-
1
-
-
83555172860
-
-
Korea KCCRMoHaWRo InSeoul: Korea Central Cancer Registry Ministry of Health and Welfare Republic of Korea
-
Korea KCCRMoHaWRo: Annual Report of the Central Cancer Registry in Korea. InSeoul: Korea Central Cancer Registry Ministry of Health and Welfare Republic of Korea, 2007, 1-114.
-
(2007)
Annual Report of the Central Cancer Registry in Korea
, pp. 1-114
-
-
-
2
-
-
33745208027
-
Familial nonmedullary thyroid carcinoma
-
Malchoff CD, Malchoff DM,: Familial nonmedullary thyroid carcinoma. Cancer Control 2006; 13: 106-110.
-
(2006)
Cancer Control
, vol.13
, pp. 106-110
-
-
Malchoff, C.D.1
Malchoff, D.M.2
-
4
-
-
0036691719
-
Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population
-
DOI 10.1007/s00268-002-6615-y
-
Uchino S, Noguchi S, Kawamoto H, et al.: Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population. World J Surg 2002; 26: 897-902. (Pubitemid 36920283)
-
(2002)
World Journal of Surgery
, vol.26
, Issue.8
, pp. 897-902
-
-
Uchino, S.1
Noguchi, S.2
Kawamoto, H.3
Yamashita, H.4
Watanabe, S.5
Yamashita, H.6
Shuto, S.7
-
5
-
-
0031032242
-
Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid
-
DOI 10.1210/jc.82.2.345
-
Burgess JR, Duffield A, Wilkinson SJ, et al.: Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid. J Clin Endocrinol Metab 1997; 82: 345-348. (Pubitemid 27068589)
-
(1997)
Journal of Clinical Endocrinology and Metabolism
, vol.82
, Issue.2
, pp. 345-348
-
-
Burgess, J.R.1
Duffield, A.2
Wilkinson, S.J.3
Ware, R.4
Greenaway, T.M.5
Percival, J.6
Hoffman, L.7
-
6
-
-
0029074897
-
Familial nonmedullary thyroid cancer. An emerging entity that warrants aggressive treatment
-
(discussion 898-899)
-
Grossman RF, Tu SH, Duh QY, et al.: Familial nonmedullary thyroid cancer. An emerging entity that warrants aggressive treatment. Arch Surg 1995; 130: 892-897 (discussion 898-899).
-
(1995)
Arch Surg
, vol.130
, pp. 892-897
-
-
Grossman, R.F.1
Tu, S.H.2
Duh, Q.Y.3
-
7
-
-
0033773933
-
Familial papillary thyroid carcinoma: Genetics, criteria for diagnosis, clinical features, and surgical treatment
-
Musholt TJ, Musholt PB, Petrich T, et al.: Familial papillary thyroid carcinoma: Genetics, criteria for diagnosis, clinical features, and surgical treatment. World J Surg 2000; 24: 1409-1417.
-
(2000)
World J Surg
, vol.24
, pp. 1409-1417
-
-
Musholt, T.J.1
Musholt, P.B.2
Petrich, T.3
-
8
-
-
16944363399
-
Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer
-
DOI 10.1086/301610
-
Bignell GR, Canzian F, Shayeghi M, et al.: Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer. Am J Hum Genet 1997; 61: 1123-1130. (Pubitemid 27492321)
-
(1997)
American Journal of Human Genetics
, vol.61
, Issue.5
, pp. 1123-1130
-
-
Bignell, G.R.1
Canzian, F.2
Shayeghi, M.3
Stark, M.4
Shugart, Y.Y.5
Biggs, P.6
Mangion, J.7
Hamoudi, R.8
Rosenblatt, J.9
Buu, P.10
Sun, S.11
Stoffer, S.S.12
Goldgar, D.E.13
Romeo, G.14
Houlston, R.S.15
Narod, S.A.16
Stratton, M.R.17
Foulkes, W.D.18
-
9
-
-
0032471912
-
A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2
-
DOI 10.1086/302164
-
Canzian F, Amati P, Harach HR, et al.: A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2. Am J Hum Genet 1998; 63: 1743-1748. (Pubitemid 30415737)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.6
, pp. 1743-1748
-
-
Canzian, F.1
Amati, P.2
Ruben Harach, H.3
Kraimps, J.-L.4
Lesueur, F.5
Barbier, J.6
Levillain, P.7
Romeo, G.8
Bonneau, D.9
-
10
-
-
0034455744
-
Papillary thyroid carcinoma associated with papillary renal neoplasia: Genetic linkage analysis of a distinct heritable tumor syndrome
-
DOI 10.1210/jc.85.5.1758
-
Malchoff CD, Sarfarazi M, Tendler B, et al.: Papillary thyroid carcinoma associated with papillary renal neoplasia: Genetic linkage analysis of a distinct heritable tumor syndrome. J Clin Endocrinol Metab 2000; 85: 1758-1764. (Pubitemid 32269272)
-
(2000)
Journal of Clinical Endocrinology and Metabolism
, vol.85
, Issue.5
, pp. 1758-1764
-
-
Malchoff, C.D.1
Sarfarazi, M.2
Tendler, B.3
Forouhar, F.4
Whalen, G.5
Joshi, V.6
Arnold, A.7
Malchoff, D.M.8
-
11
-
-
0034917504
-
Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21
-
DOI 10.1086/321979
-
McKay JD, Lesueur F, Jonard L, et al.: Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21. Am J Hum Genet 2001; 69: 440-446. (Pubitemid 32695216)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.2
, pp. 440-446
-
-
McKay, J.D.1
Lesueur, F.2
Jonard, L.3
Pastore, A.4
Williamson, J.5
Hoffman, L.6
Burgess, J.7
Duffield, A.8
Papotti, M.9
Stark, M.10
Sobol, H.11
Maes, B.12
Murat, A.13
Kaariainen, H.14
Bertholon-Gregoire, M.15
Zini, M.16
Rossing, M.A.17
Toubert, M.-E.18
Bonichon, F.19
Cavarec, M.20
Bernard, A.-M.21
Boneu, A.22
Leprat, F.23
Haas, O.24
Lasset, C.25
Schlumberger, M.26
Canzian, F.27
Goldgar, D.E.28
Romeo, G.29
more..
-
12
-
-
6044219917
-
Alternative mutations of BRAF, RET and NTRK1 are associated with similar but distinct gene expression patterns in papillary thyroid cancer
-
DOI 10.1038/sj.onc.1207980
-
Frattini M, Ferrario C, Bressan P, et al.: Alternative mutations of BRAF, RET and NTRK1 are associated with similar but distinct gene expression patterns in papillary thyroid cancer. Oncogene 2004; 23: 7436-7440. (Pubitemid 39382146)
-
(2004)
Oncogene
, vol.23
, Issue.44
, pp. 7436-7440
-
-
Frattini, M.1
Ferrario, C.2
Bressan, P.3
Balestra, D.4
De Cecco, L.5
Mondellini, P.6
Bongarzone, I.7
Collini, P.8
Gariboldi, M.9
Pilotti, S.10
Pierotti, M.A.11
Greco, A.12
-
13
-
-
33748923108
-
Absence of germline mutations in genes within the MAP kinase pathway in familial non-medullary thyroid cancer
-
Hou P, Xing M,: Absence of germline mutations in genes within the MAP kinase pathway in familial non-medullary thyroid cancer. Cell Cycle 2006; 5: 2036-2039. (Pubitemid 44435312)
-
(2006)
Cell Cycle
, vol.5
, Issue.17
, pp. 2036-2039
-
-
Hou, P.1
Xing, M.2
-
14
-
-
41349093968
-
Familial non-medullary thyroid carcinoma (FNMTC): Analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations
-
DOI 10.1677/ERC-07-0214
-
Cavaco BM, Batista PF, Martins C, et al.: Familial non-medullary thyroid carcinoma (FNMTC): Analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations. Endocr Relat Cancer 2008; 15: 207-215. (Pubitemid 351449740)
-
(2008)
Endocrine-Related Cancer
, vol.15
, Issue.1
, pp. 207-215
-
-
Cavaco, B.M.1
Batista, P.F.2
Martins, C.3
Banito, A.4
Do Rosario, F.5
Limbert, E.6
Sobrinho, L.G.7
Leite, V.8
-
15
-
-
0029900132
-
Semiautomated assessment of loss of heterozygosity and replication error in tumors
-
Canzian F, Salovaara R, Hemminki A, et al.: Semiautomated assessment of loss of heterozygosity and replication error in tumors. Cancer Res 1996; 56: 3331-3337. (Pubitemid 26242985)
-
(1996)
Cancer Research
, vol.56
, Issue.14
, pp. 3331-3337
-
-
Canzian, F.1
Salovaara, R.2
Hemminki, A.3
Kristo, P.4
Chadwick, R.B.5
Aaltonen, L.A.6
De La Chapelle, A.7
-
16
-
-
33646549545
-
Does familial non-medullary thyroid cancer adversely affect survival?
-
DOI 10.1007/s00268-005-0398-x
-
Triponez F, Wong M, Sturgeon C, et al.: Does familial non-medullary thyroid cancer adversely affect survival? World J Surg 2006; 30: 787-793. (Pubitemid 43724107)
-
(2006)
World Journal of Surgery
, vol.30
, Issue.5
, pp. 787-793
-
-
Triponez, F.1
Wong, M.2
Sturgeon, C.3
Caron, N.4
Ginzinger, D.G.5
Segal, M.R.6
Kebebew, E.7
Duh, Q.-Y.8
Clark, O.H.9
-
17
-
-
0030896374
-
Familial nonmedullary thyroid carcinoma: A meta-review of case series
-
Loh KC,: Familial nonmedullary thyroid carcinoma: A meta-review of case series. Thyroid 1997; 7: 107-113.
-
(1997)
Thyroid
, vol.7
, pp. 107-113
-
-
Loh, K.C.1
-
18
-
-
21244457181
-
BRAF mutation in thyroid cancer
-
DOI 10.1677/erc.1.0978
-
Xing M,: BRAF mutation in thyroid cancer. Endocr Relat Cancer 2005; 12: 245-262. (Pubitemid 40896444)
-
(2005)
Endocrine-Related Cancer
, vol.12
, Issue.2
, pp. 245-262
-
-
Xing, M.1
-
19
-
-
0031783481
-
Prevalences of Gsα, ras, p53 mutations and ret/PTC rearrangement in differentiated thyroid tumours in a Korean population
-
DOI 10.1046/j.1365-2265.1998.00515.x
-
Park KY, Koh JM, Kim YI, et al.: Prevalences of Gs alpha, ras, p53 mutations and ret/PTC rearrangement in differentiated thyroid tumours in a Korean population. Clin Endocrinol (Oxf) 1998; 49: 317-323. (Pubitemid 28448941)
-
(1998)
Clinical Endocrinology
, vol.49
, Issue.3
, pp. 317-323
-
-
Park, K.Y.1
Koh, J.M.2
Kim, Y.I.3
Park, H.J.4
Gong, G.5
Hong, S.J.6
Ahn, I.M.7
-
20
-
-
0037564807
-
Specific pattern of RAS oncogene mutations in follicular thyroid tumors
-
Vasko V, Ferrand M, Di Cristofaro J, et al.: Specific pattern of RAS oncogene mutations in follicular thyroid tumors. J Clin Endocrinol Metab 2003; 88: 2745-2752. (Pubitemid 36724451)
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, Issue.6
, pp. 2745-2752
-
-
Vasko, V.1
Ferrand, M.2
Di Cristofaro, J.3
Carayon, P.4
Henry, J.F.5
De Micco, C.6
-
21
-
-
0032430664
-
The interactive effect of Ras, HER2, P53 and Bcl-2 expression in predicting the survival of non-small cell lung cancer patients
-
DOI 10.1016/S0169-5002(98)00086-5, PII S0169500298000865
-
Kim YC, Park KO, Kern JA, et al.: The interactive effect of Ras, HER2, P53 and Bcl-2 expression in predicting the survival of non-small cell lung cancer patients. Lung Cancer 1998; 22: 181-190. (Pubitemid 29067392)
-
(1998)
Lung Cancer
, vol.22
, Issue.3
, pp. 181-190
-
-
Kim, Y.-C.1
Park, K.-O.2
Kern, J.A.3
Park, C.-S.4
Lim, S.-C.5
Jang, A.-S.6
Yang, J.-B.7
-
22
-
-
5444224121
-
Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status
-
DOI 10.1093/hmg/ddh238
-
Oliveira C, Westra JL, Arango D, et al.: Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status. Hum Mol Genet 2004; 13: 2303-2311. (Pubitemid 39359927)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.19
, pp. 2303-2311
-
-
Oliveira, C.1
Westra, J.L.2
Arango, D.3
Ollikainen, M.4
Domingo, E.5
Ferreira, A.6
Velho, S.7
Niessen, R.8
Lagerstedt, K.9
Alhopuro, P.10
Laiho, P.11
Veiga, I.12
Teixeira, M.R.13
Ligtenberg, M.14
Kleibeuker, J.H.15
Sijmons, R.H.16
Plukker, J.T.17
Imai, K.18
Lage, P.19
Hamelin, R.20
Albuquerque, C.21
Schwartz Jr., S.22
Lindblom, A.23
Peltomaki, P.24
Yamamoto, H.25
Aaltonen, L.A.26
Seruca, R.27
Hofstra, R.M.W.28
more..
-
23
-
-
0033304605
-
- symporter
-
Neumann S, Willgerodt H, Ackermann F, et al.: Linkage of familial euthyroid goiter to the multinodular goiter-1 locus and exclusion of the candidate genes thyroglobulin, thyroperoxidase, and Na+/I- symporter. J Clin Endocrinol Metab 1999; 84: 3750-3756. (Pubitemid 30645236)
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, Issue.10
, pp. 3750-3756
-
-
Neumann, S.1
Willgerodt, H.2
Ackermann, F.3
Reske, A.4
Jung, M.5
Reis, A.6
Paschke, R.7
-
24
-
-
17944368989
-
A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: Confirmation of linkage to TCO1
-
DOI 10.1210/jc.86.8.3701
-
Bevan S, Pal T, Greenberg CR, et al.: A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: Confirmation of linkage to TCO1. J Clin Endocrinol Metab 2001; 86: 3701-3704. (Pubitemid 32755963)
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, Issue.8
, pp. 3701-3704
-
-
Bevan, S.1
Pal, T.2
Greenberg, C.R.3
Green, H.4
Wixey, J.5
Bignell, G.6
Narod, S.A.7
Foulkes, W.D.8
Stratton, M.R.9
Houlston, R.S.10
-
25
-
-
2942753918
-
Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer
-
McKay JD, Thompson D, Lesueur F, et al.: Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer. J Med Genet 2004; 41: 407-412. (Pubitemid 38788034)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.6
, pp. 407-412
-
-
McKay, J.D.1
Thompson, D.2
Lesueur, F.3
Stankov, K.4
Pastore, A.5
Watfah, C.6
Strolz, S.7
Riccabona, G.8
Moncayo, R.9
Romeo, G.10
Goldgar, D.E.11
-
26
-
-
45749141296
-
Loss of heterozygosity at 19p13.2 and 2q21 in tumours from familial clusters of non-medullary thyroid carcinoma
-
DOI 10.1007/s10689-007-9160-x
-
Prazeres HJ, Rodrigues F, Soares P, et al.: Loss of heterozygosity at 19p13.2 and 2q21 in tumours from familial clusters of non-medullary thyroid carcinoma. Fam Cancer 2008; 7: 141-149. (Pubitemid 351871906)
-
(2008)
Familial Cancer
, vol.7
, Issue.2
, pp. 141-149
-
-
Prazeres, H.J.1
Rodrigues, F.2
Soares, P.3
Naidenov, P.4
Figueiredo, P.5
Campos, B.6
Lacerda, M.7
Martins, T.C.8
-
27
-
-
3242884228
-
Allelic loss on chromosomes 2q21 and 19p13.2 in oxyphilic thyroid tumors
-
DOI 10.1002/ijc.20259
-
Stankov K, Pastore A, Toschi L, et al.: Allelic loss on chromosomes 2q21 and 19p 13.2 in oxyphilic thyroid tumors. Int J Cancer 2004; 111: 463-467. (Pubitemid 38998831)
-
(2004)
International Journal of Cancer
, vol.111
, Issue.3
, pp. 463-467
-
-
Stankov, K.1
Pastore, A.2
Toschi, L.3
McKay, J.4
Lesueur, F.5
Kraimps, J.L.6
Bonneau, D.7
Gibelin, H.8
Levillain, P.9
Volante, M.10
Papotti, M.11
Romeo, G.12
-
28
-
-
0031909301
-
Allelic deletion at chromosome 9p21(p16) and 17p13(p53) in microdissected sporadic dysplastic nevus
-
DOI 10.1016/S0046-8177(98)90221-0
-
Park WS, Vortmeyer AO, Pack S, et al.: Allelic deletion at chromosome 9p21(p16) and 17p13(p53) in microdissected sporadic dysplastic nevus. Hum Pathol 1998; 29: 127-130. (Pubitemid 28099506)
-
(1998)
Human Pathology
, vol.29
, Issue.2
, pp. 127-130
-
-
Park, W.-S.1
Vortmeyer, A.O.2
Pack, S.3
Duray, P.H.4
Boni, R.5
Guerami, A.A.6
Emmert-Buck, M.R.7
Liotta, L.A.8
Zhuang, Z.9
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