-
3
-
-
0027508442
-
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease
-
Published erratum in N. Engl. J. Med., 331: 1535, 1994
-
(1993)
N. Engl. J. Med
, vol.329
, pp. 1531-1538
-
-
Neumann, H.P.1
Berger, D.P.2
Sigmund, G.3
Blum, U.4
Schmidt, D.5
Parmer, R.J.6
Volk, B.7
Kirste, G.8
-
4
-
-
0028981766
-
Germ-line mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype
-
(1995)
Hum. Mutat
, vol.5
, pp. 66-75
-
-
Chen, F.1
Kishida, T.2
Yao, M.3
Hustad, T.4
Glavac, D.5
Dean, M.6
Gnarra, J.R.7
Orcutt, M.L.8
Duh, F.M.9
Glenn, G.10
Green, J.11
Hsia, Y.E.12
Lamiell, J.13
Li, H.14
Wei, M.H.15
Schmidt, L.16
Tory, K.17
Kuzmin, I.18
Stackhouse, T.19
Latif, F.20
Linehan, W.M.21
Lerman, M.22
Zbar, B.23
more..
-
5
-
-
4644256817
-
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis
-
(1996)
J. Am. Med. Assoc
, 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
Gharib, H.25
Thibodeau, S.N.26
Lacroix, A.27
Frilling, A.28
Ponder, B.A.29
Mulligan, L.M.30
more..
-
7
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
(1993)
Nature (Lond.)
, 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
Ponder, M.A.11
Telenius, H.12
Tunnacliffe, A.13
Ponder, B.A.14
-
8
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
(1993)
Science (Washington DC)
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
Yao, M.4
Duh, F.M.5
Orcutt, M.L.6
Stackhouse, T.7
Kuzmin, I.8
Modi, W.9
Geil, L.10
Schmidt, L.11
Zhou, F.12
Li, H.13
Wei, M.W.14
Chen, F.15
Glenn, G.16
Choyke, P.17
Walther, M.M.18
Weng, Y.19
Duan, D.20
Dean, M.21
Glavac, D.22
Richards, F.M.23
Crossey, P.A.24
Ferguson-Smith, M.A.25
Le Paslier, D.26
Chumakov, I.27
Cohen, D.28
Chinault, A.C.29
Maher, E.R.30
Linehan, W.M.31
Zbar, B.32
Lerman, M.I.33
more..
-
9
-
-
7844234770
-
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene
-
(1998)
Hum. Mutat
, vol.12
, pp. 417-423
-
-
Stolle, C.1
Glenn, G.2
Zbar, B.3
Humphreys, J.S.4
Choyke, P.5
Walther, M.6
Pack, S.7
Hurley, K.8
Andrey, C.9
Klausner, R.10
Linehan, W.M.11
-
10
-
-
0028788184
-
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas
-
(1995)
J. Med. Genet
, vol.32
, pp. 934-937
-
-
Eng, C.1
Crossey, P.A.2
Mulligan, L.M.3
Healey, C.S.4
Houghton, C.5
Prowse, A.6
Chew, S.L.7
Dahia, P.L.8
O'Riordan, J.L.9
Toledo, S.P.10
Smith, D.P.11
Maher, E.R.12
Ponder, B.A.13
-
11
-
-
10144242640
-
Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases
-
(1996)
J. Clin. Endocrinol. Metab
, vol.81
, pp. 2881-2884
-
-
Hofstra, R.M.1
Stelwagen, T.2
Stulp, R.P.3
De Jong, D.4
Hulsbeek, M.5
Kamsteeg, E.J.6
Van den Berg, A.7
Landsvater, R.M.8
Vermey, A.9
Molenaar, W.M.10
Lips, C.J.11
Buys, C.H.12
-
13
-
-
0030804006
-
Genetic predisposition to phaeochromocytoma: Analysis of candidate genes GDNF, RET, and VHL
-
(1997)
Hum. Mol. Genet
, vol.6
, pp. 1051-1056
-
-
Woodward, E.R.1
Eng, C.2
McMahon, R.3
Voutilainen, R.4
Affara, N.A.5
Ponder, B.A.6
Maher, E.R.7
-
14
-
-
0034602950
-
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
-
(2000)
Science (Washington DC)
, vol.287
, pp. 848-851
-
-
Baysal, B.E.1
Ferrell, R.E.2
Willett-Brozick, J.E.3
Lawrence, E.C.4
Myssiorek, D.5
Bosch, A.6
Van der Mey, A.7
Taschner, P.E.8
Rubinstein, W.S.9
Myers, E.N.10
Richard, C.W.11
Cornelisse, C.J.12
Devilee, P.13
Devlin, B.14
-
17
-
-
0003137731
-
Dominant genes and phakomatoses associated with multiple primary cancers
-
Neugut, A. T. Meadows, and L. Robison (eds.), Multiple Primary Cancers. Philadelphia: Lippincott, Williams and Wilkins
-
(1999)
, pp. 165-195
-
-
Eng, C.1
Maher, E.R.2
-
18
-
-
0033843623
-
Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumors
-
(2000)
Am. J. Pathol
, vol.156
, pp. 1693-1700
-
-
Gimm, O.1
Perren, A.2
Weng, L.P.3
Marsh, D.J.4
Yeh, J.J.5
Ziebold, U.6
Gil, E.7
Hinze, R.8
Delbridge, L.9
Lees, J.A.10
Mutter, G.L.11
Robinson, B.G.12
Komminoth, P.13
Dralle, H.14
Eng, C.15
-
20
-
-
0027155194
-
Deletion mapping of chromosome 1p and 22q in pheochromocytoma
-
(1993)
Jpn. J. Cancer Res
, vol.84
, pp. 402-408
-
-
Shin, E.1
Fujita, S.2
Takami, K.3
Kurahashi, H.4
Kurita, Y.5
Kobayashi, T.6
Mori, T.7
Nishisho, I.8
Takai, S.9
-
23
-
-
12944275670
-
High frequency of hypermethylation at the 14-3-3 σ locus leads to gene silencing in breast cancer
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 6049-6054
-
-
Ferguson, A.T.1
Evron, E.2
Umbricht, C.B.3
Pandita, T.K.4
Chan, T.A.5
Hermeking, H.6
Marks, J.R.7
Lambers, A.R.8
Futreal, P.A.9
Stampfer, M.R.10
Sukumar, S.11
-
24
-
-
0028000277
-
Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing
-
(1994)
Am. J. Pathol
, vol.145
, pp. 922-929
-
-
Komminoth, P.1
Kunz, E.2
Hiort, O.3
Schroder, S.4
Matias-Guiu, X.5
Christiansen, G.6
Roth, J.7
Heitz, P.U.8
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