-
1
-
-
0022535165
-
Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entity
-
Farndon JR, Leight GS, Dilley WG, Baylin SB, Smallridge RC, Harrison TS, Wells SA Jr 1986 Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entity. Br J Surg 73:278-281.
-
(1986)
Br J Surg
, vol.73
, pp. 278-281
-
-
Farndon, J.R.1
Leight, G.S.2
Dilley, W.G.3
Baylin, S.B.4
Smallridge, R.C.5
Harrison, T.S.6
Wells Jr., S.A.7
-
2
-
-
0028819736
-
Medullary thyroid carcinoma: Recent advances and management update
-
Marsh DJ, Learoyd DL, Robinson BG 1995 Medullary thyroid carcinoma: Recent advances and management update. Thyroid 5:407-424.
-
(1995)
Thyroid
, vol.5
, pp. 407-424
-
-
Marsh, D.J.1
Learoyd, D.L.2
Robinson, B.G.3
-
3
-
-
0035034136
-
Diagnosis and therapy of sporadic and familial medullary thyroid carcinoma
-
Gimm O, Sutter T, Dralle H 2001 Diagnosis and therapy of sporadic and familial medullary thyroid carcinoma. J Cancer Res Oncol 127:156-165.
-
(2001)
J Cancer Res Oncol
, vol.127
, pp. 156-165
-
-
Gimm, O.1
Sutter, T.2
Dralle, H.3
-
4
-
-
0036256094
-
Inheritable forms of medullary thyroid carcinoma
-
Bachelot A, Lombardo F, Baudin E, Bidart JM, Schlumberger M 2002 Inheritable forms of medullary thyroid carcinoma. Biochimie 84:61-66.
-
(2002)
Biochimie
, vol.84
, pp. 61-66
-
-
Bachelot, A.1
Lombardo, F.2
Baudin, E.3
Bidart, J.M.4
Schlumberger, M.5
-
5
-
-
0023229266
-
A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10
-
London
-
Mathew CG, Chin KS, Easton DF, Thorpe K, Carter C, Liou GI, Fong SL, Bridges CD, Haak H, Kruseman AC, Schifter S, Hansen HH, Telenius H, Telenius-Berg M, Ponder BAJ 1987 A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10. Nature (London) 328: 527-528.
-
(1987)
Nature
, vol.328
, pp. 527-528
-
-
Mathew, C.G.1
Chin, K.S.2
Easton, D.F.3
Thorpe, K.4
Carter, C.5
Liou, G.I.6
Fong, S.L.7
Bridges, C.D.8
Haak, H.9
Kruseman, A.C.10
Schifter, S.11
Hansen, H.H.12
Telenius, H.13
Telenius-Berg, M.14
Ponder, B.A.J.15
-
6
-
-
0023204382
-
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage
-
London
-
Simpson NE, Kidd KK, Goodfellow PJ, McDermid H, Myers S, Kidd JR, Kackson CE, Duncan AM, Farrer LA, Brasch K, Castiglione C, Genel M, Gertner J, Greenberg CR, Gusella JF, Holden JAA, White BN 1987 Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage. Nature (London) 328:528-530.
-
(1987)
Nature
, vol.328
, pp. 528-530
-
-
Simpson, N.E.1
Kidd, K.K.2
Goodfellow, P.J.3
McDermid, H.4
Myers, S.5
Kidd, J.R.6
Kackson, C.E.7
Duncan, A.M.8
Farrer, L.A.9
Brasch, K.10
Castiglione, C.11
Genel, M.12
Gertner, J.13
Greenberg, C.R.14
Gusella, J.F.15
Holden, J.A.A.16
White, B.N.17
-
7
-
-
0025007367
-
Linkage of multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A
-
Norum RA, Lafreniere RG, O'Neal LW, Nikolai TF, Delaney JP, Sisson JC, Sobol H, Lenoir GM, Ponder BA, Willard HF, Jackson CE 1990 Linkage of multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A. Genomics 8:313-317.
-
(1990)
Genomics
, vol.8
, pp. 313-317
-
-
Norum, R.A.1
Lafreniere, R.G.2
O'Neal, L.W.3
Nikolai, T.F.4
Delaney, J.P.5
Sisson, J.C.6
Sobol, H.7
Lenoir, G.M.8
Ponder, B.A.9
Willard, H.F.10
Jackson, C.E.11
-
8
-
-
0026061598
-
Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A
-
Lairmore TC, Howe JR, Korte JA, Dilley WG, Aine L, Aine E, Wells SA Jr, Donnis-Keller H 1991 Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A. Genomics 9:181-192.
-
(1991)
Genomics
, vol.9
, pp. 181-192
-
-
Lairmore, T.C.1
Howe, J.R.2
Korte, J.A.3
Dilley, W.G.4
Aine, L.5
Aine, E.6
Wells Jr., S.A.7
Donnis-Keller, H.8
-
9
-
-
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 SAJ 1993 Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 2:851-856.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 851-856
-
-
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.J.10
-
10
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
London
-
Mulligan LM, Kwok JB, Healey CS, Elsdon MJ, Eng C, Gardner E, Love DR, More 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 (London) 363:458-460.
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.2
Healey, C.S.3
Elsdon, M.J.4
Eng, C.5
Gardner, E.6
Love, D.R.7
More, 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
-
11
-
-
0027977002
-
Single missense mutation in the tyrosine kinase catalytic domain of the RET proto-oncogene is associated with multiple endocrine neoplasia type 2B
-
Carlson KM, Dou S, Chi D, Scavarda N, Toshima K, Kackson CE, Wells SA Jr, Goodfellow PJ, Donis-Keller H 1994 Single missense mutation in the tyrosine kinase catalytic domain of the RET proto-oncogene is associated with multiple endocrine neoplasia type 2B. Proc Natl Acad USA 91:1579-1583.
-
(1994)
Proc Natl Acad USA
, vol.91
, pp. 1579-1583
-
-
Carlson, K.M.1
Dou, S.2
Chi, D.3
Scavarda, N.4
Toshima, K.5
Kackson, C.E.6
Wells Jr., S.A.7
Goodfellow, P.J.8
Donis-Keller, H.9
-
12
-
-
0028006092
-
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumors
-
Eng C, Smith DP, Mulligan LM, Nagi MA, Healey CS, Ponder MA, Gardner E, Scheumann GFW, Jackson CE, Tunnacliffe A, Ponder BAJ 1994 Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumors. Hum Mol Genet 3:237-241.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 237-241
-
-
Eng, C.1
Smith, D.P.2
Mulligan, L.M.3
Nagi, M.A.4
Healey, C.S.5
Ponder, M.A.6
Gardner, E.7
Scheumann, G.F.W.8
Jackson, C.E.9
Tunnacliffe, A.10
Ponder, B.A.J.11
-
13
-
-
0028174024
-
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
-
Hofstra RM, Landsvater RM, Ceccherini I, Stulp RP, Stelwagen T, Luo Y, Pasini B, Hoppener JW, van Amstel HK, Romeo G, Lips CJM, Buys CHCM 1994 A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature 367:375-376.
-
(1994)
Nature
, vol.367
, pp. 375-376
-
-
Hofstra, R.M.1
Landsvater, R.M.2
Ceccherini, I.3
Stulp, R.P.4
Stelwagen, T.5
Luo, Y.6
Pasini, B.7
Hoppener, J.W.8
Van Amstel, H.K.9
Romeo, G.10
Lips, C.J.M.11
Buys, C.H.C.M.12
-
14
-
-
0028881998
-
International RET Mutation Consortium. Genotype-phenotype correlation in multiple endocrine neoplasia type 2: Report of the International RET Mutation Consortium
-
Mulligan LM, Marsh DJ, Robinson BG, Schuffenecker I, Zedenius J, Lips CJM, Gagel RF, Takai SI, Noll WW, Fink M, Raue F, Lacroix A, Thibodeau SN, Frilling A, Ponder BAJ, Eng C 1995 International RET Mutation Consortium. Genotype-phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium. J Intern Med 238:343-346.
-
(1995)
J Intern Med
, vol.238
, pp. 343-346
-
-
Mulligan, L.M.1
Marsh, D.J.2
Robinson, B.G.3
Schuffenecker, I.4
Zedenius, J.5
Lips, C.J.M.6
Gagel, R.F.7
Takai, S.I.8
Noll, W.W.9
Fink, M.10
Raue, F.11
Lacroix, A.12
Thibodeau, S.N.13
Frilling, A.14
Ponder, B.A.J.15
Eng, C.16
-
15
-
-
9344234978
-
Mutations of the RET proto-oncogene in German MEN families: Relation between genotype and phenotype
-
Frank-Raue K, Hppner W, Frilling A, Kotzerke J, Dralle H, Haase R, Mann K, Seif F, Kirchner R, Rendl J, Deckart HF, Ritter MM, Hampel R, Klempa J, Scholz GH, Raue F, GMTCS Group 1996 Mutations of the RET proto-oncogene in German MEN families: relation between genotype and phenotype. J Clin Endocrinol Metab 81:1780-1783.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 1780-1783
-
-
Frank-Raue, K.1
Hppner, W.2
Frilling, A.3
Kotzerke, J.4
Dralle, H.5
Haase, R.6
Mann, K.7
Seif, F.8
Kirchner, R.9
Rendl, J.10
Deckart, H.F.11
Ritter, M.M.12
Hampel, R.13
Klempa, J.14
Scholz, G.H.15
Raue, F.16
-
16
-
-
85047682409
-
Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
Brandi ML, Gagel RF, Angeli A, Bilezikian JP, Beck-Peccoz P, Bordi C, Conte-Devolx B, Falchetti A, Gheri RG, Libroia A, Lips CJ, Lombardi G, Mannelli M, Pacini F, Ponder BA, Raue F, Skogseid B, Tamburrano G, Thakker RV, Thompson NW, Tomassetti P, Tonelli F, Wells SA Jr, Marx SJ 2001 Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 86:5658-5671.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 5658-5671
-
-
Brandi, M.L.1
Gagel, R.F.2
Angeli, A.3
Bilezikian, J.P.4
Beck-Peccoz, P.5
Bordi, C.6
Conte-Devolx, B.7
Falchetti, A.8
Gheri, R.G.9
Libroia, A.10
Lips, C.J.11
Lombardi, G.12
Mannelli, M.13
Pacini, F.14
Ponder, B.A.15
Raue, F.16
Skogseid, B.17
Tamburrano, G.18
Thakker, R.V.19
Thompson, N.W.20
Tomassetti, P.21
Tonelli, F.22
Wells Jr., S.A.23
Marx, S.J.24
more..
-
17
-
-
0031049753
-
The different RET-activating capability of mutations of cysteine 620 or cysteine 634 correlates with the multiple endocrine neoplasia type 2 disease phenotype
-
Carlomagno F, Salvatore G, Cirafici AM, De Vita G, Melillo RM, de Franciscis V, Billaud M, Fusco A, Santoro M 1997 The different RET-activating capability of mutations of cysteine 620 or cysteine 634 correlates with the multiple endocrine neoplasia type 2 disease phenotype. Cancer Res 57:391-395.
-
(1997)
Cancer Res
, vol.57
, pp. 391-395
-
-
Carlomagno, F.1
Salvatore, G.2
Cirafici, A.M.3
De Vita, G.4
Melillo, R.M.5
De Franciscis, V.6
Billaud, M.7
Fusco, A.8
Santoro, M.9
-
18
-
-
0032481129
-
Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines
-
Chappuis-Flament S, Pasini A, De Vita G, Segouffin-Cariou C, Fusco A, Attie T, Lenoir GM, Santoro M, Billaud M 1998 Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines. Oncogene 17:2851-2861.
-
(1998)
Oncogene
, vol.17
, pp. 2851-2861
-
-
Chappuis-Flament, S.1
Pasini, A.2
De Vita, G.3
Segouffin-Cariou, C.4
Fusco, A.5
Attie, T.6
Lenoir, G.M.7
Santoro, M.8
Billaud, M.9
-
19
-
-
0033054334
-
Co-segregation of MEN2 and Hirschsprung's disease: The same mutation of RET with both gain and loss-of-function?
-
Takahashi M, Iwashita T, Santoro M, Lyonnet S, Lenoir GM, Billaud M 1999 Co-segregation of MEN2 and Hirschsprung's disease: The same mutation of RET with both gain and loss-of-function? Hum Mutat 13:331-336.
-
(1999)
Hum Mutat
, vol.13
, pp. 331-336
-
-
Takahashi, M.1
Iwashita, T.2
Santoro, M.3
Lyonnet, S.4
Lenoir, G.M.5
Billaud, M.6
-
20
-
-
0030828048
-
Germline mutation of RET codon 883 in two cases of de novo MEN 2B
-
Smith DP, Houghton C, Ponder BA 1997 Germline mutation of RET codon 883 in two cases of de novo MEN 2B. Oncogene 15:1213-1217.
-
(1997)
Oncogene
, vol.15
, pp. 1213-1217
-
-
Smith, D.P.1
Houghton, C.2
Ponder, B.A.3
-
21
-
-
0030722592
-
Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation
-
Gimm O, Marsh DJ, Andrew SD, Frilling A, Dahia PL, Mulligan LM, Zajac JD, Robinson BG, Eng C 1997 Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation. J Clin Endocrinol Metab 82:3902-3904.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3902-3904
-
-
Gimm, O.1
Marsh, D.J.2
Andrew, S.D.3
Frilling, A.4
Dahia, P.L.5
Mulligan, L.M.6
Zajac, J.D.7
Robinson, B.G.8
Eng, C.9
-
22
-
-
0037629965
-
RET codon 634 mutations in multiple endocrine neoplasia type 2: Variable clinical features and clinical outcome
-
Punales MK, Graf H, Gross JL, Maia AL 2003 RET codon 634 mutations in multiple endocrine neoplasia type 2: Variable clinical features and clinical outcome. J Clin Endocrinol Metab 88:2644-2649.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 2644-2649
-
-
Punales, M.K.1
Graf, H.2
Gross, J.L.3
Maia, A.L.4
-
23
-
-
0035125612
-
Routine measurement of serum calcitonin is useful for early detection of medullary thyroid carcinoma in patients with nodular thyroid diseases
-
Harm JR, Lee MS, Min YK, Lee MK, Kim KW, Nam SJ, Yang JH, Chung JH 2001 Routine measurement of serum calcitonin is useful for early detection of medullary thyroid carcinoma in patients with nodular thyroid diseases. Thyroid 11:73-80.
-
(2001)
Thyroid
, vol.11
, pp. 73-80
-
-
Harm, J.R.1
Lee, M.S.2
Min, Y.K.3
Lee, M.K.4
Kim, K.W.5
Nam, S.J.6
Yang, J.H.7
Chung, J.H.8
-
24
-
-
0141795908
-
Head and Neck Sites. Thyroid
-
Greene FL, Page DL, Fleming ID, Fritz AG, Balch CM, Haller DG, Morrow M (eds.) Springer-Verlag, New York
-
American Joint Committee on Cancer 2002 Head and Neck Sites. Thyroid. In: Greene FL, Page DL, Fleming ID, Fritz AG, Balch CM, Haller DG, Morrow M (eds.) AJCC Cancer Staging Manual, 6th ed. Springer-Verlag, New York, pp. 77-87.
-
(2002)
AJCC Cancer Staging Manual, 6th Ed.
, pp. 77-87
-
-
-
25
-
-
0028838075
-
A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC
-
Eng C, Smith DP, Mulligan LM, Healey CS, Zvelebil MJ, Stonehouse TJ, Ponder MA, Jackson CE, Waterfield MD, Ponder BA 1995 A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC. Oncogene 10:509-513.
-
(1995)
Oncogene
, vol.10
, pp. 509-513
-
-
Eng, C.1
Smith, D.P.2
Mulligan, L.M.3
Healey, C.S.4
Zvelebil, M.J.5
Stonehouse, T.J.6
Ponder, M.A.7
Jackson, C.E.8
Waterfield, M.D.9
Ponder, B.A.10
-
26
-
-
0030896418
-
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours and Hirschsprung disease
-
Eng C, Mulligan LM 1997 Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours and Hirschsprung disease. Hum Mutat 9:97-109.
-
(1997)
Hum Mutat
, vol.9
, pp. 97-109
-
-
Eng, C.1
Mulligan, L.M.2
-
27
-
-
0033729031
-
Multiple endocrine neoplasia type 2 and RET: From neoplasia to neurogenesis
-
Hansford JR, Mulligan LM 2000 Multiple endocrine neoplasia type 2 and RET: From neoplasia to neurogenesis. J Med Genet 37:817-827.
-
(2000)
J Med Genet
, vol.37
, pp. 817-827
-
-
Hansford, J.R.1
Mulligan, L.M.2
-
28
-
-
0029028664
-
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma
-
Eng C, Mulligan LM, Smith DP, Healey CS, Frilling A, Raue F, Neumann HPH, Ponder MA, Ponder BAJ 1995 Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma. Clin Endocrinol 43:123-127.
-
(1995)
Clin Endocrinol
, vol.43
, pp. 123-127
-
-
Eng, C.1
Mulligan, L.M.2
Smith, D.P.3
Healey, C.S.4
Frilling, A.5
Raue, F.6
Neumann, H.P.H.7
Ponder, M.A.8
Ponder, B.A.J.9
-
29
-
-
10244245097
-
Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinoma
-
Wohllk N, Cote GJ, Bugalho MM, Ordonez N, Evans DB, Goepfert H, Khorana S, Schultz P, Richards CS, Gagel RF 1996 Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinoma. J Clin Endocrinol Metab 81:3740-3745.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 3740-3745
-
-
Wohllk, N.1
Cote, G.J.2
Bugalho, M.M.3
Ordonez, N.4
Evans, D.B.5
Goepfert, H.6
Khorana, S.7
Schultz, P.8
Richards, C.S.9
Gagel, R.F.10
-
30
-
-
0031695617
-
RET protooncogene mutations in patients with apparently sporadic medullary thyroid carcinoma
-
Huang CN, Wu SL, Chang TC, Huang SH, Chang TJ 1998 RET protooncogene mutations in patients with apparently sporadic medullary thyroid carcinoma. J Formos Med Assoc 97:541-546.
-
(1998)
J Formos Med Assoc
, vol.97
, pp. 541-546
-
-
Huang, C.N.1
Wu, S.L.2
Chang, T.C.3
Huang, S.H.4
Chang, T.J.5
-
31
-
-
0035281583
-
Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients
-
Wiench M, Wygoda Z, Gubala E, Wloch J, Lisowska K, Krassowski J, Scieglinska D, Fiszer-Kierzkowska A, Lange D, Kula D, Zeman M, Roskosz J, Kukulska A, Krawczyk Z, Jarzab B 2001 Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients. J Clin Oncol 19:1374-1380.
-
(2001)
J Clin Oncol
, vol.19
, pp. 1374-1380
-
-
Wiench, M.1
Wygoda, Z.2
Gubala, E.3
Wloch, J.4
Lisowska, K.5
Krassowski, J.6
Scieglinska, D.7
Fiszer-Kierzkowska, A.8
Lange, D.9
Kula, D.10
Zeman, M.11
Roskosz, J.12
Kukulska, A.13
Krawczyk, Z.14
Jarzab, B.15
-
32
-
-
0034839109
-
Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population
-
Ruiz A, Antinolo G, Fernandez RM, Eng C, Marcos I, Borrego S 2001 Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population. Clin Endocrinol 55:399-402.
-
(2001)
Clin Endocrinol
, vol.55
, pp. 399-402
-
-
Ruiz, A.1
Antinolo, G.2
Fernandez, R.M.3
Eng, C.4
Marcos, I.5
Borrego, S.6
-
33
-
-
0035404426
-
Germline mutations of the ret proto-oncogene in Chilean patients with hereditary and sporadic medullary thyroid carcinoma
-
Wohllk N, Becker P, Youlton R, Cote GJ, Gagel RF 2001 Germline mutations of the ret proto-oncogene in Chilean patients with hereditary and sporadic medullary thyroid carcinoma. Rev Med Chil 129:713-718.
-
(2001)
Rev Med Chil
, vol.129
, pp. 713-718
-
-
Wohllk, N.1
Becker, P.2
Youlton, R.3
Cote, G.J.4
Gagel, R.F.5
-
34
-
-
0034935625
-
Large-scale analysis of mutations in RET exon 16 in sporadic medullary thyroid carcinomas in Japan
-
Takano T, Miyauchi A, Yoshida H, Hasegawa Y, Kuma K, Amino N 2001 Large-scale analysis of mutations in RET exon 16 in sporadic medullary thyroid carcinomas in Japan. Jpn J Cancer Res 92:645-648.
-
(2001)
Jpn J Cancer Res
, vol.92
, pp. 645-648
-
-
Takano, T.1
Miyauchi, A.2
Yoshida, H.3
Hasegawa, Y.4
Kuma, K.5
Amino, N.6
-
35
-
-
15144343501
-
Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs a Calcitonine
-
Schuffenecker I, Virally-Monod M, Brohet R, Goldgar D, Conte-Devolx B, Leclerc L, Chabre O, Boneu A, Caron J, Houdent C, Modigliani E, Rohmer V, Schlumberger M, Eng C, Guillausseau PJ, Lenoir GM 1998 Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs a Calcitonine. J Clin Endocrinol Metab 83:487-491.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 487-491
-
-
Schuffenecker, I.1
Virally-Monod, M.2
Brohet, R.3
Goldgar, D.4
Conte-Devolx, B.5
Leclerc, L.6
Chabre, O.7
Boneu, A.8
Caron, J.9
Houdent, C.10
Modigliani, E.11
Rohmer, V.12
Schlumberger, M.13
Eng, C.14
Guillausseau, P.J.15
Lenoir, G.M.16
-
36
-
-
0003128327
-
Medullary thyroid carcinoma
-
Braverman LE, Utiger RD (eds.) Lippincott Williams & Wilkins, Philadelphia
-
Ball DW, Baylin SB, De Bustros AC 2000 Medullary thyroid carcinoma. In: Braverman LE, Utiger RD (eds.) Werner & Ingbar's The Thyroid: A Fundamental and Clinical Text, 8th ed. Lippincott Williams & Wilkins, Philadelphia, pp. 930-943.
-
(2000)
Werner & Ingbar's the Thyroid: A Fundamental and Clinical Text, 8th Ed.
, pp. 930-943
-
-
Ball, D.W.1
Baylin, S.B.2
De Bustros, A.C.3
-
37
-
-
0029944584
-
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma
-
Eng C, Mulligan LM, Healey CS, Houghton C, Frilling A, Raue F, Thomas GA, Ponder BAJ 1996 Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma. Cancer Res 56:2167-2170.
-
(1996)
Cancer Res
, vol.56
, pp. 2167-2170
-
-
Eng, C.1
Mulligan, L.M.2
Healey, C.S.3
Houghton, C.4
Frilling, A.5
Raue, F.6
Thomas, G.A.7
Ponder, B.A.J.8
-
38
-
-
0032461085
-
Mutation of the RET proto-oncogene is correlated with RET immunostaining in subpopulations of cells in sporadic medullary thyroid carcinoma
-
Eng C, Thomas G, Mulligan L, Healey CS, Houghton C, Frilling A, Raue F, Williams E, Ponder B 1998 Mutation of the RET proto-oncogene is correlated with RET immunostaining in subpopulations of cells in sporadic medullary thyroid carcinoma. J Clin Endocrinol Metab 88: 4310-4313.
-
(1998)
J Clin Endocrinol Metab
, vol.88
, pp. 4310-4313
-
-
Eng, C.1
Thomas, G.2
Mulligan, L.3
Healey, C.S.4
Houghton, C.5
Frilling, A.6
Raue, F.7
Williams, E.8
Ponder, B.9
-
39
-
-
0028199074
-
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC
-
Mulligan LM, Eng C, Healey CS, Clayton D, Kwok JBJ, Gardner E, Ponder MA, Frilling A, Jackson CE, Lehnert H, Neumann HPH, Thibodeau SN, Ponder BAJ 1994 Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. Nat Genet 6:70-74.
-
(1994)
Nat Genet
, vol.6
, pp. 70-74
-
-
Mulligan, L.M.1
Eng, C.2
Healey, C.S.3
Clayton, D.4
Kwok, J.B.J.5
Gardner, E.6
Ponder, M.A.7
Frilling, A.8
Jackson, C.E.9
Lehnert, H.10
Neumann, H.P.H.11
Thibodeau, S.N.12
Ponder, B.A.J.13
-
40
-
-
0031723231
-
Mutations of ret proto-oncogenes in 3 Korean families with MEN 2A: Clinical use of new restriction sites for genetic diagnosis
-
Lee MS, Hwang DY, Kim YH, Chung JH, Oh YS, Lee MK, Kim KW 1998 Mutations of ret proto-oncogenes in 3 Korean families with MEN 2A: Clinical use of new restriction sites for genetic diagnosis. Endocr J 45:555-561.
-
(1998)
Endocr J
, vol.45
, pp. 555-561
-
-
Lee, M.S.1
Hwang, D.Y.2
Kim, Y.H.3
Chung, J.H.4
Oh, Y.S.5
Lee, M.K.6
Kim, K.W.7
-
41
-
-
8444249722
-
Early detection of medullary thyroid cancer by screening of the RET proto-oncogene germ line point mutation in family members affected with hereditary medullary thyroid cancer
-
Kim SW, Kim TY, Park YJ, Kim WB, Shin CS, Park DJ, Park KS, Kim SY, Cho BY, Lee HK 2001 Early detection of medullary thyroid cancer by screening of the RET proto-oncogene germ line point mutation in family members affected with hereditary medullary thyroid cancer. J Korean Soc Endocrinol 16:54-64.
-
(2001)
J Korean Soc Endocrinol
, vol.16
, pp. 54-64
-
-
Kim, S.W.1
Kim, T.Y.2
Park, Y.J.3
Kim, W.B.4
Shin, C.S.5
Park, D.J.6
Park, K.S.7
Kim, S.Y.8
Cho, B.Y.9
Lee, H.K.10
-
42
-
-
0036187804
-
RET oligonucleotide microarray for the detection of RET mutations in multiple endocrine neoplasia type 2 syndromes
-
Kim IJ, Kang HC, Park JH, Ku JL, Lee JS, Kwon HJ, Yoon KA, Heo SC, Yang HY, Cho BY, Kim SY, Oh SK, Youn YK, Park DJ, Lee MS, Lee KW, Park JG 2002 RET oligonucleotide microarray for the detection of RET mutations in multiple endocrine neoplasia type 2 syndromes. Clin Cancer Res 8:457-463.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 457-463
-
-
Kim, I.J.1
Kang, H.C.2
Park, J.H.3
Ku, J.L.4
Lee, J.S.5
Kwon, H.J.6
Yoon, K.A.7
Heo, S.C.8
Yang, H.Y.9
Cho, B.Y.10
Kim, S.Y.11
Oh, S.K.12
Youn, Y.K.13
Park, D.J.14
Lee, M.S.15
Lee, K.W.16
Park, J.G.17
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