-
2
-
-
0034331355
-
Multiple endocrine neoplasia type 2 and the practice of molecular medicine
-
Eng C. Multiple endocrine neoplasia type 2 and the practice of molecular medicine. Rev Endocr Metab Disord. 1:2000;283-290.
-
(2000)
Rev Endocr Metab Disord
, vol.1
, pp. 283-290
-
-
Eng, C.1
-
3
-
-
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., Pacini F., Fink M., Niederle B., Zedenius J., Nordenskjold M., Komminoth P., Hendy G.N., Mulligan L.M. The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. international RET mutation consortium analysis JAMA. 276:1996;1575-1579.
-
(1996)
JAMA
, 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.17
Pacini, F.18
Fink, M.19
Niederle, B.20
Zedenius, J.21
Nordenskjold, M.22
Komminoth, P.23
Hendy, G.N.24
Mulligan, L.M.25
more..
-
4
-
-
0033729031
-
Multiple endocrine neoplasia type 2 and RET: From neoplasia to neurogenesis
-
Hansford J.R., Mulligan L.M. Multiple endocrine neoplasia type 2 and RET. from neoplasia to neurogenesis J Med Genet. 37:2000;817-827.
-
(2000)
J Med Genet
, vol.37
, pp. 817-827
-
-
Hansford, J.R.1
Mulligan, L.M.2
-
5
-
-
0027374562
-
Expression of the c-ret oncogene during mouse embryogenesis
-
Panchis V., Mankoo M., Costantini F. Expression of the c-ret oncogene during mouse embryogenesis. Development. 119:1993;1005-1017.
-
(1993)
Development
, vol.119
, pp. 1005-1017
-
-
Panchis, V.1
Mankoo, M.2
Costantini, F.3
-
6
-
-
0028174023
-
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
-
Schuchardt A., D'Agati V., Larsson-Blomberg L., Costantini F., Panchnis V. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature. 367:1994;380-383.
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
Costantini, F.4
Panchnis, V.5
-
7
-
-
0028916234
-
Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease
-
Borst M.J., VanCamp J.M., Peacock B.A., Decker R.A. Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease. Surgery. 117:1995;386-391.
-
(1995)
Surgery
, vol.117
, pp. 386-391
-
-
Borst, M.J.1
VanCamp, J.M.2
Peacock, B.A.3
Decker, R.A.4
-
8
-
-
0031915455
-
Occurrence of MEN 2a in familial Hirschsprung's disease: A new indication for genetic testing of the RET proto-oncogene
-
Decker R.A., Peacock M.L. Occurrence of MEN 2a in familial Hirschsprung's disease. a new indication for genetic testing of the RET proto-oncogene J Pediatr Surg. 33:1998;207-214.
-
(1998)
J Pediatr Surg
, vol.33
, pp. 207-214
-
-
Decker, R.A.1
Peacock, M.L.2
-
9
-
-
0034690117
-
Unilateral renal agenesis in a family with medullary thyroid carcinoma
-
Lore F., Cairano G., Talidis F. Unilateral renal agenesis in a family with medullary thyroid carcinoma. N Engl J Med. 342:2000;1218-1219.
-
(2000)
N Engl J Med
, vol.342
, pp. 1218-1219
-
-
Lore, F.1
Cairano, G.2
Talidis, F.3
-
11
-
-
0031964670
-
Hirschsprung disease in MEN 2A: Increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation
-
Decker R.A., Peacock M.L., Watson P. Hirschsprung disease in MEN 2A. increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation Hum Mol Genet. 7:1998;129-134.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 129-134
-
-
Decker, R.A.1
Peacock, M.L.2
Watson, P.3
-
12
-
-
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 G.M., Billaud M. Co-segregation of MEN2 and Hirschsprung's disease. the same mutation of RET with both gain and loss-of-function? Hum Mutat. 13:1999;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
-
13
-
-
0030739287
-
Biological properties of Ret with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and Hirschsprung's disease phenotype
-
Ito S., Iwashita T., Asai N., Murakami H., Iwata Y., Sobue G., Takahashi M. Biological properties of Ret with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and Hirschsprung's disease phenotype. Cancer Res. 57:1997;2870-2872.
-
(1997)
Cancer Res
, vol.57
, pp. 2870-2872
-
-
Ito, S.1
Iwashita, T.2
Asai, N.3
Murakami, H.4
Iwata, Y.5
Sobue, G.6
Takahashi, M.7
-
14
-
-
0031741050
-
Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease
-
Borrego S., Eng C., Sanchez B., Saez M.E., Navarro E., Antinolo G. Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease. J Clin Endocrinol Metab. 83:1998;3361-3364.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 3361-3364
-
-
Borrego, S.1
Eng, C.2
Sanchez, B.3
Saez, M.E.4
Navarro, E.5
Antinolo, G.6
|