaw, W.C.3
Kaffe, S.4
Sekhon, G.S.5
Stallard, R.6
-
43
-
-
0345293849
-
A functional neo-centromere formed through activation of a latent human centromere and consisting of non-satellite DNA
-
Du Sart D, Cancilla MR, Earle E, Mao J-i, Saffery R, Tainton KM, Kalistis P, Martyn J, Barry AE, Choo KHA. A functional neo-centromere formed through activation of a latent human centromere and consisting of non-satellite DNA. Nat Genet 1997; 16: 144-153.
-
(1997)
Nat Genet
, vol.16
, pp. 144-153
-
-
Du Sart, D.1
Cancilla, M.R.2
Earle, E.3
Mao, J.-I.4
Saffery, R.5
Tainton, K.M.6
Kalistis, P.7
Martyn, J.8
Barry, A.E.9
Choo, K.H.A.10
-
44
-
-
0027522464
-
Specific induction of uncoiling and recombination by azacytidine in clasical satellite-containing constitutive heterochromatin
-
Kokalj-Vokac N, Almeida A, Viegas-Péquignot E, Jeanpierre M, Malfoy B, Dutrillaux B. Specific induction of uncoiling and recombination by azacytidine in clasical satellite-containing constitutive heterochromatin. Cytogenet Cell Genet 1993; 61: 11-15.
-
(1993)
Cytogenet Cell Genet
, vol.61
, pp. 11-15
-
-
Kokalj-Vokac, N.1
Almeida, A.2
Viegas-Péquignot, E.3
Jeanpierre, M.4
Malfoy, B.5
Dutrillaux, B.6
-
45
-
-
0028050758
-
Human α-satellite DNAs are not susceptible to undercondensation after 5-azacytidine treatment
-
Fernandez JL, Goyanes V, Lopez-Fernandez C, Gosalvez J. Human α-satellite DNAs are not susceptible to undercondensation after 5-azacytidine treatment. Cytogenet Cell Genet 1994; 65: 92-94.
-
(1994)
Cytogenet Cell Genet
, vol.65
, pp. 92-94
-
-
Fernandez, J.L.1
Goyanes, V.2
Lopez-Fernandez, C.3
Gosalvez, J.4
-
46
-
-
0031692007
-
Masquerading repeats: Paralogous pitfalls of the human genome
-
Eicher EE. Masquerading repeats: paralogous pitfalls of the human genome. Genome Res 1996; 8: 758-762.
-
(1996)
Genome Res
, vol.8
, pp. 758-762
-
-
Eicher, E.E.1
-
47
-
-
0024345905
-
Human β-satellite DNA: Genomic organization of a sequence definition of a class of highly repetitive tandem DNA
-
Waye JS, Willard HF. Human β-satellite DNA: genomic organization of a sequence definition of a class of highly repetitive tandem DNA. Proc Natl Acad Sci USA 1989; 86: 6250-6254.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 6250-6254
-
-
Waye, J.S.1
Willard, H.F.2
-
48
-
-
0031872199
-
Mobile genetic elements, chiasmata, and the unique organization of beta-heterochromatin
-
Holmquist GP, Kapitonov VV, Jurka J. Mobile genetic elements, chiasmata, and the unique organization of beta-heterochromatin. Cytogenet Cell Genet 1998; 80: 113-116.
-
(1998)
Cytogenet Cell Genet
, vol.80
, pp. 113-116
-
-
Holmquist, G.P.1
Kapitonov, V.V.2
Jurka, J.3
-
49
-
-
0031848871
-
Beta-heterochromatin in mammals: Evidence from studies in Microtus agrestis based on the extensive accumulation of L1 and non-L1 retrotransposons in the heterochromatin
-
Neitzel H, Kalscheuer V, Henschel S, Digweed M, Sperling K. Beta-heterochromatin in mammals: evidence from studies in Microtus agrestis based on the extensive accumulation of L1 and non-L1 retrotransposons in the heterochromatin. Cytogenet Cell Genet 1998; 80: 165-172.
-
(1998)
Cytogenet Cell Genet
, vol.80
, pp. 165-172
-
-
Neitzel, H.1
Kalscheuer, V.2
Henschel, S.3
Digweed, M.4
Sperling, K.5
-
50
-
-
0028060062
-
Molecular cytogenetic characterization of two types of chromosome 9 variants
-
Wang JCC, Miller WA. Molecular cytogenetic characterization of two types of chromosome 9 variants. Cytogenet Cell Genet 1994; 67: 190-192.
-
(1994)
Cytogenet Cell Genet
, vol.67
, pp. 190-192
-
-
Wang, J.C.C.1
Miller, W.A.2
-
51
-
-
0029853176
-
Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9
-
Samonte RV, Conte RA, Ramesh KH, Verma RS. Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9. Hum Genet 1998; 98: 576-580.
-
(1998)
Hum Genet
, vol.98
, pp. 576-580
-
-
Samonte, R.V.1
Conte, R.A.2
Ramesh, K.H.3
Verma, R.S.4
-
52
-
-
0024421064
-
Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum
-
Arnoldus EPJ, Peters ACB, Bots GTAM, Raap AK, van de Ploeg M. Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum. Hum Genet 1989; 83: 231-234.
-
(1989)
Hum Genet
, vol.83
, pp. 231-234
-
-
Arnoldus, E.P.J.1
Peters, A.C.B.2
Bots, G.T.A.M.3
Raap, A.K.4
Van De Ploeg, M.5
-
53
-
-
0025869612
-
Interphase cytogenetics reveals somatic pairing of chromosome 17 centromeres in normal human brain tissue, but not trisomy 7 or sex-chromosome loss
-
Arnoldus EPJ, Noordermeer IA, Peters ACB, Raap AK, Van der Ploeg M. Interphase cytogenetics reveals somatic pairing of chromosome 17 centromeres in normal human brain tissue, but not trisomy 7 or sex-chromosome loss. Cytogenet Cell Genet 1991; 56: 214-216.
-
(1991)
Cytogenet Cell Genet
, vol.56
, pp. 214-216
-
-
Arnoldus, E.P.J.1
Noordermeer, I.A.2
Peters, A.C.B.3
Raap, A.K.4
Van Der Ploeg, M.5
-
54
-
-
0030586134
-
Evidence for somatic pairing of chromosome 7 and 10 homologs in a follicular lymphoma
-
Atkin NB, Jackson Z. Evidence for somatic pairing of chromosome 7 and 10 homologs in a follicular lymphoma. Cancer Genet Cytogenet 1996; 89: 129-131.
-
(1996)
Cancer Genet Cytogenet
, vol.89
, pp. 129-131
-
-
Atkin, N.B.1
Jackson, Z.2
-
55
-
-
0029943141
-
Perturbation of nuclear architecture by long distance chromosome interactions
-
Dernburg AF, Broman KW, Fung JC, Marshall WF, Philips J, Agard DA, Sedat JW. Perturbation of nuclear architecture by long distance chromosome interactions. Cell 1997; 85: 745-759.
-
(1997)
Cell
, vol.85
, pp. 745-759
-
-
Dernburg, A.F.1
Broman, K.W.2
Fung, J.C.3
Marshall, W.F.4
Philips, J.5
Agard, D.A.6
Sedat, J.W.7
-
56
-
-
0029898246
-
Dicentric (1;15) in myeloid disorders
-
Michaux L, Dierlamm J, Mecucci C, Meeus P, Ameye G, Libouton J-M, Verhoef G, Ferrant A, Louwagie A, Verellen-Dumoulin C, Van Den Berghe H. Dicentric (1;15) in myeloid disorders. Cancer Genet Cytogenet 1996; 88: 86-90.
-
(1996)
Cancer Genet Cytogenet
, vol.88
, pp. 86-90
-
-
Michaux, L.1
Dierlamm, J.2
Mecucci, C.3
Meeus, P.4
Ameye, G.5
Libouton, J.-M.6
Verhoef, G.7
Ferrant, A.8
Louwagie, A.9
Verellen-Dumoulin, C.10
Van Den Berghe, H.11
-
57
-
-
0023914812
-
Dicentric chromosome in the bone marrow of a child with megakaryoblastic leukaemia and Down's syndrome
-
Wilkie AO, Kitchen C, Oakhill A, Howell RT, Berry PJ. Dicentric chromosome in the bone marrow of a child with megakaryoblastic leukaemia and Down's syndrome. J Clin Pathol 1988; 41: 378-380.
-
(1988)
J Clin Pathol
, vol.41
, pp. 378-380
-
-
Wilkie, A.O.1
Kitchen, C.2
Oakhill, A.3
Howell, R.T.4
Berry, P.J.5
-
59
-
-
0025368831
-
Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemia. A possible association with acquired pseudo-Pelger-Huet anomaly and small vacuolated granulocytes
-
Lai JL, Zandecki M, Fenaux P, Le Baron F, Bauters F, Cosson A, Deminatti M. Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemia. A possible association with acquired pseudo-Pelger-Huet anomaly and small vacuolated granulocytes. Cancer Genet Cytogenet 1990; 46: 173-183.
-
(1990)
Cancer Genet Cytogenet
, vol.46
, pp. 173-183
-
-
Lai, J.L.1
Zandecki, M.2
Fenaux, P.3
Le Baron, F.4
Bauters, F.5
Cosson, A.6
Deminatti, M.7
-
60
-
-
0030783859
-
dic(5;17): A recurring abnormality in malignant myeloid disorders associated with mutations of TP53
-
Wang P, Spielberger RT, Thangavelu M, Zhao N, Davis EM, lannantuoni K, Larson RA, Le Beau MM. dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53. Genes Chromos Cancer 1997; 20: 282-291.
-
(1997)
Genes Chromos Cancer
, vol.20
, pp. 282-291
-
-
Wang, P.1
Spielberger, R.T.2
Thangavelu, M.3
Zhao, N.4
Davis, E.M.5
Lannantuoni, K.6
Larson, R.A.7
Le Beau, M.M.8
-
61
-
-
0025063464
-
Cytogenetics of pre-B-cell acute lymphoblastic leukemia with emphasis on prognostic implications of the t(1;19)
-
Raimondi SC, Behm FG, Roberson PK, Williams DL, Pui CH, Crist WM, Look AT, Rivera GK. Cytogenetics of pre-B-cell acute lymphoblastic leukemia with emphasis on prognostic implications of the t(1;19). J Clin Oncol 1990; 8: 1380-1388.
-
(1990)
J Clin Oncol
, vol.8
, pp. 1380-1388
-
-
Raimondi, S.C.1
Behm, F.G.2
Roberson, P.K.3
Williams, D.L.4
Pui, C.H.5
Crist, W.M.6
Look, A.T.7
Rivera, G.K.8
-
62
-
-
0025914808
-
New recurring chromosomal translocations in childhood acute lymphoblastic leukemia
-
Raimondi SC, Privitera E, Williams DL, Look AT, Behm F, Rivera GK, Crist WM, Pui CH. New recurring chromosomal translocations in childhood acute lymphoblastic leukemia. Blood 1991; 77: 2016-2022.
-
(1991)
Blood
, vol.77
, pp. 2016-2022
-
-
Raimondi, S.C.1
Privitera, E.2
Williams, D.L.3
Look, A.T.4
Behm, F.5
Rivera, G.K.6
Crist, W.M.7
Pui, C.H.8
-
63
-
-
0025167170
-
Inv(12)(p13q11) and dicentric chromosomes in a secondary leukaemia with basophilia
-
Huret JL, Brizard A, Guilhot F, Couet D, Schoenwald M, Savage JR, Tanzer J. Inv(12)(p13q11) and dicentric chromosomes in a secondary leukaemia with basophilia. Haematologica 1990; 75: 473-476.
-
(1990)
Haematologica
, vol.75
, pp. 473-476
-
-
Huret, J.L.1
Brizard, A.2
Guilhot, F.3
Couet, D.4
Schoenwald, M.5
Savage, J.R.6
Tanzer, J.7
-
64
-
-
0025306590
-
Two additional cases of t dic(9:12) in acute lymphocytic leukemia (ALL): Prognosis in ALL with dic(9;12)
-
Huret JL, Heerema NA, Brizard A, Provisor AJ, Benz-Lemoine E, Guilhot F, Savage JR, Tanzer J. Two additional cases of t dic(9:12) in acute lymphocytic leukemia (ALL): prognosis in ALL with dic(9;12). Leukemia 1990; 4: 423-425.
-
(1990)
Leukemia
, vol.4
, pp. 423-425
-
-
Huret, J.L.1
Heerema, N.A.2
Brizard, A.3
Provisor, A.J.4
Benz-Lemoine, E.5
Guilhot, F.6
Savage, J.R.7
Tanzer, J.8
-
65
-
-
0030071115
-
Dicentric (9;12) in pre-B acute lymphoblastic leukemia (ALL) in an infant
-
Stark B, Jeison M, Luria D, Cohen IJ, Goshen Y, Fisher S, Zaizov R. Dicentric (9;12) in pre-B acute lymphoblastic leukemia (ALL) in an infant. Leukemia 1996; 10: 183-184.
-
(1996)
Leukemia
, vol.10
, pp. 183-184
-
-
Stark, B.1
Jeison, M.2
Luria, D.3
Cohen, I.J.4
Goshen, Y.5
Fisher, S.6
Zaizov, R.7
-
66
-
-
15644381022
-
Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12
-
Streubel B, Sauerland C, Heil G, Freund M, Bartels H, Lengfelder E, Wandt H, Ludwig WD, Nowotny H, Baldus M, Grothaus-Pinke B, Buchner T, Fonatsch C. Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12. Br J Haematol 1998; 100: 521-533.
-
(1998)
Br J Haematol
, vol.100
, pp. 521-533
-
-
Streubel, B.1
Sauerland, C.2
Heil, G.3
Freund, M.4
Bartels, H.5
Lengfelder, E.6
Wandt, H.7
Ludwig, W.D.8
Nowotny, H.9
Baldus, M.10
Grothaus-Pinke, B.11
Buchner, T.12
Fonatsch, C.13
-
67
-
-
0024230806
-
A recurring chromosome rearrangement, dic(16;22), in acute nonlymphocytic leukemia
-
Li YS, Anastasi J, Larson RA, Le Beau MM, Vardiman JW, Rowley JD. A recurring chromosome rearrangement, dic(16;22), in acute nonlymphocytic leukemia. Cancer Genet Cytogenet 1988; 35: 143-150.
-
(1988)
Cancer Genet Cytogenet
, vol.35
, pp. 143-150
-
-
Li, Y.S.1
Anastasi, J.2
Larson, R.A.3
Le Beau, M.M.4
Vardiman, J.W.5
Rowley, J.D.6
-
68
-
-
0027769539
-
Whole arm translocation t(17;18): A non-random abnormality of myeloid cell proliferation
-
Jonveaux P, Derré J, Berger R. Whole arm translocation t(17;18): a non-random abnormality of myeloid cell proliferation. Leukemia 1993; 7: 1987-1989.
-
(1993)
Leukemia
, vol.7
, pp. 1987-1989
-
-
Jonveaux, P.1
Derré, J.2
Berger, R.3
-
69
-
-
0032145185
-
Acute promyelocytic leukemia with a dicentric chromosome involving chromosomes 11, 17, and 18
-
Chong YY, Wong CC, Lau LC, Knight L, Lim P, Lui WO, Yong MH, Goh YT, Tan P. Acute promyelocytic leukemia with a dicentric chromosome involving chromosomes 11, 17, and 18. Cancer Genet Cytogenet 1998; 105: 69-73.
-
(1998)
Cancer Genet Cytogenet
, vol.105
, pp. 69-73
-
-
Chong, Y.Y.1
Wong, C.C.2
Lau, L.C.3
Knight, L.4
Lim, P.5
Lui, W.O.6
Yong, M.H.7
Goh, Y.T.8
Tan, P.9
-
71
-
-
0032104102
-
Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization
-
Maljaei SH, Brito-Babapulle V, Hiorns LR, Catovsky D. Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization. Cancer Genet Cytogenet 1998; 103: 110-116.
-
(1998)
Cancer Genet Cytogenet
, vol.103
, pp. 110-116
-
-
Maljaei, S.H.1
Brito-Babapulle, V.2
Hiorns, L.R.3
Catovsky, D.4
-
72
-
-
0031789470
-
Pre-B acute lymphoblastic leukemia in a 3-year-old boy with pre-acute myelogenous leukemia myelodysplastic syndrome: Cytogenetic evidence of common early progenitor cell ontogeny
-
Rossbach HC, Sutcliffe MJ, Chamizo W, Haag MM, Grana NH, Washington KR, Barbosa JL. Pre-B acute lymphoblastic leukemia in a 3-year-old boy with pre-acute myelogenous leukemia myelodysplastic syndrome: cytogenetic evidence of common early progenitor cell ontogeny. J Pediat Hematol Oncol 1998; 20: 347-352.
-
(1998)
J Pediat Hematol Oncol
, vol.20
, pp. 347-352
-
-
Rossbach, H.C.1
Sutcliffe, M.J.2
Chamizo, W.3
Haag, M.M.4
Grana, N.H.5
Washington, K.R.6
Barbosa, J.L.7
-
73
-
-
0022606752
-
Specific chromosome markers involved with chronic T lymphocyte tumors
-
Zech L, Godal T, Hammarstrom L, Mellstedt H, Smith CI, Totterman T, Went M. Specific chromosome markers involved with chronic T lymphocyte tumors. Cancer Genet Cytogenet 1986; 21: 67-77.
-
(1986)
Cancer Genet Cytogenet
, vol.21
, pp. 67-77
-
-
Zech, L.1
Godal, T.2
Hammarstrom, L.3
Mellstedt, H.4
Smith, C.I.5
Totterman, T.6
Went, M.7
-
74
-
-
0023869490
-
An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma
-
Fan Y-S, Baer MR, Jani Sait SN, Dal Cin P, Prentice TC, Preisler HD, Sandberg AA. An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma. Cancer Genet Cytogenet 1988; 30: 133-137.
-
(1988)
Cancer Genet Cytogenet
, vol.30
, pp. 133-137
-
-
Fan, Y.-S.1
Baer, M.R.2
Jani Sait, S.N.3
Dal Cin, P.4
Prentice, T.C.5
Preisler, H.D.6
Sandberg, A.A.7
-
75
-
-
0016761632
-
Chromosome band analysis in 19 cases of chronic myeloid leukemia: 9 chronic, 10 blastic two with Ph1 (22q-) translocation on 17 short arm
-
Engel E, McGee BJ, Flexner JM, Krantz SB. Chromosome band analysis in 19 cases of chronic myeloid leukemia: 9 chronic, 10 blastic two with Ph1 (22q-) translocation on 17 short arm. Ann Génét 1975; 18: 239-240.
-
(1975)
Ann Génét
, vol.18
, pp. 239-240
-
-
Engel, E.1
McGee, B.J.2
Flexner, J.M.3
Krantz, S.B.4
-
76
-
-
0019519175
-
Isochromosome (17q) in Philadelphia chromosome (Ph1)-negative juvenile chronic myelocytic leukemia
-
Casalone R, Francesconi D, Pasquali F, Comotti B, Vaccari F. Isochromosome (17q) in Philadelphia chromosome (Ph1)-negative juvenile chronic myelocytic leukemia. Cancer Genet Cytogenet 1981; 3: 145-148.
-
(1981)
Cancer Genet Cytogenet
, vol.3
, pp. 145-148
-
-
Casalone, R.1
Francesconi, D.2
Pasquali, F.3
Comotti, B.4
Vaccari, F.5
-
77
-
-
0019504551
-
Dicentric isochromosome for the long arm of chromosome #17, dic i(17q), in a patient with chronic myelogenous leukemia (CML)
-
Whang-Peng J, Lee E, Knutsen T, Solanki D. Dicentric isochromosome for the long arm of chromosome #17, dic i(17q), in a patient with chronic myelogenous leukemia (CML). Cancer Genet Cytogenet 1981; 3: 233-236.
-
(1981)
Cancer Genet Cytogenet
, vol.3
, pp. 233-236
-
-
Whang-Peng, J.1
Lee, E.2
Knutsen, T.3
Solanki, D.4
-
78
-
-
0020396312
-
The isochromosome (17q) in chronic myelocytic leukaemia: Mechanism of origin, centromeric function and clonal evolution
-
Pasquali F, Panarello C, Bernasconi P, Casalone R. The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolution. Hum Genet 1982; 62: 89-90.
-
(1982)
Hum Genet
, vol.62
, pp. 89-90
-
-
Pasquali, F.1
Panarello, C.2
Bernasconi, P.3
Casalone, R.4
-
79
-
-
0023234636
-
Philadelphia chromosome-positive acute leukemia: Morphologic and clinical correlations
-
Helenglass G, Testa JR, Schiffer CA. Philadelphia chromosome-positive acute leukemia: morphologic and clinical correlations. Am J Hematol 1987; 25: 311-324.
-
(1987)
Am J Hematol
, vol.25
, pp. 311-324
-
-
Helenglass, G.1
Testa, J.R.2
Schiffer, C.A.3
-
80
-
-
0022889221
-
Dicentric chromosome 17 in patients with leukemia
-
Testa JR, Cohen BC. Dicentric chromosome 17 in patients with leukemia. Cancer Genet Cytogenet 1986; 23: 47-52.
-
(1986)
Cancer Genet Cytogenet
, vol.23
, pp. 47-52
-
-
Testa, J.R.1
Cohen, B.C.2
-
81
-
-
0026483865
-
Detection of an i(17q) chromosome by fluorescent in situ hybridization with a chromosome 17 alpha satellite DNA probe
-
Nakagawa H, Inazawa J, Misawa S, Tanaka S, Takashima T, Taniwaki M, Abe T, Kashima K. Detection of an i(17q) chromosome by fluorescent in situ hybridization with a chromosome 17 alpha satellite DNA probe. Cancer Genet Cytogenet 1992; 62: 140-143.
-
(1992)
Cancer Genet Cytogenet
, vol.62
, pp. 140-143
-
-
Nakagawa, H.1
Inazawa, J.2
Misawa, S.3
Tanaka, S.4
Takashima, T.5
Taniwaki, M.6
Abe, T.7
Kashima, K.8
-
82
-
-
0025778881
-
Acute myeloid leukemias with chromosomal abnormalities involving the 21q22 region identified by their in vitro responsiveness to interleukin-5
-
Touw I, Donath J, Pouwels K, van Buitenen C, Schipper P, Santini V, Hagemeijer A, Lowenberg B, Delwel R. Acute myeloid leukemias with chromosomal abnormalities involving the 21q22 region identified by their in vitro responsiveness to interleukin-5. Leukemia 1991; 5: 687-692.
-
(1991)
Leukemia
, vol.5
, pp. 687-692
-
-
Touw, I.1
Donath, J.2
Pouwels, K.3
Van Buitenen, C.4
Schipper, P.5
Santini, V.6
Hagemeijer, A.7
Lowenberg, B.8
Delwel, R.9
-
83
-
-
0021288796
-
'Masked' Phl chromosome abnormalities in CML: A report of two unique cases
-
Bernstein R, Pinto MR, Rosendorff J, Kramer S, Mendelow B. 'Masked' Phl chromosome abnormalities in CML: a report of two unique cases. Blood 1994; 63: 399-406.
-
(1994)
Blood
, vol.63
, pp. 399-406
-
-
Bernstein, R.1
Pinto, M.R.2
Rosendorff, J.3
Kramer, S.4
Mendelow, B.5
-
84
-
-
0028846257
-
Isodicentric (X)(q13) in haematological malignancies: Presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature
-
Dierlam J, Michaux L, Criel A, Wlodarska I, Zeller W, Louwagie A, Michaux J-L, Mecucci C, Van Den Berghe H. Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature. Br J Haematol 1995; 91: 885-891.
-
(1995)
Br J Haematol
, vol.91
, pp. 885-891
-
-
Dierlam, J.1
Michaux, L.2
Criel, A.3
Wlodarska, I.4
Zeller, W.5
Louwagie, A.6
Michaux, J.-L.7
Mecucci, C.8
Van Den Berghe, H.9
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