-
1
-
-
0028887421
-
Identification of the von Hippel-Lindau (VHL) gene. Its role in renal cancer
-
Linehan, W. M , Lerman, M I., and Zbar, B. Identification of the von Hippel-Lindau (VHL) gene. Its role in renal cancer JAMA, 273: 564-570, 1995.
-
(1995)
JAMA
, vol.273
, pp. 564-570
-
-
Linehan, W.M.1
Lerman, M.I.2
Zbar, B.3
-
2
-
-
0018736628
-
Hereditary renal-cell carcinoma associated with a chromosomal translocation
-
Cohen, A J., Li, F. P., Berg, S., Marchetto, D. J., Tsai, S., Jacobs, S. C., and Brown, R. S Hereditary renal-cell carcinoma associated with a chromosomal translocation. N. Engl J Med., 301: 592-595, 1979.
-
(1979)
N. Engl J Med.
, vol.301
, pp. 592-595
-
-
Cohen, A.J.1
Li, F.P.2
Berg, S.3
Marchetto, D.J.4
Tsai, S.5
Jacobs, S.C.6
Brown, R.S.7
-
3
-
-
0021167530
-
Involvement of band 3p14 in t(3;8) hereditary renal carcinoma
-
Wang, N., and Perkins, K. L. Involvement of band 3p14 in t(3;8) hereditary renal carcinoma. Cancer Genet Cytogenet., 11: 479-481, 1984.
-
(1984)
Cancer Genet Cytogenet.
, vol.11
, pp. 479-481
-
-
Wang, N.1
Perkins, K.L.2
-
4
-
-
0029045840
-
Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3
-
Paradee, W., Mullins, C., He, Z., Glover, T., Wilke, C., Opalka, B., Schutte, J., and Smith, D. I. Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3. Genomics, 27: 358-361, 1995.
-
(1995)
Genomics
, vol.27
, pp. 358-361
-
-
Paradee, W.1
Mullins, C.2
He, Z.3
Glover, T.4
Wilke, C.5
Opalka, B.6
Schutte, J.7
Smith, D.I.8
-
5
-
-
0023220797
-
Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer
-
Naylor, S. L., Johnson, B. E., Minna, J D , and Sakaguchi, A. Y Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer Nature (Lond.), 329: 451-454, 1987.
-
(1987)
Nature (Lond.)
, vol.329
, pp. 451-454
-
-
Naylor, S.L.1
Johnson, B.E.2
Minna, J.D.3
Sakaguchi, A.Y.4
-
6
-
-
0023233027
-
Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung
-
Brauch, H , Johnson, B., Hovis, J , Yano, T , Gazdar, A., Pettengill, O. S., Graziano, S., Sorenson, G. D., Poiesz, B J., Minna, J., Linehan, M , and Zbar, B Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung. N Engl. J. Med., 317. 1109-1113, 1987.
-
(1987)
N Engl. J. Med.
, vol.317
, pp. 1109-1113
-
-
Brauch, H.1
Johnson, B.2
Hovis, J.3
Yano, T.4
Gazdar, A.5
Pettengill, O.S.6
Graziano, S.7
Sorenson, G.D.8
Poiesz, B.J.9
Minna, J.10
Linehan, M.11
Zbar, B.12
-
7
-
-
0023181644
-
Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma
-
Zbar, B., Brauch, H., Talmadge, C., and Linehan, M. Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma. Nature (Lond.), 327: 721-724, 1987.
-
(1987)
Nature (Lond.)
, vol.327
, pp. 721-724
-
-
Zbar, B.1
Brauch, H.2
Talmadge, C.3
Linehan, M.4
-
8
-
-
0028133288
-
Loss of heterozygosity on the short arm of chromosome 3 in mesothelioma cell lines and solid tumors
-
Zeiger, M. A., Gnarra, J. R., Zbar, B., Linehan, W. M., and Pass, H. I. Loss of heterozygosity on the short arm of chromosome 3 in mesothelioma cell lines and solid tumors Genes Chromosomes & Cancer, 11: 15-20, 1994
-
(1994)
Genes Chromosomes & Cancer
, vol.11
, pp. 15-20
-
-
Zeiger, M.A.1
Gnarra, J.R.2
Zbar, B.3
Linehan, W.M.4
Pass, H.I.5
-
9
-
-
0029057487
-
Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma
-
Zeiger, M. A., Zbar, B., Keiser, H , Linehan, W M., and Gnarra, J. R. Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma. Genes Chromosomes & Cancer, 13: 151-156, 1995.
-
(1995)
Genes Chromosomes & Cancer
, vol.13
, pp. 151-156
-
-
Zeiger, M.A.1
Zbar, B.2
Keiser, H.3
Linehan, W.M.4
Gnarra, J.R.5
-
10
-
-
0023235930
-
Loss of heterozygosity for a chromosome 3 sequence presumably at 3p21 in small cell lung cancer
-
Mooibroek, H., Osinga, J., Postmus, P E., Carritt, B , and Buys, C. H. Loss of heterozygosity for a chromosome 3 sequence presumably at 3p21 in small cell lung cancer. Cancer Genet. Cytogenet., 27: 361-365, 1987
-
(1987)
Cancer Genet. Cytogenet.
, vol.27
, pp. 361-365
-
-
Mooibroek, H.1
Osinga, J.2
Postmus, P.E.3
Carritt, B.4
Buys, C.H.5
-
11
-
-
0342591692
-
Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines
-
Kastury, K., Baffa, R., Druck, T , Ohta, M., Cotticelli, M. G., Inoue, H., Negrini, M., Rugge, M., Huang, D., Croce, C. M., Palazzo, J., and Huebner, K. Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines. Cancer Res., 56. 978-983, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 978-983
-
-
Kastury, K.1
Baffa, R.2
Druck, T.3
Ohta, M.4
Cotticelli, M.G.5
Inoue, H.6
Negrini, M.7
Rugge, M.8
Huang, D.9
Croce, C.M.10
Palazzo, J.11
Huebner, K.12
-
12
-
-
0028672618
-
Detection of genetic loss in tumors by representational difference analysis
-
Lisitsyn, N. A., Leach, F S., Vogelstein, B., and Wigler, M. H. Detection of genetic loss in tumors by representational difference analysis. Cold Spring Harbor Symp. Quant. Biol., 59. 585-587, 1994
-
(1994)
Cold Spring Harbor Symp. Quant. Biol.
, vol.59
, pp. 585-587
-
-
Lisitsyn, N.A.1
Leach, F.S.2
Vogelstein, B.3
Wigler, M.H.4
-
13
-
-
0027504088
-
Antioncogenes and human cancer
-
Knudson, A. G. Antioncogenes and human cancer. Proc. Natl. Acad. Sci. USA, 90: 10914-10921, 1993.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 10914-10921
-
-
Knudson, A.G.1
-
14
-
-
0028939263
-
Comparative genomic analysis of tumors: Detection of DNA losses and amplification
-
Lisitsyn, N. A., Lisitsina, N. M., Dalbagni, G., Barker, P , Sanchez, C. A., Gnarra, J., Linehan, W. M., Reid, B. J., and Wigler, M. H. Comparative genomic analysis of tumors: detection of DNA losses and amplification. Proc Natl. Acad. Sci. USA, 92: 151-155, 1995.
-
(1995)
Proc Natl. Acad. Sci. USA
, vol.92
, pp. 151-155
-
-
Lisitsyn, N.A.1
Lisitsina, N.M.2
Dalbagni, G.3
Barker, P.4
Sanchez, C.A.5
Gnarra, J.6
Linehan, W.M.7
Reid, B.J.8
Wigler, M.H.9
-
15
-
-
13344279424
-
The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3,8) breakpoint, is abnormal in digestive tract cancers
-
Ohta, M., Hiroshi, I., Cotticelli, M G., Kastury, K., Baffa, R , Palazzo, J., Siprashvili, Z., Mori, M., McCue, P., Druck, T., Croce, C. M., and Huebner, K. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3,8) breakpoint, is abnormal in digestive tract cancers. Cell, 84: 587-597, 1996.
-
(1996)
Cell
, vol.84
, pp. 587-597
-
-
Ohta, M.1
Hiroshi, I.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
-
16
-
-
0029562527
-
Cloning of the Schizosaccharomyces pombe gene encoding diadenosine 5′,5‴-p-1,p-4-tetraphosphate [ap(4)a] asymmetrical hydrolase: Sequence similarity with the histidine triad (HIT) protein family
-
Huang, Y., Garrison, P N , and Barnes, L. D Cloning of the Schizosaccharomyces pombe gene encoding diadenosine 5′,5‴-p-1,p-4-tetraphosphate [ap(4)a] asymmetrical hydrolase: sequence similarity with the histidine triad (HIT) protein family. Biochem. J., 312: 925-932, 1995.
-
(1995)
Biochem. J.
, vol.312
, pp. 925-932
-
-
Huang, Y.1
Garrison, P.N.2
Barnes, L.D.3
-
17
-
-
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. 17-26, 1996
-
(1996)
Cell
, vol.85
, pp. 17-26
-
-
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
-
18
-
-
0029066689
-
Inactivation of the type II TGF-β receptor in colon cancer cells with microsatellite instability
-
Washington DC
-
Markowitz, S., Wang, J., Myeroff, L., Parsons, R., Sun, L., Lutterbaugh, J., Fan, R. S., Zborowska, E., Kinzler, K. W., Vogelstein, B , Brattain, M., and Willcon, J. K. V. Inactivation of the type II TGF-β receptor in colon cancer cells with microsatellite instability. Science (Washington DC), 268: 1336-1338, 1995
-
(1995)
Science
, vol.268
, pp. 1336-1338
-
-
Markowitz, S.1
Wang, J.2
Myeroff, L.3
Parsons, R.4
Sun, L.5
Lutterbaugh, J.6
Fan, R.S.7
Zborowska, E.8
Kinzler, K.W.9
Vogelstein, B.10
Brattain, M.11
Willcon, J.K.V.12
-
19
-
-
0023216178
-
Cell Culture of human colon adenomas and carcinomas
-
Willson, J Cell Culture of human colon adenomas and carcinomas Cancer Res., 47: 2704-2713, 1987.
-
(1987)
Cancer Res.
, vol.47
, pp. 2704-2713
-
-
Willson, J.1
-
20
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
Leach, F. S., Nicolaides, N C., Papadopoulos, N., Liu, B., Jen, J , Parsons, R., Peltomäki, P., Sistonen, P., Aaltonen, L. A., Nystrom-Lahti, M., Guan, X-Y., Zhang, J., Meltzer, P. S., Yu, J-W., Kao, F-T , Chen, D. J., Cerosaletti, K. M., Fournier, R. E K., Todd, S., Lewis, T., Leach, R J., Naylor, S. L., Weissenbach, J , Mecklin, J-P , Järvinen, H., Peterson, G M., Hamilton, S. R., Green, J., Jass, J , Watson, P., Lynch, H T., Trent, J. M., de la Chapelle, A., Kinzler, K. W., and Vogelstein, B Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell, 75: 1215-1225, 1993.
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.C.2
Papadopoulos, N.3
Liu, B.4
Jen, J.5
Parsons, R.6
Peltomäki, P.7
Sistonen, P.8
Aaltonen, L.A.9
Nystrom-Lahti, M.10
Guan, X.-Y.11
Zhang, J.12
Meltzer, P.S.13
Yu, J.-W.14
Kao, F.-T.15
Chen, D.J.16
Cerosaletti, K.M.17
Fournier, R.E.K.18
Todd, S.19
Lewis, T.20
Leach, R.J.21
Naylor, S.L.22
Weissenbach, J.23
Mecklin, J.-P.24
Järvinen, H.25
Peterson, G.M.26
Hamilton, S.R.27
Green, J.28
Jass, J.29
Watson, P.30
Lynch, H.T.31
Trent, J.M.32
De La Chapelle, A.33
Kinzler, K.W.34
Vogelstein, B.35
more..
-
21
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Washington DC
-
Papadopoulos, N., Nicolaides, N C., Wei, Y-F., Ruben, S. M., Carter, K. C., Rosen, C A., Haseltine, W. A., Fleischmann, R. D., Fraser, C. M , Adams, M. D., Venter, J. C., Hamilton, S. R., Peterson, G. M , Watson, P., Lynch, H. T., Peltomaki, P., Mecklin, J-P , de la Chapelle, A., Kinzler, K W., and Vogelstein, B. Mutation of a mutL homolog in hereditary colon cancer. Science (Washington DC), 263: 1625-1629, 1994.
-
(1994)
Science
, vol.263
, pp. 1625-1629
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Wei, Y.-F.3
Ruben, S.M.4
Carter, K.C.5
Rosen, C.A.6
Haseltine, W.A.7
Fleischmann, R.D.8
Fraser, C.M.9
Adams, M.D.10
Venter, J.C.11
Hamilton, S.R.12
Peterson, G.M.13
Watson, P.14
Lynch, H.T.15
Peltomaki, P.16
Mecklin, J.-P.17
De La Chapelle, A.18
Kinzler, K.W.19
Vogelstein, B.20
more..
-
22
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu, B., Parsons, R., Papadopoulos, N , Nicolaides, N. C., Lynch, H. T., Watson, P., Jass, J. R , Dunlop, M., Wyllie, A., Peltomaki, P., de la Chapelle, A., Hamilton, S. R., Vogelstein, B., and Kinzler, K. W. Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med., 2: 169-174, 1996.
-
(1996)
Nat Med.
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.2
Papadopoulos, N.3
Nicolaides, N.C.4
Lynch, H.T.5
Watson, P.6
Jass, J.R.7
Dunlop, M.8
Wyllie, A.9
Peltomaki, P.10
De La Chapelle, A.11
Hamilton, S.R.12
Vogelstein, B.13
Kinzler, K.W.14
-
23
-
-
0025634118
-
p53 gene mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis
-
Baker, S J., Preisinger, A. C., Jessup, J M., Paraskeva, C , Markowitz, S., Willson, J. K , Hamilton, S., and Vogelstein, B. p53 gene mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis. Cancer Res., 50: 7717-7722, 1990.
-
(1990)
Cancer Res.
, vol.50
, pp. 7717-7722
-
-
Baker, S.J.1
Preisinger, A.C.2
Jessup, J.M.3
Paraskeva, C.4
Markowitz, S.5
Willson, J.K.6
Hamilton, S.7
Vogelstein, B.8
-
24
-
-
0028875562
-
Allelotype of pancreatic adenocarcinoma using xenograft enrichment
-
Hahn, S. A., Seymour, A. B., Hoque, A T , Schutte, M., da Costa, L. T., Redston, M. S., Caldas, C., Weinstein, C. L., Fischer, A., Yeo, C. J., Hruban, R. H., and Kern, S. E. Allelotype of pancreatic adenocarcinoma using xenograft enrichment. Cancer Res , 55: 4670-4675, 1995.
-
(1995)
Cancer Res
, vol.55
, pp. 4670-4675
-
-
Hahn, S.A.1
Seymour, A.B.2
Hoque, A.T.3
Schutte, M.4
Da Costa, L.T.5
Redston, M.S.6
Caldas, C.7
Weinstein, C.L.8
Fischer, A.9
Yeo, C.J.10
Hruban, R.H.11
Kern, S.E.12
-
25
-
-
0026068837
-
Stability of critical genetic lesions in human colorectal carcinoma xenografts
-
McQueen, H. A., Wyllie, A. H., Piris, J., Foster, E., and Bird, C. C. Stability of critical genetic lesions in human colorectal carcinoma xenografts. Br. J. Cancer, 63: 94-96, 1991.
-
(1991)
Br. J. Cancer
, vol.63
, pp. 94-96
-
-
McQueen, H.A.1
Wyllie, A.H.2
Piris, J.3
Foster, E.4
Bird, C.C.5
-
26
-
-
0027314411
-
Microsatellite instability in cancer of the proximal colon
-
Washington DC
-
Thibodeau, S. N., Bren, G., and Schaid, D. Microsatellite instability in cancer of the proximal colon. Science (Washington DC), 260: 816-819, 1993.
-
(1993)
Science
, vol.260
, pp. 816-819
-
-
Thibodeau, S.N.1
Bren, G.2
Schaid, D.3
-
27
-
-
0027285475
-
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
-
Ionov, Y., Peinado, M. A , Malkhosyan, S , Shibata, D., and Perucho, M. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature (Lond.), 363: 558-561, 1993.
-
(1993)
Nature (Lond.)
, vol.363
, pp. 558-561
-
-
Ionov, Y.1
Peinado, M.A.2
Malkhosyan, S.3
Shibata, D.4
Perucho, M.5
-
28
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancer
-
Washington DC
-
Aaltonen, L. A., Peltomäki, P , Leach, F. S., Sistonen, P., Pylkkanen, L., Mecklin, J. P., Jarvinen, H., Powell, S. M., Jen, J., Hamilton, S. R., Petersen, G. M., Kinzler, K. W , Vogelstein, B., and de La Chapelle, A. Clues to the pathogenesis of familial colorectal cancer. Science (Washington DC), 260: 812-816, 1993.
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomäki, P.2
Leach, F.S.3
Sistonen, P.4
Pylkkanen, L.5
Mecklin, J.P.6
Jarvinen, H.7
Powell, S.M.8
Jen, J.9
Hamilton, S.R.10
Petersen, G.M.11
Kinzler, K.W.12
Vogelstein, B.13
De La Chapelle, A.14
-
29
-
-
0029089259
-
Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspectives
-
Marra, G., and Boland, C. R Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives. J. Natl. Cancer Inst., 87: 1114-1125, 1995.
-
(1995)
J. Natl. Cancer Inst.
, vol.87
, pp. 1114-1125
-
-
Marra, G.1
Boland, C.R.2
-
30
-
-
0026234101
-
Identification and characterization of the gene for neurofibromatosis type 1
-
White, R., Viskochil, D , and O'Connell, P Identification and characterization of the gene for neurofibromatosis type 1. Curr. Opin. Neurobiol., 1: 462-467, 1991.
-
(1991)
Curr. Opin. Neurobiol.
, vol.1
, pp. 462-467
-
-
White, R.1
Viskochil, D.2
O'Connell, P.3
-
31
-
-
0025876136
-
The hunt for the neurofibromatosis gene
-
Goldberg, N. S., and Collins, F. S. The hunt for the neurofibromatosis gene. Arch. Dermatol., 127: 1705-1707, 1991.
-
(1991)
Arch. Dermatol.
, vol.127
, pp. 1705-1707
-
-
Goldberg, N.S.1
Collins, F.S.2
-
32
-
-
0025978395
-
cDNA sequence and genomic structure of Ev12b, a gene lying within an intron of the neurofibromatosis type 1 gene
-
Cawthon, R. M., Andersen, L B , Buchberg, A. M., Xu, G. F , O'Connell, P., Viskochil, D., Weiss, R. B , Wallace, M. R., Marchuk, D. A., Culver, M., Stevens, J., Jenkins, N. A., Copeland, N. G., Collins, F. S., and White, R. cDNA sequence and genomic structure of Ev12b, a gene lying within an intron of the neurofibromatosis type 1 gene. Genomics, 9: 446-460, 1991.
-
(1991)
Genomics
, vol.9
, pp. 446-460
-
-
Cawthon, R.M.1
Andersen, L.B.2
Buchberg, A.M.3
Xu, G.F.4
O'Connell, P.5
Viskochil, D.6
Weiss, R.B.7
Wallace, M.R.8
Marchuk, D.A.9
Culver, M.10
Stevens, J.11
Jenkins, N.A.12
Copeland, N.G.13
Collins, F.S.14
White, R.15
-
33
-
-
0026011110
-
The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene
-
Viskochil, D., Cawthon, R , O'Connell, P., Xu, G F., Stevens, J., Culver, M., Carey, J., and White, R. The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene. Mol. Cell. Biol., 11: 906-912, 1991.
-
(1991)
Mol. Cell. Biol.
, vol.11
, pp. 906-912
-
-
Viskochil, D.1
Cawthon, R.2
O'Connell, P.3
Xu, G.F.4
Stevens, J.5
Culver, M.6
Carey, J.7
White, R.8
-
34
-
-
0025167973
-
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations
-
O'Connell, P., Viskochil, D., Buchberg, A. M., Fountain, J., Cawthon, R. M., Culver, M., Stevens, J , Rich, D. C , Ledbetter, D. H , Wallace, M., Carey, J. C., Jenkins, N. A., Copeland, N. G., Collins, F. S., and White, R. The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations. Genomics, 7. 547-554, 1990.
-
(1990)
Genomics
, vol.7
, pp. 547-554
-
-
O'Connell, P.1
Viskochil, D.2
Buchberg, A.M.3
Fountain, J.4
Cawthon, R.M.5
Culver, M.6
Stevens, J.7
Rich, D.C.8
Ledbetter, D.H.9
Wallace, M.10
Carey, J.C.11
Jenkins, N.A.12
Copeland, N.G.13
Collins, F.S.14
White, R.15
-
35
-
-
0023910775
-
Translocation t(3:8)(p14.2:q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes
-
Glover, T. W , Coyle-Morris, J F., Li, F. P., Brown, R. S., Berger, C. S., Gemmill, R. M., and Hecht, F. Translocation t(3:8)(p14.2:q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes. Cancer Genet. Cytogenet., 31: 69-73, 1988.
-
(1988)
Cancer Genet. Cytogenet.
, vol.31
, pp. 69-73
-
-
Glover, T.W.1
Coyle-Morris, J.F.2
Li, F.P.3
Brown, R.S.4
Berger, C.S.5
Gemmill, R.M.6
Hecht, F.7
-
37
-
-
15844390729
-
Evaluation of candidate tumor suppressor genes on chromosome 18 in colorectal cancers
-
in press
-
Thiagalingam, S , Lengauer, C., Leach, F. S., Schutte, M., Hahn, S., Overhauser, J., Wilson, J. K V., Markowitz, S., Hamilton, S. R , Kern, S. E., Kinzler, K. W., and Vogelstein, B. Evaluation of candidate tumor suppressor genes on chromosome 18 in colorectal cancers. Nat Genet , in press, 1996.
-
(1996)
Nat Genet
-
-
Thiagalingam, S.1
Lengauer, C.2
Leach, F.S.3
Schutte, M.4
Hahn, S.5
Overhauser, J.6
Wilson, J.K.V.7
Markowitz, S.8
Hamilton, S.R.9
Kern, S.E.10
Kinzler, K.W.11
Vogelstein, B.12
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