-
1
-
-
0018908108
-
An identical translocation between chromosome 1 and 7 in three patients with myelofibrosis and myeloid metaplasia
-
Geraedts JP, den Ottolander G J, Ploem JE, Muntinghe OG. An identical translocation between chromosome 1 and 7 in three patients with myelofibrosis and myeloid metaplasia. Br J Haematol. 1980;44:569-575.
-
(1980)
Br J Haematol
, vol.44
, pp. 569-575
-
-
Geraedts, J.P.1
Den Ottolander, G.J.2
Ploem, J.E.3
Muntinghe, O.G.4
-
2
-
-
0019500493
-
Acute nonlymphocytic leukemia, preleukemia, and acute myeloproliferative syndrome secondary to treatment of other malignant diseases: Clinical and cytogenetic characteristics and results of in vitro culture of bone marrow and HLA typing
-
Pedersen-Bjergaard J, Philip P, Mortensen BT, et al. Acute nonlymphocytic leukemia, preleukemia, and acute myeloproliferative syndrome secondary to treatment of other malignant diseases: clinical and cytogenetic characteristics and results of in vitro culture of bone marrow and HLA typing. Blood. 1981;57:712-723.
-
(1981)
Blood
, vol.57
, pp. 712-723
-
-
Pedersen-Bjergaard, J.1
Philip, P.2
Mortensen, B.T.3
-
3
-
-
0022381732
-
Combined trisomy 1q and monosomy 7q due to translocation 1;7 in myelodysplastic syndromes
-
Mecucci C, Ghione F, Tricot G, Van den Berghe H. Combined trisomy 1q and monosomy 7q due to translocation 1;7 in myelodysplastic syndromes. Cancer Genet Cytogenet. 1985;18:193-197.
-
(1985)
Cancer Genet Cytogenet
, vol.18
, pp. 193-197
-
-
Mecucci, C.1
Ghione, F.2
Tricot, G.3
Van den Berghe, H.4
-
4
-
-
0022372555
-
Translocation 1;7 in hematologic disorders: A brief review of 22 cases
-
Scheres JM, Hustinx TW, Geraedts JP, Leeksma OH, Meltzer PS. Translocation 1;7 in hematologic disorders: a brief review of 22 cases. Cancer Genet Cytogenet. 1985;18:207-213.
-
(1985)
Cancer Genet Cytogenet
, vol.18
, pp. 207-213
-
-
Scheres, J.M.1
Hustinx, T.W.2
Geraedts, J.P.3
Leeksma, O.H.4
Meltzer, P.S.5
-
5
-
-
0022645855
-
Unbalanced 1;7 translocation and therapy-induced hematologic disorders: A possible relationship
-
Morrison-DeLap SJ, Kuffel DG, Dewald GW, Letendre L. Unbalanced 1;7 translocation and therapy-induced hematologic disorders: a possible relationship. Am J Hematol. 1986;21:39-47.
-
(1986)
Am J Hematol
, vol.21
, pp. 39-47
-
-
Morrison-DeLap, S.J.1
Kuffel, D.G.2
Dewald, G.W.3
Letendre, L.4
-
7
-
-
0027025363
-
Der(1;7) (q10;p10) in three patients with malignant hematologic disorders
-
Yokoo H, Okada Y, Tominaga K, et al. der(1;7) (q10;p10) in three patients with malignant hematologic disorders. Rinsho Ketsueki. 1992;33:1829-1833.
-
(1992)
Rinsho Ketsueki
, vol.33
, pp. 1829-1833
-
-
Yokoo, H.1
Okada, Y.2
Tominaga, K.3
-
8
-
-
0031788987
-
Cytogenetically unrelated clones in therapy-related myelodysplasia and acute myeloid leukemia: Experience from the Copenhagen series updated to 180 consecutive cases
-
Pedersen-Bjergaard J, Timshel S, Andersen MK, Andersen AS, Philip P. Cytogenetically unrelated clones in therapy-related myelodysplasia and acute myeloid leukemia: experience from the Copenhagen series updated to 180 consecutive cases. Genes Chromosomes Cancer. 1998;23:337-349.
-
(1998)
Genes Chromosomes Cancer
, vol.23
, pp. 337-349
-
-
Pedersen-Bjergaard, J.1
Timshel, S.2
Andersen, M.K.3
Andersen, A.S.4
Philip, P.5
-
9
-
-
0033984674
-
Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centromere
-
Andersen MK, Pedersen-Bjergaard J. Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centromere. Leukemia. 2000;14:105-111.
-
(2000)
Leukemia
, vol.14
, pp. 105-111
-
-
Andersen, M.K.1
Pedersen-Bjergaard, J.2
-
10
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P, Cox C, LeBeau MM, et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood. 1997;89:2079-2088.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
-
11
-
-
0034995677
-
The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex
-
Mauritzson N, Johansson B, Rylander L, et al. The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex. Br J Haematol. 2001;113:347-356.
-
(2001)
Br J Haematol
, vol.113
, pp. 347-356
-
-
Mauritzson, N.1
Johansson, B.2
Rylander, L.3
-
12
-
-
0024336174
-
Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7
-
Alitalo T, Willard HF, de la Chapelle A. Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7. Cytogenet Cell Genet. 1989;50:49-53.
-
(1989)
Cytogenet Cell Genet
, vol.50
, pp. 49-53
-
-
Alitalo, T.1
Willard, H.F.2
De La Chapelle, A.3
-
13
-
-
0026703382
-
Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies
-
Kibbelaar RE, Mulder JW, van Kamp H, et al. Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies. Genes Chromosomes Cancer. 1992;4:128-134.
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 128-134
-
-
Kibbelaar, R.E.1
Mulder, J.W.2
Van Kamp, H.3
-
14
-
-
0034489876
-
FISH demonstrates treatment-related chromosome damage in myeloid but not plasma cells in primary systemic amyloidosis
-
Fonseca R, Rajkumar SV, Ahmann GJ, et al. FISH demonstrates treatment-related chromosome damage in myeloid but not plasma cells in primary systemic amyloidosis. Leuk Lymphoma. 2000;39:391-395.
-
(2000)
Leuk Lymphoma
, vol.39
, pp. 391-395
-
-
Fonseca, R.1
Rajkumar, S.V.2
Ahmann, G.J.3
-
15
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
Seabright M. A rapid banding technique for human chromosomes. Lancet. 1971;2:971-972.
-
(1971)
Lancet
, vol.2
, pp. 971-972
-
-
Seabright, M.1
-
16
-
-
0033400204
-
A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumors
-
Yang Y, Kiss H, Kost-Alimova M, et al. A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumors. Genomics. 1999;62:147-155.
-
(1999)
Genomics
, vol.62
, pp. 147-155
-
-
Yang, Y.1
Kiss, H.2
Kost-Alimova, M.3
-
17
-
-
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
-
18
-
-
0034839213
-
The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers
-
Tapia-Paez I, Kost-Alimova M, Hu P, et al. The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers. Hum Genet. 2001;109:167-177.
-
(2001)
Hum Genet
, vol.109
, pp. 167-177
-
-
Tapia-Paez, I.1
Kost-Alimova, M.2
Hu, P.3
-
19
-
-
0023064191
-
Genomic organization of alpha satellite DNA on human chromosome 7: Evidence for two distinct alphoid domains on a single chromosome
-
Waye JS, England SB, Willard HF. Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome. Mol Cell Biol. 1987;7:349-356.
-
(1987)
Mol Cell Biol
, vol.7
, pp. 349-356
-
-
Waye, J.S.1
England, S.B.2
Willard, H.F.3
-
20
-
-
0028335709
-
The C-terminal SH3 domain of the mouse c-Crk protein negatively regulates tyrosine-phosphorylation of Crk associated p130 in rat 3Y1 cells
-
Ogawa S, Toyoshima H, Kozutsumi H, et al. The C-terminal SH3 domain of the mouse c-Crk protein negatively regulates tyrosine-phosphorylation of Crk associated p130 in rat 3Y1 cells. Oncogene. 1994;9:1669-1678.
-
(1994)
Oncogene
, vol.9
, pp. 1669-1678
-
-
Ogawa, S.1
Toyoshima, H.2
Kozutsumi, H.3
-
21
-
-
0030884929
-
Human centromeric DNAs
-
Lee C, Wevrick R, Fisher 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
Fisher, R.B.3
Ferguson-Smith, M.A.4
Lin, C.C.5
-
22
-
-
0032055381
-
Centromeres: The missing link in the development of human artificial chromosomes
-
Willard HF. Centromeres: the missing link in the development of human artificial chromosomes. Curr Opin Genet Dev. 1998;8:219-225.
-
(1998)
Curr Opin Genet Dev
, vol.8
, pp. 219-225
-
-
Willard, H.F.1
-
23
-
-
0030696619
-
Alphoid repetitive DNA in human chromosomes
-
Jorgensen AL. Alphoid repetitive DNA in human chromosomes. Dan Med Bull. 1997;44:522-534.
-
(1997)
Dan Med Bull
, vol.44
, pp. 522-534
-
-
Jorgensen, A.L.1
-
24
-
-
0024429163
-
Molecular characterization of human minichromosomes with centromere from chromosome 1 in human-hamster hybrid cells
-
Carine K, Jacquemin-Sablon A, Waltzer E, Mascarello J, Scheffler IE. Molecular characterization of human minichromosomes with centromere from chromosome 1 in human-hamster hybrid cells. Somat Cell Mol Genet. 1989;15:445-460.
-
(1989)
Somat Cell Mol Genet
, vol.15
, pp. 445-460
-
-
Carine, K.1
Jacquemin-Sablon, A.2
Waltzer, E.3
Mascarello, J.4
Scheffler, I.E.5
-
25
-
-
0002666536
-
Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: Implications for development of centromere-based genetic linkage maps
-
Willard HF, Waye JS, Skolnick MH, Schwartz CE, Powers VE, England SB. Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. Proc Natl Acad Sci U S A. 1986;83:5611-5615.
-
(1986)
Proc Natl Acad Sci U S A
, vol.83
, pp. 5611-5615
-
-
Willard, H.F.1
Waye, J.S.2
Skolnick, M.H.3
Schwartz, C.E.4
Powers, V.E.5
England, S.B.6
-
26
-
-
0024379003
-
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: High-frequency array-length polymorphism and meiotic stability
-
Wevrick R, Willard HF. Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability. Proc Natl Acad Sci U S A. 1989;86:9394-9398.
-
(1989)
Proc Natl Acad Sci U S A
, vol.86
, pp. 9394-9398
-
-
Wevrick, R.1
Willard, H.F.2
-
27
-
-
0034879060
-
Alpha-satellite DNA of primates: Old and new families
-
Alexandrov I, Kazakov A, Tumeneva I, Shepelev V, Yurov Y. Alpha-satellite DNA of primates: old and new families. Chromosoma. 2001;110:253-266.
-
(2001)
Chromosoma
, vol.110
, pp. 253-266
-
-
Alexandrov, I.1
Kazakov, A.2
Tumeneva, I.3
Shepelev, V.4
Yurov, Y.5
-
28
-
-
0018392825
-
Cloning of human satellite III DNA: Different components are on different chromosomes
-
Cooke HJ, Hindley J. Cloning of human satellite III DNA: different components are on different chromosomes. Nucleic Acids Res. 1979;6:3177-3197.
-
(1979)
Nucleic Acids Res
, vol.6
, pp. 3177-3197
-
-
Cooke, H.J.1
Hindley, J.2
-
29
-
-
0028354712
-
Chromosomal localization of human satellites 2 and 3 by a FISH method using oligonucleotides as probes
-
Tagarro I, Fernandez-Peralta AM, Gonzalez-Aguilera JJ. Chromosomal localization of human satellites 2 and 3 by a FISH method using oligonucleotides as probes. Hum Genet. 1994;93:383-388.
-
(1994)
Hum Genet
, vol.93
, pp. 383-388
-
-
Tagarro, I.1
Fernandez-Peralta, A.M.2
Gonzalez-Aguilera, J.J.3
-
30
-
-
0025806731
-
Physical map of the centromeric region of human chromosome 7: Relationship between two distinct alpha satellite arrays
-
Wevrick R, Willard HF. Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays. Nucleic Acids Res. 1991;19:2295-2301.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 2295-2301
-
-
Wevrick, R.1
Willard, H.F.2
-
31
-
-
0030943877
-
Cytologic characterization of two distinct alpha satellite DNA domains on human chromosome 7, using double-labeling hybridizations in fluorescence and electron microscopy on a melanoma cell line
-
Fetni R, Richer CL, Malfoy B, Dutrillaux B, Lemieux N. Cytologic characterization of two distinct alpha satellite DNA domains on human chromosome 7, using double-labeling hybridizations in fluorescence and electron microscopy on a melanoma cell line. Cancer Genet Cytogenet. 1997;96:17-22.
-
(1997)
Cancer Genet Cytogenet
, vol.96
, pp. 17-22
-
-
Fetni, R.1
Richer, C.L.2
Malfoy, B.3
Dutrillaux, B.4
Lemieux, N.5
-
32
-
-
0023414542
-
Chromosome-specific alpha satellite DNA from human chromosome 1: Hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA
-
Waye JS, Durfy SJ, Pinkel D, et al. Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase 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
-
33
-
-
0035812788
-
Genomic and genetic definition of a functional human centromere
-
Schueler MG, Higgins AW, Rudd MK, Gustashaw K, Willard HF. Genomic and genetic definition of a functional human centromere. Science. 2001;294:109-115.
-
(2001)
Science
, vol.294
, pp. 109-115
-
-
Schueler, M.G.1
Higgins, A.W.2
Rudd, M.K.3
Gustashaw, K.4
Willard, H.F.5
-
34
-
-
0035098011
-
Molecular and cytological analysis of a 5.5 Mb minichromosome
-
Auriche C, Donini P, Ascenzioni F. Molecular and cytological analysis of a 5.5 Mb minichromosome. EMBO Rep. 2001;2:102-107.
-
(2001)
EMBO Rep
, vol.2
, pp. 102-107
-
-
Auriche, C.1
Donini, P.2
Ascenzioni, F.3
-
35
-
-
0027083417
-
Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7
-
Wevrick R, Willard VP, Willard HF. Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7. Genomics. 1992;14:912-923.
-
(1992)
Genomics
, vol.14
, pp. 912-923
-
-
Wevrick, R.1
Willard, V.P.2
Willard, H.F.3
-
36
-
-
0027722155
-
Therapy-related myelodysplasia and acute myeloid leukemia: Cytogenetic characteristics of 115 consecutive cases and risk in seven cohorts of patients treated intensively for malignant diseases in the Copenhagen series
-
Pedersen-Bjergaard J, Philip P, Larsen SO, et al. Therapy-related myelodysplasia and acute myeloid leukemia: cytogenetic characteristics of 115 consecutive cases and risk in seven cohorts of patients treated intensively for malignant diseases in the Copenhagen series. Leukemia. 1993;7:1975-1986.
-
(1993)
Leukemia
, vol.7
, pp. 1975-1986
-
-
Pedersen-Bjergaard, J.1
Philip, P.2
Larsen, S.O.3
-
37
-
-
0028871987
-
Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia
-
Pedersen-Bjergaard J, Pedersen M, Roulston D, Philip P. Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia. Blood. 1995;86:3542-3552.
-
(1995)
Blood
, vol.86
, pp. 3542-3552
-
-
Pedersen-Bjergaard, J.1
Pedersen, M.2
Roulston, D.3
Philip, P.4
|