-
1
-
-
0032080482
-
Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas
-
Bridge J.A., Nelson M., Orndal C., Bhatia P., Neff J.R. Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas. Cancer. 82:1998;1657-1663.
-
(1998)
Cancer
, vol.82
, pp. 1657-1663
-
-
Bridge, J.A.1
Nelson, M.2
Orndal, C.3
Bhatia, P.4
Neff, J.R.5
-
2
-
-
0028091147
-
Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses
-
Mertens F., Rydholm A., Kreicbergs A., Willen H., Jonsson K., Heim S., Mitelman F., Mandahl N. Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses. Genes Chromosomes Cancer. 9:1994;8-12.
-
(1994)
Genes Chromosomes Cancer
, vol.9
, pp. 8-12
-
-
Mertens, F.1
Rydholm, A.2
Kreicbergs, A.3
Willen, H.4
Jonsson, K.5
Heim, S.6
Mitelman, F.7
Mandahl, N.8
-
3
-
-
0034020664
-
Recurrent anomalies of 6q25 in chondromyxoid fibroma
-
Safar A., Nelson M., Neff J.R., Maale G.E., Bayani J., Squire J., Bridge J.A. Recurrent anomalies of 6q25 in chondromyxoid fibroma. Hum Pathol. 31:2000;306-311.
-
(2000)
Hum Pathol
, vol.31
, pp. 306-311
-
-
Safar, A.1
Nelson, M.2
Neff, J.R.3
Maale, G.E.4
Bayani, J.5
Squire, J.6
Bridge, J.A.7
-
4
-
-
0036752209
-
Cytogenetic and molecular cytogenetic evidence of recurrent 8q24.1 loss in osteochondroma
-
Feely M.G., Boehm A.K., Bridge R.S., Krallman P.A., Neff J.R., Nelson M., Bridge J.A. Cytogenetic and molecular cytogenetic evidence of recurrent 8q24.1 loss in osteochondroma. Cancer Genet Cytogenet. 137(2):2002;102-107.
-
(2002)
Cancer Genet Cytogenet
, vol.137
, Issue.2
, pp. 102-107
-
-
Feely, M.G.1
Boehm, A.K.2
Bridge, R.S.3
Krallman, P.A.4
Neff, J.R.5
Nelson, M.6
Bridge, J.A.7
-
5
-
-
0032006991
-
Evidence of an association between 6q13-21 chromosome aberrations and locally aggressive behavior in patients with cartilage tumors
-
Sawyer J.R., Swanson C.M., Lukacs J.L., Nicholas R.W., North P.E., Thomas J.R. Evidence of an association between 6q13-21 chromosome aberrations and locally aggressive behavior in patients with cartilage tumors. Cancer. 82:1998;474-483.
-
(1998)
Cancer
, vol.82
, pp. 474-483
-
-
Sawyer, J.R.1
Swanson, C.M.2
Lukacs, J.L.3
Nicholas, R.W.4
North, P.E.5
Thomas, J.R.6
-
7
-
-
0025707275
-
Chromosomal rearrangements in chondromatous tumors
-
Mandahl N., Heim S., Arheden K., Rydholm A., Willen H., Mitelman F. Chromosomal rearrangements in chondromatous tumors. Cancer. 65:1990;242-248.
-
(1990)
Cancer
, vol.65
, pp. 242-248
-
-
Mandahl, N.1
Heim, S.2
Arheden, K.3
Rydholm, A.4
Willen, H.5
Mitelman, F.6
-
8
-
-
0032527876
-
Solitary enchondroma with clonal chromosomal abnormalities
-
Gunawan B., Weber M., Bergmann F., Wildberger J., Fuzesi L. Solitary enchondroma with clonal chromosomal abnormalities. Cancer Genet Cytogenet. 104:1998;161-164.
-
(1998)
Cancer Genet Cytogenet
, vol.104
, pp. 161-164
-
-
Gunawan, B.1
Weber, M.2
Bergmann, F.3
Wildberger, J.4
Fuzesi, L.5
-
9
-
-
0036156440
-
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group
-
Tallini G., Dorfman H., Brys P., Dal Cin P., de Wever I., Fletcher C.D., Jonson K., Mandahl N., Mertens F., Mitelman F., Rosai J., Rydholm A., Samson I., Sciot R., Van den Bergh H., Vanni R., Willen H. Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. J Pathol. 196:2002;194-203.
-
(2002)
J Pathol
, vol.196
, pp. 194-203
-
-
Tallini, G.1
Dorfman, H.2
Brys, P.3
Dal Cin, P.4
De Wever, I.5
Fletcher, C.D.6
Jonson, K.7
Mandahl, N.8
Mertens, F.9
Mitelman, F.10
Rosai, J.11
Rydholm, A.12
Samson, I.13
Sciot, R.14
Van den Bergh, H.15
Vanni, R.16
Willen, H.17
-
10
-
-
0027422876
-
Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions
-
Bridge J.A., Bhatia P.S., Anderson J.R., Neff J.R. Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions. Cancer Genet Cytogenet. 69:1993;79-90.
-
(1993)
Cancer Genet Cytogenet
, vol.69
, pp. 79-90
-
-
Bridge, J.A.1
Bhatia, P.S.2
Anderson, J.R.3
Neff, J.R.4
-
12
-
-
0027472230
-
Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma
-
Mandahl N., Willen H., Rydholm A., Heim S., Mitelman F. Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma. Genes Chromosomes Cancer. 6:1993;121-123.
-
(1993)
Genes Chromosomes Cancer
, vol.6
, pp. 121-123
-
-
Mandahl, N.1
Willen, H.2
Rydholm, A.3
Heim, S.4
Mitelman, F.5
-
13
-
-
0034656173
-
Supernumerary ring chromosomes derived from the long arm of chromosome 12 as the primary cytogenetic anomaly in a rare soft tissue chondroma
-
Shadan F.F., Mascarello J.T., Newbury R.O., Dennis T., Spallone P., Stock A.D. Supernumerary ring chromosomes derived from the long arm of chromosome 12 as the primary cytogenetic anomaly in a rare soft tissue chondroma. Cancer Genet Cytogenet. 118:2000;144-147.
-
(2000)
Cancer Genet Cytogenet
, vol.118
, pp. 144-147
-
-
Shadan, F.F.1
Mascarello, J.T.2
Newbury, R.O.3
Dennis, T.4
Spallone, P.5
Stock, A.D.6
-
15
-
-
0031728109
-
The pericentromeric inversion, inv (6)(p25q13), is a novel diagnostic marker in chondromyxoid fibroma
-
Granter S.R., Renshaw A.A., Kozakewich H.P., Fletcher J.A. The pericentromeric inversion, inv (6)(p25q13), is a novel diagnostic marker in chondromyxoid fibroma. Mod Pathol. 11:1998;1071-1074.
-
(1998)
Mod Pathol
, vol.11
, pp. 1071-1074
-
-
Granter, S.R.1
Renshaw, A.A.2
Kozakewich, H.P.3
Fletcher, J.A.4
-
16
-
-
0036144612
-
Cytogenetic aberrations and their prognostic impact in chondrosarcoma
-
Mandahl N., Gustafson P., Mertens F., Akerman M., Baldetorp B., Gisselsson D., Knuutila S., Bauer H.C., Larsson O. Cytogenetic aberrations and their prognostic impact in chondrosarcoma. Genes Chromosomes Cancer. 33:2002;188-200.
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 188-200
-
-
Mandahl, N.1
Gustafson, P.2
Mertens, F.3
Akerman, M.4
Baldetorp, B.5
Gisselsson, D.6
Knuutila, S.7
Bauer, H.C.8
Larsson, O.9
-
17
-
-
0033870238
-
Online access to CGH data of DNA sequence copy number changes
-
Knuutila S., Autio K., Aalto Y. Online access to CGH data of DNA sequence copy number changes. Am J Pathol. 157:2000;689.
-
(2000)
Am J Pathol
, vol.157
, pp. 689
-
-
Knuutila, S.1
Autio, K.2
Aalto, Y.3
-
18
-
-
0030928950
-
Identification of a zinc-finger gene at 6q25: A chromosomal region implicated in development of many solid tumors
-
Abdollahi A., Roberts D., Godwin A.K., Schultz D.C., Sonoda G., Testa J.R., Hamilton T.C. Identification of a zinc-finger gene at 6q25. a chromosomal region implicated in development of many solid tumors Oncogene. 14:1997;1973-1979.
-
(1997)
Oncogene
, vol.14
, pp. 1973-1979
-
-
Abdollahi, A.1
Roberts, D.2
Godwin, A.K.3
Schultz, D.C.4
Sonoda, G.5
Testa, J.R.6
Hamilton, T.C.7
-
19
-
-
0033547301
-
LOT1 is a growth suppressor gene down-regulated by the epidermal growth factor receptor ligands and encodes a nuclear zinc-finger protein
-
Abdollahi A., Bao R., Hamilton T.C. LOT1 is a growth suppressor gene down-regulated by the epidermal growth factor receptor ligands and encodes a nuclear zinc-finger protein. Oncogene. 18:1999;6477-6487.
-
(1999)
Oncogene
, vol.18
, pp. 6477-6487
-
-
Abdollahi, A.1
Bao, R.2
Hamilton, T.C.3
-
20
-
-
0031006549
-
AIM1, a novel non-lens member of the betagamma-crystallin superfamily, is associated with the control of tumorigenicity in human malignant melanoma
-
Ray M.E., Wistow G., Su Y.A., Meltzer P.S., Trent J.M. AIM1, a novel non-lens member of the betagamma-crystallin superfamily, is associated with the control of tumorigenicity in human malignant melanoma. Proc Natl Acad Sci USA. 94:1997;3229-3234.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 3229-3234
-
-
Ray, M.E.1
Wistow, G.2
Su, Y.A.3
Meltzer, P.S.4
Trent, J.M.5
-
21
-
-
18244383816
-
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma
-
Gisselsson D., Palsson E., Hoglund M., Domanski H., Mertens F., Pandis N., Sciot R., Dal Cin P., Bridge J.A., Mandahl N. Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma. Genes Chromosomes Cancer. 33:2002;133-140.
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 133-140
-
-
Gisselsson, D.1
Palsson, E.2
Hoglund, M.3
Domanski, H.4
Mertens, F.5
Pandis, N.6
Sciot, R.7
Dal Cin, P.8
Bridge, J.A.9
Mandahl, N.10
-
22
-
-
0033590604
-
Co-amplification and overexpression of CDK4, SAS and MDM2 occurs frequently in human parosteal osteosarcomas
-
Wunder J.S., Eppert K., Burrow S.R., Gokgoz N., Bell R.S., Andrulis I.L., Gogkoz N. Co-amplification and overexpression of CDK4, SAS and MDM2 occurs frequently in human parosteal osteosarcomas. Oncogene. 18:1999;783-788.
-
(1999)
Oncogene
, vol.18
, pp. 783-788
-
-
Wunder, J.S.1
Eppert, K.2
Burrow, S.R.3
Gokgoz, N.4
Bell, R.S.5
Andrulis, I.L.6
Gogkoz, N.7
-
23
-
-
0027508958
-
MDM2 gene amplification in metastatic osteosarcoma
-
Ladanyi M., Cha C., Lewis R., Jhanwar S.C., Huvos A.G., Healey J.H. MDM2 gene amplification in metastatic osteosarcoma. Cancer Res. 53:1993;16-18.
-
(1993)
Cancer Res
, vol.53
, pp. 16-18
-
-
Ladanyi, M.1
Cha, C.2
Lewis, R.3
Jhanwar, S.C.4
Huvos, A.G.5
Healey, J.H.6
-
24
-
-
0031689788
-
Clinicopathologic implications of MDM2, p53 and K-ras gene alterations in osteosarcomas: MDM2 amplification and p53 mutations found in progressive tumors
-
Yokoyama R., Schneider-Stock R., Radig K., Wex T., Roessner A. Clinicopathologic implications of MDM2, p53 and K-ras gene alterations in osteosarcomas. MDM2 amplification and p53 mutations found in progressive tumors Pathol Res Pract. 194:1998;615-621.
-
(1998)
Pathol Res Pract
, vol.194
, pp. 615-621
-
-
Yokoyama, R.1
Schneider-Stock, R.2
Radig, K.3
Wex, T.4
Roessner, A.5
-
25
-
-
0029088063
-
Recurrent rearrangements in the high mobility group protein gene, HMGI- C, in benign mesenchymal tumours
-
Schoenmakers E.F., Wanschura S., Mols R., Bullerdiek J., Van den Bergh H., Van de Ven W.J. Recurrent rearrangements in the high mobility group protein gene, HMGI- C, in benign mesenchymal tumours. Nat Genet. 10:1995;436-444.
-
(1995)
Nat Genet
, vol.10
, pp. 436-444
-
-
Schoenmakers, E.F.1
Wanschura, S.2
Mols, R.3
Bullerdiek, J.4
Van den Bergh, H.5
Van de Ven, W.J.6
-
26
-
-
0026621537
-
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)
-
Aman P., Ron D., Mandahl N., Fioretos T., Heim S., Arheden K., Willen H., Rydholm A., Mitelman F. Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11). Genes Chromosomes Cancer. 5:1992;278-285.
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 278-285
-
-
Aman, P.1
Ron, D.2
Mandahl, N.3
Fioretos, T.4
Heim, S.5
Arheden, K.6
Willen, H.7
Rydholm, A.8
Mitelman, F.9
-
27
-
-
0027183108
-
EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts
-
Zucman J., Delattre O., Desmaze C., Epstein A.L., Stenman G., Speleman F., Fletchers C.D., Aurias A., Thomas G. EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts. Nat Genet. 4:1993;341-345.
-
(1993)
Nat Genet
, vol.4
, pp. 341-345
-
-
Zucman, J.1
Delattre, O.2
Desmaze, C.3
Epstein, A.L.4
Stenman, G.5
Speleman, F.6
Fletchers, C.D.7
Aurias, A.8
Thomas, G.9
-
28
-
-
0344573926
-
Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group
-
Fletcher C.D., Dal Cin P., de Wever I., Mandahl N., Mertens F., Mitelman F., Rosai J., Rydholm A., Sciot R., Tallini G., Van den Bergh H., Vanni R., Willen H. Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. Am J Pathol. 154:1999;1841-1847.
-
(1999)
Am J Pathol
, vol.154
, pp. 1841-1847
-
-
Fletcher, C.D.1
Dal Cin, P.2
De Wever, I.3
Mandahl, N.4
Mertens, F.5
Mitelman, F.6
Rosai, J.7
Rydholm, A.8
Sciot, R.9
Tallini, G.10
Van den Bergh, H.11
Vanni, R.12
Willen, H.13
-
29
-
-
0026647561
-
Chromosome rearrangements at 12q13 in two cases of chondrosarcomas
-
Hirabayashi Y., Yoshida M.A., Ikeuchi T., Ishida T., Kojima T., Higaki S., Machinami R., Tonomura A. Chromosome rearrangements at 12q13 in two cases of chondrosarcomas. Cancer Genet Cytogenet. 60:1992;35-40.
-
(1992)
Cancer Genet Cytogenet
, vol.60
, pp. 35-40
-
-
Hirabayashi, Y.1
Yoshida, M.A.2
Ikeuchi, T.3
Ishida, T.4
Kojima, T.5
Higaki, S.6
Machinami, R.7
Tonomura, A.8
-
30
-
-
0027429622
-
Chromosome aberrations and cytogenetic intratumor heterogeneity in chondrosarcomas
-
Orndal C., Mandahl N., Rydholm A., Willen H., Brosjo O., Mitelman F. Chromosome aberrations and cytogenetic intratumor heterogeneity in chondrosarcomas. J Cancer Res Clin Oncol. 120:1993;51-56.
-
(1993)
J Cancer Res Clin Oncol
, vol.120
, pp. 51-56
-
-
Orndal, C.1
Mandahl, N.2
Rydholm, A.3
Willen, H.4
Brosjo, O.5
Mitelman, F.6
-
31
-
-
0028029732
-
Cytogenetic findings in 19 malignant bone tumors
-
Ozisik Y.Y., Meloni A.M., Peier A., Altungoz O., Spanier S.S., Zalupski M.M., Leong S.P., Sandberg A.A. Cytogenetic findings in 19 malignant bone tumors. Cancer. 74:1994;2268-2275.
-
(1994)
Cancer
, vol.74
, pp. 2268-2275
-
-
Ozisik, Y.Y.1
Meloni, A.M.2
Peier, A.3
Altungoz, O.4
Spanier, S.S.5
Zalupski, M.M.6
Leong, S.P.7
Sandberg, A.A.8
-
32
-
-
0002945571
-
Extraskeletal and skeletal myxoid chondrosarcoma: A multiparameter analysis of three cases including cytogenetic analysis and fluorescence in situ hybridization
-
Rao U.N., Surti U., Hoffner L., Howard T., Leger W., Contis L., Yaw K. Extraskeletal and skeletal myxoid chondrosarcoma. a multiparameter analysis of three cases including cytogenetic analysis and fluorescence in situ hybridization Mol Diagn. 1:1996;99-107.
-
(1996)
Mol Diagn
, vol.1
, pp. 99-107
-
-
Rao, U.N.1
Surti, U.2
Hoffner, L.3
Howard, T.4
Leger, W.5
Contis, L.6
Yaw, K.7
-
33
-
-
0030987571
-
Chromosomal abnormalities in low grade chondrosarcoma and a review of the literature
-
Swarts S.J., Neff J.R., Nelson M., Johansson S., Bridge J.A. Chromosomal abnormalities in low grade chondrosarcoma and a review of the literature. Cancer Genet Cytogenet. 98:1997;126-130.
-
(1997)
Cancer Genet Cytogenet
, vol.98
, pp. 126-130
-
-
Swarts, S.J.1
Neff, J.R.2
Nelson, M.3
Johansson, S.4
Bridge, J.A.5
-
34
-
-
0036095457
-
Translocation der(13;21)(q10;q10) in Skeletal and Extraskeletal Mesenchymal Chondrosarcoma
-
Naumann S., Krallman P.A., Unni K.K., Fidler M.E., Neff J.R. Translocation der(13;21)(q10;q10) in Skeletal and Extraskeletal Mesenchymal Chondrosarcoma. Mod Pathol. 15:2002;572-576.
-
(2002)
Mod Pathol
, vol.15
, pp. 572-576
-
-
Naumann, S.1
Krallman, P.A.2
Unni, K.K.3
Fidler, M.E.4
Neff, J.R.5
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