-
1
-
-
2642614615
-
-
Thesis. Brisbane, Queensland, Australia: University of Queensland
-
Leonard, J. H. Biology of Merkel cell carcinoma (Thesis). Brisbane, Queensland, Australia: University of Queensland, 1997.
-
(1997)
Biology of Merkel Cell Carcinoma
-
-
Leonard, J.H.1
-
2
-
-
0021880983
-
Biology of disease, neuroendocrine (Merkel) cells of the skin: Hyperplasias, dysplasias and neoplasms
-
Gould, V. E., Moll, R., Moll, I., Lee, I., and Franke, W. W. Biology of disease, neuroendocrine (Merkel) cells of the skin: hyperplasias, dysplasias and neoplasms. Lab. Invest., 52: 334-353, 1985.
-
(1985)
Lab. Invest.
, vol.52
, pp. 334-353
-
-
Gould, V.E.1
Moll, R.2
Moll, I.3
Lee, I.4
Franke, W.W.5
-
3
-
-
0028832033
-
Radiation therapy in the treatment of Merkel cell carcinoma
-
Meeuwissen, J. A., Bourne, R. G., and Kearsley, J. H. Radiation therapy in the treatment of Merkel cell carcinoma. Int. J. Radiat. Oncol. Biol. Phys., 15: 325-331, 1995.
-
(1995)
Int. J. Radiat. Oncol. Biol. Phys.
, vol.15
, pp. 325-331
-
-
Meeuwissen, J.A.1
Bourne, R.G.2
Kearsley, J.H.3
-
4
-
-
0022615480
-
Cytogenetic study of a Merkel cell carcinoma
-
Kusyk, C. J., and Romsdahl, M. M. Cytogenetic study of a Merkel cell carcinoma. Cancer Genet. Cytogenet., 20: 311-316, 1986.
-
(1986)
Cancer Genet. Cytogenet.
, vol.20
, pp. 311-316
-
-
Kusyk, C.J.1
Romsdahl, M.M.2
-
5
-
-
17744419604
-
Tumeur neuroendocrine de la peau. Mise en évidence d'anomalies chromosomiques dans les cellules tumorales
-
Hopfner, C., Teyssier, J. R., Eychenne, D., Lesaunier, F., Nollez, F., and Adnet, J. J. Tumeur neuroendocrine de la peau. Mise en évidence d'anomalies chromosomiques dans les cellules tumorales. Presse Med, 16: 731, 1987.
-
(1987)
Presse Med
, vol.16
, pp. 731
-
-
Hopfner, C.1
Teyssier, J.R.2
Eychenne, D.3
Lesaunier, F.4
Nollez, F.5
Adnet, J.J.6
-
6
-
-
0023238786
-
Establishment, and characterization of a neuroendocrine skin carcinoma cell line
-
Rosen, S. T., Gould, V. E., Salwen, H. R., Herst, C. V., Le Beau, M. M., Lee, I., Bauer, K., Marder, R. J., Andersen, R., Kies, M. S., Moll, R., Franke, W. W., and Radosevich, J. A. Establishment, and characterization of a neuroendocrine skin carcinoma cell line. Lab. Invest., 56. 302-312, 1987.
-
(1987)
Lab. Invest.
, vol.56
, pp. 302-312
-
-
Rosen, S.T.1
Gould, V.E.2
Salwen, H.R.3
Herst, C.V.4
Le Beau, M.M.5
Lee, I.6
Bauer, K.7
Marder, R.J.8
Andersen, R.9
Kies, M.S.10
Moll, R.11
Franke, W.W.12
Radosevich, J.A.13
-
7
-
-
0023854206
-
Cytogenetic studies in primary and metastatic neuroendocrine Merkel cell carcinoma
-
Sozzi, G., Bertoglio, M. G., Pilotti, S., Rilke, F., Pierotti, M. A., and Porta, G. D. Cytogenetic studies in primary and metastatic neuroendocrine Merkel cell carcinoma. Cancer Genet. Cytogenet., 30: 151-158, 1988.
-
(1988)
Cancer Genet. Cytogenet.
, vol.30
, pp. 151-158
-
-
Sozzi, G.1
Bertoglio, M.G.2
Pilotti, S.3
Rilke, F.4
Pierotti, M.A.5
Porta, G.D.6
-
8
-
-
0023730731
-
Short communication: Deletion 7q, trisomy 6 and 11 in a case of Merkel cell carcinoma
-
Sandbrick, F., Müller, L., Fiebig, H. H., and Kovacs, G. Short communication: deletion 7q, trisomy 6 and 11 in a case of Merkel cell carcinoma. Cancer Genet. Cytogenet., 33: 305-309: 1988.
-
(1988)
Cancer Genet. Cytogenet.
, vol.33
, pp. 305-309
-
-
Sandbrick, F.1
Müller, L.2
Fiebig, H.H.3
Kovacs, G.4
-
9
-
-
0024517677
-
Involvement of chromosome 22 in a Merkel cell carcinoma in a patient with previous meningioma
-
Shabtai, F., Sternberg, A., Klar, D., Reiss, R., and Halbrecht, I. Involvement of chromosome 22 in a Merkel cell carcinoma in a patient with previous meningioma. Cancer Genet. Cytogenet., 38: 43-48: 1989.
-
(1989)
Cancer Genet. Cytogenet.
, vol.38
, pp. 43-48
-
-
Shabtai, F.1
Sternberg, A.2
Klar, D.3
Reiss, R.4
Halbrecht, I.5
-
10
-
-
0024419917
-
Non random cytogenetic changes characterize Merkel cell carcinoma
-
Koduru, P. R., Dicostanzo, D. P., Jhanwar S. C. Non random cytogenetic changes characterize Merkel cell carcinoma. Dis. Markers, 7: 153-161, 1989.
-
(1989)
Dis. Markers
, vol.7
, pp. 153-161
-
-
Koduru, P.R.1
Dicostanzo, D.P.2
Jhanwar, S.C.3
-
11
-
-
0026027661
-
Cytogenetic study in a bone marrow metastatic Merkel cell carcinoma
-
Smadja, N., de Gramont, A., Gonzalez-Canali, G., Louvet, C., Wattel, E., and Krulik, M. Cytogenetic study in a bone marrow metastatic Merkel cell carcinoma. Cancer Genet. Cytogenet., 51: 85-87, 1991.
-
(1991)
Cancer Genet. Cytogenet.
, vol.51
, pp. 85-87
-
-
Smadja, N.1
De Gramont, A.2
Gonzalez-Canali, G.3
Louvet, C.4
Wattel, E.5
Krulik, M.6
-
12
-
-
0027156440
-
Chromosomes 1, 11 and 13 are frequently involved in karyotypic abnormalities seen in metastatic Merkel cell carcinoma
-
Leonard, J. H., Leonard, P., and Kearsley, J. H. Chromosomes 1, 11 and 13 are frequently involved in karyotypic abnormalities seen in metastatic Merkel cell carcinoma. Cancer Genet. Cytogenet., 67: 65-70, 1993.
-
(1993)
Cancer Genet. Cytogenet.
, vol.67
, pp. 65-70
-
-
Leonard, J.H.1
Leonard, P.2
Kearsley, J.H.3
-
13
-
-
0028128254
-
Chromosomal evolution in a Merkel cell carcinoma
-
Schlegelberger, B., Bartels, H., and Sterry, W. Chromosomal evolution in a Merkel cell carcinoma. Cancer Genet. Cytogenet., 75: 74-76, 1994.
-
(1994)
Cancer Genet. Cytogenet.
, vol.75
, pp. 74-76
-
-
Schlegelberger, B.1
Bartels, H.2
Sterry, W.3
-
14
-
-
0028211586
-
Deletion of chromosome arm 1p in a Merkel cell carcinoma (MCC)
-
Gibas, Z., Weil, S., Chen, S. T., and McCue, P. A. Deletion of chromosome arm 1p in a Merkel cell carcinoma (MCC). Genes Chromosomes Cancer, 9: 216-220, 1994.
-
(1994)
Genes Chromosomes Cancer
, vol.9
, pp. 216-220
-
-
Gibas, Z.1
Weil, S.2
Chen, S.T.3
McCue, P.A.4
-
15
-
-
0028125273
-
Merkel cell carcinoma. Histopathology, immunohistochemistry, and cytogenetic analysis
-
Tope, W. D., and Sangüeza, A. P. Merkel cell carcinoma. Histopathology, immunohistochemistry, and cytogenetic analysis. Dermatol, Surg. Oncol., 20: 648-652, 1994.
-
(1994)
Dermatol, Surg. Oncol.
, vol.20
, pp. 648-652
-
-
Tope, W.D.1
Sangüeza, A.P.2
-
16
-
-
0029791365
-
Chromosome 6 trisomy as sole anomaly in a primary Merkel cell carcinoma
-
Larsimont, D., and Verhest, A. Chromosome 6 trisomy as sole anomaly in a primary Merkel cell carcinoma. Virchows Arch., 428: 305-309, 1996.
-
(1996)
Virchows Arch.
, vol.428
, pp. 305-309
-
-
Larsimont, D.1
Verhest, A.2
-
17
-
-
0030294876
-
Cytogenetic study of neuroendocrine carcinoma of Merkel cells
-
Vasquez-Mazariego, Y., Vallcorba, I., Ferro, M. T., Lopez-Yarto, A., Garcia-Sagredo, J. M., Cabello, P., Resino, M., Munoz, R., Mayayo, M., and San Roman C. Cytogenetic study of neuroendocrine carcinoma of Merkel cells. Cancer Genet. Cytogenet., 92: 79-81, 1996.
-
(1996)
Cancer Genet. Cytogenet.
, vol.92
, pp. 79-81
-
-
Vasquez-Mazariego, Y.1
Vallcorba, I.2
Ferro, M.T.3
Lopez-Yarto, A.4
Garcia-Sagredo, J.M.5
Cabello, P.6
Resino, M.7
Munoz, R.8
Mayayo, M.9
San Roman, C.10
-
18
-
-
0027368906
-
Merkel cell carcinoma: In vitro and in vivo characteristics of a new cell line
-
Ronan, S. G., Green, A. D., Shilkaitis, A., Huang, T. S. W., and Das Gupta, T. K. Merkel cell carcinoma: in vitro and in vivo characteristics of a new cell line. J. Am. Acad. Dermatol., 29: 715-722, 1993.
-
(1993)
J. Am. Acad. Dermatol.
, vol.29
, pp. 715-722
-
-
Ronan, S.G.1
Green, A.D.2
Shilkaitis, A.3
Huang, T.S.W.4
Das Gupta, T.K.5
-
19
-
-
0025633279
-
Primary culture of cells arising from a neuroendocrine skin carcinoma
-
English, K. B., Hammond, E. H., and Stayner, N. Primary culture of cells arising from a neuroendocrine skin carcinoma. Am. J. Dermatol., 12: 589-597, 1990.
-
(1990)
Am. J. Dermatol.
, vol.12
, pp. 589-597
-
-
English, K.B.1
Hammond, E.H.2
Stayner, N.3
-
20
-
-
0028316009
-
Establishment and characterization of two Merkel cell tumor cultures
-
Moll, I., Bohnert, E., Herbst, C., Förster, W., Moll, R., and Franke, W. W. Establishment and characterization of two Merkel cell tumor cultures. J. Invest. Dermatol., 102: 346-353, 1994.
-
(1994)
J. Invest. Dermatol.
, vol.102
, pp. 346-353
-
-
Moll, I.1
Bohnert, E.2
Herbst, C.3
Förster, W.4
Moll, R.5
Franke, W.W.6
-
21
-
-
0030039683
-
Deletion mapping of the short arm of chromosome 3 in Merkel cell carcinoma
-
Leonard, J. H., Williams, G., Walters, M. K., Nancarrow, D. J., and Rabbitts, P. H. Deletion mapping of the short arm of chromosome 3 in Merkel cell carcinoma. Genes Chromosomes Cancer 15: 102-107, 1996.
-
(1996)
Genes Chromosomes Cancer
, vol.15
, pp. 102-107
-
-
Leonard, J.H.1
Williams, G.2
Walters, M.K.3
Nancarrow, D.J.4
Rabbitts, P.H.5
-
22
-
-
0030953421
-
Loss of heterozygosity of chromosome 13 in Merkel cell carcinoma
-
Leonard, J. H., Hayward, N. Loss of heterozygosity of chromosome 13 in Merkel cell carcinoma. Genes Chromosomes Cancer, 20: 43-97, 1997.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 43-97
-
-
Leonard, J.H.1
Hayward, N.2
-
23
-
-
0027429650
-
Characterisation of cell lines established from Merkel cell (small cell) cancer of the skin
-
Leonard, J. H., Bell, J. R., and Kearsley, J. H. Characterisation of cell lines established from Merkel cell (small cell) cancer of the skin. Int. J. Cancer, 55: 803-810, 1993.
-
(1993)
Int. J. Cancer
, vol.55
, pp. 803-810
-
-
Leonard, J.H.1
Bell, J.R.2
Kearsley, J.H.3
-
24
-
-
0028945237
-
Characterization of four Merkel cell carcinoma adherent cell lines
-
Leonard, J. H., Dash, P., Holland, P., Kearsley, J. H., and Bell, J. R. Characterization of four Merkel cell carcinoma adherent cell lines. Int. J. Cancer. 60: 100-107, 1994.
-
(1994)
Int. J. Cancer.
, vol.60
, pp. 100-107
-
-
Leonard, J.H.1
Dash, P.2
Holland, P.3
Kearsley, J.H.4
Bell, J.R.5
-
25
-
-
0030789270
-
Comparative genomic hybridization analysis of human neuroblastomas: Detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines
-
Van Roy, N., Jauch, A., Van Gele, M., Laureys, G., Versteeg, R., De Paepe, A., Cremer, T., and Speleman, F. Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines. Cancer Genet. Cytogenet., 97: 135-142, 1997.
-
(1997)
Cancer Genet. Cytogenet.
, vol.97
, pp. 135-142
-
-
Van Roy, N.1
Jauch, A.2
Van Gele, M.3
Laureys, G.4
Versteeg, R.5
De Paepe, A.6
Cremer, T.7
Speleman, F.8
-
26
-
-
0004136246
-
-
N. Ford, C. Nolan, and M. Ferguson (eds.), Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Sambrook, J., Fritsch, E. F., and Maniatis, T. In N. Ford, C. Nolan, and M. Ferguson (eds.), Molecular Cloning: A Laboratory Manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1989.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
27
-
-
0027537408
-
Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridisation
-
du Manoir, S., Speicher, M. R., Joos, S., Schröck, E., Popp, S., Döhner, H., Kovacs, G., Robert-Nicoud, M., Lichter, P., and Cremer, T. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridisation. Hum. Genet., 90: 590-610, 1993.
-
(1993)
Hum. Genet.
, vol.90
, pp. 590-610
-
-
Du Manoir, S.1
Speicher, M.R.2
Joos, S.3
Schröck, E.4
Popp, S.5
Döhner, H.6
Kovacs, G.7
Robert-Nicoud, M.8
Lichter, P.9
Cremer, T.10
-
28
-
-
0028934697
-
Quantitative analysis of comparative genomic hybridization
-
du Manoir, S., Schröck, E., Bentz, M., Speicher, M. R., Joos, S., Ried, T., Lichter P., and Cremer, T. Quantitative analysis of comparative genomic hybridization. Cytometry, 19: 27-41, 1995.
-
(1995)
Cytometry
, vol.19
, pp. 27-41
-
-
Du Manoir, S.1
Schröck, E.2
Bentz, M.3
Speicher, M.R.4
Joos, S.5
Ried, T.6
Lichter, P.7
Cremer, T.8
-
29
-
-
0031418167
-
Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridization analysis
-
Van Gele, M., Van Roy, N., Jauch, A., Laureys, G., Schelfhout, V., De Potter, C. R., Brock, P., Uyttebroeck, A., Sciot, R., Schuuring, E., Versteeg, R., and Speleman, F. Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridization analysis. Eur. J. Cancer, 33: 1979-1982; 1997.
-
(1997)
Eur. J. Cancer
, vol.33
, pp. 1979-1982
-
-
Van Gele, M.1
Van Roy, N.2
Jauch, A.3
Laureys, G.4
Schelfhout, V.5
De Potter, C.R.6
Brock, P.7
Uyttebroeck, A.8
Sciot, R.9
Schuuring, E.10
Versteeg, R.11
Speleman, F.12
-
30
-
-
0028027866
-
Identification of frequent novel genetic alterations in small cell lung carcinoma
-
Levin, N, A., Brzoska, P., Gupta, N., Minna, J. D., Gray J. W., and Christman M. F. Identification of frequent novel genetic alterations in small cell lung carcinoma. Cancer Res., 54: 5086-5091, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 5086-5091
-
-
Levin, N.A.1
Brzoska, P.2
Gupta, N.3
Minna, J.D.4
Gray, J.W.5
Christman, M.F.6
-
31
-
-
0028351198
-
Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization
-
Ried, T., Petersen, I., Holtgreve-Grez, H., Speicher, M. R., Schröck, E., du Manoir, S., and Cremer, T. Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization. Cancer Res., 54: 1801-1806, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 1801-1806
-
-
Ried, T.1
Petersen, I.2
Holtgreve-Grez, H.3
Speicher, M.R.4
Schröck, E.5
Du Manoir, S.6
Cremer, T.7
-
32
-
-
0029030266
-
Identification of novel regions of altered DNA copy number in small cell lung tumors
-
Levin, N. A., Brzoska, P. M., Warnock, M. L., Gray, J. W., and Christman, M. F. Identification of novel regions of altered DNA copy number in small cell lung tumors. Genes Chromosomes Cancer, 13: 175-185, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.13
, pp. 175-185
-
-
Levin, N.A.1
Brzoska, P.M.2
Warnock, M.L.3
Gray, J.W.4
Christman, M.F.5
-
33
-
-
0031012404
-
Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p
-
Petersen, I., Langreck, H., Wolf, G., Schwendel, A., Psille, R., Vogt, P., Reichel M. B., Ried, T., and Dietel, M. Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p. Br. J. Cancer, 75: 79-86, 1997.
-
(1997)
Br. J. Cancer
, vol.75
, pp. 79-86
-
-
Petersen, I.1
Langreck, H.2
Wolf, G.3
Schwendel, A.4
Psille, R.5
Vogt, P.6
Reichel, M.B.7
Ried, T.8
Dietel, M.9
-
34
-
-
0029976382
-
Loss of heterozygosity studies in squamous cell carcinomas of the head and neck
-
Ransom, D. T., Leonard, J. H., Kearsley, J. H., Turbett, G. R., Heel, K., Sosars, V., Hayward, N. K., and Bishop, J. F. Loss of heterozygosity studies in squamous cell carcinomas of the head and neck. Head Neck, 18: 248-253, 1996.
-
(1996)
Head Neck
, vol.18
, pp. 248-253
-
-
Ransom, D.T.1
Leonard, J.H.2
Kearsley, J.H.3
Turbett, G.R.4
Heel, K.5
Sosars, V.6
Hayward, N.K.7
Bishop, J.F.8
-
35
-
-
0029055452
-
Frequent novel DNA copy number increase in squamous cell head and neck tumors
-
Brzoska, P. M., Levin, N. A., Fu, K. K., Kaplan, M. J., Singer, M. I., Gray, J. W, and Christman, M. F. Frequent novel DNA copy number increase in squamous cell head and neck tumors. Cancer Res., 55: 3055-3059, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 3055-3059
-
-
Brzoska, P.M.1
Levin, N.A.2
Fu, K.K.3
Kaplan, M.J.4
Singer, M.I.5
Gray, J.W.6
Christman, M.F.7
-
36
-
-
0028920353
-
Comparative genomic hybridization detects novel deletions and amplifications in head and neck squamous cell carcinomas
-
Speicher, M. R., Howe, C., Crotty, P., du Manoir, S., Costa, J., and Ward, D. C. Comparative genomic hybridization detects novel deletions and amplifications in head and neck squamous cell carcinomas. Cancer Res., 55: 1010-1013, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 1010-1013
-
-
Speicher, M.R.1
Howe, C.2
Crotty, P.3
Du Manoir, S.4
Costa, J.5
Ward, D.C.6
-
37
-
-
2642647160
-
Chromosomes in lung cancer
-
S. R. Wolman and S. Sell (eds.), Totowa, NJ Humana Press Inc.
-
Bell, D. W., and Testa, J. R. Chromosomes in lung cancer. In: S. R. Wolman and S. Sell (eds.), Human Cytogenetic Cancer Markers, pp. 247-255. Totowa, NJ Humana Press Inc., 1997.
-
(1997)
Human Cytogenetic Cancer Markers
, pp. 247-255
-
-
Bell, D.W.1
Testa, J.R.2
-
38
-
-
0028269349
-
Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region
-
Van Dyke, D. L., Worsham, M. J., Benninger, M. S., Krause, C. J., Baker, S. R., Wolf, G. T., Drumheller, T., Tilley, B. C., Carey, T. E. Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region. Genes Chromosomes Cancer, 9: 192-206, 1994.
-
(1994)
Genes Chromosomes Cancer
, vol.9
, pp. 192-206
-
-
Van Dyke, D.L.1
Worsham, M.J.2
Benninger, M.S.3
Krause, C.J.4
Baker, S.R.5
Wolf, G.T.6
Drumheller, T.7
Tilley, B.C.8
Carey, T.E.9
-
39
-
-
0030999555
-
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
-
Mitelman, F., Mertens, F., and Johansson, B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat. Genet., 15: 417-474, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 417-474
-
-
Mitelman, F.1
Mertens, F.2
Johansson, B.3
-
40
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Washington DC
-
Latif, F., Tory, K., Gnarra, J., Yao, M., Duh, F., Orcutt, M. L., Stackhouse, T., Kuzmin, I., Modi, W., Geil, L., Schmidt, L., Zhou, F., Li, H., Wei, M. H., Chen, F., Glenn, G., Choyko, P., McClellan, M. W., Weng, Y., Duan, D. R., Dean, M., Glavac, D., Richards, F. M., Crossey, P. A., Ferguson-Smith, M. A., Le Paslier, D., Chumakov, I., Cohen, D., Chinault, A. C. Maher, E. R., Linehan, W. M., Zbar, B., and Lerman, M. I. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science (Washington DC), 260: 1317-1320, 1993.
-
(1993)
Science
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
Yao, M.4
Duh, F.5
Orcutt, M.L.6
Stackhouse, T.7
Kuzmin, I.8
Modi, W.9
Geil, L.10
Schmidt, L.11
Zhou, F.12
Li, H.13
Wei, M.H.14
Chen, F.15
Glenn, G.16
Choyko, P.17
McClellan, M.W.18
Weng, Y.19
Duan, D.R.20
Dean, M.21
Glavac, D.22
Richards, F.M.23
Crossey, P.A.24
Ferguson-Smith, M.A.25
Le Paslier, D.26
Chumakov, I.27
Cohen, D.28
Chinault, A.C.29
Maher, E.R.30
Linehan, W.M.31
Zbar, B.32
Lerman, M.I.33
more..
-
41
-
-
0028987709
-
Assignment of the human beta-catenin gene (CTNNB1) to 3p22-3p21.3 by fluorescence in situ hybridisation
-
Van Hengel, J., Nollet, F., Berx, G., Van Roy, N., Speleman, F., and Van Roy, F. Assignment of the human beta-catenin gene (CTNNB1) to 3p22-3p21.3 by fluorescence in situ hybridisation. Cytogenet. Cell Genet., 70: 68-70, 1995.
-
(1995)
Cytogenet. Cell Genet.
, vol.70
, pp. 68-70
-
-
Van Hengel, J.1
Nollet, F.2
Berx, G.3
Van Roy, N.4
Speleman, F.5
Van Roy, F.6
-
42
-
-
13344279424
-
The human FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated translocation breakpoint, is abnormal in digestive tract cancers
-
Ohta, M., Inoue, H., Cotticelli, M. G., Kastury, K., Baffa, R., Palazzo, J., Siprashvili, Z., Mori, M., McCue, P., Druck, T., Croce, C. M., and Huebner, K. The human FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated translocation breakpoint, is abnormal in digestive tract cancers. Cell, 84: 587-597, 1996.
-
(1996)
Cell
, vol.84
, pp. 587-597
-
-
Ohta, M.1
Inoue, H.2
Cotticelli, M.G.3
Kastury, K.4
Baffa, R.5
Palazzo, J.6
Siprashvili, Z.7
Mori, M.8
McCue, P.9
Druck, T.10
Croce, C.M.11
Huebner, K.12
-
43
-
-
15844384990
-
The FHIT gene at 3p14.2 is abnormal in lung cancer
-
Sozzi, G., Veronese, M. L., Negrini, M., Baffa, R., Cotticelli, M. G., Inoue, H., Tornielli, S., Pilotti, S., De Gregorio, L., Pastorino, U., Pierotti, M. A., Ohta, M., Huebner, K., and Croce, C. M. The FHIT gene at 3p14.2 is abnormal in lung cancer. Cell, 85: 1-20, 1996.
-
(1996)
Cell
, vol.85
, pp. 1-20
-
-
Sozzi, G.1
Veronese, M.L.2
Negrini, M.3
Baffa, R.4
Cotticelli, M.G.5
Inoue, H.6
Tornielli, S.7
Pilotti, S.8
De Gregorio, L.9
Pastorino, U.10
Pierotti, M.A.11
Ohta, M.12
Huebner, K.13
Croce, C.M.14
-
44
-
-
9344225158
-
Aberrant FHIT transcripts in Merkel cell carcinoma
-
Sozzi, G., Alder, H., Tornielli, S., Corletto, V., Baffa, R., Veronese, M. L., Negrini, M., Pilotti, S., Pierotti, M. A., Huebner, K., and Croce, C. M. Aberrant FHIT transcripts in Merkel cell carcinoma. Cancer Res., 56: 2472-2472, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 2472-2472
-
-
Sozzi, G.1
Alder, H.2
Tornielli, S.3
Corletto, V.4
Baffa, R.5
Veronese, M.L.6
Negrini, M.7
Pilotti, S.8
Pierotti, M.A.9
Huebner, K.10
Croce, C.M.11
-
45
-
-
0029975245
-
Distinct areas of allelic loss on chromosomal region 10p and 10q in human prostate cancer
-
Trybus, T. M., Burgress, A. C., Wojno K. J., Glover, T. W., and Macoska, J. A. Distinct areas of allelic loss on chromosomal region 10p and 10q in human prostate cancer. Cancer Res., 56: 2263-2267, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 2263-2267
-
-
Trybus, T.M.1
Burgress, A.C.2
Wojno, K.J.3
Glover, T.W.4
Macoska, J.A.5
-
46
-
-
0026329715
-
Common regions of deletion on chromosomes 5q, 6q. and 10q in renal cell carcinoma
-
Morita, R., Susumu, S., Ishikawa, J., Ogawa, O., Yoshida, O., Yamakawa, K., and Nakamura, Y. Common regions of deletion on chromosomes 5q, 6q. and 10q in renal cell carcinoma. Cancer Res., 51: 5817-5820, 1991.
-
(1991)
Cancer Res.
, vol.51
, pp. 5817-5820
-
-
Morita, R.1
Susumu, S.2
Ishikawa, J.3
Ogawa, O.4
Yoshida, O.5
Yamakawa, K.6
Nakamura, Y.7
-
47
-
-
0028955264
-
Allelic loss of sequences from the long arm of chromosome 10 and replication errors in endometrial cancers
-
Peiffer, S. L., Herzog, T. J., Tribune, D. J., Mutch, D. G., Gersell, D. J., Goodfellow P. J. Allelic loss of sequences from the long arm of chromosome 10 and replication errors in endometrial cancers. Cancer Res., 55: 1922-1926, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 1922-1926
-
-
Peiffer, S.L.1
Herzog, T.J.2
Tribune, D.J.3
Mutch, D.G.4
Gersell, D.J.5
Goodfellow, P.J.6
-
48
-
-
0028264298
-
Loss of heterozygosity for 10q22-qter in malignant melanoma progression
-
Herbst, R. A., Weiss, J., Ehnis, A., Cavanee, W. K., and Arden, K. C. Loss of heterozygosity for 10q22-qter in malignant melanoma progression. Cancer Res., 54: 3111-3114, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 3111-3114
-
-
Herbst, R.A.1
Weiss, J.2
Ehnis, A.3
Cavanee, W.K.4
Arden, K.C.5
-
49
-
-
17144436629
-
Identification of a candidate tumor suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
-
Steck, P. A., Pershouse, M. A., Jasser, S. A., Yung, W. K. A., Lin, H., Ligon, A. H., Langford, L. A., Baumgard, M. L., Hattier, T., Davis, T., Frye, C., Hu, R., Swedlund, B., Teng, D. H. F., and Tavtigian, S. V. Identification of a candidate tumor suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat. Genet., 15: 356-362, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 356-362
-
-
Steck, P.A.1
Pershouse, M.A.2
Jasser, S.A.3
Yung, W.K.A.4
Lin, H.5
Ligon, A.H.6
Langford, L.A.7
Baumgard, M.L.8
Hattier, T.9
Davis, T.10
Frye, C.11
Hu, R.12
Swedlund, B.13
Teng, D.H.F.14
Tavtigian, S.V.15
-
50
-
-
0031052844
-
Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinoma
-
Marsh, D. J., Zheng, Z., Zedenius, J., Kremeer, H., Padberg, G. W., Larsson, C., Longy, M., and Eng, C. Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinoma. Cancer Res., 57: 500-503, 1997.
-
(1997)
Cancer Res.
, vol.57
, pp. 500-503
-
-
Marsh, D.J.1
Zheng, Z.2
Zedenius, J.3
Kremeer, H.4
Padberg, G.W.5
Larsson, C.6
Longy, M.7
Eng, C.8
-
51
-
-
0027171632
-
Homozygous deletion and frequent allelic loss of chromosome 8p22 loci in human prostate cancer
-
Bova, G. S., Carter, B. S., Bussemakers, M. J., Emi, M., Fujiwara, Y., Kyprianou, N., Jacobs, S. C., Robinson, J. C., Epstein, J. I., and Walsh, P. C. Homozygous deletion and frequent allelic loss of chromosome 8p22 loci in human prostate cancer. Cancer Res., 53: 3869-3873, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 3869-3873
-
-
Bova, G.S.1
Carter, B.S.2
Bussemakers, M.J.3
Emi, M.4
Fujiwara, Y.5
Kyprianou, N.6
Jacobs, S.C.7
Robinson, J.C.8
Epstein, J.I.9
Walsh, P.C.10
-
52
-
-
0028918829
-
Identification of gains and losses of DNA sequences in primary bladder cancer by comparative genomic hybridization
-
Kallioniemi, A., Kallioniemi, O. P., Citro, G., Sauter, G., DeVries, S., Kerschmann, R., Caroll, P., and Waldman, F. Identification of gains and losses of DNA sequences in primary bladder cancer by comparative genomic hybridization. Genes Chromosomes Cancer, 12: 213-219, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.12
, pp. 213-219
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Citro, G.3
Sauter, G.4
DeVries, S.5
Kerschmann, R.6
Caroll, P.7
Waldman, F.8
-
53
-
-
0030040471
-
Genetic aberrations detected by comparative genomic hybridization are associated with clinical outcome in renal cell carcinoma
-
Moch, H., Presti, J. C., Sauter, G., Buchholz, N., Jordan, P., Mihatsch, M. J., and Waldman, F. M. Genetic aberrations detected by comparative genomic hybridization are associated with clinical outcome in renal cell carcinoma. Cancer Res., 56: 27-30, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 27-30
-
-
Moch, H.1
Presti, J.C.2
Sauter, G.3
Buchholz, N.4
Jordan, P.5
Mihatsch, M.J.6
Waldman, F.M.7
-
54
-
-
0027406542
-
Evidence for the presence of two tumor suppressor genes on chromosome 8p for colorectal carcinoma
-
Fujiwara, Y., Emi, M., Ohata, H., Kato, Y., Nakajima, T., Mori, T., and Nakamura, Y. Evidence for the presence of two tumor suppressor genes on chromosome 8p for colorectal carcinoma. Cancer Res., 53: 1172-1174, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 1172-1174
-
-
Fujiwara, Y.1
Emi, M.2
Ohata, H.3
Kato, Y.4
Nakajima, T.5
Mori, T.6
Nakamura, Y.7
-
55
-
-
0031022784
-
Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization
-
Marchio, A., Meddeb, M., Pineau, P., Danglot, G., Tiollais, P., Bernheim, A., and Dejean, A. Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization. Genes Chromosomes Cancer, 18: 59-65, 1997.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 59-65
-
-
Marchio, A.1
Meddeb, M.2
Pineau, P.3
Danglot, G.4
Tiollais, P.5
Bernheim, A.6
Dejean, A.7
-
56
-
-
0028840532
-
Loss of heterozygosity on the short arm of chromosome 8 in male breast carcinomas
-
Chuaqui, R. F., Sanz-Ortega, J., Vocke, C., Linehan, W. M., Sanz-Esponera, J., Zhuang, Z., Emmert-Buck, M. R., and Merino, M. J. Loss of heterozygosity on the short arm of chromosome 8 in male breast carcinomas. Cancer Res., 55: 4995-4998, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 4995-4998
-
-
Chuaqui, R.F.1
Sanz-Ortega, J.2
Vocke, C.3
Linehan, W.M.4
Sanz-Esponera, J.5
Zhuang, Z.6
Emmert-Buck, M.R.7
Merino, M.J.8
-
57
-
-
0030014483
-
Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behavior in breast cancer
-
Yaremko, M. L., Kutza, C. Lysak, J., Mick, R., Recant, W. M., and Westbrook, C. A. Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behavior in breast cancer. Genes Chromosomes Cancer, 16: 189-195, 1996.
-
(1996)
Genes Chromosomes Cancer
, vol.16
, pp. 189-195
-
-
Yaremko, M.L.1
Kutza, C.2
Lysak, J.3
Mick, R.4
Recant, W.M.5
Westbrook, C.A.6
-
58
-
-
0021063273
-
Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumor
-
Schwab, M., Alitalo, K., Klempnauer, K. H., Varmus, H. E., Bishop, J. M., Gilbert, F., Brodeur, G., Goldstein, M., and Trent, J. M. Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumor. Nature (Lond.), 305: 245-248, 1983.
-
(1983)
Nature (Lond.)
, vol.305
, pp. 245-248
-
-
Schwab, M.1
Alitalo, K.2
Klempnauer, K.H.3
Varmus, H.E.4
Bishop, J.M.5
Gilbert, F.6
Brodeur, G.7
Goldstein, M.8
Trent, J.M.9
-
59
-
-
0029030524
-
Ip36: Every subband a suppressor?
-
Versteeg, R., Caron, H., Cheng, N. C., van der Drift, P., Slater, R., Westerveld, A., Voute, P. A., Delattre, O., Laureys, G., Van Roy, N., and Speleman, F. Ip36: Every subband a suppressor? Eur. J. Cancer, 31A: 538-541, 1995.
-
(1995)
Eur. J. Cancer
, vol.31 A
, pp. 538-541
-
-
Versteeg, R.1
Caron, H.2
Cheng, N.C.3
Van Der Drift, P.4
Slater, R.5
Westerveld, A.6
Voute, P.A.7
Delattre, O.8
Laureys, G.9
Van Roy, N.10
Speleman, F.11
-
60
-
-
0029736825
-
Characterization of genomic alterations associated with glioma progression by comparative genomic hybridization
-
Weber, R. G., Sabel, M., Reifenberger J., Sommer, C., Oberstraβ, J., Reifenberger, G., Kiessling, M., and Cremer, T. Characterization of genomic alterations associated with glioma progression by comparative genomic hybridization. Oncogene, 13: 983-994, 1996.
-
(1996)
Oncogene
, vol.13
, pp. 983-994
-
-
Weber, R.G.1
Sabel, M.2
Reifenberger, J.3
Sommer, C.4
Oberstraß, J.5
Reifenberger, G.6
Kiessling, M.7
Cremer, T.8
-
61
-
-
0025324441
-
Chromosome mapping of the human RAS-related RAP1A, RAP1B, and RAP2 genes to chromosomes 1p12→p13, 12q14, and 13q34. respectively
-
Rousseau-Merck, M. F., Pizon, V., Tavitian, A., and Berger, R. Chromosome mapping of the human RAS-related RAP1A, RAP1B, and RAP2 genes to chromosomes 1p12→p13, 12q14, and 13q34. respectively. Cytogenet. Cell Genet., 53: 2-4, 1990.
-
(1990)
Cytogenet. Cell Genet.
, vol.53
, pp. 2-4
-
-
Rousseau-Merck, M.F.1
Pizon, V.2
Tavitian, A.3
Berger, R.4
-
62
-
-
0029955911
-
Comparative genomic hybridization (CGH) discloses chromosomal and subchromosomal copy number changes in Merkel cell carcinomas
-
Harle, M., Arens, N., Moll, I., Back, W., Schulz, T., and Scherthan, H. Comparative genomic hybridization (CGH) discloses chromosomal and subchromosomal copy number changes in Merkel cell carcinomas. J. Cutan. Pathol., 23: 391-397, 1996.
-
(1996)
J. Cutan. Pathol.
, vol.23
, pp. 391-397
-
-
Harle, M.1
Arens, N.2
Moll, I.3
Back, W.4
Schulz, T.5
Scherthan, H.6
-
63
-
-
0027998424
-
Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridization
-
Speicher, M. R., Prescher, G., du Manoir, S., Jauch, A., Horsthemke, B., Bornfeld, N., Becher, R., and Cremer, T. Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridization. Cancer Res., 54: 3817-3823, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 3817-3823
-
-
Speicher, M.R.1
Prescher, G.2
Du Manoir, S.3
Jauch, A.4
Horsthemke, B.5
Bornfeld, N.6
Becher, R.7
Cremer, T.8
-
64
-
-
0028004226
-
Comparative genomic hybridization, allelic imbalance, and fluorescence in situ hybridization on chromosome 8 in prostate cancer
-
Cher, M. L., MacGrogan, D., Bookstein, R., Brown, J. A., Jenkins, R. B., and Jensen R. H. Comparative genomic hybridization, allelic imbalance, and fluorescence in situ hybridization on chromosome 8 in prostate cancer. Genes Chromosomes Cancer, 11: 153-162, 1994.
-
(1994)
Genes Chromosomes Cancer
, vol.11
, pp. 153-162
-
-
Cher, M.L.1
MacGrogan, D.2
Bookstein, R.3
Brown, J.A.4
Jenkins, R.B.5
Jensen, R.H.6
-
65
-
-
0028848334
-
Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization
-
Joos, S., Bergerheim, U. S. R., Pan, Y., Matsuyama, H., Bentz, M., du Manoir, S., and Lichter, P. Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization. Genes Chromosomes Cancer, 14: 267-276, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 267-276
-
-
Joos, S.1
Bergerheim, U.S.R.2
Pan, Y.3
Matsuyama, H.4
Bentz, M.5
Du Manoir, S.6
Lichter, P.7
-
66
-
-
0028887369
-
Genetic changes in primary and recurrent prostate cancer by comparative genomic hybridization
-
Visakorpi, T., Kallioniemi, A. H., Syvänen, A-C., Hyytinen, E. R., Karhu, R., Tammela, T., Isola, J. J., and Kallioniemi, O-P. Genetic changes in primary and recurrent prostate cancer by comparative genomic hybridization. Cancer Res., 55: 342-347, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 342-347
-
-
Visakorpi, T.1
Kallioniemi, A.H.2
Syvänen, A.-C.3
Hyytinen, E.R.4
Karhu, R.5
Tammela, T.6
Isola, J.J.7
Kallioniemi, O.-P.8
-
67
-
-
0026724911
-
c-myc oncogene expression in ocular melanomas
-
Royds, J. A., Sharrard, R. M., Parsons, M. A., Lawry, J., Rees, R., Cottam, D., Wagner, B., and Rennie, I. G. c-myc oncogene expression in ocular melanomas. Graefe's Arch. Clin. Exp. Ophthalmol., 230: 366-371, 1992.
-
(1992)
Graefe's Arch. Clin. Exp. Ophthalmol.
, vol.230
, pp. 366-371
-
-
Royds, J.A.1
Sharrard, R.M.2
Parsons, M.A.3
Lawry, J.4
Rees, R.5
Cottam, D.6
Wagner, B.7
Rennie, I.G.8
-
68
-
-
0000778884
-
EEN encodes for a member of a new family of proteins containing an Src homology 3 domain and is the third gene located on chromosome 19p13 that fuses to MLL in human leukemia
-
So, C. W., Caldas, C., Liu, M. M., Chen, S. J., Huang, Q. H., Gu, L. J., Sham, M. H., and Wiedemann, L. M. EEN encodes for a member of a new family of proteins containing an Src homology 3 domain and is the third gene located on chromosome 19p13 that fuses to MLL in human leukemia. Proc. Natl. Acad. Sci. USA, 94: 2563-2568, 1997.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 2563-2568
-
-
So, C.W.1
Caldas, C.2
Liu, M.M.3
Chen, S.J.4
Huang, Q.H.5
Gu, L.J.6
Sham, M.H.7
Wiedemann, L.M.8
|