-
1
-
-
0026780698
-
The translocation (6;9)(p23;q34) shows consistent rearrangement of two genes and defines a myeloproliferative disorder with specific clinical features
-
Soekarman D, von Lindern M, Daenen S, de Jong B, Fonatch C, Heinze B et al. The translocation (6;9)(p23;q34) shows consistent rearrangement of two genes and defines a myeloproliferative disorder with specific clinical features. Blood 1992; 79: 2990-2997.
-
(1992)
Blood
, vol.79
, pp. 2990-2997
-
-
Soekarman, D.1
von Lindern, M.2
Daenen, S.3
de Jong, B.4
Fonatch, C.5
Heinze, B.6
-
2
-
-
4344608433
-
Acute myeloid leukemia with t(6;9)(p23;q34) is associated with dysplasia and a high frequency of FLT3 mutations
-
Oyarzo MP, Lin P, Glassman A, Bueso-Ramos CE, Luthra R, Medeiros J. Acute myeloid leukemia with t(6;9)(p23;q34) is associated with dysplasia and a high frequency of FLT3 mutations. Hematopathology 2004; 122: 348-358.
-
(2004)
Hematopathology
, vol.122
, pp. 348-358
-
-
Oyarzo, M.P.1
Lin, P.2
Glassman, A.3
Bueso-Ramos, C.E.4
Luthra, R.5
Medeiros, J.6
-
3
-
-
0031028263
-
A recurring translocation, t(3;6)(q27;p21), in non-Hodgkin's lymphoma results in replacement of the 5′ regulatory region of BCL-6 with a novel H4 histone gene
-
Akasaka T, Miura I, Takahashi N, Akasaka H, Yonetani N, Ohno H et al. A recurring translocation, t(3;6)(q27;p21), in non-Hodgkin's lymphoma results in replacement of the 5′ regulatory region of BCL-6 with a novel H4 histone gene. Cancer Res 1997; 57: 7-12.
-
(1997)
Cancer Res
, vol.57
, pp. 7-12
-
-
Akasaka, T.1
Miura, I.2
Takahashi, N.3
Akasaka, H.4
Yonetani, N.5
Ohno, H.6
-
4
-
-
0034797156
-
Splicing factor SRP20 is a novel partner of BCL6 in a t(3;6)(q27;p21) translocation in transformed follicular lymphoma
-
Chen W, Itoyama T, Chaganti RSK. Splicing factor SRP20 is a novel partner of BCL6 in a t(3;6)(q27;p21) translocation in transformed follicular lymphoma. Genes Chromosome Cancer 2001; 32: 281-284.
-
(2001)
Genes Chromosome Cancer
, vol.32
, pp. 281-284
-
-
Chen, W.1
Itoyama, T.2
Chaganti, R.S.K.3
-
5
-
-
0035525788
-
Cyclin D3 is a target of t(6;14)(p21.1;q32.3) of mature B-cell malignancies
-
Sonoki T, Harder L, Horsman DE, Karran L, Taniguchi I, Willis TG et al. Cyclin D3 is a target of t(6;14)(p21.1;q32.3) of mature B-cell malignancies. Blood 2001; 98: 2837-2844.
-
(2001)
Blood
, vol.98
, pp. 2837-2844
-
-
Sonoki, T.1
Harder, L.2
Horsman, D.E.3
Karran, L.4
Taniguchi, I.5
Willis, T.G.6
-
6
-
-
0035412392
-
Cyclin D3 at 6p21 is dysregulated by recurrent chromosomal translocations to immunoglobulin loci in multiple myeloma
-
Shaughnessy J, Gabrera A, Qi Y, Brents L, Zhan F, Tian E et al. Cyclin D3 at 6p21 is dysregulated by recurrent chromosomal translocations to immunoglobulin loci in multiple myeloma. Blood 2001; 98: 217-223.
-
(2001)
Blood
, vol.98
, pp. 217-223
-
-
Shaughnessy, J.1
Gabrera, A.2
Qi, Y.3
Brents, L.4
Zhan, F.5
Tian, E.6
-
7
-
-
84984756503
-
Deregulation of MUM/IRF4 by chromosomal translocation in multiple myeloma
-
Iida S, Rao PH, Butler M, Corradini P, Boccadoro M, Klein B et al. Deregulation of MUM/IRF4 by chromosomal translocation in multiple myeloma. Nat Genet 1997; 17: 226-230.
-
(1997)
Nat Genet
, vol.17
, pp. 226-230
-
-
Iida, S.1
Rao, P.H.2
Butler, M.3
Corradini, P.4
Boccadoro, M.5
Klein, B.6
-
8
-
-
0025818349
-
Cytogeentics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL)
-
Johansson B, Mertens F, Heim S, Kristoffersson U, Mitelman F. Cytogeentics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL). Eur J Haematol 1991; 47: 17-27.
-
(1991)
Eur J Haematol
, vol.47
, pp. 17-27
-
-
Johansson, B.1
Mertens, F.2
Heim, S.3
Kristoffersson, U.4
Mitelman, F.5
-
9
-
-
0023940274
-
The short arm of chromosome 6 is nonrandomly rearranged in secondary myelodysplastic syndromes
-
Mecucci C, Michaux J-L, Louwagie A, Boogaerts M, Van Den Berghe H. The short arm of chromosome 6 is nonrandomly rearranged in secondary myelodysplastic syndromes. Cancer Genet Cytogenet 1988; 31: 147-155.
-
(1988)
Cancer Genet Cytogenet
, vol.31
, pp. 147-155
-
-
Mecucci, C.1
Michaux, J.-L.2
Louwagie, A.3
Boogaerts, M.4
Van Den Berghe, H.5
-
10
-
-
0024455497
-
Chromosome 6p rearrangements appear to be secondary changes in various haematological malignancies
-
Huret JL, Schoenwald M, Brizard A, Guilhot F, Vilmer E, Tanzer J. Chromosome 6p rearrangements appear to be secondary changes in various haematological malignancies. Leukemia Res 1989; 13: 819-824.
-
(1989)
Leukemia Res
, vol.13
, pp. 819-824
-
-
Huret, J.L.1
Schoenwald, M.2
Brizard, A.3
Guilhot, F.4
Vilmer, E.5
Tanzer, J.6
-
11
-
-
0026710302
-
Unbalanced 6p translocation as primary karyotipic anomaly in secondary acute nonlymphocytic leukemia
-
Mancini M, Mecucci C, Cedrone M, Rondinelli MB, Aloe-Spiriti A, Alimena G. Unbalanced 6p translocation as primary karyotipic anomaly in secondary acute nonlymphocytic leukemia. Cancer Genet Cytogenet 1992; 60: 93-95.
-
(1992)
Cancer Genet Cytogenet
, vol.60
, pp. 93-95
-
-
Mancini, M.1
Mecucci, C.2
Cedrone, M.3
Rondinelli, M.B.4
Aloe-Spiriti, A.5
Alimena, G.6
-
13
-
-
0029867401
-
Derivative (6)t(1;6)(q22;p21) revealed in bone marrow cells by FISH 9 months before diagnosis of acute T-lymphoblastic leukemia
-
Michalovà K, Lemez P, Bartsch O, Brezinova J, Zemanova Z, Jelinek J et al. Derivative (6)t(1;6)(q22;p21) revealed in bone marrow cells by FISH 9 months before diagnosis of acute T-lymphoblastic leukemia. Cancer Genet Cytogenet 1996; 86: 131-135.
-
(1996)
Cancer Genet Cytogenet
, vol.86
, pp. 131-135
-
-
Michalovà, K.1
Lemez, P.2
Bartsch, O.3
Brezinova, J.4
Zemanova, Z.5
Jelinek, J.6
-
14
-
-
0034005973
-
Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodysplastic syndrome following treatment for a primitive neuroectodermal tumor
-
Mathew S, Head D, Rodriguez-Galindo C, Raimondi S. Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodysplastic syndrome following treatment for a primitive neuroectodermal tumor. Leukemia Lymphoma 2000; 37: 213-218.
-
(2000)
Leukemia Lymphoma
, vol.37
, pp. 213-218
-
-
Mathew, S.1
Head, D.2
Rodriguez-Galindo, C.3
Raimondi, S.4
-
16
-
-
2942720402
-
Submicroscopic deletions in 5q- associated malignancies
-
Crescenzi B, La Starza R, Romoli S, Beacci D, Matteucci C, Barba G et al. Submicroscopic deletions in 5q- associated malignancies. Haematologica 2004; 89: 281-285.
-
(2004)
Haematologica
, vol.89
, pp. 281-285
-
-
Crescenzi, B.1
La Starza, R.2
Romoli, S.3
Beacci, D.4
Matteucci, C.5
Barba, G.6
-
17
-
-
20344407088
-
The hypereosinophilic syndrome: Fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases
-
La Starza R, Specchia G, Cuneo A, Beacci D, Nozzoli C, Luciano L et al. The hypereosinophilic syndrome: Fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases. Haematologica 2005; 90: 596-601.
-
(2005)
Haematologica
, vol.90
, pp. 596-601
-
-
La Starza, R.1
Specchia, G.2
Cuneo, A.3
Beacci, D.4
Nozzoli, C.5
Luciano, L.6
-
18
-
-
18444390564
-
Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization investigations on the U937-I cell line
-
Matteucci C, La Starza R, Crescenzi B, Falzetti D, Romoli S, Emiliani C et al. Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization investigations on the U937-I cell line. Cancer Genet Cytogenet 2002; 135: 28-34.
-
(2002)
Cancer Genet Cytogenet
, vol.135
, pp. 28-34
-
-
Matteucci, C.1
La Starza, R.2
Crescenzi, B.3
Falzetti, D.4
Romoli, S.5
Emiliani, C.6
-
19
-
-
0036934475
-
Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976-1993 and on 5098 unselected cases reported in the literature 1974-2001
-
Mauritzson N, Albin M, Rylander L, Billstrom R, Ahlgren T, Mikoczy Z et al. Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976-1993 and on 5098 unselected cases reported in the literature 1974-2001. Leukemia 2002; 16: 2366-2378.
-
(2002)
Leukemia
, vol.16
, pp. 2366-2378
-
-
Mauritzson, N.1
Albin, M.2
Rylander, L.3
Billstrom, R.4
Ahlgren, T.5
Mikoczy, Z.6
-
20
-
-
0015891353
-
A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents
-
Sasaki MS, Tonomura A. A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents. Cancer Res 1973; 33: 1829-1836.
-
(1973)
Cancer Res
, vol.33
, pp. 1829-1836
-
-
Sasaki, M.S.1
Tonomura, A.2
-
21
-
-
0033763360
-
MLL amplification in acute leukaemia: A United Kingdom Cancer Cytogenetics Group (UKCCG) study
-
Cuthbert G, Thompson K, McCullough S, Watmore A, Dickinson H, Telford N et al. MLL amplification in acute leukaemia: A United Kingdom Cancer Cytogenetics Group (UKCCG) study. Leukemia 2000; 14: 1885-1891.
-
(2000)
Leukemia
, vol.14
, pp. 1885-1891
-
-
Cuthbert, G.1
Thompson, K.2
McCullough, S.3
Watmore, A.4
Dickinson, H.5
Telford, N.6
-
22
-
-
0033934638
-
Double minute chromosomes and c-MYC amplification in a child with secondary myelodysplastic syndrome after treatment for acute lymphoblastic leukemia
-
Mathew S, Lorsbach RB, Shearer P, Sandlund JT, Raimondi SC. Double minute chromosomes and c-MYC amplification in a child with secondary myelodysplastic syndrome after treatment for acute lymphoblastic leukemia. Leukemia 2000; 14: 1314-1315.
-
(2000)
Leukemia
, vol.14
, pp. 1314-1315
-
-
Mathew, S.1
Lorsbach, R.B.2
Shearer, P.3
Sandlund, J.T.4
Raimondi, S.C.5
-
23
-
-
0037047628
-
Recent segmental duplications in the human genome
-
Bailey JA, Gu Z, Clark RA, Reinert K, Samonte RV, Schwartz S et al. Recent segmental duplications in the human genome. Science 2002; 297: 1003-1007.
-
(2002)
Science
, vol.297
, pp. 1003-1007
-
-
Bailey, J.A.1
Gu, Z.2
Clark, R.A.3
Reinert, K.4
Samonte, R.V.5
Schwartz, S.6
-
24
-
-
0036468807
-
Genome architecture, rearrangements and genomic disorders
-
Stankiewicz P, Lupski JR. Genome architecture, rearrangements and genomic disorders. Trends Genet 2002; 18: 74-82.
-
(2002)
Trends Genet
, vol.18
, pp. 74-82
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
25
-
-
0034028921
-
Structure of chromosomal duplicons and their role in mediating human genomic disorders
-
Ji Y, Eicher EE, Schwartz S, Nicholls RD. Structure of chromosomal duplicons and their role in mediating human genomic disorders. Genome Res 2000; 10: 597-610.
-
(2000)
Genome Res
, vol.10
, pp. 597-610
-
-
Ji, Y.1
Eicher, E.E.2
Schwartz, S.3
Nicholls, R.D.4
-
26
-
-
0037162516
-
A 76 Kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: Possible involvement in the genesis of the philadelphia chromosome translocation
-
Saglio G, Storlazzi CT, Giugliano E, Surace C, Anelli L, Rege-Cambrin G et al. A 76 Kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: Possible involvement in the genesis of the philadelphia chromosome translocation. Proc Natl Acad Sci USA 2002; 99: 9882-9887.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 9882-9887
-
-
Saglio, G.1
Storlazzi, C.T.2
Giugliano, E.3
Surace, C.4
Anelli, L.5
Rege-Cambrin, G.6
-
27
-
-
0035071955
-
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements
-
Giglio S, Broman KW, Matsumoto N, Calvari V, Gimelli G, Neumann T et al. Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements. Am J Hum Genet 2001; 68: 874-883.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 874-883
-
-
Giglio, S.1
Broman, K.W.2
Matsumoto, N.3
Calvari, V.4
Gimelli, G.5
Neumann, T.6
-
28
-
-
0036071427
-
Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation
-
Giglio S, Calvari V, gregato G, Gimelli G, Camanini S, Giorda R et al. Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation. Am J Hum Genet 2002; 71: 276-285.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 276-285
-
-
Giglio, S.1
Calvari, V.2
Gregato, G.3
Gimelli, G.4
Camanini, S.5
Giorda, R.6
-
29
-
-
0035011834
-
Alteration of chromosome arm 6p is characteristic of primary mediastinal B-cell lymphoma, as identified by genome-wide allelotyping
-
Rigaud G, Moore PS, Taruscio D, Scardoni M, Montresor M, Menestrina F et al. Alteration of chromosome arm 6p is characteristic of primary mediastinal B-cell lymphoma, as identified by genome-wide allelotyping. Genes Chromosomes Cancer 2001; 31: 191-195.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 191-195
-
-
Rigaud, G.1
Moore, P.S.2
Taruscio, D.3
Scardoni, M.4
Montresor, M.5
Menestrina, F.6
-
30
-
-
0345714858
-
Frequent amplification and rearrangement of chromosomal bands 6p12p21 and 17p11.2 in osteosarcoma
-
Lau CC, Harris CP, Lu X-Y, Perloky L, Gogineni S, Chintagumpala M et al. Frequent amplification and rearrangement of chromosomal bands 6p12p21 and 17p11.2 in osteosarcoma. Genes Chromosomes Cancer 2004; 39: 11-21.
-
(2004)
Genes Chromosomes Cancer
, vol.39
, pp. 11-21
-
-
Lau, C.C.1
Harris, C.P.2
Lu, X-.Y.3
Perloky, L.4
Gogineni, S.5
Chintagumpala, M.6
-
31
-
-
0031974484
-
Comparison of DNA copy number changes in malignant mesothelioma, adenocarcinoma and large-cell anaplastic carcinoma of the lung
-
Bjorkqvist AM, Tammilehto L, Nordling S, Nu'minen M, Anttilla S, Mattson K et al. Comparison of DNA copy number changes in malignant mesothelioma, adenocarcinoma and large-cell anaplastic carcinoma of the lung. Br J Cancer 1998; 77: 260-269.
-
(1998)
Br J Cancer
, vol.77
, pp. 260-269
-
-
Bjorkqvist, A.M.1
Tammilehto, L.2
Nordling, S.3
Nu'minen, M.4
Anttilla, S.5
Mattson, K.6
-
32
-
-
19944430329
-
Candidate genes in breast cancer revealed by microarray-based comparative genomic hybridization of archived tissue
-
Nessling M, Richter K, Schwaenen C, Roerig P, Wrobel G, Wessendorf S et al. Candidate genes in breast cancer revealed by microarray-based comparative genomic hybridization of archived tissue. Cancer Res 2005; 65: 439-447.
-
(2005)
Cancer Res
, vol.65
, pp. 439-447
-
-
Nessling, M.1
Richter, K.2
Schwaenen, C.3
Roerig, P.4
Wrobel, G.5
Wessendorf, S.6
-
33
-
-
0036329794
-
Genetic alterations in epithelial ovarian tumors analyzed by comparative genomic hybridization
-
Hauptmann S, Denkert C, Koch I, Petersen S, Scluns K, Reles A et al. Genetic alterations in epithelial ovarian tumors analyzed by comparative genomic hybridization. Hum Pathol 2002; 33: 632-641.
-
(2002)
Hum Pathol
, vol.33
, pp. 632-641
-
-
Hauptmann, S.1
Denkert, C.2
Koch, I.3
Petersen, S.4
Scluns, K.5
Reles, A.6
-
34
-
-
0036170837
-
Genomic amplification in retinoblastoma narrowed to 0.6 mega-base on chromosome 6p containing a kinesin-like gene, RBKIN
-
Chen D, Pajovic S, Duckett A, Brown VD, Squire JA, Gallie BL. Genomic amplification in retinoblastoma narrowed to 0.6 mega-base on chromosome 6p containing a kinesin-like gene, RBKIN. Cancer Res 2002; 62: 967-971.
-
(2002)
Cancer Res
, vol.62
, pp. 967-971
-
-
Chen, D.1
Pajovic, S.2
Duckett, A.3
Brown, V.D.4
Squire, J.A.5
Gallie, B.L.6
-
35
-
-
0035146240
-
Concomitant loss of chromosome 3 and whole arm losses and gains of chromosome 1, 6, or 8 in metastasizing primary uveal melanoma
-
Aalto Y, Eriksson L, Seregard S, Larsson O, Knuutila S. Concomitant loss of chromosome 3 and whole arm losses and gains of chromosome 1, 6, or 8 in metastasizing primary uveal melanoma. Invest Ophthalmol Vis Sci 2001; 42: 313-317.
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 313-317
-
-
Aalto, Y.1
Eriksson, L.2
Seregard, S.3
Larsson, O.4
Knuutila, S.5
-
36
-
-
4243052846
-
Translocations involving 6p22 in acute myeloid leukaemia at relapse: Breakpoint characterization using microarray-based comparative genomic hybridization
-
Tchinda J, Dijkhuizen T, van der Vlies P, Kok K, Horst J. Translocations involving 6p22 in acute myeloid leukaemia at relapse: Breakpoint characterization using microarray-based comparative genomic hybridization. Br J Haematol 2004; 126: 495-500.
-
(2004)
Br J Haematol
, vol.126
, pp. 495-500
-
-
Tchinda, J.1
Dijkhuizen, T.2
van der Vlies, P.3
Kok, K.4
Horst, J.5
-
37
-
-
0032883699
-
Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6
-
Somberger KS, Weremowicz S, Williams AJ, Quade BJ, Ligon AH, Pedeutour F et al. Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6. Cancer Genet Cytogenet 1999; 114: 9-16.
-
(1999)
Cancer Genet Cytogenet
, vol.114
, pp. 9-16
-
-
Somberger, K.S.1
Weremowicz, S.2
Williams, A.J.3
Quade, B.J.4
Ligon, A.H.5
Pedeutour, F.6
-
38
-
-
0037108434
-
Overexpression of FKBP51 in idiopathic myelofibrosis regulates the growth factor independence of megakaryocyte progenitors
-
Giraudier S, Chagraoui H, Komura E, Barnache S, Blanchet B, LeCouedic JP et al. Overexpression of FKBP51 in idiopathic myelofibrosis regulates the growth factor independence of megakaryocyte progenitors. Blood 2002; 100: 2932-2940.
-
(2002)
Blood
, vol.100
, pp. 2932-2940
-
-
Giraudier, S.1
Chagraoui, H.2
Komura, E.3
Barnache, S.4
Blanchet, B.5
LeCouedic, J.P.6
-
39
-
-
0035057424
-
Duplication or amplification of chromosome 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents
-
Andersen MK, Christiansen DH, Kirchhoff M, Pedersen-Bjergaard J. Duplication or amplification of chromosome 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents. Genes Chromosomes Cancer 2001; 31: 337-349.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 337-349
-
-
Andersen, M.K.1
Christiansen, D.H.2
Kirchhoff, M.3
Pedersen-Bjergaard, J.4
-
40
-
-
13544273521
-
Amplification or duplication of chromosome band 21q22 with multiple copies of the AML1 gene and mutation of the TP53 gene in therapy-related MDS and AML
-
Andersen MK, Christiansen DH, Pedersen-Bjegaard J. Amplification or duplication of chromosome band 21q22 with multiple copies of the AML1 gene and mutation of the TP53 gene in therapy-related MDS and AML. Leukemia 2005; 19: 197-200.
-
(2005)
Leukemia
, vol.19
, pp. 197-200
-
-
Andersen, M.K.1
Christiansen, D.H.2
Pedersen-Bjegaard, J.3
|