-
1
-
-
0021299457
-
Genetic aspects of multiple endocrine neoplasia
-
Schimke RN. 1984 Genetic aspects of multiple endocrine neoplasia. Annu Rev Med 35:25-31.
-
(1984)
Annu Rev Med
, vol.35
, pp. 25-31
-
-
Schimke, R.N.1
-
2
-
-
0014402822
-
Syndrome of bilateral pheochromoctyoma, medullary thyroid carcinoma and multiple neuromas
-
Schimke RN, Hartmann WH, Prout TW, Rimoin DL. 1968 Syndrome of bilateral pheochromoctyoma, medullary thyroid carcinoma and multiple neuromas. N Engl J Med 279:1-7.
-
(1968)
N Engl J Med
, vol.279
, pp. 1-7
-
-
Schimke, R.N.1
Hartmann, W.H.2
Prout, T.W.3
Rimoin, D.L.4
-
3
-
-
0014317788
-
Multiple mucosal neuromas, phaeochromocytoma and medullary carcinoma of the thyroid - A syndrome
-
Gorlin RJ, Sedano HO, Vickers RA, Cervenka J. 1968 Multiple mucosal neuromas, phaeochromocytoma and medullary carcinoma of the thyroid - a syndrome. Cancer 22:293-299.
-
(1968)
Cancer
, vol.22
, pp. 293-299
-
-
Gorlin, R.J.1
Sedano, H.O.2
Vickers, R.A.3
Cervenka, J.4
-
4
-
-
0029836333
-
The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung disease
-
Eng C. 1996 The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung disease. N Engl J Med 335:943-951.
-
(1996)
N Engl J Med
, vol.335
, pp. 943-951
-
-
Eng, C.1
-
5
-
-
4644256817
-
The relationship between specific RET protooncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET Mutation Consortium analysis
-
Eng C, Clayton D, Schuffenecker I, et al. 1996 The relationship between specific RET protooncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET Mutation Consortium analysis. JAMA 276:1575-1579.
-
(1996)
JAMA
, vol.276
, pp. 1575-1579
-
-
Eng, C.1
Clayton, D.2
Schuffenecker, I.3
-
6
-
-
0028881998
-
Genotype-phenotype correlation in MEN 2: Report of the International RET Mutation Consortium
-
Mulligan LM, Marsh DJ, Robinson BG, et al. 1995 Genotype-phenotype correlation in MEN 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
-
7
-
-
0030896418
-
Mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2, related sporadic tumours and Hirschsprung diseaes
-
Eng C, Mulligan LM. 1997 Mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2, related sporadic tumours and Hirschsprung diseaes. Hum Mutat 9:97-109.
-
(1997)
Hum Mutat
, vol.9
, pp. 97-109
-
-
Eng, C.1
Mulligan, L.M.2
-
8
-
-
0029588614
-
No mutation at codon 918 of the RET gene in a family with multiple endocrine neoplasia type 2B
-
Toogood AA, Eng C, Smith DP, Ponder BAJ, Shalet SM. 1995 No mutation at codon 918 of the RET gene in a family with multiple endocrine neoplasia type 2B. Clin Endocrinol 43:759-762.
-
(1995)
Clin Endocrinol
, vol.43
, pp. 759-762
-
-
Toogood, A.A.1
Eng, C.2
Smith, D.P.3
Ponder, B.A.J.4
Shalet, S.M.5
-
10
-
-
0023228919
-
Deletion of genes on chromosome 1 in endocrine neoplasia
-
Mathew CGP, Smith BA, Thorp K, et al. 1987 Deletion of genes on chromosome 1 in endocrine neoplasia. Nature 328:524-526.
-
(1987)
Nature
, vol.328
, pp. 524-526
-
-
Mathew, C.G.P.1
Smith, B.A.2
Thorp, K.3
-
11
-
-
0028566385
-
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene
-
Mulligan LM, Eng C, Attié T, et al. 1994 Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene. Hum Mol Genet 3:2163-2167.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2163-2167
-
-
Mulligan, L.M.1
Eng, C.2
Attié, T.3
-
12
-
-
0031004088
-
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
-
Liaw D, Marsh DJ, Li J, et al. 1997 Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nature Genet 16:64-67.
-
(1997)
Nature Genet
, vol.16
, pp. 64-67
-
-
Liaw, D.1
Marsh, D.J.2
Li, J.3
-
13
-
-
9844248826
-
Allelic imbalance, including deletion of PTENIMMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation
-
in press
-
Marsh DJ, Dahia PLM, Coulon V, et al. 1997 Allelic imbalance, including deletion of PTENIMMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation. Genes Chrom Cancer, in press
-
(1997)
Genes Chrom Cancer
-
-
Marsh, D.J.1
Dahia, P.L.M.2
Coulon, V.3
-
14
-
-
0023158426
-
R E T transforming gene encodes a fusion protein homologous to tyrosine kinases
-
Takahashi M, Cooper GM. 1987 R E T transforming gene encodes a fusion protein homologous to tyrosine kinases. Mol Cell Biol 3:1378-1385.
-
(1987)
Mol Cell Biol
, vol.3
, pp. 1378-1385
-
-
Takahashi, M.1
Cooper, G.M.2
-
15
-
-
0024208663
-
Cloning and expression of the ret proto-oncogene encoding a receptor tyrosine kinase with two potential transmembrane domains
-
Takahashi M, Buma Y, Iwamoto T, Inaguma Y, Ikeda H, Hiai H. 1988 Cloning and expression of the ret proto-oncogene encoding a receptor tyrosine kinase with two potential transmembrane domains. Oncogene 3:571-578.
-
(1988)
Oncogene
, vol.3
, pp. 571-578
-
-
Takahashi, M.1
Buma, Y.2
Iwamoto, T.3
Inaguma, Y.4
Ikeda, H.5
Hiai, H.6
-
16
-
-
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, et al. 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
-
17
-
-
0029002147
-
RET mutations in exons 13 and 14 of FMTC patients
-
Bolino A, Schuffenecker I, Luo Y, et al. 1995 RET mutations in exons 13 and 14 of FMTC patients. Oncogene 10:2415-2419.
-
(1995)
Oncogene
, vol.10
, pp. 2415-2419
-
-
Bolino, A.1
Schuffenecker, I.2
Luo, Y.3
-
18
-
-
0029944584
-
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma
-
Eng C, Mulligan LM, Healey CS, et al. 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
-
19
-
-
0023885305
-
The protein kinase family: Conserved features and deduced phylogeny of the catalytic domain
-
Hanks SK, Quinn AM, Hunter T. 1988 The protein kinase family: conserved features and deduced phylogeny of the catalytic domain. Science 241:42-52.
-
(1988)
Science
, vol.241
, pp. 42-52
-
-
Hanks, S.K.1
Quinn, A.M.2
Hunter, T.3
-
20
-
-
0028938721
-
Catalytic specificity of protein-tyrosine kinases is critical for selective signalling
-
Songyang Z, Carraway III KL, Eck MJ, et al. 1995 Catalytic specificity of protein-tyrosine kinases is critical for selective signalling. Nature 373:536-539.
-
(1995)
Nature
, vol.373
, pp. 536-539
-
-
Songyang, Z.1
Carraway III, K.L.2
Eck, M.J.3
-
21
-
-
13344286328
-
RET activation by germline MEN2A and MEN2B mutations
-
Borrello MG, Smith DP, Pasini B, et al. 1995 RET activation by germline MEN2A and MEN2B mutations. Oncogene 11:2419-2427.
-
(1995)
Oncogene
, vol.11
, pp. 2419-2427
-
-
Borrello, M.G.1
Smith, D.P.2
Pasini, B.3
-
22
-
-
0028914683
-
Activation of RET as a dominant transforming gene by germline mutations of MEN 2A and MEN 2B
-
Santoro M, Carlomagno F, Romano A, et al. 1995 Activation of RET as a dominant transforming gene by germline mutations of MEN 2A and MEN 2B. Science 267:381-383.
-
(1995)
Science
, vol.267
, pp. 381-383
-
-
Santoro, M.1
Carlomagno, F.2
Romano, A.3
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