-
1
-
-
0020679049
-
Patient with 13 chromosome deletion: Evidence that the retinoblastoma gene is a recessive cancer gene
-
Benedict WF, Murphree AL, Banerjee A, Spina CA, Sparkes MD, Sparkes RS (1983) Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene. Science 219:973-975
-
(1983)
Science
, vol.219
, pp. 973-975
-
-
Benedict, W.F.1
Murphree, A.L.2
Banerjee, A.3
Spina, C.A.4
Sparkes, M.D.5
Sparkes, R.S.6
-
2
-
-
0028221943
-
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
-
Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindhlom A, Tannergard P, Bollag RJ, Godwin AR, Ward DC, Nordenskjold M, Fishel R, Kolodner R, Liskay RM (1994) Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature 368:258-261
-
(1994)
Nature
, vol.368
, pp. 258-261
-
-
Bronner, C.E.1
Baker, S.M.2
Morrison, P.T.3
Warren, G.4
Smith, L.G.5
Lescoe, M.K.6
Kane, M.7
Earabino, C.8
Lipford, J.9
Lindhlom, A.10
Tannergard, P.11
Bollag, R.J.12
Godwin, A.R.13
Ward, D.C.14
Nordenskjold, M.15
Fishel, R.16
Kolodner, R.17
Liskay, R.M.18
-
3
-
-
0025099787
-
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
-
Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Kral A, Yeger H, Lewis WH, Jones C, Housman DE (1990) Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 60:509-520
-
(1990)
Cell
, vol.60
, pp. 509-520
-
-
Call, K.M.1
Glaser, T.2
Ito, C.Y.3
Buckler, A.J.4
Pelletier, J.5
Haber, D.A.6
Rose, E.A.7
Kral, A.8
Yeger, H.9
Lewis, W.H.10
Jones, C.11
Housman, D.E.12
-
4
-
-
0020518746
-
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
-
Cavenee WK, Dryja TP, Phillips RA, Benedict WF, Godbout R, Gallie BL, Murphree AL, Strong LC, White RL (1983) Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature 305:779-784
-
(1983)
Nature
, vol.305
, pp. 779-784
-
-
Cavenee, W.K.1
Dryja, T.P.2
Phillips, R.A.3
Benedict, W.F.4
Godbout, R.5
Gallie, B.L.6
Murphree, A.L.7
Strong, L.C.8
White, R.L.9
-
5
-
-
0015749593
-
A general theory of carcinogenesis
-
Comings DE (1973) A general theory of carcinogenesis. Proc Natl Acad Sci USA 70:3324-3328
-
(1973)
Proc Natl Acad Sci USA
, vol.70
, pp. 3324-3328
-
-
Comings, D.E.1
-
6
-
-
0025086953
-
p53 functions as a cell cycle control protein in osteosarcomas
-
Diller L, Kassel J, Nelson CE, Gryka MA, Litwak G, Gebhardt M, Bressac B, Ozturk M, Baker SJ, Vogelstein B, Friend SH (1990) p53 functions as a cell cycle control protein in osteosarcomas. Mol Cell Biol 10:5772-5781
-
(1990)
Mol Cell Biol
, vol.10
, pp. 5772-5781
-
-
Diller, L.1
Kassel, J.2
Nelson, C.E.3
Gryka, M.A.4
Litwak, G.5
Gebhardt, M.6
Bressac, B.7
Ozturk, M.8
Baker, S.J.9
Vogelstein, B.10
Friend, S.H.11
-
7
-
-
0027303248
-
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
-
Donis-Keller H, Dou S, Chi D, Carlson KM, Toshima K, Lairmore TC, Howe JR, Moley JF, Goodfellow P, Wells SA (1993) Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 2:851
-
(1993)
Hum Mol Genet
, vol.2
, pp. 851
-
-
Donis-Keller, H.1
Dou, S.2
Chi, D.3
Carlson, K.M.4
Toshima, K.5
Lairmore, T.C.6
Howe, J.R.7
Moley, J.F.8
Goodfellow, P.9
Wells, S.A.10
-
8
-
-
0022623369
-
Second primary neoplasms in patients with retinoblastoma
-
Draper GJ, Sanders BM, Kingston JE (1986) Second primary neoplasms in patients with retinoblastoma. Br J Cancer 53:661-671
-
(1986)
Br J Cancer
, vol.53
, pp. 661-671
-
-
Draper, G.J.1
Sanders, B.M.2
Kingston, J.E.3
-
9
-
-
0025092693
-
Ulcerative colitis and colorectal cancer: A population-based study
-
Ekbom A, Helmick C, Zack M, Adami H-O (1990) Ulcerative colitis and colorectal cancer: a population-based study. N Engl J Med 323:1228-1233
-
(1990)
N Engl J Med
, vol.323
, pp. 1228-1233
-
-
Ekbom, A.1
Helmick, C.2
Zack, M.3
Adami, H.-O.4
-
10
-
-
0025312728
-
A genetic model of colorectal tumorigenesis
-
Fearon ER, Vogelstein B (1990) A genetic model of colorectal tumorigenesis. Cell 61:759-767
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
11
-
-
0021338486
-
Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours
-
Fearon ER, Vogelstein B, Feinberg AP (1984) Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours. Nature 309:176-178
-
(1984)
Nature
, vol.309
, pp. 176-178
-
-
Fearon, E.R.1
Vogelstein, B.2
Feinberg, A.P.3
-
12
-
-
0025056930
-
Identification of a chromosome 18q gene that is altered in colorectal cancers
-
Fearon ER, Cho KR, Nigro JM, Kern SE, Simons JW, Ruppert JM, Hamilton SR, Preisinger AC, Thomas G, Kinzler KW, Vogelstein B (1990) Identification of a chromosome 18q gene that is altered in colorectal cancers. Science 247:49-56
-
(1990)
Science
, vol.247
, pp. 49-56
-
-
Fearon, E.R.1
Cho, K.R.2
Nigro, J.M.3
Kern, S.E.4
Simons, J.W.5
Ruppert, J.M.6
Hamilton, S.R.7
Preisinger, A.C.8
Thomas, G.9
Kinzler, K.W.10
Vogelstein, B.11
-
13
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary non-polyposis colon cancer
-
Fishel R, Lescoe MK, Rao MRS, Copeland NG, Jenkins NA, Garber J, Kane M, Kolodner R (1993) The human mutator gene homolog MSH2 and its association with hereditary non-polyposis colon cancer. Cell 75:1027-1038
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.1
Lescoe, M.K.2
Rao, M.R.S.3
Copeland, N.G.4
Jenkins, N.A.5
Garber, J.6
Kane, M.7
Kolodner, R.8
-
14
-
-
0017060019
-
Sporadic bilateral retinoblastoma and 13q-chromosomal deletion
-
Francke U, Kung F (1976) Sporadic bilateral retinoblastoma and 13q-chromosomal deletion. Med Pediatr Oncol 2:379-385
-
(1976)
Med Pediatr Oncol
, vol.2
, pp. 379-385
-
-
Francke, U.1
Kung, F.2
-
16
-
-
0022506980
-
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
-
Friend SH, Bernards R, Rogelj S, Weinberg RA, Rapaport JM, Albert DM, Dryja TP (1986) A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma. Nature 323:643-646
-
(1986)
Nature
, vol.323
, pp. 643-646
-
-
Friend, S.H.1
Bernards, R.2
Rogelj, S.3
Weinberg, R.A.4
Rapaport, J.M.5
Albert, D.M.6
Dryja, T.P.7
-
17
-
-
0023222707
-
Structural evidence for the authenticity of the human retinoblastoma gene
-
Fung Y-KT, Murphree AL, T'Ang A, Qian J, Hinrichs SH, Benedict WF (1987) Structural evidence for the authenticity of the human retinoblastoma gene. Science 236:1657-1661
-
(1987)
Science
, vol.236
, pp. 1657-1661
-
-
Fung, Y.-K.T.1
Murphree, A.L.2
T'Ang, A.3
Qian, J.4
Hinrichs, S.H.5
Benedict, W.F.6
-
18
-
-
0028073794
-
BRCA1 mutations in primary breast and ovarian cancers
-
Futreal PA, Liu Q, Shattuck-Eidens D, Cochran C, Harshman K, Tavtigian S, Bennett LM, Haugen-Strano A, Swensen J, Miki Y, Eddington K, McClure M, Frye C, Weaver-Feldhaus J, Ding W, Gholami Z, Söderkvist P, Terry L, Jhanwar S, Berchuck A, Iglehart JD, Marks J, Ballinger DG, Barrett JC, Skolnick MH, Kamb A, Wiseman R (1994) BRCA1 mutations in primary breast and ovarian cancers. Science 266:120-122
-
(1994)
Science
, vol.266
, pp. 120-122
-
-
Futreal, P.A.1
Liu, Q.2
Shattuck-Eidens, D.3
Cochran, C.4
Harshman, K.5
Tavtigian, S.6
Bennett, L.M.7
Haugen-Strano, A.8
Swensen, J.9
Miki, Y.10
Eddington, K.11
McClure, M.12
Frye, C.13
Weaver-Feldhaus, J.14
Ding, W.15
Gholami, Z.16
Söderkvist, P.17
Terry, L.18
Jhanwar, S.19
Berchuck, A.20
Iglehart, J.D.21
Marks, J.22
Ballinger, D.G.23
Barrett, J.C.24
Skolnick, M.H.25
Kamb, A.26
Wiseman, R.27
more..
-
19
-
-
0025098654
-
Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping
-
Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GAP (1990) Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping. Nature 343:774-778
-
(1990)
Nature
, vol.343
, pp. 774-778
-
-
Gessler, M.1
Poustka, A.2
Cavenee, W.3
Neve, R.L.4
Orkin, S.H.5
Bruns, G.A.P.6
-
20
-
-
0020512716
-
Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma
-
Godbout R, Dryja TP, Squire J, Gallie BL, Phillips RA (1983) Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma. Nature 304:451-453
-
(1983)
Nature
, vol.304
, pp. 451-453
-
-
Godbout, R.1
Dryja, T.P.2
Squire, J.3
Gallie, B.L.4
Phillips, R.A.5
-
21
-
-
0025938038
-
Identification and characterization of the familial adenomatous polyposis coli gene
-
Groden J, Thliveris A, Samowitz W, Carlson M, Gelbert L, Albertsen H, Joslyn G, Stevens J, Spirio L, Robertson M, Sargeant L, Krapcho K, Wolff E, Burt R, Hughes JP, Warrington J, McPherson J, Wasmuth J, LePaslier D, Abderrahim H, Cohen D, Leppert M, White R (1991) Identification and characterization of the familial adenomatous polyposis coli gene. Cell 66:589-600
-
(1991)
Cell
, vol.66
, pp. 589-600
-
-
Groden, J.1
Thliveris, A.2
Samowitz, W.3
Carlson, M.4
Gelbert, L.5
Albertsen, H.6
Joslyn, G.7
Stevens, J.8
Spirio, L.9
Robertson, M.10
Sargeant, L.11
Krapcho, K.12
Wolff, E.13
Burt, R.14
Hughes, J.P.15
Warrington, J.16
McPherson, J.17
Wasmuth, J.18
LePaslier, D.19
Abderrahim, H.20
Cohen, D.21
Leppert, M.22
White, R.23
more..
-
22
-
-
0028171234
-
p53 protein expression in ulcertative colitis-associated colorectal dysplasia and carcinoma
-
Harpaz N, Peck AL, Yin J, Fiel I, Hontanosas M, Tong TR, Laurin JN, Abraham JM, Greenwald BD, Meltzer SJ (1994) p53 protein expression in ulcertative colitis-associated colorectal dysplasia and carcinoma. Human Pathol 25:1069-1074
-
(1994)
Human Pathol
, vol.25
, pp. 1069-1074
-
-
Harpaz, N.1
Peck, A.L.2
Yin, J.3
Fiel, I.4
Hontanosas, M.5
Tong, T.R.6
Laurin, J.N.7
Abraham, J.M.8
Greenwald, B.D.9
Meltzer, S.J.10
-
23
-
-
0016793355
-
Retinoblastoma: A model of hereditary fragile chromosomal regions
-
Hashem N, Khalifa SH (1975) Retinoblastoma: a model of hereditary fragile chromosomal regions. Hum Hered 25:35-49
-
(1975)
Hum Hered
, vol.25
, pp. 35-49
-
-
Hashem, N.1
Khalifa, S.H.2
-
24
-
-
0018148959
-
Model for the incidence of embryonal cancers: Application to retinoblastoma
-
Hethcote HW, Knudson AG (1978) Model for the incidence of embryonal cancers: application to retinoblastoma Proc Natl Acad Sci USA 75:2453-2457
-
(1978)
Proc Natl Acad Sci USA
, vol.75
, pp. 2453-2457
-
-
Hethcote, H.W.1
Knudson, A.G.2
-
25
-
-
0026920079
-
Inactivation of both APC alleles in an early stage of colon adenomas in a patient with familial adenomatous polyposis (FAP)
-
Ichii S, Horii A, Nakatsuru S, Furuyama J, Utsunomiya J, Nakamura Y (1992) Inactivation of both APC alleles in an early stage of colon adenomas in a patient with familial adenomatous polyposis (FAP). Hum Mol Genet 1:387-390
-
(1992)
Hum Mol Genet
, vol.1
, pp. 387-390
-
-
Ichii, S.1
Horii, A.2
Nakatsuru, S.3
Furuyama, J.4
Utsunomiya, J.5
Nakamura, Y.6
-
26
-
-
0019638461
-
Interstitial deletion of short arm of chromosome 11 limited to Wilms' tumor cells in a patient without aniridia
-
Kaneko Y, Egues MC, Rowley JD (1981) Interstitial deletion of short arm of chromosome 11 limited to Wilms' tumor cells in a patient without aniridia. Cancer Res 41:4577-4578
-
(1981)
Cancer Res
, vol.41
, pp. 4577-4578
-
-
Kaneko, Y.1
Egues, M.C.2
Rowley, J.D.3
-
27
-
-
0026496885
-
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia
-
Kastan MB, Zhan Q, El Deiry WS, Carrier F, Jacks T, Walsh WV, Plunkett BS, Vogelstein B, Fornace AJ (1992) A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia. Cell 71:587-597
-
(1992)
Cell
, vol.71
, pp. 587-597
-
-
Kastan, M.B.1
Zhan, Q.2
El Deiry, W.S.3
Carrier, F.4
Jacks, T.5
Walsh, W.V.6
Plunkett, B.S.7
Vogelstein, B.8
Fornace, A.J.9
-
28
-
-
0026695813
-
Genetic changes of both p53 alleles associated with the conversion from colorectal adenoma to early carcinoma in familial adenomatous polyposis
-
Kikuchi-Yanoshita R, Konishi M, Ito S, Seki M, Tanaka K, Maeda Y, lino H, Fukayama M, Koike M, Mori T, Sakuraba H, Fukunari H, Iwama T, Miyaki M (1992) Genetic changes of both p53 alleles associated with the conversion from colorectal adenoma to early carcinoma in familial adenomatous polyposis. Cancer Res 52:3965-3971
-
(1992)
Cancer Res
, vol.52
, pp. 3965-3971
-
-
Kikuchi-Yanoshita, R.1
Konishi, M.2
Ito, S.3
Seki, M.4
Tanaka, K.5
Maeda, Y.6
Lino, H.7
Fukayama, M.8
Koike, M.9
Mori, T.10
Sakuraba, H.11
Fukunari, H.12
Iwama, T.13
Miyaki, M.14
-
29
-
-
0023611733
-
The approaching era of the tumor-suppressor genes
-
Klein G (1987) The approaching era of the tumor-suppressor genes. Science 238:1539-1545
-
(1987)
Science
, vol.238
, pp. 1539-1545
-
-
Klein, G.1
-
30
-
-
0015043748
-
Mutation and cancer: Statistical study of retinoblastoma
-
Knudson AG (1971) Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA 68:820-823
-
(1971)
Proc Natl Acad Sci USA
, vol.68
, pp. 820-823
-
-
Knudson, A.G.1
-
31
-
-
0001201784
-
Mutation and human cancer
-
Knudson AG (1973) Mutation and human cancer. Adv Cancer Res 17:317-352
-
(1973)
Adv Cancer Res
, vol.17
, pp. 317-352
-
-
Knudson, A.G.1
-
32
-
-
0017819319
-
Retinoblastoma: A prototypic hereditary neoplasm
-
Knudson AG (1978) Retinoblastoma: a prototypic hereditary neoplasm. Semin Oncol 5:57-60
-
(1978)
Semin Oncol
, vol.5
, pp. 57-60
-
-
Knudson, A.G.1
-
33
-
-
0021879645
-
Hereditary cancer, oncogenes, and antioncogenes
-
Knudson AG (1985) Hereditary cancer, oncogenes, and antioncogenes. Cancer Res 45:1437-1443
-
(1985)
Cancer Res
, vol.45
, pp. 1437-1443
-
-
Knudson, A.G.1
-
34
-
-
0026873214
-
Stem cell regulation, tissue ontogeny, and oncogenic events
-
Knudson AG (1992) Stem cell regulation, tissue ontogeny, and oncogenic events. Sem Cancer Biol 3:99-106
-
(1992)
Sem Cancer Biol
, vol.3
, pp. 99-106
-
-
Knudson, A.G.1
-
35
-
-
0027504088
-
Antioncogenes and human cancer
-
Knudson AG (1993) Antioncogenes and human cancer. Proc Natl Acad Sei USA 90:10914-10921
-
(1993)
Proc Natl Acad Sei USA
, vol.90
, pp. 10914-10921
-
-
Knudson, A.G.1
-
36
-
-
0015295131
-
Mutation and cancer: A model for Wilms' tumor of the kidney
-
Knudson AG, Strong LC (1972a) Mutation and cancer: a model for Wilms' tumor of the kidney. J Natl Cancer Inst 48:313-324
-
(1972)
J Natl Cancer Inst
, vol.48
, pp. 313-324
-
-
Knudson, A.G.1
Strong, L.C.2
-
37
-
-
0015402175
-
Mutation and cancer: Neuroblastoma and pheochromocytoma
-
Knudson AG, Strong LC (1972b) Mutation and cancer: neuroblastoma and pheochromocytoma. Am J Hum Genet 24:514-532
-
(1972)
Am J Hum Genet
, vol.24
, pp. 514-532
-
-
Knudson, A.G.1
Strong, L.C.2
-
40
-
-
0021327569
-
Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour
-
Koufos A, Hansen MF, Lampkin DB, Workman ML, Copeland NG, Jenkins NA, Cavenee WK (1984) Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour. Nature 309:170-172
-
(1984)
Nature
, vol.309
, pp. 170-172
-
-
Koufos, A.1
Hansen, M.F.2
Lampkin, D.B.3
Workman, M.L.4
Copeland, N.G.5
Jenkins, N.A.6
Cavenee, W.K.7
-
41
-
-
0016168585
-
Computer-assisted analysis of chromosomal abnormalities: Detection of a deletion in aniridia/Wilms' tumor syndrome
-
Ladda R, Atkins L, Littlefield J, Neurath P, Marimuthu KM (1974) Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia/Wilms' tumor syndrome. Science 185:784-787
-
(1974)
Science
, vol.185
, pp. 784-787
-
-
Ladda, R.1
Atkins, L.2
Littlefield, J.3
Neurath, P.4
Marimuthu, K.M.5
-
42
-
-
0018348655
-
Tantigen is bound to a host protein in SV40-transformed cells
-
Lane DP, Crawford LW (1979) Tantigen is bound to a host protein in SV40-transformed cells. Nature 278:261-263
-
(1979)
Nature
, vol.278
, pp. 261-263
-
-
Lane, D.P.1
Crawford, L.W.2
-
43
-
-
0027145633
-
Mutations of a mutS homolog in hereditary non-polyposis colorectal cancer
-
Leach FS, Nicolaides NC, Papadopoulos N, Liu B, Jen J, Parsons R, Peltomäki P, Sistonen P, Aaltonen LA, Nyström-Lahti M, Guan X-Y, Zhang J, Meltzer PS, Yu J-W, Kao F-T, Chen DJ, Cerosaletti KM, Fournier REK, Todd S, Lewis T, Leach RJ, Naylor SL, Weissenbach J, Mecklin J-P, Järvinen H, Petersen GM, Hamilton SR, Green J, Jass J, Watson P, Lynch HT, Trent JM, Chapelle A de la, Kinzler KW, Vogelstein B (1993) Mutations of a mutS homolog in hereditary non-polyposis colorectal cancer. Cell 75:1215-1225
-
(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
Nyström-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
Petersen, 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..
-
44
-
-
0023106062
-
Human retinoblastoma susceptibility gene: Cloning, identification, and sequence
-
Lee W-H, Bookstein R, Hong F, Young L-J, Shew J-Y, Lee EY-HP (1987) Human retinoblastoma susceptibility gene: cloning, identification, and sequence. Science 235:1394-1399
-
(1987)
Science
, vol.235
, pp. 1394-1399
-
-
Lee, W.-H.1
Bookstein, R.2
Hong, F.3
Young, L.-J.4
Shew, J.-Y.5
Lee, E.Y.-H.P.6
-
45
-
-
0016650416
-
Familial breast cancer, soft-tissue sarcomas, and other neoplasms
-
Li FP, Fraumeni JF (1975) Familial breast cancer, soft-tissue sarcomas, and other neoplasms. Ann Intern Med 83:833-834
-
(1975)
Ann Intern Med
, vol.83
, pp. 833-834
-
-
Li, F.P.1
Fraumeni, J.F.2
-
46
-
-
0018760324
-
Characterization of a 54 K dalton cellular SV40 tumor antigen present in SV40 transformed cells and uninfected embryonal carcinoma cells
-
Linzer DIH, Levine AJ (1979) Characterization of a 54 K dalton cellular SV40 tumor antigen present in SV40 transformed cells and uninfected embryonal carcinoma cells. Cell 17:43-52
-
(1979)
Cell
, vol.17
, pp. 43-52
-
-
Linzer, D.I.H.1
Levine, A.J.2
-
47
-
-
0025633582
-
Germline p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
-
Malkin D, Li FP, Strong LC, Fraumeni JF, Nelson CE, Kim DH, Kassel J, Gryka MA, Bischoff FZ, Tainsky MA, Friend SH (1990) Germline p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science 250:1233-1238
-
(1990)
Science
, vol.250
, pp. 1233-1238
-
-
Malkin, D.1
Li, F.P.2
Strong, L.C.3
Fraumeni, J.F.4
Nelson, C.E.5
Kim, D.H.6
Kassel, J.7
Gryka, M.A.8
Bischoff, F.Z.9
Tainsky, M.A.10
Friend, S.H.11
-
48
-
-
0023576046
-
Rearrangement of the p53 gene in human osteogenic sarcomas
-
Masuda HC, Miller C, Koeffler HP, Battifora H, Cline MJ (1987) Rearrangement of the p53 gene in human osteogenic sarcomas. Proc Natl Acad Sci USA 84:7716-7719
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 7716-7719
-
-
Masuda, H.C.1
Miller, C.2
Koeffler, H.P.3
Battifora, H.4
Cline, M.J.5
-
49
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JBJ, Healey CS, Elsdon MJ, Eng C, Gardner E, Love DR, Mole SE, Moore JK, Papi L, Ponder MA, Telenius H, Tunnacliffe A, Ponder BAJ (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363:458-460
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.J.2
Healey, C.S.3
Elsdon, M.J.4
Eng, C.5
Gardner, E.6
Love, D.R.7
Mole, S.E.8
Moore, J.K.9
Papi, L.10
Ponder, M.A.11
Telenius, H.12
Tunnacliffe, A.13
Ponder, B.A.J.14
-
50
-
-
0023220797
-
Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer
-
Naylor SL, Johnson BE, Minna JD, Sakaguchi AY (1987) Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer. Nature 329:451-454
-
(1987)
Nature
, vol.329
, pp. 451-454
-
-
Naylor, S.L.1
Johnson, B.E.2
Minna, J.D.3
Sakaguchi, A.Y.4
-
51
-
-
0025899162
-
Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients
-
Nishisho I, Nakamura Y, Miyoski Y, Miki Y, Ando H, Horii A, Koyama K, Utsunomiya J, Baba S, Hedge P, Markham A, Krush AJ, Petersen G, Hamilton SR, Nilbert MC, Levy DB, Bryan TM, Preisinger AC, Smith KJ, Su L-K, Kinzler KW, Vogelstein B (1991) Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 253:665-669
-
(1991)
Science
, vol.253
, pp. 665-669
-
-
Nishisho, I.1
Nakamura, Y.2
Miyoski, Y.3
Miki, Y.4
Ando, H.5
Horii, A.6
Koyama, K.7
Utsunomiya, J.8
Baba, S.9
Hedge, P.10
Markham, A.11
Krush, A.J.12
Petersen, G.13
Hamilton, S.R.14
Nilbert, M.C.15
Levy, D.B.16
Bryan, T.M.17
Preisinger, A.C.18
Smith, K.J.19
Su, L.-K.20
Kinzler, K.W.21
Vogelstein, B.22
more..
-
52
-
-
0021343902
-
Development of homozygosity for chromosome 11p markers in Wilms' tumor
-
Orkin SH, Goldman DS, Sallan SE (1984) Development of homozygosity for chromosome 11p markers in Wilms' tumor. Nature 309:172-174
-
(1984)
Nature
, vol.309
, pp. 172-174
-
-
Orkin, S.H.1
Goldman, D.S.2
Sallan, S.E.3
-
53
-
-
0029047954
-
Loss of Apc heterozygosity and abnormal tissue building in nascent intestinal polyps in mice carrying a truncated Apc gene
-
Oshima M, Oshima H, Kitagawa K, Kobayashi M, Itakura C, Taketo M (1995) Loss of Apc heterozygosity and abnormal tissue building in nascent intestinal polyps in mice carrying a truncated Apc gene. Proc Natl Acad Sci USA 92:4482-4486
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 4482-4486
-
-
Oshima, M.1
Oshima, H.2
Kitagawa, K.3
Kobayashi, M.4
Itakura, C.5
Taketo, M.6
-
54
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos N, Nicolaides NC, Wei YF, Ruben SM, Carter KC, Rosen CA, Haseltine WA, Reischmann RD, Fraser CM, Adams MD, Venter JC, Hamilton SR, Petersen GM, Watson P, Lynch HT, Peltomäki P, Mecklin J-P, Chapelle A de la, Kinzler KW, Vogelstein B (1994) Mutation of a mutL homolog in hereditary colon cancer. Science 263:1625-1629
-
(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
Reischmann, R.D.8
Fraser, C.M.9
Adams, M.D.10
Venter, J.C.11
Hamilton, S.R.12
Petersen, G.M.13
Watson, P.14
Lynch, H.T.15
Peltomäki, P.16
Mecklin, J.-P.17
De La Chapelle, A.18
Kinzler, K.W.19
Vogelstein, B.20
more..
-
55
-
-
0021338485
-
Loss of Harvey ras allele in sporadic Wilms' tumour
-
Reeve AE, Housiaux PJ, Gardner RJM, Chewings WE, Grindley RM, Millow LJ (1984) Loss of Harvey ras allele in sporadic Wilms' tumour. Nature 309:174-176
-
(1984)
Nature
, vol.309
, pp. 174-176
-
-
Reeve, A.E.1
Housiaux, P.J.2
Gardner, R.J.M.3
Chewings, W.E.4
Grindley, R.M.5
Millow, L.J.6
-
56
-
-
0017883401
-
Chromosomal imbalance in the aniridia-Wilms' tumor association: 11p interstitial deletion
-
Riccardi VM, Sujansky E, Smith AC, Francke U (1978) Chromosomal imbalance in the aniridia-Wilms' tumor association: 11p interstitial deletion. Pediatrics 61:604-610
-
(1978)
Pediatrics
, vol.61
, pp. 604-610
-
-
Riccardi, V.M.1
Sujansky, E.2
Smith, A.C.3
Francke, U.4
-
57
-
-
0027394231
-
The APC gene product in normal and tumor cells
-
Smith KJ, Johnson KA, Bryan TM, Hill DE, Markowitz S, Willson JKV, Paraskeva C, Petersen GM, Hamilton SR, Vogelstein B, Kinzler KW (1993) The APC gene product in normal and tumor cells. Proc Natl Acad Sci USA 90:2846-2850
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2846-2850
-
-
Smith, K.J.1
Johnson, K.A.2
Bryan, T.M.3
Hill, D.E.4
Markowitz, S.5
Willson, J.K.V.6
Paraskeva, C.7
Petersen, G.M.8
Hamilton, S.R.9
Vogelstein, B.10
Kinzler, K.W.11
-
58
-
-
0019190556
-
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14
-
Sparkes RS, Sparkes MC, Wilson MG, Towner JW, Benedict W, Murphree AL, Yunis JJ (1980) Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14. Science 208:1042-1044
-
(1980)
Science
, vol.208
, pp. 1042-1044
-
-
Sparkes, R.S.1
Sparkes, M.C.2
Wilson, M.G.3
Towner, J.W.4
Benedict, W.5
Murphree, A.L.6
Yunis, J.J.7
-
59
-
-
0020659338
-
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D
-
Sparkes RS, Murphree AL, Lingua RW, Sparkes MC, Field LL, Funderburk SJ, Benedict WF (1983) Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D. Science 219-.971-973
-
(1983)
Science
, vol.219
, pp. 971-973
-
-
Sparkes, R.S.1
Murphree, A.L.2
Lingua, R.W.3
Sparkes, M.C.4
Field, L.L.5
Funderburk, S.J.6
Benedict, W.F.7
-
60
-
-
0028979727
-
Adenomatous polyposis coli gene mutations in ulcerative colitis-associated dysplasias and cancers versus sporadic colon neoplasms
-
Tarmin L, Yin J, Harpaz N, Kozam M, Noordzij J, Antonio L, Jiang H-Y, Chan O, Cymes K, Meltzer, SJ (1995) Adenomatous polyposis coli gene mutations in ulcerative colitis-associated dysplasias and cancers versus sporadic colon neoplasms. Cancer Res 55:2035-2038
-
(1995)
Cancer Res
, vol.55
, pp. 2035-2038
-
-
Tarmin, L.1
Yin, J.2
Harpaz, N.3
Kozam, M.4
Noordzij, J.5
Antonio, L.6
Jiang, H.-Y.7
Chan, O.8
Cymes, K.9
Meltzer, S.J.10
-
61
-
-
0020038032
-
Specific chromosome defect associated with human small-cell lung cancer: Deletion 3p(14-23)
-
Whang-Peng J, Kao-Shan CS, Lee EC (1982) Specific chromosome defect associated with human small-cell lung cancer: deletion 3p(14-23). Science 215:181-182
-
(1982)
Science
, vol.215
, pp. 181-182
-
-
Whang-Peng, J.1
Kao-Shan, C.S.2
Lee, E.C.3
|