-
1
-
-
0029928160
-
APC gene: Database of germline and somatic mutations in human tumors and cell lines
-
Beroud C, Soussi T. APC gene: database of germline and somatic mutations in human tumors and cell lines. Nucleic Acids Res 1996, 24:121-124
-
(1996)
Nucleic Acids Res
, vol.24
, pp. 121-124
-
-
Beroud, C.1
Soussi, T.2
-
2
-
-
0031017268
-
Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines
-
Kane MF, Loda M, Gaida GM, Lipman J, Mishra R, Goldman H, Jessup JM, Kolodner R: Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines. Cancer Res 1997, 57:808-811
-
(1997)
Cancer Res
, vol.57
, pp. 808-811
-
-
Kane, M.F.1
Loda, M.2
Gaida, G.M.3
Lipman, J.4
Mishra, R.5
Goldman, H.6
Jessup, J.M.7
Kolodner, R.8
-
3
-
-
0027163231
-
Association between meningioma and Cowden's disease
-
Lyons CJ, Wilson CB, Horton JC: Association between meningioma and Cowden's disease. Neurology 1993, 43:1436-1437
-
(1993)
Neurology
, vol.43
, pp. 1436-1437
-
-
Lyons, C.J.1
Wilson, C.B.2
Horton, J.C.3
-
4
-
-
0031004088
-
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
-
Liaw D, Marsh DJ, Li J, Dahia PLM, Wang SI, Zheng ZM, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R: Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet 1997, 16:64-67
-
(1997)
Nat Genet
, vol.16
, pp. 64-67
-
-
Liaw, D.1
Marsh, D.J.2
Li, J.3
Dahia, P.L.M.4
Wang, S.I.5
Zheng, Z.M.6
Bose, S.7
Call, K.M.8
Tsou, H.C.9
Peacocke, M.10
Eng, C.11
Parsons, R.12
-
5
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
Li J, Yen C, Liaw D, Podsypanina K, Bose S, Wang SI, Puc J, Miliaresis C, Rodgers L, McCombie R, Bigner SH, Giovanella BC, Ittmann M, Tycko B, Hibshoosh H, Wigler MH, Parsons R: PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science 1997, 275:1943-1947
-
(1997)
Science
, vol.275
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
Podsypanina, K.4
Bose, S.5
Wang, S.I.6
Puc, J.7
Miliaresis, C.8
Rodgers, L.9
McCombie, R.10
Bigner, S.H.11
Giovanella, B.C.12
Ittmann, M.13
Tycko, B.14
Hibshoosh, H.15
Wigler, M.H.16
Parsons, R.17
-
6
-
-
17144436629
-
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
-
Steck PA, Pershouse MA, Jasser SA, Yung WKA, Lin H, Ligon AH, Langford LA, Baumgard ML, Hattier T, Davis T, Frye C, Hu R, Swedlund B, Teng DHF, Tavtigian SV: Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat Genet 1997, 15:356-362
-
(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
-
7
-
-
0030801275
-
Mutation analysis of the putative tumor suppressor gene PTEN/ MMAC1 in primary breast carcinomas
-
Rhei E, Kang L, Bogomolniy F, Federici MG, Borgen PI, Boyd J: Mutation analysis of the putative tumor suppressor gene PTEN/ MMAC1 in primary breast carcinomas. Cancer Res 1997, 57:3657-3659
-
(1997)
Cancer Res
, vol.57
, pp. 3657-3659
-
-
Rhei, E.1
Kang, L.2
Bogomolniy, F.3
Federici, M.G.4
Borgen, P.I.5
Boyd, J.6
-
8
-
-
0030777104
-
Disruption of the MMAC1/PTEN gene by deletion or mutation is a frequent event in malignant melanoma
-
Guldberg P, thor Straten P, Birck A, Ahrenkiel V, Kirkin AF, Zeuthen J: Disruption of the MMAC1/PTEN gene by deletion or mutation is a frequent event in malignant melanoma. Cancer Res 1997, 57:3660-3663
-
(1997)
Cancer Res
, vol.57
, pp. 3660-3663
-
-
Guldberg, P.1
Thor Straten, P.2
Birck, A.3
Ahrenkiel, V.4
Kirkin, A.F.5
Zeuthen, J.6
-
9
-
-
0030761409
-
Mutations in PTEN are frequent in endometrial carcinoma but rare in other common gynecological malignancies
-
Tashiro H, Blazes MS, Wu R, Cho KR, Bose S, Wang SI, Li J, Parsons R, Ellenson LH: Mutations in PTEN are frequent in endometrial carcinoma but rare in other common gynecological malignancies. Cancer Res 1997, 57:3935-3940
-
(1997)
Cancer Res
, vol.57
, pp. 3935-3940
-
-
Tashiro, H.1
Blazes, M.S.2
Wu, R.3
Cho, K.R.4
Bose, S.5
Wang, S.I.6
Li, J.7
Parsons, R.8
Ellenson, L.H.9
-
10
-
-
0030799909
-
Somatic mutations of PTEN in glioblastoma multiforme
-
Wang SI, Puc J, Li J, Bruce JN, Cairns P, Sidransky D, Parsons R: Somatic mutations of PTEN in glioblastoma multiforme. Cancer Res 1997, 57:4183-4186
-
(1997)
Cancer Res
, vol.57
, pp. 4183-4186
-
-
Wang, S.I.1
Puc, J.2
Li, J.3
Bruce, J.N.4
Cairns, P.5
Sidransky, D.6
Parsons, R.7
-
11
-
-
0030817576
-
PTEN gene mutations are seen in high-grade but not in low-grade gliomas
-
Rasheed BK, Stenzel TT, McLendon RE, Parsons R, Friedman AH, Friedman HS, Bigner DD, Bigner SH: PTEN gene mutations are seen in high-grade but not in low-grade gliomas Cancer Res 1997, 57: 4187-4190
-
(1997)
Cancer Res
, vol.57
, pp. 4187-4190
-
-
Rasheed, B.K.1
Stenzel, T.T.2
McLendon, R.E.3
Parsons, R.4
Friedman, A.H.5
Friedman, H.S.6
Bigner, D.D.7
Bigner, S.H.8
-
12
-
-
0030730905
-
Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors
-
Dahia PL, Marsh DJ, Zheng Z, Zedenius J, Komminoth P, Frisk T, Wallin G, Parsons R, Longy M, Larsson C, Eng C: Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors Cancer Res 1997, 57:4710-4713
-
(1997)
Cancer Res
, vol.57
, pp. 4710-4713
-
-
Dahia, P.L.1
Marsh, D.J.2
Zheng, Z.3
Zedenius, J.4
Komminoth, P.5
Frisk, T.6
Wallin, G.7
Parsons, R.8
Longy, M.9
Larsson, C.10
Eng, C.11
-
13
-
-
0030781053
-
PTEN/MMAC1 mutations in endormetrial cancers
-
Risinger JI, Hayes AK, Berchuck A, Barrett JC. PTEN/MMAC1 mutations in endormetrial cancers. Cancer Res 1997, 57:4736-4738
-
(1997)
Cancer Res
, vol.57
, pp. 4736-4738
-
-
Risinger, J.I.1
Hayes, A.K.2
Berchuck, A.3
Barrett, J.C.4
-
14
-
-
0031203265
-
Germline mutations in PTEN are present in Bannayan-Zonnona syndrome
-
Marsh DJ, Dahia PL, Zheng Z, Liaw D, Parsons R, Gorlin RJ, Eng C: Germline mutations in PTEN are present in Bannayan-Zonnona syndrome. Nat Genet 1997, 16:333-334
-
(1997)
Nat Genet
, vol.16
, pp. 333-334
-
-
Marsh, D.J.1
Dahia, P.L.2
Zheng, Z.3
Liaw, D.4
Parsons, R.5
Gorlin, R.J.6
Eng, C.7
-
15
-
-
15444339425
-
Exclusion of PTEN/MMAC1/TEP1 and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome (JPS)
-
Marsh DJ, Roth S, Lunetta KL, Hemminki A, Dahia PLM, Sistonen P, Zheng ZM, Caron S, vanrsouw NJ, Bodmer WF, Cottrell SE, Dunlop MG, Eccles D, Hodgson SV, Jarvinen H, Kellokumpu I, Markie D, Neale K, Phillips R, Rozen P, Syngal S, Vijg J, Tomlmson IPM, Aaltonen LA, Eng C: Exclusion of PTEN/MMAC1/TEP1 and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome (JPS). Cancer Res 1997, 57:5017-5020
-
(1997)
Cancer Res
, vol.57
, pp. 5017-5020
-
-
Marsh, D.J.1
Roth, S.2
Lunetta, K.L.3
Hemminki, A.4
Dahia, P.L.M.5
Sistonen, P.6
Zheng, Z.M.7
Caron, S.8
Vanrsouw, N.J.9
Bodmer, W.F.10
Cottrell, S.E.11
Dunlop, M.G.12
Eccles, D.13
Hodgson, S.V.14
Jarvinen, H.15
Kellokumpu, I.16
Markie, D.17
Neale, K.18
Phillips, R.19
Rozen, P.20
Syngal, S.21
Vijg, J.22
Tomlmson, I.P.M.23
Aaltonen, L.A.24
Eng, C.25
more..
-
16
-
-
0031612533
-
PTEN germ-line mutations in juvenile polyposis coli
-
Olschwang S, Serova-Sinilnikova OM, Lenoir GM, Thomas G. PTEN germ-line mutations in juvenile polyposis coli. Nat Genet 1998, 18: 12-14
-
(1998)
Nat Genet
, vol.18
, pp. 12-14
-
-
Olschwang, S.1
Serova-Sinilnikova, O.M.2
Lenoir, G.M.3
Thomas, G.4
-
18
-
-
0031012344
-
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
-
Hemminki A, Tomlinson I, Markie D, Jarvinen H, Sistonen P, Bjorkqvist AM, Knuutila S, Salovaara R, Bodmer W, Shibata D, delaChapelle A, Aaltonen LA: Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. Nat Genet 1997, 15:87-90
-
(1997)
Nat Genet
, vol.15
, pp. 87-90
-
-
Hemminki, A.1
Tomlinson, I.2
Markie, D.3
Jarvinen, H.4
Sistonen, P.5
Bjorkqvist, A.M.6
Knuutila, S.7
Salovaara, R.8
Bodmer, W.9
Shibata, D.10
DelaChapelle, A.11
Aaltonen, L.A.12
-
19
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
Hemminki A, Markie D, Tomlinson IPM, Avizienyte E, Roth S, Loukola A, Bignell G, Warren W, Aminoff M, Hoglund P, Jarvinen H, Kristo P, Pelin K, Ridanpaa M, Salovaara R, Toro T, Bodmer W, Olschwang S, Olsen AS, Stratton MR, delaChapelle A, Aaltonen LA: A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 1998; 391:184-187
-
(1998)
Nature
, vol.391
, pp. 184-187
-
-
Hemminki, A.1
Markie, D.2
Tomlinson, I.P.M.3
Avizienyte, E.4
Roth, S.5
Loukola, A.6
Bignell, G.7
Warren, W.8
Aminoff, M.9
Hoglund, P.10
Jarvinen, H.11
Kristo, P.12
Pelin, K.13
Ridanpaa, M.14
Salovaara, R.15
Toro, T.16
Bodmer, W.17
Olschwang, S.18
Olsen, A.S.19
Stratton, M.R.20
DelaChapelle, A.21
Aaltonen, L.A.22
more..
-
20
-
-
0031213644
-
Allele loss in colorectal cancer at the Cowden disease/juvenile polyposis locus on 10q
-
Frayling IM, Bodmer WF, Tomlinson IP: Allele loss in colorectal cancer at the Cowden disease/juvenile polyposis locus on 10q. Cancer Genet Cytogenet 1997, 97:64-69
-
(1997)
Cancer Genet Cytogenet
, vol.97
, pp. 64-69
-
-
Frayling, I.M.1
Bodmer, W.F.2
Tomlinson, I.P.3
-
21
-
-
0031908348
-
Defects in mismatch repair occur after APC mutations in the pathogenesis of sporadic colorectal tumours
-
Homfray TFR, Cottrell SE, Ilyas M, Rowan A, Talbot IC, Bodmer WF, Tomlinson IPM: Defects in mismatch repair occur after APC mutations in the pathogenesis of sporadic colorectal tumours. Hum Mutat 1998, 11:114-120
-
(1998)
Hum Mutat
, vol.11
, pp. 114-120
-
-
Homfray, T.F.R.1
Cottrell, S.E.2
Ilyas, M.3
Rowan, A.4
Talbot, I.C.5
Bodmer, W.F.6
Tomlinson, I.P.M.7
-
22
-
-
0031049128
-
Genetic alterations and epithelial dysplasia in juvenile polyposis syndromes and sporadic juvenile polyps
-
Wu TT, Rezai B, Rashid A, Luce MC, Cayouette MC, Kim C, Sani N, Mishra L, Moskaluk CA, Yardley JH, Hamilton SR: Genetic alterations and epithelial dysplasia in juvenile polyposis syndromes and sporadic juvenile polyps. Am J Pathol 1997, 150:939-947
-
(1997)
Am J Pathol
, vol.150
, pp. 939-947
-
-
Wu, T.T.1
Rezai, B.2
Rashid, A.3
Luce, M.C.4
Cayouette, M.C.5
Kim, C.6
Sani, N.7
Mishra, L.8
Moskaluk, C.A.9
Yardley, J.H.10
Hamilton, S.R.11
-
23
-
-
0027193630
-
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutions
-
Sheffield VC, Beck JS, Kwitek AE, Sandstrom DW, Stone EM: The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutions. Genomics 1993, 16:325-332
-
(1993)
Genomics
, vol.16
, pp. 325-332
-
-
Sheffield, V.C.1
Beck, J.S.2
Kwitek, A.E.3
Sandstrom, D.W.4
Stone, E.M.5
-
24
-
-
0027982001
-
Comparative sensitivity of alternative single-strand conformation polymorphism (SSCP) methods
-
Vidal PA, Moller DE: Comparative sensitivity of alternative single-strand conformation polymorphism (SSCP) methods. Biotechniques 1994, 17:490-492
-
(1994)
Biotechniques
, vol.17
, pp. 490-492
-
-
Vidal, P.A.1
Moller, D.E.2
-
25
-
-
0028198386
-
Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene
-
Ravnik GM, Glavac D, Dean M: Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene. Hum Mol Genet 1994, 3:801-807
-
(1994)
Hum Mol Genet
, vol.3
, pp. 801-807
-
-
Ravnik, G.M.1
Glavac, D.2
Dean, M.3
-
26
-
-
0030770814
-
Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease
-
Arch EM, Goodman BK, Van Wesep RA, Liaw D, Clarke K, Parsons R, McKusick VA, Geraghty MT: Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease. Am J Med Genet 1997, 71:489-493
-
(1997)
Am J Med Genet
, vol.71
, pp. 489-493
-
-
Arch, E.M.1
Goodman, B.K.2
Van Wesep, R.A.3
Liaw, D.4
Clarke, K.5
Parsons, R.6
McKusick, V.A.7
Geraghty, M.T.8
-
27
-
-
0030843274
-
Methylation of the BRCA1 gene in sporadic breast cancer
-
Dobrovic A, Simpfendorfer D: Methylation of the BRCA1 gene in sporadic breast cancer. Cancer Res 1997, 57:3347-3350
-
(1997)
Cancer Res
, vol.57
, pp. 3347-3350
-
-
Dobrovic, A.1
Simpfendorfer, D.2
|