-
2
-
-
0025326726
-
A major segment of the neurofibromatosis type 1 gene. cDNA sequence, genomic structure, and point mutations
-
Cawthon, R M., Weiss, R , Xu, G , Viskochil, D , Culver, M., Stevens, J., Robertson, M , Dunn, D., Gesteland, R , O'Connell, P , and White, R A major segment of the neurofibromatosis type 1 gene. cDNA sequence, genomic structure, and point mutations. Cell, 62. 193-201, 1990.
-
(1990)
Cell
, vol.62
, pp. 193-201
-
-
Cawthon, R.M.1
Weiss, R.2
Xu, G.3
Viskochil, D.4
Culver, M.5
Stevens, J.6
Robertson, M.7
Dunn, D.8
Gesteland, R.9
O'Connell, P.10
White, R.11
-
3
-
-
0025369709
-
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
-
Viskochil, D , Buchberg, A. M., Xu, G., Cawthon, R M., Stevens, J., Wolf, R. K , Culver, M., Carey, J. C , Copeland, N. G , Jenkins, N A , White, R., and O'Connell, P Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell, 62. 187-192, 1990.
-
(1990)
Cell
, vol.62
, pp. 187-192
-
-
Viskochil, D.1
Buchberg, A.M.2
Xu, G.3
Cawthon, R.M.4
Stevens, J.5
Wolf, R.K.6
Culver, M.7
Carey, J.C.8
Copeland, N.G.9
Jenkins, N.A.10
White, R.11
O'Connell, P.12
-
4
-
-
0025297599
-
Type 1 neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients
-
Washington DC
-
Wallace, M R , Marchuk, D. A , Andersen, L. B , Letcher, R., Odeh, H. M., Saulino, A M., Fountain, J. W , Brereton, A , Nicholson, J , Mitchell, A L., Brownstein, B H., and Collins, F S. Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. Science (Washington DC), 249: 181-186, 1990.
-
(1990)
Science
, vol.249
, pp. 181-186
-
-
Wallace, M.R.1
Marchuk, D.A.2
Andersen, L.B.3
Letcher, R.4
Odeh, H.M.5
Saulino, A.M.6
Fountain, J.W.7
Brereton, A.8
Nicholson, J.9
Mitchell, A.L.10
Brownstein, B.H.11
Collins, F.S.12
-
5
-
-
0026505197
-
Somatic mutations in the neurofibromatosis 1 gene in human tumors
-
Li, Y , Bollag, G., Clark, R., Stevens, J., Conroy, L., Fults, D., Ward, K., Friedman, E., Samowitz, W , Robertson, M., Bradley, P., McGormick, F , White, R., and Cawthon, R. Somatic mutations in the neurofibromatosis 1 gene in human tumors Cell, 69: 275-281, 1992.
-
(1992)
Cell
, vol.69
, pp. 275-281
-
-
Li, Y.1
Bollag, G.2
Clark, R.3
Stevens, J.4
Conroy, L.5
Fults, D.6
Ward, K.7
Friedman, E.8
Samowitz, W.9
Robertson, M.10
Bradley, P.11
McGormick, F.12
White, R.13
Cawthon, R.14
-
6
-
-
0027502579
-
Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines
-
Andersen, L. B , Fountain, J. W., Gutmann, D. H., Tarlé, S. A., Glover, T. W , Dracopoli, N C , Housman, D. E , and Collins, F S. Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines. Nat. Genet., 3: 118-121, 1993.
-
(1993)
Nat. Genet.
, vol.3
, pp. 118-121
-
-
Andersen, L.B.1
Fountain, J.W.2
Gutmann, D.H.3
Tarlé, S.A.4
Glover, T.W.5
Dracopoli, N.C.6
Housman, D.E.7
Collins, F.S.8
-
7
-
-
0027468594
-
Somatic deletion of neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
-
Legius, E., Marchuk, D. A , Collins, F S., and Glover, T. W. Somatic deletion of neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. Nat. Genet., 3: 122-126, 1993.
-
(1993)
Nat. Genet.
, vol.3
, pp. 122-126
-
-
Legius, E.1
Marchuk, D.A.2
Collins, F.S.3
Glover, T.W.4
-
8
-
-
0027439597
-
Neurofibromatosis type 1 gene mutations in neuroblastoma
-
The, I , Murthy, A. E., Hannigan, G. E., Jacoby, L. B., Menon, A. G., Gusella, J. F., and Bernards. A. Neurofibromatosis type 1 gene mutations in neuroblastoma. Nat. Genet , 3. 62-66, 1993.
-
(1993)
Nat. Genet
, vol.3
, pp. 62-66
-
-
The, I.1
Murthy, A.E.2
Hannigan, G.E.3
Jacoby, L.B.4
Menon, A.G.5
Gusella, J.F.6
Bernards, A.7
-
9
-
-
0029060246
-
Cytogenetic findings in malignant peripheral nerve sheath tumors
-
Mertens, F , Rydholm, A., Bauer, H. F. C , Limon, J., Nedoszytko, B., Szadowska, A , Willén, H., Heim, S., Mitelman. F., and Mandahl, N. Cytogenetic findings in malignant peripheral nerve sheath tumors. Int J Cancer, 61. 793-798, 1995.
-
(1995)
Int J Cancer
, vol.61
, pp. 793-798
-
-
Mertens, F.1
Rydholm, A.2
Bauer, H.F.C.3
Limon, J.4
Nedoszytko, B.5
Szadowska, A.6
Willén, H.7
Heim, S.8
Mitelman, F.9
Mandahl, N.10
-
10
-
-
0028631156
-
Cytogenetic analysis of soft tissue sarcomas: Recurrent chromosome abnormalities in malignant peripheral nerve sheath tumors (MPNST)
-
Jhanwar, S. C , Chen, Q., Li, F. P , Brennan, M F, and Woodruff, J. M. Cytogenetic analysis of soft tissue sarcomas: recurrent chromosome abnormalities in malignant peripheral nerve sheath tumors (MPNST) Cancer Genet. Cytogenet., 78: 138-144, 1994.
-
(1994)
Cancer Genet. Cytogenet.
, vol.78
, pp. 138-144
-
-
Jhanwar, S.C.1
Chen, Q.2
Li, F.P.3
Brennan, M.F.4
Woodruff, J.M.5
-
11
-
-
0024387728
-
Mutations in the p53 gene occur in diverse human tumour types
-
Nigro, J. M., Baker, S. J , Preisinger, A. C., Jessup, J. M., Hosteller, R., Cleary, K., Bigner, S. H., Davidson, N., Baylin, S., Devilee, P., Glover, T , Collins, F S., Weston, A., Modali, R , Harris, C C , and Vogelstein, B. Mutations in the p53 gene occur in diverse human tumour types. Nature (Lond), 342: 705-708, 1989
-
(1989)
Nature (Lond)
, vol.342
, pp. 705-708
-
-
Nigro, J.M.1
Baker, S.J.2
Preisinger, A.C.3
Jessup, J.M.4
Hosteller, R.5
Cleary, K.6
Bigner, S.H.7
Davidson, N.8
Baylin, S.9
Devilee, P.10
Glover, T.11
Collins, F.S.12
Weston, A.13
Modali, R.14
Harris, C.C.15
Vogelstein, B.16
-
12
-
-
0025108408
-
Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis
-
Menon, A. G., Anderson, K. M., Riccardi, V. M., Chung, R Y., Whaley, J. M , Yandell, D. W., Farmer, G. E., Freiman, R. N., Lee, J K., Li, F. P , Barker, D , Ledbetter, D. H., Kleider, A., Martuza, R. L., Gusella, J. F., and Seizinger, B. R. Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis. Proc. Natl. Acad. Sci. USA, 87: 5435-5439, 1990.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 5435-5439
-
-
Menon, A.G.1
Anderson, K.M.2
Riccardi, V.M.3
Chung, R.Y.4
Whaley, J.M.5
Yandell, D.W.6
Farmer, G.E.7
Freiman, R.N.8
Lee, J.K.9
Li, F.P.10
Barker, D.11
Ledbetter, D.H.12
Kleider, A.13
Martuza, R.L.14
Gusella, J.F.15
Seizinger, B.R.16
-
13
-
-
0028146806
-
TP53 mutations are frequent in malignant NF1 tumors
-
Legius, E., Dierick, H., Wu, R., Hall, B. K., Marynen, P., Cassiman, J-J., and Glover, T. W. TP53 mutations are frequent in malignant NF1 tumors. Genes Chromosomes & Cancer, 10: 250-255, 1994.
-
(1994)
Genes Chromosomes & Cancer
, vol.10
, pp. 250-255
-
-
Legius, E.1
Dierick, H.2
Wu, R.3
Hall, B.K.4
Marynen, P.5
Cassiman, J.-J.6
Glover, T.W.7
-
14
-
-
0028819644
-
Alterations at chromosome 17 loci in peripheral nerve sheath tumors
-
Lothe, R A., Slettan, A, Sæter, G , Brogger, A., Børresen, A-L., and Nesland, J-M. Alterations at chromosome 17 loci in peripheral nerve sheath tumors. J Neuropathol. & Exp. Neurol , 54: 65-73, 1995.
-
(1995)
J Neuropathol. & Exp. Neurol
, vol.54
, pp. 65-73
-
-
Lothe, R.A.1
Slettan, A.2
Sæter, G.3
Brogger, A.4
Børresen, A.-L.5
Nesland, J.-M.6
-
15
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Washington DC
-
Kallioniemi, A., Kallioniemi, O-P., Sudar, D. Rutovitz, D., Gray, J., Waldman, F., and Pinkel, D. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science (Washington DC). 258: 818-821, 1992.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.-P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.5
Waldman, F.6
Pinkel, D.7
-
16
-
-
0027966172
-
Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors
-
Kallioniemi, O-P , Kallioniemt, A., Piper, J., Isola, J., Waldman, F. M., Gray, J. W., and Pinkel, D. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Genes Chromosomes & Cancer, 10, 231-243, 1994.
-
(1994)
Genes Chromosomes & Cancer
, vol.10
, pp. 231-243
-
-
Kallioniemi, O.-P.1
Kallioniemt, A.2
Piper, J.3
Isola, J.4
Waldman, F.M.5
Gray, J.W.6
Pinkel, D.7
-
17
-
-
0028907211
-
Computer image analysis of comparative genomic hybridization
-
Piper, J , Rutovitz, D., Sudar, D , Kallioniemi A., Kallioniemi, O-P , Waldman, F M., Gray, J. W., and Pinkel, D. Computer image analysis of comparative genomic hybridization Cytometry, 19 10-26, 1995.
-
(1995)
Cytometry
, vol.19
, pp. 10-26
-
-
Piper, J.1
Rutovitz, D.2
Sudar, D.3
Kallioniemi, A.4
Kallioniemi, O.-P.5
Waldman, F.M.6
Gray, J.W.7
Pinkel, D.8
-
18
-
-
0004055327
-
-
New York: Wiley-Liss, Inc.
-
Heim, S., and Mirelman, F Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells, Ed 2. New York: Wiley-Liss, Inc., 1995.
-
(1995)
Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells, Ed 2
-
-
Heim, S.1
Mirelman, F.2
-
19
-
-
0028276710
-
Mutation spectrum of the retinoblastoma gene in osteosarcomas
-
Wadayama, B-I, Toguchida, J., Shimizu, T., Ishizaki, K , Sasaki, M S., Kotoura, Y., and Yamamuro, T. Mutation spectrum of the retinoblastoma gene in osteosarcomas. Cancer Res., 54 3042-3048, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 3042-3048
-
-
Wadayama, B.-I.1
Toguchida, J.2
Shimizu, T.3
Ishizaki, K.4
Sasaki, M.S.5
Kotoura, Y.6
Yamamuro, T.7
-
21
-
-
0028105914
-
Stifled by inhibitions
-
Peters, G Stifled by inhibitions. Nature (Lond.), 371: 204-205, 1994
-
(1994)
Nature (Lond.)
, vol.371
, pp. 204-205
-
-
Peters, G.1
-
22
-
-
0028206724
-
Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization
-
Kallioniemi, A. Kallioniemi, O-P , Piper, J, Tanner, M., Stokke, T., Chen, L., Smith, H S , Pinkel, D , Gray, J. W., and Waldman, F. M. Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization. Proc. Natl. Acad. Sci. USA. 96: 2156-2160, 1994.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 2156-2160
-
-
Kallioniemi, A.1
Kallioniemi, O.-P.2
Piper, J.3
Tanner, M.4
Stokke, T.5
Chen, L.6
Smith, H.S.7
Pinkel, D.8
Gray, J.W.9
Waldman, F.M.10
-
23
-
-
0028001095
-
Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection
-
Guan, X-Y , Meltzer, P. S., Dalton, W. S., and Trent, J. M. Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection. Nat Genet., 8: 155-161, 1994.
-
(1994)
Nat Genet.
, vol.8
, pp. 155-161
-
-
Guan, X.-Y.1
Meltzer, P.S.2
Dalton, W.S.3
Trent, J.M.4
-
24
-
-
0024957180
-
Molecular genetic analysis in von Recklinghausen neurofibromatosis: Loss of heterozygosity for chromosome 17
-
Skuse, G. R., Kosciolek, B. A , and Rowley, P T. Molecular genetic analysis in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17 Genes Chromosomes & Cancer, 1: 36-41, 1989.
-
(1989)
Genes Chromosomes & Cancer
, vol.1
, pp. 36-41
-
-
Skuse, G.R.1
Kosciolek, B.A.2
Rowley, P.T.3
-
25
-
-
0025804020
-
Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis
-
Glover, T. W., Stein, C. K , Legius, E., Andersen, L. B., Brereton, A , and Johnson, S Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis. Genes Chromosomes & Cancer, 3: 62-70, 1991.
-
(1991)
Genes Chromosomes & Cancer
, vol.3
, pp. 62-70
-
-
Glover, T.W.1
Stein, C.K.2
Legius, E.3
Andersen, L.B.4
Brereton, A.5
Johnson, S.6
-
26
-
-
0028990263
-
Involvement of chromosomes 17 and 22 in dermatofibrosarcoma protuberans
-
Minoletti, F., Miozzo, M., Pedeutour, F. Sard, L., Pilotti, S, Azzarelli, A., Turc-Carel, C., Pierotti, M. A. and Sozzi. G. Involvement of chromosomes 17 and 22 in dermatofibrosarcoma protuberans. Genes Chromosomes & Cancer, 13: 62-65, 1995.
-
(1995)
Genes Chromosomes & Cancer
, vol.13
, pp. 62-65
-
-
Minoletti, F.1
Miozzo, M.2
Pedeutour, F.3
Sard, L.4
Pilotti, S.5
Azzarelli, A.6
Turc-Carel, C.7
Pierotti, M.A.8
Sozzi, G.9
-
27
-
-
0029006919
-
Ring 22 chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences
-
Pedeutour, F., Simon, M-P., Minoletti, F . Sozzi, G , Pierotti, M. A , Hecht, F., and Turc-Carel, C. Ring 22 chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences. Cancer Res., 55: 2400-2403, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 2400-2403
-
-
Pedeutour, F.1
Simon, M.-P.2
Minoletti, F..3
Sozzi, G.4
Pierotti, M.A.5
Hecht, F.6
Turc-Carel, C.7
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