-
1
-
-
0027248156
-
Genetics, natural-history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer-an updated review
-
Lynch H.T., Smyrk T.C., Watson P., Lanspa S.J., Lynch J.F., Lynch P.M., Cavalieri R.J., Boland C.R. Genetics, natural-history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer-an updated review. Gastroenterology. 104:1993;1535-1549
-
(1993)
Gastroenterology
, vol.104
, pp. 1535-1549
-
-
Lynch, H.T.1
Smyrk, T.C.2
Watson, P.3
Lanspa, S.J.4
Lynch, J.F.5
Lynch, P.M.6
Cavalieri, R.J.7
Boland, C.R.8
-
2
-
-
10544255347
-
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
-
Kruse R., Lamberti C., Wang Y., Ruelfs C., Bruns A., Esche C., Lehmann P., Ruzicka T., Rutten A., Friedl W., Propping P. Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene? Hum Genet. 98:1996;747-750
-
(1996)
Hum Genet
, vol.98
, pp. 747-750
-
-
Kruse, R.1
Lamberti, C.2
Wang, Y.3
Ruelfs, C.4
Bruns, A.5
Esche, C.6
Lehmann, P.7
Ruzicka, T.8
Rutten, A.9
Friedl, W.10
Propping, P.11
-
3
-
-
0029775147
-
The genetic basis of Muir-Torre syndrome includes the hMLH1 locus
-
Bapat B., Xia L., Madlensky L., Mitri A., Tonin P., Narod S.A., Gallinger S. The genetic basis of Muir-Torre syndrome includes the hMLH1 locus. Am J Hum Genet. 59:1996;736-739
-
(1996)
Am J Hum Genet
, vol.59
, pp. 736-739
-
-
Bapat, B.1
Xia, L.2
Madlensky, L.3
Mitri, A.4
Tonin, P.5
Narod, S.A.6
Gallinger, S.7
-
4
-
-
0014061877
-
Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face
-
Muir E.G., Bell A.J., Barlow K.A. Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face. Br J Surg. 54:1967;191-195
-
(1967)
Br J Surg
, vol.54
, pp. 191-195
-
-
Muir, E.G.1
Bell, A.J.2
Barlow, K.A.3
-
5
-
-
0014358038
-
Multiple sebaceous tumors
-
Torre D. Multiple sebaceous tumors. Arch Dermatol. 98:1968;549-551
-
(1968)
Arch Dermatol
, vol.98
, pp. 549-551
-
-
Torre, D.1
-
6
-
-
0033752013
-
Hereditary non-polyposis colorectal cancer associated with disseminated superficial porokeratosis. Microsatellite instability in skin tumours
-
Takata M., Shirasaki F., Nakatani T., Takehara K. Hereditary non-polyposis colorectal cancer associated with disseminated superficial porokeratosis. Microsatellite instability in skin tumours. Br J Dermatol. 143:2000;851-855
-
(2000)
Br J Dermatol
, vol.143
, pp. 851-855
-
-
Takata, M.1
Shirasaki, F.2
Nakatani, T.3
Takehara, K.4
-
7
-
-
0033376697
-
Microsatellite instability in benign skin lesions in hereditary non-polyposis colorectal cancer syndrome
-
Swale V.J., Quinn A.G., Wheeler J.M., Beck N.E., Dove-Edwin I., Thomas H.J.W., Bodmer W.F., Bataille V.A. Microsatellite instability in benign skin lesions in hereditary non-polyposis colorectal cancer syndrome. J Invest Dermatol. 113:1999;901-905
-
(1999)
J Invest Dermatol
, vol.113
, pp. 901-905
-
-
Swale, V.J.1
Quinn, A.G.2
Wheeler, J.M.3
Beck, N.E.4
Dove-Edwin, I.5
Thomas, H.J.W.6
Bodmer, W.F.7
Bataille, V.A.8
-
8
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal-cancer
-
Aaltonen L.A., Peltomaki 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., Delachapelle A. Clues to the pathogenesis of familial colorectal-cancer. Science. 260:1993;812-816
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomaki, 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
Delachapelle, A.14
-
9
-
-
0028585821
-
Structure of the human MSH2 locus and analysis of 2 Muir-Torre kindreds for MSH2 mutations
-
Kolodner R.D., Hall N.R., Lipford J., Kane M.F., Rao M.R.S., Morrison P., Wirth L., Finan P.J., Burn J., Chapman P., Earabino C., Merchant E., Bishop D.T. Structure of the human MSH2 locus and analysis of 2 Muir-Torre kindreds for MSH2 mutations. Genomics. 24:1994;516-526
-
(1994)
Genomics
, vol.24
, pp. 516-526
-
-
Kolodner, R.D.1
Hall, N.R.2
Lipford, J.3
Kane, M.F.4
Rao, M.R.S.5
Morrison, P.6
Wirth, L.7
Finan, P.J.8
Burn, J.9
Chapman, P.10
Earabino, C.11
Merchant, E.12
Bishop, D.T.13
-
10
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon-cancer
-
Fishel R., Lescoe M.K., Rao M.R.S., Copeland N.G., Jenkins N.A., Garber J., Kane M., Kolodner R. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon-cancer. Cell. 75:1993;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
-
11
-
-
0032534069
-
A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
-
Boland C., Thibodeau S., Hamilton S., Sidransky D., Eshleman J., Burt R., Meltzer S., Rodriguez-Bigas M., Fodde R., Ranzani G., Srivastava S. A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res. 58:1998;5248-5257
-
(1998)
Cancer Res
, vol.58
, pp. 5248-5257
-
-
Boland, C.1
Thibodeau, S.2
Hamilton, S.3
Sidransky, D.4
Eshleman, J.5
Burt, R.6
Meltzer, S.7
Rodriguez-Bigas, M.8
Fodde, R.9
Ranzani, G.10
Srivastava, S.11
-
12
-
-
0029066689
-
Inactivation of the type-II TGF-β receptor in colon cancer cells with microsatellite instability
-
Markowitz S., Wang J., Myeroff L., Parsons R., Sun L.Z., Lutterbaugh J., Fan R.S., Zborowska E., Kinzler K.W., Vogelstein B., Brattain M., Willson J.K.V. Inactivation of the type-II TGF-β receptor in colon cancer cells with microsatellite instability. Science. 268:1995;1336-1338
-
(1995)
Science
, vol.268
, pp. 1336-1338
-
-
Markowitz, S.1
Wang, J.2
Myeroff, L.3
Parsons, R.4
Sun, L.Z.5
Lutterbaugh, J.6
Fan, R.S.7
Zborowska, E.8
Kinzler, K.W.9
Vogelstein, B.10
Brattain, M.11
Willson, J.K.V.12
-
13
-
-
0031895510
-
The BAX gene, the promoter of apoptosis, is mutated in genetically unstable cancers of the colorectum, stomach, and endometrium
-
Ouyang H., Furukawa T., Abe T., Kato Y., Horii A. The BAX gene, the promoter of apoptosis, is mutated in genetically unstable cancers of the colorectum, stomach, and endometrium. Clin Cancer Res. 4:1998;1071-1074
-
(1998)
Clin Cancer Res
, vol.4
, pp. 1071-1074
-
-
Ouyang, H.1
Furukawa, T.2
Abe, T.3
Kato, Y.4
Horii, A.5
-
15
-
-
16944361874
-
Mutation of hMSH3 and hMSH6 mismatch repair genes in genetically unstable human colorectal and gastric carcinomas
-
Yin J., Kong D.H., Wang S.N., Zou T.T., Souza R.F., Smolinski K.N., Lynch P.M., Hamilton S.R., Sugimura H., Powell S.M., Young J., Abraham J.M., Meltzer S.J. Mutation of hMSH3 and hMSH6 mismatch repair genes in genetically unstable human colorectal and gastric carcinomas. Hum Mutat. 10:1997;474-478
-
(1997)
Hum Mutat
, vol.10
, pp. 474-478
-
-
Yin, J.1
Kong, D.H.2
Wang, S.N.3
Zou, T.T.4
Souza, R.F.5
Smolinski, K.N.6
Lynch, P.M.7
Hamilton, S.R.8
Sugimura, H.9
Powell, S.M.10
Young, J.11
Abraham, J.M.12
Meltzer, S.J.13
-
16
-
-
0035020167
-
Hereditary nonpolyposis colorectal cancer with gynecologic malignancies: Report of two families in Taiwan
-
Chen C.H., Huang R.L., Yu M.S., Wong L.J.C., Chao T.F., Chu T.Y. Hereditary nonpolyposis colorectal cancer with gynecologic malignancies: report of two families in Taiwan. J Formos Med Assoc. 100:2001;269-273
-
(2001)
J Formos Med Assoc
, vol.100
, pp. 269-273
-
-
Chen, C.H.1
Huang, R.L.2
Yu, M.S.3
Wong, L.J.C.4
Chao, T.F.5
Chu, T.Y.6
-
17
-
-
0036244746
-
A research-based tumor tissue bank of gynecologic oncology: Characteristics of nucleic acids extracted from normal and tumor tissues from different sites
-
Chu T.Y., Hwang K.S., Yu M.H., Lee H.S., Lai H.C., Liu J.Y. A research-based tumor tissue bank of gynecologic oncology: characteristics of nucleic acids extracted from normal and tumor tissues from different sites. Int J Gynecol Cancer. 12:2002;171-176
-
(2002)
Int J Gynecol Cancer
, vol.12
, pp. 171-176
-
-
Chu, T.Y.1
Hwang, K.S.2
Yu, M.H.3
Lee, H.S.4
Lai, H.C.5
Liu, J.Y.6
-
18
-
-
0029971551
-
Overexpression of the proto-oncogene C-jun in association with low-risk type-specific human papillomavirus infection in condyloma acuminata
-
Yang Y.F., Tsao Y.P., Yin C.S., Chen S.L., Chu T.Y. Overexpression of the proto-oncogene C-jun in association with low-risk type-specific human papillomavirus infection in condyloma acuminata. J Med Virol. 48:1996;302-307
-
(1996)
J Med Virol
, vol.48
, pp. 302-307
-
-
Yang, Y.F.1
Tsao, Y.P.2
Yin, C.S.3
Chen, S.L.4
Chu, T.Y.5
-
19
-
-
0028785603
-
Microsatellite instability and mutations of the transforming growth-factor-β type II receptor gene in colorectal cancer
-
Parsons R., Myeroff L.L., Liu B., Willson J.K.V., Markowitz S.D., Kinzler K.W., Vogelstein B. Microsatellite instability and mutations of the transforming growth-factor-β type II receptor gene in colorectal cancer. Cancer Res. 55:1995;5548-5550
-
(1995)
Cancer Res
, vol.55
, pp. 5548-5550
-
-
Parsons, R.1
Myeroff, L.L.2
Liu, B.3
Willson, J.K.V.4
Markowitz, S.D.5
Kinzler, K.W.6
Vogelstein, B.7
-
20
-
-
0028231090
-
The 1993-94 Genethon human genetic-linkage map
-
Gyapay G., Morissette J., Vignal A., Dib C., Fizames C., Millasseau P., Marc S., Bernardi G., Lathrop M., Weissenbach J. The 1993-94 Genethon human genetic-linkage map. Nat Genet. 7:1994;246-339
-
(1994)
Nat Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
21
-
-
0028362315
-
Instability of short tandem repeats (microsatellites) in human cancers
-
Wooster R., Cletonjansen A.M., Collins N., Mangion J., Cornelis R.S., Cooper C.S., Gusterson B.A., Ponder B.A.J., Vondeimling A., Wiestler O.D., Cornelisse C.J., Devilee P., Stratton M.R. Instability of short tandem repeats (microsatellites) in human cancers. Nat Genet. 6:1994;152-156
-
(1994)
Nat Genet
, vol.6
, pp. 152-156
-
-
Wooster, R.1
Cletonjansen, A.M.2
Collins, N.3
Mangion, J.4
Cornelis, R.S.5
Cooper, C.S.6
Gusterson, B.A.7
Ponder, B.A.J.8
Vondeimling, A.9
Wiestler, O.D.10
Cornelisse, C.J.11
Devilee, P.12
Stratton, M.R.13
-
23
-
-
0035986651
-
Highly aggressive leiomyosarcoma associated with Lynch II syndrome: Increasing the range of extracolonic cancers related with hereditary non-polyposis colonic cancer
-
Arana V.M., del Pino Y.B., Garcia-Castro C., Gonzalez-Aguilera J.J., Fernandez-Peralta A., Hermoso F.G. Highly aggressive leiomyosarcoma associated with Lynch II syndrome: increasing the range of extracolonic cancers related with hereditary non-polyposis colonic cancer. Ann Oncol. 13:2002;807-808
-
(2002)
Ann Oncol
, vol.13
, pp. 807-808
-
-
Arana, V.M.1
Del Pino, Y.B.2
Garcia-Castro, C.3
Gonzalez-Aguilera, J.J.4
Fernandez-Peralta, A.5
Hermoso, F.G.6
-
25
-
-
0031012850
-
Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma
-
Simon M.P., Pedeutour F., Sirvent N., Grosgeorge J., Minoletti F., Coindre J.M., Terrier-Lacombe M.J., Mandahl N., Craver R.D., Blin N., Sozzi G., Turc-Carel C., O'Brien K.P., Kedra D., Fransson I., Guilbaud C., Dumanski J.P. Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma. Nat Genet. 15:1997;95-98
-
(1997)
Nat Genet
, vol.15
, pp. 95-98
-
-
Simon, M.P.1
Pedeutour, F.2
Sirvent, N.3
Grosgeorge, J.4
Minoletti, F.5
Coindre, J.M.6
Terrier-Lacombe, M.J.7
Mandahl, N.8
Craver, R.D.9
Blin, N.10
Sozzi, G.11
Turc-Carel, C.12
O'Brien, K.P.13
Kedra, D.14
Fransson, I.15
Guilbaud, C.16
Dumanski, J.P.17
-
26
-
-
0032505090
-
Transforming activity of the chimeric sequence formed by the fusion of collagen gene COL1A1 and the platelet-derived growth factor beta-chain gene in dermatofibrosarcoma protuberans
-
Greco A., Fusetti L., Villa R., Sozzi G., Minoletti F., Mauri P., Pierotti M.A. Transforming activity of the chimeric sequence formed by the fusion of collagen gene COL1A1 and the platelet-derived growth factor beta-chain gene in dermatofibrosarcoma protuberans. Oncogene. 17:1998;1313-1319
-
(1998)
Oncogene
, vol.17
, pp. 1313-1319
-
-
Greco, A.1
Fusetti, L.2
Villa, R.3
Sozzi, G.4
Minoletti, F.5
Mauri, P.6
Pierotti, M.A.7
-
27
-
-
0031616146
-
Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers
-
Okamura S., Koyama K., Miyoshi Y., Monden M., Takami M. Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers. J Hum Genet. 43:1998;143-145
-
(1998)
J Hum Genet
, vol.43
, pp. 143-145
-
-
Okamura, S.1
Koyama, K.2
Miyoshi, Y.3
Monden, M.4
Takami, M.5
-
28
-
-
0031769438
-
Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: Examination of mutations found in hereditary nonpolyposis colorectal cancer
-
Guerrette S., Wilson T., Gradia S., Fishel R. Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer. Mol Cell Biol. 18:1998;6616-6623
-
(1998)
Mol Cell Biol
, vol.18
, pp. 6616-6623
-
-
Guerrette, S.1
Wilson, T.2
Gradia, S.3
Fishel, R.4
-
29
-
-
0029919109
-
Hereditary cancer: Two hits revisited
-
Knudson A.G. Hereditary cancer: two hits revisited. J Cancer Res Clin Oncol. 122:1996;135-140
-
(1996)
J Cancer Res Clin Oncol
, vol.122
, pp. 135-140
-
-
Knudson, A.G.1
-
30
-
-
0029783835
-
Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair
-
Risinger J.I., Umar A., Boyd J., Berchuck A., Kunkel T.A., Barrett J.C. Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair. Nat Genet. 14:1996;102-105
-
(1996)
Nat Genet
, vol.14
, pp. 102-105
-
-
Risinger, J.I.1
Umar, A.2
Boyd, J.3
Berchuck, A.4
Kunkel, T.A.5
Barrett, J.C.6
-
31
-
-
0028785602
-
A transforming growth factor-β receptor type II gene mutation common in colon and gastric but rare in endometrial cancers with microsatellite instability
-
Myeroff L.L., Parsons R., Kim S.J., Hedrick L., Cho K.R., Orth K., Mathis M., Kinzler K.W., Lutterbaugh J., Park K., Bang Y.J., Lee H.Y., Park J.G., Lynch H.T., Roberts A.B., Vogelstein B., Markowitz S.D. A transforming growth factor-β receptor type II gene mutation common in colon and gastric but rare in endometrial cancers with microsatellite instability. Cancer Res. 55:1995;5545-5547
-
(1995)
Cancer Res
, vol.55
, pp. 5545-5547
-
-
Myeroff, L.L.1
Parsons, R.2
Kim, S.J.3
Hedrick, L.4
Cho, K.R.5
Orth, K.6
Mathis, M.7
Kinzler, K.W.8
Lutterbaugh, J.9
Park, K.10
Bang, Y.J.11
Lee, H.Y.12
Park, J.G.13
Lynch, H.T.14
Roberts, A.B.15
Vogelstein, B.16
Markowitz, S.D.17
-
32
-
-
0033521859
-
Frequent aberration of the transforming growth factor-β receptor II gene in cell lines but no apparent mutation in pre-invasive and invasive carcinomas of the uterine cervix
-
Chu T.Y., Lai J.S., Shen C.Y., Liu H.S., Chao C.F. Frequent aberration of the transforming growth factor-β receptor II gene in cell lines but no apparent mutation in pre-invasive and invasive carcinomas of the uterine cervix. Int J Cancer. 80:1999;506-510
-
(1999)
Int J Cancer
, vol.80
, pp. 506-510
-
-
Chu, T.Y.1
Lai, J.S.2
Shen, C.Y.3
Liu, H.S.4
Chao, C.F.5
-
33
-
-
0032848660
-
Repression of the gene encoding the TGF-β type II receptor is a major target of the EWS-FLI1 oncoprotein
-
Hahm K.B., Cho K.N., Lee C., Im Y.H., Chang J., Choi S.G., Sorensen P.H.B., Thiele C.J., Kim S.J. Repression of the gene encoding the TGF-β type II receptor is a major target of the EWS-FLI1 oncoprotein. Nat Genet. 23:1999;222-227
-
(1999)
Nat Genet
, vol.23
, pp. 222-227
-
-
Hahm, K.B.1
Cho, K.N.2
Lee, C.3
Im, Y.H.4
Chang, J.5
Choi, S.G.6
Sorensen, P.H.B.7
Thiele, C.J.8
Kim, S.J.9
-
34
-
-
0033855479
-
Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation
-
Planck M., Wenngren E., Borg A., Olsson H., Nilbert M. Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation. Genes Chromosomes Cancer. 29:2000;33-39
-
(2000)
Genes Chromosomes Cancer
, vol.29
, pp. 33-39
-
-
Planck, M.1
Wenngren, E.2
Borg, A.3
Olsson, H.4
Nilbert, M.5
|