-
1
-
-
2642577062
-
Embryonal rhabdomyosarcoma
-
Fletcher C.D.M., Unni K.K., and Mertens F. (Eds), IARC Press, Lyon
-
Parham D.M., and Barr F.G. Embryonal rhabdomyosarcoma. In: Fletcher C.D.M., Unni K.K., and Mertens F. (Eds). Pathology and genetics of tumours of soft tissue and bone. World Health Organization Classification of Tumours (2002), IARC Press, Lyon 146-149
-
(2002)
Pathology and genetics of tumours of soft tissue and bone. World Health Organization Classification of Tumours
, pp. 146-149
-
-
Parham, D.M.1
Barr, F.G.2
-
2
-
-
0032732984
-
Genes, chromosomes, and rhabdomyosarcoma
-
Anderson J., Gordon A., Pritchard-Jones K., and Shipley J. Genes, chromosomes, and rhabdomyosarcoma. Genes Chromosomes Cancer 26 (1999) 275-285
-
(1999)
Genes Chromosomes Cancer
, vol.26
, pp. 275-285
-
-
Anderson, J.1
Gordon, A.2
Pritchard-Jones, K.3
Shipley, J.4
-
3
-
-
0035142423
-
Cytogenetic abnormalities in 42 rhabdomyosarcoma: a United Kingdom Cancer Cytogenetics Group Study
-
Gordon T., McManus A., Anderson J., Min T., Swansbury J., Pritchard-Jones K., Shipley J., and United Kingdom Children's Cancer Study Group; United Kingdom Cancer Cytogenetics Group. Cytogenetic abnormalities in 42 rhabdomyosarcoma: a United Kingdom Cancer Cytogenetics Group Study. Med Pediatr Oncol 36 (2001) 259-267
-
(2001)
Med Pediatr Oncol
, vol.36
, pp. 259-267
-
-
Gordon, T.1
McManus, A.2
Anderson, J.3
Min, T.4
Swansbury, J.5
Pritchard-Jones, K.6
Shipley, J.7
-
4
-
-
33847708861
-
-
Mitelman F, Johansson B, Mertens F, editors. Mitelman database of chromosome aberrations in cancer [Internet]. Updated June 2006. Available from http://cgap.nci.nih.gov/Chromosomes/Mitelman.
-
-
-
-
5
-
-
0034088133
-
Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hybridization and fluorescence in situ hybridization: an Intergroup Rhabdomyosarcoma study
-
Bridge J.A., Liu J., Weibolt V., Baker K.S., Perry D., Kruger R., Qualman S., Barr F., Sorensen P., Triche T., and Suijkerbuijk R. Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hybridization and fluorescence in situ hybridization: an Intergroup Rhabdomyosarcoma study. Genes Chromosomes Cancer 27 (2000) 337-344
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 337-344
-
-
Bridge, J.A.1
Liu, J.2
Weibolt, V.3
Baker, K.S.4
Perry, D.5
Kruger, R.6
Qualman, S.7
Barr, F.8
Sorensen, P.9
Triche, T.10
Suijkerbuijk, R.11
-
6
-
-
18244374534
-
Genomic gains and losses are similar in genetic and histologic subtypes of rhabdomyosarcoma, whereas amplification predominates in embryonal with anaplasia and alveolar subtypes
-
Bridge J.A., Liu J., Qualman S.J., Suijkerbuijk R., Wenger G., Zhang J., Wan X., Baker K.S., Sorensen P., and Barr F.G. Genomic gains and losses are similar in genetic and histologic subtypes of rhabdomyosarcoma, whereas amplification predominates in embryonal with anaplasia and alveolar subtypes. Genes Chromosomes Cancer 33 (2002) 310-321
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 310-321
-
-
Bridge, J.A.1
Liu, J.2
Qualman, S.J.3
Suijkerbuijk, R.4
Wenger, G.5
Zhang, J.6
Wan, X.7
Baker, K.S.8
Sorensen, P.9
Barr, F.G.10
-
7
-
-
0023925987
-
Chromosomal analysis of sixteen human rhabdomyosarcomas
-
Wang-Wuu S., Soukup S., Ballard E., Gotwals B., and Lampkin B. Chromosomal analysis of sixteen human rhabdomyosarcomas. Cancer Res 48 (1988) 983-987
-
(1988)
Cancer Res
, vol.48
, pp. 983-987
-
-
Wang-Wuu, S.1
Soukup, S.2
Ballard, E.3
Gotwals, B.4
Lampkin, B.5
-
8
-
-
0027392707
-
Alveolar rhabdomyosarcoma with the t(2;13): cytogenetic findings and clinicopathologic correlations
-
Douglass E.C., Shapiro D.N., Valentine M., Rowe S.T., Carroll A.J., Raney R.B., Ragab A.H., Abella S.M., and Parham D.M. Alveolar rhabdomyosarcoma with the t(2;13): cytogenetic findings and clinicopathologic correlations. Med Pediatr Oncol 21 (1993) 83-87
-
(1993)
Med Pediatr Oncol
, vol.21
, pp. 83-87
-
-
Douglass, E.C.1
Shapiro, D.N.2
Valentine, M.3
Rowe, S.T.4
Carroll, A.J.5
Raney, R.B.6
Ragab, A.H.7
Abella, S.M.8
Parham, D.M.9
-
9
-
-
0029932287
-
der(16)t(1;16)(q21;q13) as a secondary change in alveolar rhabdomyosarcoma: a case report and review of the literature
-
McManus A.P., Min T., Swansbury G.J., Gusterson B.A., Pinkerton C.R., and Shipley J.M. der(16)t(1;16)(q21;q13) as a secondary change in alveolar rhabdomyosarcoma: a case report and review of the literature. Cancer Genet Cytogenet 87 (1996) 179-181
-
(1996)
Cancer Genet Cytogenet
, vol.87
, pp. 179-181
-
-
McManus, A.P.1
Min, T.2
Swansbury, G.J.3
Gusterson, B.A.4
Pinkerton, C.R.5
Shipley, J.M.6
-
11
-
-
0023785269
-
Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16)
-
Mugneret F., Lizard S., Aurias A., and Turc-Carel C. Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16). Cancer Genet Cytogenet 32 (1988) 239-245
-
(1988)
Cancer Genet Cytogenet
, vol.32
, pp. 239-245
-
-
Mugneret, F.1
Lizard, S.2
Aurias, A.3
Turc-Carel, C.4
-
12
-
-
0025346123
-
A second nonrandom translocation der(16)t(1;16)(q21;q13) in Ewing's sarcoma and peripheral neuroectodermal tumor
-
Douglass E.C., Rowe S.T., Valentine M., Parham D., Meyer W.H., and Thompson E.I. A second nonrandom translocation der(16)t(1;16)(q21;q13) in Ewing's sarcoma and peripheral neuroectodermal tumor. Cytogenet Cell Genet 53 (1990) 87-90
-
(1990)
Cytogenet Cell Genet
, vol.53
, pp. 87-90
-
-
Douglass, E.C.1
Rowe, S.T.2
Valentine, M.3
Parham, D.4
Meyer, W.H.5
Thompson, E.I.6
-
13
-
-
0028817596
-
Translocation (1;16) identified by chromosome painting, and PRimed IN Situ-labeling (PRINS): report of two cases and review of the cytogenetic literature
-
Hindkjaer J., Hammoudah S.A.F.M., Bendix Hansen K., Jensen P.D., Koch J., and Pedersen B. Translocation (1;16) identified by chromosome painting, and PRimed IN Situ-labeling (PRINS): report of two cases and review of the cytogenetic literature. Cancer Genet Cytogenet 79 (1995) 15-20
-
(1995)
Cancer Genet Cytogenet
, vol.79
, pp. 15-20
-
-
Hindkjaer, J.1
Hammoudah, S.A.F.M.2
Bendix Hansen, K.3
Jensen, P.D.4
Koch, J.5
Pedersen, B.6
-
14
-
-
0029905059
-
Demonstration of the translocation der(16)t(1;16)(q12;q11.2) in interphase nuclei of Ewing tumors
-
Hattinger C.M., Rumpler S., Ambros I.M., Strehl S., Lion T., Zoubek A., Gadner H., and Ambros P.F. Demonstration of the translocation der(16)t(1;16)(q12;q11.2) in interphase nuclei of Ewing tumors. Genes Chromosomes Cancer 17 (1996) 141-150
-
(1996)
Genes Chromosomes Cancer
, vol.17
, pp. 141-150
-
-
Hattinger, C.M.1
Rumpler, S.2
Ambros, I.M.3
Strehl, S.4
Lion, T.5
Zoubek, A.6
Gadner, H.7
Ambros, P.F.8
-
15
-
-
8044259637
-
Additional chromosome 1q aberrations and der(16)t(1;16), correlation to the phenotypic expression and clinical behavior of the Ewing family of tumors
-
Stark B., Mor C., Jeison M., Gobuzov R., Cohen I.J., Goshen Y., Stein J., Fisher S., Ash S., Yaniv I., and Zaizov R. Additional chromosome 1q aberrations and der(16)t(1;16), correlation to the phenotypic expression and clinical behavior of the Ewing family of tumors. J Neurooncol 31 (1997) 3-8
-
(1997)
J Neurooncol
, vol.31
, pp. 3-8
-
-
Stark, B.1
Mor, C.2
Jeison, M.3
Gobuzov, R.4
Cohen, I.J.5
Goshen, Y.6
Stein, J.7
Fisher, S.8
Ash, S.9
Yaniv, I.10
Zaizov, R.11
-
16
-
-
0030683962
-
Der(16)t(1;16)(q21;q13) as a secondary structural aberration in yet a third sarcoma, extraskeleatl myxoid chondrosarcoma
-
Day S.J., Nelson M., Rosenthal H., Vergara G.G., and Bridge J.A. Der(16)t(1;16)(q21;q13) as a secondary structural aberration in yet a third sarcoma, extraskeleatl myxoid chondrosarcoma. Genes Chromosomes Cancer 20 (1997) 425-427
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 425-427
-
-
Day, S.J.1
Nelson, M.2
Rosenthal, H.3
Vergara, G.G.4
Bridge, J.A.5
-
17
-
-
0028798282
-
Cytogenetic and immunohistochemical profile of myxoid liposarcoma
-
Gibas Z., Miettinen M., Limon J., Nedoszytko B., Mrozek K., Roszkiewicz A., Rys J., Niezabitowski A., and Debiec-Rychter M. Cytogenetic and immunohistochemical profile of myxoid liposarcoma. Am J Clin Pathol 103 (1995) 20-26
-
(1995)
Am J Clin Pathol
, vol.103
, pp. 20-26
-
-
Gibas, Z.1
Miettinen, M.2
Limon, J.3
Nedoszytko, B.4
Mrozek, K.5
Roszkiewicz, A.6
Rys, J.7
Niezabitowski, A.8
Debiec-Rychter, M.9
-
18
-
-
0043066830
-
Inconspicuous insertion 22;12 in myxoid/round cell liposarcoma accompanied by the secondary structural abnormality der(16)t(1;16)
-
Birch N.C., Antonescu C.R., Nelson M., Sarran L., Neff J.R., Seemayer T., and Bridge J.A. Inconspicuous insertion 22;12 in myxoid/round cell liposarcoma accompanied by the secondary structural abnormality der(16)t(1;16). J Mol Diagn 5 (2003) 191-194
-
(2003)
J Mol Diagn
, vol.5
, pp. 191-194
-
-
Birch, N.C.1
Antonescu, C.R.2
Nelson, M.3
Sarran, L.4
Neff, J.R.5
Seemayer, T.6
Bridge, J.A.7
-
19
-
-
0141891868
-
Protocol for the examination of specimens from patients (children and adults) with rhabdomyosarcoma
-
Qualman S.J., Bowen J., Parham D.M., Branton P.A., and Meyer W.H. Protocol for the examination of specimens from patients (children and adults) with rhabdomyosarcoma. Arch Pathol Lab Med 127 (2003) 1290-1297
-
(2003)
Arch Pathol Lab Med
, vol.127
, pp. 1290-1297
-
-
Qualman, S.J.1
Bowen, J.2
Parham, D.M.3
Branton, P.A.4
Meyer, W.H.5
-
21
-
-
3042843645
-
Cytogenetic and molecular cytogenetic findings in 43 aneurysmal bone cysts: aberrations of 17p mapped to 17p13.2 by fluorescence in situ hybridization
-
Althof P.A., Ohmori K., Zhou M., Bailey J.M., Bridge R.S., Nelson M., Neff J.R., and Bridge J.A. Cytogenetic and molecular cytogenetic findings in 43 aneurysmal bone cysts: aberrations of 17p mapped to 17p13.2 by fluorescence in situ hybridization. Mod Pathol 17 (2004) 518-525
-
(2004)
Mod Pathol
, vol.17
, pp. 518-525
-
-
Althof, P.A.1
Ohmori, K.2
Zhou, M.3
Bailey, J.M.4
Bridge, R.S.5
Nelson, M.6
Neff, J.R.7
Bridge, J.A.8
-
23
-
-
33646884148
-
Use of a novel FISH assay on paraffin-embedded tissues as an adjunct to diagnosis of alveolar rhabdomyosarcoma
-
Nishio J., Althof P.A., Bailey J.M., Zhou M., Neff J.R., Barr F.G., Parham D.M., Teot L., Qualman S.J., and Bridge J.A. Use of a novel FISH assay on paraffin-embedded tissues as an adjunct to diagnosis of alveolar rhabdomyosarcoma. Lab Invest 86 (2006) 547-556
-
(2006)
Lab Invest
, vol.86
, pp. 547-556
-
-
Nishio, J.1
Althof, P.A.2
Bailey, J.M.3
Zhou, M.4
Neff, J.R.5
Barr, F.G.6
Parham, D.M.7
Teot, L.8
Qualman, S.J.9
Bridge, J.A.10
-
24
-
-
0031003597
-
Detection of gene fusions in rhabdomyosarcoma by reverse transcriptase-polymerase chain reaction assay of archival samples
-
Edwards R.H., Chatten J., Xiong Q.B., and Barr F.G. Detection of gene fusions in rhabdomyosarcoma by reverse transcriptase-polymerase chain reaction assay of archival samples. Diagn Mol Pathol 6 (1997) 91-97
-
(1997)
Diagn Mol Pathol
, vol.6
, pp. 91-97
-
-
Edwards, R.H.1
Chatten, J.2
Xiong, Q.B.3
Barr, F.G.4
-
25
-
-
0031902298
-
Der(16)t(1;16) is a secondary chromosome aberration in at least eighteen different types of human cancer
-
Mrozek K., and Bloomfield C.D. Der(16)t(1;16) is a secondary chromosome aberration in at least eighteen different types of human cancer. Genes Chromosomes Cancer 23 (1998) 78-80
-
(1998)
Genes Chromosomes Cancer
, vol.23
, pp. 78-80
-
-
Mrozek, K.1
Bloomfield, C.D.2
-
26
-
-
0028899822
-
Der(16)t(1;16) is a nonrandom secondary chromosome aberration in many types of human neoplasia, including myxoid liposarcoma, rhabdomyosarcoma and Philadelphia chromosome-positive acute lymphoblastic leukemia
-
Mrozek K., Arthur D.C., Karakousis C.P., Koduru P.R.K., Le Beau M.M., Pettenati M.J., Tantravahi R., Mrozek E., Perez-Mesa C., Rao U.N.M., Frankel S.R., Davey F.R., and Bloomfield C.D. Der(16)t(1;16) is a nonrandom secondary chromosome aberration in many types of human neoplasia, including myxoid liposarcoma, rhabdomyosarcoma and Philadelphia chromosome-positive acute lymphoblastic leukemia. Int J Oncol 6 (1995) 531-538
-
(1995)
Int J Oncol
, vol.6
, pp. 531-538
-
-
Mrozek, K.1
Arthur, D.C.2
Karakousis, C.P.3
Koduru, P.R.K.4
Le Beau, M.M.5
Pettenati, M.J.6
Tantravahi, R.7
Mrozek, E.8
Perez-Mesa, C.9
Rao, U.N.M.10
Frankel, S.R.11
Davey, F.R.12
Bloomfield, C.D.13
-
28
-
-
0029097446
-
Comparative genomic hybridization analysis of human sarcomas: I. Occurrence of genomic imbalances and identification of a novel major amplicon at 1q21-q22 in soft tissue sarcomas
-
Forus A., Weghuis D.O., Smeets D., Fodstad O., Myklebost O., and Guerts van Kessel A. Comparative genomic hybridization analysis of human sarcomas: I. Occurrence of genomic imbalances and identification of a novel major amplicon at 1q21-q22 in soft tissue sarcomas. Genes Chromosomes Cancer 14 (1995) 8-14
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 8-14
-
-
Forus, A.1
Weghuis, D.O.2
Smeets, D.3
Fodstad, O.4
Myklebost, O.5
Guerts van Kessel, A.6
-
29
-
-
0031858675
-
Molecular characterization of a novel amplicon at 1q21-q22 frequently observed in human sarcomas
-
Forus A., Berner J.M., Meza-Zepeda L.A., Saeter G., Mischke D., Fodstad O., and Myklebost O. Molecular characterization of a novel amplicon at 1q21-q22 frequently observed in human sarcomas. Br J Cancer 78 (1998) 495-503
-
(1998)
Br J Cancer
, vol.78
, pp. 495-503
-
-
Forus, A.1
Berner, J.M.2
Meza-Zepeda, L.A.3
Saeter, G.4
Mischke, D.5
Fodstad, O.6
Myklebost, O.7
-
30
-
-
0034018449
-
A novel and consistent amplicon at 13q31 associated with alveolar rhabdomyosarcoma
-
Gordon A.T., Brinkschmidt C., Anderson J., Coleman N., Dockhorn-Dworniczak B., Pritchard-Jones K., and Shipley J. A novel and consistent amplicon at 13q31 associated with alveolar rhabdomyosarcoma. Genes Chromosomes Cancer 28 (2000) 220-226
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 220-226
-
-
Gordon, A.T.1
Brinkschmidt, C.2
Anderson, J.3
Coleman, N.4
Dockhorn-Dworniczak, B.5
Pritchard-Jones, K.6
Shipley, J.7
-
31
-
-
1342267079
-
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
-
Nilsson M., Meza-Zepeda L.A., Mertens F., Forus A., Myklebost O., and Mandahl N. Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas. Int J Cancer 109 (2004) 363-369
-
(2004)
Int J Cancer
, vol.109
, pp. 363-369
-
-
Nilsson, M.1
Meza-Zepeda, L.A.2
Mertens, F.3
Forus, A.4
Myklebost, O.5
Mandahl, N.6
-
32
-
-
27944448457
-
Mapping and characterization of the amplicon near APOA2 in 1q23 in human sarcomas by FISH and array CGH
-
Kresse S.H., Berner J.M., Meza-Zepeda L.A., Gregory S.G., Kuo W.L., Gray J.W., Forus A., and Myklebost O. Mapping and characterization of the amplicon near APOA2 in 1q23 in human sarcomas by FISH and array CGH. Mol Cancer 4 (2005) 39
-
(2005)
Mol Cancer
, vol.4
, pp. 39
-
-
Kresse, S.H.1
Berner, J.M.2
Meza-Zepeda, L.A.3
Gregory, S.G.4
Kuo, W.L.5
Gray, J.W.6
Forus, A.7
Myklebost, O.8
-
33
-
-
0030962761
-
Allelotype of pediatric rhabdomyosarcoma
-
Visser M., Sijmons C., Bras J., Arceci R.J., Godfried M., Valentijn L.J., Voute P.A., and Baas F. Allelotype of pediatric rhabdomyosarcoma. Oncogene 15 (1997) 1309-1314
-
(1997)
Oncogene
, vol.15
, pp. 1309-1314
-
-
Visser, M.1
Sijmons, C.2
Bras, J.3
Arceci, R.J.4
Godfried, M.5
Valentijn, L.J.6
Voute, P.A.7
Baas, F.8
-
34
-
-
33646591281
-
Chromosome 16 tumor-suppressor genes in breast cancer
-
Rakha E.A., Green A.R., Powe D.G., Roylance R., and Ellias I.O. Chromosome 16 tumor-suppressor genes in breast cancer. Genes Chromosomes Cancer 45 (2006) 527-535
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 527-535
-
-
Rakha, E.A.1
Green, A.R.2
Powe, D.G.3
Roylance, R.4
Ellias, I.O.5
-
35
-
-
2442707675
-
Integration of high-resolution array comparative genomic hybridization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23-qter and identifies underlying candidate tumor suppressor genes in prostate cancer
-
Watson J.E.V., Doggett N.A., Albertson D.G., Andaya A., Chinnaiyan A., Van Dekken H., Ginzinger D., Haqq C., James K., Kamkar S., Kowbel D., Pinkel D., Schmitt L., Simko J.P., Volik S., Weinberg V.K., Paris P.L., and Collins C. Integration of high-resolution array comparative genomic hybridization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23-qter and identifies underlying candidate tumor suppressor genes in prostate cancer. Oncogene 23 (2004) 3487-3494
-
(2004)
Oncogene
, vol.23
, pp. 3487-3494
-
-
Watson, J.E.V.1
Doggett, N.A.2
Albertson, D.G.3
Andaya, A.4
Chinnaiyan, A.5
Van Dekken, H.6
Ginzinger, D.7
Haqq, C.8
James, K.9
Kamkar, S.10
Kowbel, D.11
Pinkel, D.12
Schmitt, L.13
Simko, J.P.14
Volik, S.15
Weinberg, V.K.16
Paris, P.L.17
Collins, C.18
-
36
-
-
0035360824
-
Loss of expression and aberrant methylation of the CDH13 (H-cadherin) gene in breast and lung cancers
-
Toyooka K.O., Toyooka S., Virmani A.K., Sathyanarayana U.G., Euhus D.M., Gilcrease M., Minna J.D., and Gazdar A.F. Loss of expression and aberrant methylation of the CDH13 (H-cadherin) gene in breast and lung cancers. Cancer Res 61 (2001) 4556-4560
-
(2001)
Cancer Res
, vol.61
, pp. 4556-4560
-
-
Toyooka, K.O.1
Toyooka, S.2
Virmani, A.K.3
Sathyanarayana, U.G.4
Euhus, D.M.5
Gilcrease, M.6
Minna, J.D.7
Gazdar, A.F.8
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