-
1
-
-
0001868499
-
Multiple endocrine neoplasia type 2 and medullary thyroid carcinoma
-
In : A.*Grossman. Blackwell Science, Oxford
-
Eng, C. Ponder, B.A.J. 1998 Multiple endocrine neoplasia type 2 and medullary thyroid carcinoma. In : A. Grossman Clinical Endocrinology. Blackwell Science, Oxford, 635 650.
-
(1998)
Clinical Endocrinology
, pp. 635-650
-
-
Eng, C.1
Ponder, B.A.J.2
-
2
-
-
0030637186
-
Recent advances in multiple endocrine neoplasia syndromes
-
Gardner, D.G. 1997 Recent advances in multiple endocrine neoplasia syndromes. Advances in Internal Medicine, 42, 597 627.
-
(1997)
Advances in Internal Medicine
, vol.42
, pp. 597-627
-
-
Gardner, D.G.1
-
3
-
-
0027231568
-
Germline mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan, L.M., Kwok, J.B., Healey, C.S., Elsdon, M.J., Eng, C., Gardner, E., Love, D.R., Mole, S.E., Moore, J.K., Papi, L., et al. 1993 Germline mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature, 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
Mole, S.E.8
Moore, J.K.9
Papi, L.10
-
4
-
-
0027303248
-
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
-
Donis-Keller, H., Dou, S., Chi, D., Carlson, K.M., Toshima, K., Lairmore, T.C., Howe, J.R., Moley, J.F., Goodfellow, P. Wells, S.A. Jr. 1993 Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Human Molecular Genetics, 2, 851 856.
-
(1993)
Human Molecular Genetics
, 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 Jr., S.A.10
-
5
-
-
0023158426
-
RET transforming gene encodes a fusion protein homologous to tyrosine kinases
-
Takahashi, M. Cooper, G.M. 1987 RET transforming gene encodes a fusion protein homologous to tyrosine kinases. Molecular Cell Biology, 7, 1378 1385.
-
(1987)
Molecular Cell Biology
, vol.7
, pp. 1378-1385
-
-
Takahashi, M.1
Cooper, G.M.2
-
6
-
-
0024208663
-
Cloning and expression of the RET proto-oncogene encoding a 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 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
-
7
-
-
4644256817
-
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET Mutation Consortium analysis
-
Eng, C., Clayton, D., Schuffenecker, I., Lenoir, G., Cote, G., Gagel, R.F., van Amstel, H.K., Lips, C.J., Nishisho, I., Takai, S.I., Marsh, D.J., Robinson, B.G., Frank-Raue, K., Raue, F., Xue, F., Noll, W.W., Romei, C.C., Pacini, F., Fink, M., Niederle, B.M., Zedenius, J., Nordenskjold, M., Komminoth, P., Hendy, G.N. Mulligan, L.M. 1996 The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET Mutation Consortium analysis. Journal of the American Medical Association, 276, 1575 1579.
-
(1996)
Journal of the American Medical Association
, vol.276
, pp. 1575-1579
-
-
Eng, C.1
Clayton, D.2
Schuffenecker, I.3
Lenoir, G.4
Cote, G.5
Gagel, R.F.6
Van Amstel, H.K.7
Lips, C.J.8
Nishisho, I.9
Takai, S.I.10
Marsh, D.J.11
Robinson, B.G.12
Frank-Raue, K.13
Raue, F.14
Xue, F.15
Noll, W.W.16
Romei, C.C.17
Pacini, F.18
Fink, M.19
Niederle, B.M.20
Zedenius, J.21
Nordenskjold, M.22
Komminoth, P.23
Hendy, G.N.24
Mulligan, L.M.25
more..
-
8
-
-
22244480355
-
RET proto-oncogene: A review and update of genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors
-
Kouvaraki, M.A., Shapiro, S.E., Perrier, N.D., Cote, G.J., Gagel, R.F., Hoff, A.O., Sherman, S.I., Lee, J.E. Evans, D.B. 2005 RET proto-oncogene: a review and update of genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors. Thyroid, 15, 531 544.
-
(2005)
Thyroid
, vol.15
, pp. 531-544
-
-
Kouvaraki, M.A.1
Shapiro, S.E.2
Perrier, N.D.3
Cote, G.J.4
Gagel, R.F.5
Hoff, A.O.6
Sherman, S.I.7
Lee, J.E.8
Evans, D.B.9
-
9
-
-
0028914683
-
Activation of RET as a dominant transforming gene by germline mutations of MEN 2A and MEN 2B
-
Santoro, M., Carlomagno, F., Romano, A., Bottaro, D.P., Dathan, N.A., Grieco, M., Fusco, A., Vecchio, G., Matoskova, B., Kraus, M.H., 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
Bottaro, D.P.4
Dathan, N.A.5
Grieco, M.6
Fusco, A.7
Vecchio, G.8
Matoskova, B.9
Kraus, M.H.10
-
10
-
-
0028838086
-
Mechanism of activation of the RET proto-oncogene by multiple endocrine neoplasia 2A mutations
-
Asai, N., Iwashita, T., Matsuyama, M. Takahashi, M. 1995 Mechanism of activation of the RET proto-oncogene by multiple endocrine neoplasia 2A mutations. Molecular Cell Biology, 3, 1613 1619.
-
(1995)
Molecular Cell Biology
, vol.3
, pp. 1613-1619
-
-
Asai, N.1
Iwashita, T.2
Matsuyama, M.3
Takahashi, M.4
-
11
-
-
13344286328
-
RET activation by germline MEN 2A and MEN 2B mutations
-
Borrello, M.G., Smith, D.P., Pasini, B., Bongarzone, I., Greco, A., Lorenzo, M.J., Arighi, E., Miranda, C., Eng, C., Alberti, L., et al. 1995 RET activation by germline MEN 2A and MEN 2B mutations. Oncogene, 11, 2419 2427.
-
(1995)
Oncogene
, vol.11
, pp. 2419-2427
-
-
Borrello, M.G.1
Smith, D.P.2
Pasini, B.3
Bongarzone, I.4
Greco, A.5
Lorenzo, M.J.6
Arighi, E.7
Miranda, C.8
Eng, C.9
Alberti, L.10
-
12
-
-
0029785832
-
Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome)
-
Morrison, P.J. Nevin, N.C. 1996 Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome). Journal of Medical Genetics, 33, 779 782.
-
(1996)
Journal of Medical Genetics
, vol.33
, pp. 779-782
-
-
Morrison, P.J.1
Nevin, N.C.2
-
13
-
-
0028174024
-
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
-
Hofstra, R.M., Landsvater, R.M., Ceccherini, I., Stulp, R.P., Stelwagen, T., Luo, Y., Pasini, B., Hoppener, J.W., van Amstel, H.K., Romeo, G., et al. 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
-
14
-
-
0028006092
-
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours
-
Eng, C., Smith, D.P., Mulligan, L.M., Nagai, M.A., Healey, C.S., Ponder, M.A., Gardner, E., Scheumann, G.F., Jackson, C.E., Tunnacliffe, A., et al. 1994 Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours. Human Molecular Genetics, 3, 237 241.
-
(1994)
Human Molecular Genetics
, vol.3
, pp. 237-241
-
-
Eng, C.1
Smith, D.P.2
Mulligan, L.M.3
Nagai, M.A.4
Healey, C.S.5
Ponder, M.A.6
Gardner, E.7
Scheumann, G.F.8
Jackson, C.E.9
Tunnacliffe, A.10
-
15
-
-
0027977002
-
Single missense mutation in the tyrosine kinase catalytic domain of the RET proto-oncogene is associated with multiple endocrine neoplasia type 2B
-
Carlson, K.M., Dou, S., Chi, D., Scavarda, N., Toshima, K., Jackson, C.E., Wells, S.A. Jr., Goodfellow, P.J. 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. Proceedings of the National Academy of Sciences of the USA, 91, 1579 1583.
-
(1994)
Proceedings of the National Academy of Sciences of the USA
, vol.91
, pp. 1579-1583
-
-
Carlson, K.M.1
Dou, S.2
Chi, D.3
Scavarda, N.4
Toshima, K.5
Jackson, C.E.6
Wells Jr., S.A.7
Goodfellow, P.J.8
Donis-Keller, H.9
-
16
-
-
0028953446
-
Detection of a germline mutation at codon 918 of the RET proto-oncogene in French MEN 2B families
-
Rossel, M., Schuffenecker, I., Schlumberger, M., Bonnardel, C., Modigliani, E., Gardet, P., Navarro, J., Luo, Y., Romeo, G., Lenoir, G., et al. 1995 Detection of a germline mutation at codon 918 of the RET proto-oncogene in French MEN 2B families. Human Genetics, 95, 403 406.
-
(1995)
Human Genetics
, vol.95
, pp. 403-406
-
-
Rossel, M.1
Schuffenecker, I.2
Schlumberger, M.3
Bonnardel, C.4
Modigliani, E.5
Gardet, P.6
Navarro, J.7
Luo, Y.8
Romeo, G.9
Lenoir, G.10
-
17
-
-
0030663857
-
The multiple endocrine neoplasia type 2B point mutation switches the specificity of the RET tyrosine kinase towards cellular substrates that are susceptible to interact with Crk and Nck
-
Bocciardi, R., Mograbi, B., Pasini, B., Borrello, M.G., Pierotti, M.A., Bourget, I., Fischer, S., Romeo, G. Rossi, B. 1997 The multiple endocrine neoplasia type 2B point mutation switches the specificity of the RET tyrosine kinase towards cellular substrates that are susceptible to interact with Crk and Nck. Oncogene, 15, 2257 2265.
-
(1997)
Oncogene
, vol.15
, pp. 2257-2265
-
-
Bocciardi, R.1
Mograbi, B.2
Pasini, B.3
Borrello, M.G.4
Pierotti, M.A.5
Bourget, I.6
Fischer, S.7
Romeo, G.8
Rossi, B.9
-
18
-
-
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, D.J., Andrew, S.D., Frilling, A., Dahia, P.L., Mulligan, L.M., Zajac, J.D., Robinson, B.G. Eng, C. 1997 Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation. Journal of Clinical Endocrinology and Metabolism, 82, 3902 3904.
-
(1997)
Journal of Clinical Endocrinology and Metabolism
, 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
-
19
-
-
0030828048
-
Germline mutation of RET codon 883 in two cases of de novo MEN 2B
-
Smith, D.P., Houghton, C. Ponder, B.A.J. 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.J.3
-
20
-
-
0029002147
-
RET mutations in exons 13 and 14 of FMTC patients
-
Bolino, A., Schuffenecker, I., Luo, Y., Seri, M., Silengo, M., Tocco, T., Chabrier, G., Houdent, C., Murat, A., Schlumberger, M 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
Seri, M.4
Silengo, M.5
Tocco, T.6
Chabrier, G.7
Houdent, C.8
Murat, A.9
Schlumberger, M.10
-
21
-
-
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, D.P., Mulligan, L.M., Healey, C.S., Zvelebil, M.J., Stonehouse, T.J., Ponder, M.A., Jackson, C.E., Waterfield, M.D. Ponder, B.A. 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
-
22
-
-
0030998008
-
Mutation of RET codon 768 is associated with the FMTC phenotype
-
Boccia, L.M., Green, J.S., Joyce, C., Eng, C., Taylor, S.A. Mulligan, L.M. 1997 Mutation of RET codon 768 is associated with the FMTC phenotype. Clinical Genetics, 5, 80 85.
-
(1997)
Clinical Genetics
, vol.5
, pp. 80-85
-
-
Boccia, L.M.1
Green, J.S.2
Joyce, C.3
Eng, C.4
Taylor, S.A.5
Mulligan, L.M.6
-
23
-
-
0031765304
-
A new hotspot for mutations in the RET proto-oncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia
-
Berndt, I., Reuter, M., Saller, B., Frank-Raue, K., Groth, P., Grussendorf, M., Raue, F., Ritter, M.M. Hoppner, W. 1998 A new hotspot for mutations in the RET proto-oncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia. Journal of Clinical Endocrinology and Metabolism, 83, 770 774.
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, pp. 770-774
-
-
Berndt, I.1
Reuter, M.2
Saller, B.3
Frank-Raue, K.4
Groth, P.5
Grussendorf, M.6
Raue, F.7
Ritter, M.M.8
Hoppner, W.9
-
24
-
-
0029848352
-
Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene
-
Fink, M., Weinhusel, A., Niederle, B. Haas, O.A. 1996 Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene. International Journal of Cancer, 69, 312 316.
-
(1996)
International Journal of Cancer
, vol.69
, pp. 312-316
-
-
Fink, M.1
Weinhusel, A.2
Niederle, B.3
Haas, O.A.4
-
25
-
-
0030819689
-
A novel point mutation in the intracellular domain of the RET proto-oncogene in a family with medullary thyroid carcinoma
-
Hofstra, R.M., Fattoruso, O., Quadro, L., Wu, Y., Libroia, A., Verga, U., Colantuoni, V. Buys, C.H. 1997 A novel point mutation in the intracellular domain of the RET proto-oncogene in a family with medullary thyroid carcinoma. Journal of Clinical Endocrinology and Metabolism, 82, 4176 4178.
-
(1997)
Journal of Clinical Endocrinology and Metabolism
, vol.82
, pp. 4176-4178
-
-
Hofstra, R.M.1
Fattoruso, O.2
Quadro, L.3
Wu, Y.4
Libroia, A.5
Verga, U.6
Colantuoni, V.7
Buys, C.H.8
-
26
-
-
0035048305
-
Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: Oncological features and biochemical properties
-
Machens, A., Gimm, O., Hinze, R., Hoppner, W., Boehm, B.O. Dralle, H. 2001 Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: oncological features and biochemical properties. Journal of Clinical Endocrinology and Metabolism, 86, 1104 1109.
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, pp. 1104-1109
-
-
MacHens, A.1
Gimm, O.2
Hinze, R.3
Hoppner, W.4
Boehm, B.O.5
Dralle, H.6
-
27
-
-
0033166442
-
Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma
-
Iwashita, T., Kato, M., Murakami, H., Asai, N., Ishiguro, Y., Ito, S., Iwata, Y., Kawai, K., Asai, M., Kurokawa, K., Kajita, H. Takahashi, M. 1999 Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma. Oncogene, 18, 3919 3922.
-
(1999)
Oncogene
, vol.18
, pp. 3919-3922
-
-
Iwashita, T.1
Kato, M.2
Murakami, H.3
Asai, N.4
Ishiguro, Y.5
Ito, S.6
Iwata, Y.7
Kawai, K.8
Asai, M.9
Kurokawa, K.10
Kajita, H.11
Takahashi, M.12
-
28
-
-
0344442410
-
A novel germ-line point mutation in RET exon 8 (Gly (533) Cys) in a large kindred with familial medullary thyroid carcinoma
-
Da Silva, A.M., Maciel, R.M., Da Silva, M.R., Toledo, S.R., De Carvalho, M.B. Cerutti, J.M. 2003 A novel germ-line point mutation in RET exon 8 (Gly (533) Cys) in a large kindred with familial medullary thyroid carcinoma. Journal of Clinical Endocrinology and Metabolism, 88, 5438 5443.
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, pp. 5438-5443
-
-
Da Silva, A.M.1
MacIel, R.M.2
Da Silva, M.R.3
Toledo, S.R.4
De Carvalho, M.B.5
Cerutti, J.M.6
-
29
-
-
18744374884
-
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases
-
Ahmed, S.A., Snow-Bailey, K., Highsmith, W.E., Sun, W., Fenwick, R.G. Mao, R. 2005 Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases. Journal of Molecular Diagnostics, 7, 283 288.
-
(2005)
Journal of Molecular Diagnostics
, vol.7
, pp. 283-288
-
-
Ahmed, S.A.1
Snow-Bailey, K.2
Highsmith, W.E.3
Sun, W.4
Fenwick, R.G.5
Mao, R.6
-
30
-
-
16444365550
-
Medullary thyroid carcinoma in a child with a new RET mutation and a RET polymorphism
-
Vandenbosch, K., Renard, M., Uyttebroeck, A., Sciot, R., Matthijs, G. Legius, E. 2005 Medullary thyroid carcinoma in a child with a new RET mutation and a RET polymorphism. Journal of Genetic Counseling, 16, 95 100.
-
(2005)
Journal of Genetic Counseling
, vol.16
, pp. 95-100
-
-
Vandenbosch, K.1
Renard, M.2
Uyttebroeck, A.3
Sciot, R.4
Matthijs, G.5
Legius, E.6
-
31
-
-
8744267477
-
Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition
-
Elisei, R., Cosci, B., Romei, C., Agate, L., Piampiani, P., Miccoli, P., Berti, P., Basolo, F., Ugolini, C., Ciampi, R., Nikiforov, Y. Pinchera, A. 2004 Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition. Journal of Clinical Endocrinology and Metabolism, 89, 5823 5827.
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, pp. 5823-5827
-
-
Elisei, R.1
Cosci, B.2
Romei, C.3
Agate, L.4
Piampiani, P.5
Miccoli, P.6
Berti, P.7
Basolo, F.8
Ugolini, C.9
Ciampi, R.10
Nikiforov, Y.11
Pinchera, A.12
-
32
-
-
3242729164
-
A novel point mutation of the RET proto-oncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma
-
Jimenez, C., Dang, G.T., Schultz, P.N., El-Naggar, A., Shapiro, S., Barnes, E.A., Evans, D.B., Vassilopoulou-Sellin, R., Gagel, R.F., Cote, G.J. Hoff, A.O. 2004 A novel point mutation of the RET proto-oncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma. Journal of Clinical Endocrinology and Metabolism, 89, 3521 3526.
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, pp. 3521-3526
-
-
Jimenez, C.1
Dang, G.T.2
Schultz, P.N.3
El-Naggar, A.4
Shapiro, S.5
Barnes, E.A.6
Evans, D.B.7
Vassilopoulou-Sellin, R.8
Gagel, R.F.9
Cote, G.J.10
Hoff, A.O.11
-
33
-
-
0028101170
-
Somatic and MEN 2A de novo mutations identified in the RET proto-oncogene by screening of sporadic MTCs
-
Zedenius, J., Wallin, G., Hamberger, B., Nordenskjold, M., Weber, G. Larsson, C. 1994 Somatic and MEN 2A de novo mutations identified in the RET proto-oncogene by screening of sporadic MTCs. Human Molecular Genetics, 3, 1259 1262.
-
(1994)
Human Molecular Genetics
, vol.3
, pp. 1259-1262
-
-
Zedenius, J.1
Wallin, G.2
Hamberger, B.3
Nordenskjold, M.4
Weber, G.5
Larsson, C.6
-
34
-
-
0029028664
-
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma
-
Eng, C., Mulligan, L.M., Smith, D.P., Healey, C.S., Frilling, A., Raue, F., Neumann, H.P., Ponder, M.A. Ponder, B.A. 1995 Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma. Clinical Endocrinology, 43, 123 127.
-
(1995)
Clinical Endocrinology
, 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.7
Ponder, M.A.8
Ponder, B.A.9
-
35
-
-
0032512688
-
Germline and somatic mutations of the RET proto-oncogene in apparently sporadic medullary thyroid carcinomas
-
Scurini, C., Quadro, L., Fattoruso, O., Verga, U., Libroia, A., Lupoli, G., Cascone, E., Marzano, L., Paracchi, S., Busnardo, B., Girelli, M.E., Bellastella, A. Colantuoni, V. 1998 Germline and somatic mutations of the RET proto-oncogene in apparently sporadic medullary thyroid carcinomas. Molecular Cell Endocrinology, 137, 51 57.
-
(1998)
Molecular Cell Endocrinology
, vol.137
, pp. 51-57
-
-
Scurini, C.1
Quadro, L.2
Fattoruso, O.3
Verga, U.4
Libroia, A.5
Lupoli, G.6
Cascone, E.7
Marzano, L.8
Paracchi, S.9
Busnardo, B.10
Girelli, M.E.11
Bellastella, A.12
Colantuoni, V.13
-
36
-
-
0027965639
-
DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the RET proto-oncogene
-
Ceccherini, I., Hofstra, R.M., Luo, Y., Stulp, R.P., Barone, V., Stelwagen, T., Bocciardi, R., Nijveen, H., Bolino, A., Seri, M., et al. 1994 DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the RET proto-oncogene. Oncogene, 9, 3025 3029.
-
(1994)
Oncogene
, vol.9
, pp. 3025-3029
-
-
Ceccherini, I.1
Hofstra, R.M.2
Luo, Y.3
Stulp, P.R.4
Barone, V.5
Stelwagen, T.6
Bocciardi, R.7
Nijveen, H.8
Bolino, A.9
Seri, M.10
-
37
-
-
0027581466
-
A polymorphic repeat at the D10S141 locus
-
Love, D.R., Gardner, E. Ponder, B.A.J. 1993 A polymorphic repeat at the D10S141 locus. Human Molecular Genetics, 2, 491.
-
(1993)
Human Molecular Genetics
, vol.2
, pp. 491
-
-
Love, D.R.1
Gardner, E.2
Ponder, B.A.J.3
-
38
-
-
0027581466
-
A polymorphic dinucleotide repeat at the ZNF22 locus
-
Love, D.R., Gardner, E. Ponder, B.A.J. 1993 A polymorphic dinucleotide repeat at the ZNF22 locus. Human Molecular Genetics, 2, 491.
-
(1993)
Human Molecular Genetics
, vol.2
, pp. 491
-
-
Love, D.R.1
Gardner, E.2
Ponder, B.A.J.3
-
39
-
-
0030034851
-
Genetic analysis of seven Mediterranean families with multiple endocrine neoplasia type 2A
-
Oriola, J., Hernandez, C., Simo, R., Barcelo, A., Casamitjana, R., Vilardell, E. Rivera-Fillat, F. 1996 Genetic analysis of seven Mediterranean families with multiple endocrine neoplasia type 2A. Clinical Endocrinology, 44, 207 212.
-
(1996)
Clinical Endocrinology
, vol.44
, pp. 207-212
-
-
Oriola, J.1
Hernandez, C.2
Simo, R.3
Barcelo, A.4
Casamitjana, R.5
Vilardell, E.6
Rivera-Fillat, F.7
-
40
-
-
2442735471
-
High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain
-
Sanchez, B., Robledo, M., Biarnes, J., Saez, M.E., Volpini, V., Benitez, J., Navarro, E., Ruiz, A., Antinolo, G. Borrego, S. 1999 High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain. Journal of Medical Genetics, 36, 68 67.
-
(1999)
Journal of Medical Genetics
, vol.36
, pp. 68-67
-
-
Sanchez, B.1
Robledo, M.2
Biarnes, J.3
Saez, M.E.4
Volpini, V.5
Benitez, J.6
Navarro, E.7
Ruiz, A.8
Antinolo, G.9
Borrego, S.10
-
41
-
-
0242693048
-
MEN 2A families: From hot spots to hot regions
-
Bugalho, M.J., Domingues, R. Sobrinho, L. 2003 MEN 2A families: From hot spots to hot regions. International Journal of Molecular Medicine, 11, 71 74.
-
(2003)
International Journal of Molecular Medicine
, vol.11
, pp. 71-74
-
-
Bugalho, M.J.1
Domingues, R.2
Sobrinho, L.3
-
42
-
-
0023885305
-
The protein kinase family: Conserved features and deduced phylogeny of catalytic domains
-
Hanks, S.K., Quinn, A.M. Hunter, T. 1988 The protein kinase family: conserved features and deduced phylogeny of catalytic domains. Science, 241, 42 52.
-
(1988)
Science
, vol.241
, pp. 42-52
-
-
Hanks, S.K.1
Quinn, A.M.2
Hunter, T.3
-
43
-
-
21144453885
-
Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence
-
Kashuk, C.S., Stone, E.A., Grice, E.A., Portnoy, M.E., Green, E.D., Sidow, A., Chakravarti, A. McCallion, A.S. 2005 Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence. Proceedings of the National Academy of Sciences of the USA, 102, 8949 8954.
-
(2005)
Proceedings of the National Academy of Sciences of the USA
, vol.102
, pp. 8949-8954
-
-
Kashuk, C.S.1
Stone, E.A.2
Grice, E.A.3
Portnoy, M.E.4
Green, E.D.5
Sidow, A.6
Chakravarti, A.7
McCallion, A.S.8
|