-
1
-
-
4644256817
-
The relationship between specific ret proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET mutation consortium analysis
-
DOI 10.1001/jama.276.19.1575
-
Eng, C., Clayton, D., Schuffenecker, I. et al 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. (Pubitemid 26384740)
-
(1996)
Journal of the American Medical Association
, vol.276
, Issue.19
, pp. 1575-1579
-
-
Eng, C.1
Clayton, D.2
Schuffenecker, I.3
Lenoir, G.4
Cote, G.5
Gagel, R.F.6
Ploos Van Amstel, H.K.7
Lips, C.J.M.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.17
Pacini, F.18
Fink, M.19
Niederle, B.20
Zedenius, J.21
Nordenskjold, M.22
Komminoth, P.23
Hendy, G.N.24
Gharib, H.25
Thibodeau, S.N.26
Lacroix, A.27
Frilling, A.28
Ponder, B.A.J.29
Mulligan, L.M.30
more..
-
2
-
-
0030896418
-
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease
-
DOI 10.1002/(SICI)1098-1004(1997)9:2<97::AID-HUMU1>3.0.CO;2-M
-
Eng, C. Mulligan, L.M. (1997) Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease. Human Mutation, 9, 97 109. (Pubitemid 27133173)
-
(1997)
Human Mutation
, vol.9
, Issue.2
, pp. 97-109
-
-
Eng, C.1
Mulligan, L.M.2
-
3
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan, L.M., Kwok, J.B., Healey, C.S. et al. (1993) Germ-line 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
-
4
-
-
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. (Pubitemid 17045226)
-
(1987)
Molecular and Cellular Biology
, vol.7
, Issue.4
, pp. 1378-1385
-
-
Takahashi, M.1
Cooper, G.M.2
-
5
-
-
0344442410
-
533Cys) in a Large Kindred with Familial Medullary Thyroid Carcinoma
-
DOI 10.1210/jc.2003-030997
-
Da Silva, A.M., Maciel, R.M., Da Silva, M.R. et al. (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. (Pubitemid 37452751)
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, Issue.11
, pp. 5438-5443
-
-
Alvares Da Silva, A.M.1
Maciel, R.M.B.2
Dias Da Silva, M.R.3
Toledo, S.R.C.4
De Carvalho, M.B.5
Cerutti, J.M.6
-
6
-
-
0028199074
-
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC
-
DOI 10.1038/ng0194-70
-
Mulligan, L.M., Eng, C., Healey, C.S. et al. (1994) Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. Nature Genetics, 6, 70 74. (Pubitemid 24191916)
-
(1994)
Nature Genetics
, vol.6
, Issue.1
, 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
-
7
-
-
0030998008
-
Mutation of RET codon 768 is associated with the FMTC phenotype
-
Boccia, L.M., Green, J.S., Joyce, C. et al. (1997) Mutation of RET codon 768 is associated with the FMTC phenotype. Clinical Genetics, 51, 81 85. (Pubitemid 27149712)
-
(1997)
Clinical Genetics
, vol.51
, Issue.2
, pp. 81-85
-
-
Boccia, L.M.1
Green, J.S.2
Joyce, C.3
Eng, C.4
Taylor, S.A.M.5
Mulligan, L.M.6
-
8
-
-
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
Al, E.4
-
9
-
-
33646015994
-
A rare RET gene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: Implications for screening
-
Kaldrymides, P., Mytakidis, N., Anagnostopoulos, T. et al. (2006) A rare RET gene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: implications for screening. Clinical Endocrinology, 64, 561 566.
-
(2006)
Clinical Endocrinology
, vol.64
, pp. 561-566
-
-
Kaldrymides, P.1
Mytakidis, N.2
Anagnostopoulos, T.3
-
10
-
-
33747080744
-
RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors
-
DOI 10.1210/er.2006-0017
-
de Groot, J.W., Links, T.P., Plukker, J.T. et al. (2006) RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors. Endocrine Review, 27, 535 560. (Pubitemid 44213230)
-
(2006)
Endocrine Reviews
, vol.27
, Issue.5
, pp. 535-560
-
-
De Groot, J.W.B.1
Links, T.P.2
Plukker, J.T.M.3
Lips, C.J.M.4
Hofstra, R.M.W.5
-
11
-
-
0027977002
-
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B
-
Carlson, K.M., Dou, S., Chi, D. et al. (1994) Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B. Proceedings of the National Academy of Sciences USA, 91, 1579 1583. (Pubitemid 24059056)
-
(1994)
Proceedings of the National Academy of Sciences of the United States of America
, vol.91
, Issue.4
, 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
-
12
-
-
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. et al. (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. (Pubitemid 27509392)
-
(1997)
Journal of Clinical Endocrinology and Metabolism
, vol.82
, Issue.11
, pp. 3902-3904
-
-
Gimm, O.1
Marsh, D.J.2
Andrew, S.D.3
Frilling, A.4
Dahia, P.L.M.5
Mulligan, L.M.6
Zajac, J.D.7
Robinson, B.G.8
Eng, C.9
-
13
-
-
22244480355
-
RET proto-oncogene: A review and update of genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors
-
DOI 10.1089/thy.2005.15.531
-
Kouvaraki, M.A., Shapiro, S.E., Perrier, N.D. et al. (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. (Pubitemid 40993726)
-
(2005)
Thyroid
, vol.15
, Issue.6
, 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
-
14
-
-
31544434233
-
Polymorphisms in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A
-
DOI 10.1158/0008-5472.CAN-05-2995
-
Lesueur, F., Cebrian, A., Robledo, M. et al. (2006) Polymorphisms in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A. Cancer Research, 66, 1177 1180. (Pubitemid 43165988)
-
(2006)
Cancer Research
, vol.66
, Issue.2
, pp. 1177-1180
-
-
Lesueur, F.1
Cebrian, A.2
Robledo, M.3
Niccoli-Sire, P.4
Svensson, K.-A.5
Pinson, S.6
Leyland, J.7
Whittaker, J.8
Pharoah, P.D.9
Ponder, B.A.J.10
-
15
-
-
85047682409
-
Consensus: Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
DOI 10.1210/jc.86.12.5658
-
Brandi, M.L., Gagel, R.F., Angeli, A. et al. (2001) Guidelines for diagnosis and therapy of MEN type 1 and type 2. Journal of Clinical Endocrinology and Metabolism, 86, 5658 5671. (Pubitemid 33152604)
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, Issue.12
, 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.M.11
Lombardi, G.12
Mannelli, M.13
Pacini, F.14
Ponder, B.A.J.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..
-
16
-
-
34548653042
-
A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A
-
Bethanis, S., Koutsodontis, G., Palouka, T. et al. (2007) A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A. Hormones (Athens), 6, 152 156.
-
(2007)
Hormones (Athens)
, vol.6
, pp. 152-156
-
-
Bethanis, S.1
Koutsodontis, G.2
Palouka, T.3
-
17
-
-
0344406081
-
Polymorphisms G691S/S904S of RET as genetic modifiers of MEN 2A
-
Robledo, M., Gil, L., Pollan, M. et al. (2003) Polymorphisms G691S/S904S of RET as genetic modifiers of MEN 2A. Cancer Research, 63, 1814 1817. (Pubitemid 36460842)
-
(2003)
Cancer Research
, vol.63
, Issue.8
, pp. 1814-1817
-
-
Robledo, M.1
Gil, L.2
Pollan, M.3
Cebrian, A.4
Ruiz, S.5
Azanedo, M.6
Benitez, J.7
Menarguez, J.8
Rojas, J.M.9
-
18
-
-
0043133692
-
Segregation of the V804L mutation and S836S polymorphism of exon 14 of the RET gene in an extended kindred with familial medullary thyroid cancer
-
DOI 10.1034/j.1399-0004.2003.00044.x
-
Patocs, A., Valkusz, Z., Igaz, P. et al. (2003) Segregation of the V804L mutation and S836S polymorphism of exon 14 of the RET gene in an extended kindred with familial medullary thyroid cancer. Clinical Genetics, 63, 219 223. (Pubitemid 36949924)
-
(2003)
Clinical Genetics
, vol.63
, Issue.3
, pp. 219-223
-
-
Patocs, A.1
Valkusz, Z.2
Igaz, P.3
Balogh, K.4
Toth, M.5
Varga, I.6
Racz, K.7
-
19
-
-
27744453187
-
Polymorphisms in exon 13 and intron 14 of the RET protooncogene: Genetic modifiers of medullary thyroid carcinoma?
-
DOI 10.1210/jc.2005-1278
-
Baumgartner-Parzer, S.M., Lang, R., Wagner, L. et al. (2005) Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma? Journal of Clinical Endocrinology and Metabolism, 90, 6232 6236. (Pubitemid 41606549)
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.90
, Issue.11
, pp. 6232-6236
-
-
Baumgartner-Parzer, S.M.1
Lang, R.2
Wagner, L.3
Heinze, G.4
Niederle, B.5
Kaserer, K.6
Waldhaasl, W.7
Vierhapper, H.8
-
20
-
-
0242288679
-
Intronic Single Nucleotide Polymorphisms in the RET Protooncogene Are Associated with a Subset of Apparently Sporadic Pheochromocytoma and May Modulate Age of Onset
-
DOI 10.1210/jc.2003-030245
-
McWhinney, S.R., Boru, G., Binkley, P.K. et al. (2003) Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset. Journal of Clinical Endocrinology and Metabolism, 88, 4911 4916. (Pubitemid 37357543)
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, Issue.10
, pp. 4911-4916
-
-
McWhinney, S.R.1
Boru, G.2
Binkley, P.K.3
Peczkowska, M.4
Januszewicz, A.A.5
Neumann, H.P.H.6
Eng, C.7
-
21
-
-
3242694881
-
RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population
-
DOI 10.1210/jc.2003-031898
-
Elisei, R., Cosci, B., Romei, C. et al. (2004) RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population. Journal of Clinical Endocrinology and Metabolism, 89, 3579 3584. (Pubitemid 38951937)
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, Issue.7
, pp. 3579-3584
-
-
Elisei, R.1
Cosci, B.2
Romei, C.3
Bottici, V.4
Sculli, M.5
Lari, R.6
Barale, R.7
Pacini, F.8
Pinchera, A.9
-
22
-
-
2442750413
-
Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression
-
Borrego, S., Saez, M.E., Ruiz, A. et al. (1999) Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression. Journal of Medical Genetics, 36, 771 774. (Pubitemid 29462322)
-
(1999)
Journal of Medical Genetics
, vol.36
, Issue.10
, pp. 771-774
-
-
Borrego, S.1
Saez, M.E.2
Ruiz, A.3
Gimm, O.4
Lopez-Alonso, M.5
Antinolo, G.6
Eng, C.7
-
23
-
-
0037217482
-
A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma
-
DOI 10.1086/345466
-
Borrego, S., Wright, F.A., Fernandez, R.M. et al. (2003) A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma. American Journal of Human Genetics, 72, 88 100. (Pubitemid 36056845)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.1
, pp. 88-100
-
-
Borrego, S.1
Wright, F.A.2
Fernandez, R.M.3
Williams, N.4
Lopez-Alonso, M.5
Davuluri, R.6
Antinolo, G.7
Eng, C.8
-
24
-
-
2342640283
-
The RET IVS1-126G>T Variant Is Strongly Associated with the Development of Sporadic Medullary Thyroid Cancer [2]
-
DOI 10.1089/105072504323031022
-
Fernandez, R.M., Robledo, M., Antinolo, G. et al. (2004) The RET IVS1-126G > T variant is strongly associated with the development of sporadic medullary thyroid cancer. Thyroid, 14, 329 331. (Pubitemid 38569286)
-
(2004)
Thyroid
, vol.14
, Issue.4
, pp. 329-331
-
-
Fernandez, R.M.1
Robledo, M.2
Antinolo, G.3
Pecina, A.4
Ruiz-Llorente, S.5
Eng, C.6
Borrego, S.7
-
25
-
-
0037052762
-
Genetic analysis of RET, GFrα1 and GDNF genes in Spanish families with multiple endocrine neoplasia type 2A
-
DOI 10.1002/ijc.10298
-
Gil, L., Azanedo, M., Pollan, M. et al. (2002) Genetic analysis of RET, GFR alpha 1 and GDNF genes in Spanish families with multiple endocrine neoplasia type 2A. International Journal of Cancer, 99, 299 304. (Pubitemid 34309490)
-
(2002)
International Journal of Cancer
, vol.99
, Issue.2
, pp. 299-304
-
-
Gil, L.1
Azanedo, M.2
Pollan, M.3
Cristobal, E.4
Arribas, B.5
Garcia-Albert, L.6
Garcia-Saiz, A.7
Maestro, M.L.8
Torres, A.9
Menarguez, J.10
Rojas, J.M.11
-
26
-
-
35448953567
-
Y791F RET mutation and early onset of medullary thyroid carcinoma in a Brazilian kindred: Evaluation of phenotype-modifying effect of germline variants [2]
-
DOI 10.1111/j.1365-2265.2007.02964.x
-
Tamanaha, R., Camacho, C.P., Ikejiri, E.S. et al. (2007) Y791F RET mutation and early onset of medullary thyroid carcinoma in a Brazilian kindred: evaluation of phenotype-modifying effect of germline variants. Clinical Endocrinology, 67, 806 808. (Pubitemid 47620447)
-
(2007)
Clinical Endocrinology
, vol.67
, Issue.5
, pp. 806-808
-
-
Tamanaha, R.1
Camacho, C.P.2
Ikejiri, E.S.3
Maciel, R.M.B.4
Cerutti, J.M.5
-
27
-
-
8444249623
-
Polymorphisms in the RET proto-oncogene and the phenotypic presentation of familial medullary thyroid carcinoma
-
DOI 10.1089/thy.2004.14.848
-
Magalhaes, P.K., de Castro, M., Elias, L.L. et al. (2004) Polymorphisms in the RET proto-oncogene and the phenotypic presentation of familial medullary thyroid carcinoma. Thyroid, 14, 848 852. (Pubitemid 39489010)
-
(2004)
Thyroid
, vol.14
, Issue.10
, pp. 848-852
-
-
Magalhaes, P.K.R.1
De Castro, M.2
Elias, L.L.K.3
Soares, E.G.4
Maciel, L.M.Z.5
-
28
-
-
35348914729
-
Genetic polymorphisms: Implications in the pathogenesis of medullary thyroid carcinoma
-
da Rocha, A.P., Magalhaes, P.K., Maia, A.L. et al. (2007) Genetic polymorphisms: implications in the pathogenesis of medullary thyroid carcinoma. Arquivos Brasileirso de Endocrinologia and Metabologia, 51, 723 730.
-
(2007)
Arquivos Brasileirso de Endocrinologia and Metabologia
, vol.51
, pp. 723-730
-
-
Da Rocha, A.P.1
Magalhaes, P.K.2
Maia, A.L.3
-
29
-
-
49649106288
-
RET genotypes in sporadic medullary thyroid cancer: Studies in a large Italian series
-
Fugazzola, L., Muzza, M., Mian, C. et al. (2008) RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series. Clinical Endocrinology, 69, 418 425.
-
(2008)
Clinical Endocrinology
, vol.69
, pp. 418-425
-
-
Fugazzola, L.1
Muzza, M.2
Mian, C.3
-
30
-
-
28344438091
-
Endothelial nitric oxide synthase gene variant modulates the relationship between serum cholesterol levels and blood pressure in the general population: New evidence for a direct effect of lipids in arterial blood pressure
-
DOI 10.1016/j.atherosclerosis.2005.03.035, PII S0021915005002613
-
Pereira, A.C., Sposito, A.C., Mota, G.F. et al. (2006) Endothelial nitric oxide synthase gene variant modulates the relationship between serum cholesterol levels and blood pressure in the general population: new evidence for a direct effect of lipids in arterial blood pressure. Atherosclerosis, 184, 193 200. (Pubitemid 41721088)
-
(2006)
Atherosclerosis
, vol.184
, Issue.1
, pp. 193-200
-
-
Pereira, A.C.1
Sposito, A.C.2
Mota, G.F.3
Cunha, R.S.4
Herkenhoff, F.L.5
Mill, J.G.6
Krieger, J.E.7
-
31
-
-
0033545406
-
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation
-
Gimm, O., Neuberg, D.S., Marsh, D.J. et al. (1999) Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation. Oncogene, 18, 1369 1373. (Pubitemid 29094889)
-
(1999)
Oncogene
, vol.18
, Issue.6
, pp. 1369-1373
-
-
Gimm, O.1
Neuberg, D.S.2
Marsh, D.J.3
Dahia, P.L.M.4
Hoang-Vu, C.5
Raue, F.6
Hinze, R.7
Dralle, H.8
Eng, C.9
-
32
-
-
33747155907
-
RET and GFRA1 germline polymorphisms in medullary thyroid cancer patients
-
Severskaia, N.V., Saenko, V.A., Il'in, A.A. et al. (2006) RET and GFRA1 germline polymorphisms in medullary thyroid cancer patients. Molecular Biology (Mosk), 40, 425 435.
-
(2006)
Molecular Biology (Mosk)
, vol.40
, pp. 425-435
-
-
Severskaia, N.V.1
Saenko, V.A.2
Il'In, A.A.3
-
33
-
-
12344292359
-
RET polymorphisms in codons 769 and 836 are not associated with predisposition to medullary thyroid carcinoma
-
DOI 10.1016/j.cdp.2004.04.002, PII S0361090X04000546
-
Wiench, M., Wloch, J., Wygoda, Z. et al. (2004) RET polymorphisms in codons 769 and 836 are not associated with predisposition to medullary thyroid carcinoma. Cancer Detection and Prevention, 28, 231 236. (Pubitemid 40125372)
-
(2004)
Cancer Detection and Prevention
, vol.28
, Issue.4
, pp. 231-236
-
-
Wiench, M.1
Wloch, J.2
Wygoda, Z.3
Gubala, E.4
Oczko, M.5
Pawlaczek, A.6
Kula, D.7
Lange, D.8
Jarzab, B.9
-
34
-
-
31144475062
-
G691S, L769L and S836S ret proto-oncogene polymorphisms are not associated with higher risk to sporadic medullary thyroid carcinoma in Chilean patients
-
Wohllk, G.N., Soto, C.E., Bravo, A.M. et al. (2005) G691S, L769L and S836S ret proto-oncogene polymorphisms are not associated with higher risk to sporadic medullary thyroid carcinoma in Chilean patients. Revista Medica de Chile, 133, 397 402.
-
(2005)
Revista Medica de Chile
, vol.133
, pp. 397-402
-
-
Wohllk, G.N.1
Soto, C.E.2
Bravo, A.M.3
-
35
-
-
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
-
DOI 10.1046/j.1365-2265.2001.01328.x
-
Ruiz, A., Antinolo, G., Fernandez, R.M. et al. (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. Clinical Endocrinology, 55, 399 402. (Pubitemid 32823050)
-
(2001)
Clinical Endocrinology
, vol.55
, Issue.3
, pp. 399-402
-
-
Ruiz, A.1
Antinolo, G.2
Fernandez, R.M.3
Eng, C.4
Marcos, I.5
Borrego, S.6
-
36
-
-
1242341217
-
Germline-sequence variants S836S and L769L in the RE arranged during Transfection (RET) proto-oncogene are not associated with predisposition to sporadic medullary carcinoma in the French population [1]
-
DOI 10.1111/j.0009-9163.2004.00172.x
-
Berard, I., Kraimps, J.L., Savagner, F. et al. (2004) Germline-sequence variants S836S and L769L in the RE arranged during Transfection (RET) proto-oncogene are not associated with predisposition to sporadic medullary carcinoma in the French population. Clinical Genetics, 65, 150 152. (Pubitemid 38220117)
-
(2004)
Clinical Genetics
, vol.65
, Issue.2
, pp. 150-152
-
-
Berard, I.1
Kraimps, J.-L.2
Savagner, F.3
Murat, A.4
Renaudin, K.5
Nicolli-Sire, P.6
Bertrand, G.7
Moisan, J.-P.8
Bezieau, S.9
-
37
-
-
1542757108
-
Novel intronic polymorphisms in the RET proto-oncogene and their association with Hirschsprung disease
-
Fitze, G., Schierz, M., Kuhlisch, E. et al. (2003) Novel intronic polymorphisms in the RET proto-oncogene and their association with Hirschsprung disease. Human Mutation, 22, 177.
-
(2003)
Human Mutation
, vol.22
, pp. 177
-
-
Fitze, G.1
Schierz, M.2
Kuhlisch, E.3
-
38
-
-
0035281583
-
Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients
-
Wiench, M., Wygoda, Z., Gubala, E. et al. (2001) Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients. Journal of Clinical Oncology, 19, 1374 1380. (Pubitemid 32202543)
-
(2001)
Journal of Clinical Oncology
, vol.19
, Issue.5
, 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
-
39
-
-
51049095458
-
Gene expression profiling of papillary thyroid carcinoma identifies transcripts correlated with BRAF mutational status and lymph node metastasis
-
Oler, G., Camacho, C.P., Hojaij, F.C. et al. (2008) Gene expression profiling of papillary thyroid carcinoma identifies transcripts correlated with BRAF mutational status and lymph node metastasis. Clinical Cancer Research, 14, 4735 4742.
-
(2008)
Clinical Cancer Research
, vol.14
, pp. 4735-4742
-
-
Oler, G.1
Camacho, C.P.2
Hojaij, F.C.3
-
40
-
-
4143052369
-
The expression of PAX8-PRARγ rearrangements is not specific to follicular thyroid carcinoma [1]
-
DOI 10.1111/j.1365-2265.2004.02061.x
-
Nakabashi, C.C., Guimaraes, G.S., Michaluart, P. Jr. et al. (2004) The expression of PAX8-PPARgamma rearrangements is not specific to follicular thyroid carcinoma. Clinical Endocrinology, 61, 280 282. (Pubitemid 39093127)
-
(2004)
Clinical Endocrinology
, vol.61
, Issue.2
, pp. 280-282
-
-
Nakabashi, C.C.D.1
Guimaraes, G.S.2
Michaluart Jr., P.3
Ward, L.S.4
Cerutti, J.M.5
Maciel, R.M.B.6
-
41
-
-
0030787520
-
Improved splice site detection in Genie
-
Reese, M.G., Eeckman, F.H., Kulp, D. et al. (1997) Improved splice site detection in Genie. Journal of Computational Biology, 4, 311 323. (Pubitemid 27355870)
-
(1997)
Journal of Computational Biology
, vol.4
, Issue.3
, pp. 311-323
-
-
Reese, M.G.1
-
42
-
-
0042242582
-
ESEfinder: A web resource to identify exonic splicing enhancers
-
DOI 10.1093/nar/gkg616
-
Cartegni, L., Wang, J., Zhu, Z. et al. (2003) ESEfinder: a web resource to identify exonic splicing enhancers. Nucleic Acids Research, 31, 3568 3571. (Pubitemid 37442199)
-
(2003)
Nucleic Acids Research
, vol.31
, Issue.13
, pp. 3568-3571
-
-
Cartegni, L.1
Wang, J.2
Zhu, Z.3
Zhang, M.Q.4
Krainer, A.R.5
-
43
-
-
0033854456
-
RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease
-
Borrego, S., Ruiz, A., Saez, M.E. et al. (2000) RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease. Journal of Medical Genetics, 37, 572 578. (Pubitemid 30604093)
-
(2000)
Journal of Medical Genetics
, vol.37
, Issue.8
, pp. 572-578
-
-
Borrego, S.1
Ruiz, A.2
Saez, M.E.3
Gimm, O.4
Gao, X.5
Lopez-Alonso, M.6
Hernandez, A.7
Wright, F.A.8
Antinolo, G.9
Eng, C.10
-
44
-
-
34249816810
-
Transcription factor NFAT, its role in cancer development, and as a potential target for chemoprevention
-
DOI 10.2174/156800907780809750
-
Lu, H. Huan, C. (2007) Transcription factor NFAT, its role in cancer development, and as a potential target for chemoprevention. Current Cancer Drug Targets, 7, 343 353. (Pubitemid 46849239)
-
(2007)
Current Cancer Drug Targets
, vol.7
, Issue.4
, pp. 343-353
-
-
Lu, H.1
Huang, C.2
-
45
-
-
16844382568
-
NFAT transcription factors: From cell cycle to tumor development
-
Viola, J.P., Carvalho, L.D., Fonseca, B.P. et al. (2005) NFAT transcription factors: from cell cycle to tumor development. Brazilian Journal of Medical and Biology Research, 38, 335 344. (Pubitemid 40485172)
-
(2005)
Brazilian Journal of Medical and Biological Research
, vol.38
, Issue.3
, pp. 335-344
-
-
Viola, J.P.B.1
Carvalho, L.D.S.2
Fonseca, B.P.F.3
Teixeira, L.K.4
-
46
-
-
20244382845
-
Identifying candidate hirschsprung disease-associated RET variants
-
DOI 10.1086/429589
-
Burzynski, G.M., Nolte, I.M., Bronda, A. et al. (2005) Identifying candidate Hirschsprung disease-associated RET variants. American Journal of Human Genetics, 76, 850 858. (Pubitemid 40563105)
-
(2005)
American Journal of Human Genetics
, vol.76
, Issue.5
, pp. 850-858
-
-
Burzynski, G.M.1
Nolte, I.M.2
Bronda, A.3
Bos, K.4
Osinga, J.5
Menacho, I.P.6
Twigt, B.7
Maas, S.8
Brooks, A.S.9
Verheij, J.B.G.M.10
Buys, C.H.C.M.11
Hofstra, R.M.W.12
-
47
-
-
27744559793
-
Polymorphisms in the initiators of RET (Rearranged during transfection) signaling pathway and susceptibility to sporadic medullary thyroid carcinoma
-
DOI 10.1210/jc.2004-2449
-
Cebrian, A., Lesueur, F., Martin, S. et al. (2005) Polymorphisms in the initiators of RET (rearranged during transfection) signaling pathway and susceptibility to sporadic medullary thyroid carcinoma. Journal of Clinical Endocrinology and Metabolism, 90, 6268 6274. (Pubitemid 41606555)
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.90
, Issue.11
, pp. 6268-6274
-
-
Cebrian, A.1
Lesueur, F.2
Martin, S.3
Leyland, J.4
Ahmed, S.5
Luccarini, C.6
Smith, P.L.7
Luben, R.8
Whittaker, J.9
Pharoah, P.D.10
Dunning, A.M.11
Ponder, B.A.J.12
-
48
-
-
0038146914
-
Splicing error in E1α pyruvate dehydrogenase mRNA caused by novel intronic mutation responsible for lactic acidosis and mental retardation
-
DOI 10.1074/jbc.M211106200
-
Mine, M., Brivet, M., Touati, G. et al. (2003) Splicing error in E1alpha pyruvate dehydrogenase mRNA caused by novel intronic mutation responsible for lactic acidosis and mental retardation. Journal of Biological Chemistry, 278, 11768 11772. (Pubitemid 36800145)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.14
, pp. 11768-11772
-
-
Mine, M.1
Brivet, M.2
Touati, G.3
Grabowski, P.4
Abitbol, M.5
Marsac, C.6
-
49
-
-
16244373960
-
The SR protein SC35 is responsible for aberrant splicing of the E1α pyruvate dehydrogenase mRNA in a case of mental retardation with lactic acidosis
-
DOI 10.1128/MCB.25.8.3286-3294.2005
-
Gabut, M., Mine, M., Marsac, C. et al. (2005) The SR protein SC35 is responsible for aberrant splicing of the E1alpha pyruvate dehydrogenase mRNA in a case of mental retardation with lactic acidosis. Molecular Cell Biology, 25, 3286 3294. (Pubitemid 40464328)
-
(2005)
Molecular and Cellular Biology
, vol.25
, Issue.8
, pp. 3286-3294
-
-
Gabut, M.1
Mine, M.2
Marsac, C.3
Brivet, M.4
Tazi, J.5
Soret, J.6
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