-
2
-
-
16744366177
-
Clinical experience over 48 years with pheochromocytoma
-
Goldstein RE, O'Neill JA, Jr., Holcomb GW, 3rd, et al. Clinical experience over 48 years with pheochromocytoma. Ann Surg 229:755-764; discussion 764-756, 1999.
-
(1999)
Ann Surg
, vol.229
, pp. 755-764
-
-
Goldstein, R.E.1
O'Neill Jr., J.A.2
Holcomb III, G.W.3
-
3
-
-
0033394457
-
Pheochromocytoma in Italy: A multicentric retrospective study
-
Mannelli M, Ianni L, Cilotti A, Conti A. Pheochromocytoma in Italy: a multicentric retrospective study. Eur J Endocrinol 141:619-624, 1999.
-
(1999)
Eur J Endocrinol
, vol.141
, pp. 619-624
-
-
Mannelli, M.1
Ianni, L.2
Cilotti, A.3
Conti, A.4
-
4
-
-
0025170981
-
Long-term evaluation following resection of apparently benign pheochromocytoma(s)/paraganglioma(s)
-
van Heerden JA, Roland CF, Carney JA, Sheps SG, Grant CS. Long-term evaluation following resection of apparently benign pheochromocytoma(s)/ paraganglioma(s). World J Surg 14:325-329, 1990.
-
(1990)
World J Surg
, vol.14
, pp. 325-329
-
-
Van Heerden, J.A.1
Roland, C.F.2
Carney, J.A.3
Sheps, S.G.4
Grant, C.S.5
-
5
-
-
0033980581
-
Changes in clinical features and long-term prognosis in patients with pheochromocytoma
-
Noshiro T, Shimizu K, Watanabe T, et al. Changes in clinical features and long-term prognosis in patients with pheochromocytoma. Am J Hypertens 13:35-43, 2000.
-
(2000)
Am J Hypertens
, vol.13
, pp. 35-43
-
-
Noshiro, T.1
Shimizu, K.2
Watanabe, T.3
-
6
-
-
0031837914
-
Pheochromocytoma, a rare cause of hypertension: Long-term follow-up of 55 surgically treated patients
-
Favia G, Lumachi F, Polistina F, D'Amico DF. Pheochromocytoma, a rare cause of hypertension: long-term follow-up of 55 surgically treated patients. World J Surg 22:689-693; discussion 694, 1998.
-
(1998)
World J Surg
, vol.22
, pp. 689-693
-
-
Favia, G.1
Lumachi, F.2
Polistina, F.3
D'Amico, D.F.4
-
7
-
-
0036240747
-
Adrenalectomy for familial pheochromocytoma in the laparoscopic era
-
Brunt LM, Lairmore TC, Doherty GM, Quasebarth MA, DeBenedetti M, Moley JF. Adrenalectomy for familial pheochromocytoma in the laparoscopic era. Ann Surg 235:713-720; discussion 720-711, 2002.
-
(2002)
Ann Surg
, vol.235
, pp. 713-720
-
-
Brunt, L.M.1
Lairmore, T.C.2
Doherty, G.M.3
Quasebarth, M.A.4
DeBenedetti, M.5
Moley, J.F.6
-
8
-
-
0037046659
-
Germ-line mutations in nonsyndromic pheochromocytoma
-
Neumann HP, Bausch B, McWhinney SR, et al. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 346:1459-1466, 2002.
-
(2002)
N Engl J Med
, vol.346
, pp. 1459-1466
-
-
Neumann, H.P.1
Bausch, B.2
McWhinney, S.R.3
-
9
-
-
0018375375
-
Paragangliomas of the head and neck region. A pathologic study of tumors fro m 71 patients
-
Lack EE, Cubilla AL, Woodruff JM. Paragangliomas of the head and neck region. A pathologic study of tumors fro m 71 patients. Hum Pathol 10:191-218, 1979.
-
(1979)
Hum Pathol
, vol.10
, pp. 191-218
-
-
Lack, E.E.1
Cubilla, A.L.2
Woodruff, J.M.3
-
11
-
-
0036468725
-
National Cancer Data Base report on malignant paragangliomas of the head and neck
-
Lee JH, Barich F, Karnell LH, et al. National Cancer Data Base report on malignant paragangliomas of the head and neck. Cancer 94:730-737, 2002.
-
(2002)
Cancer
, vol.94
, pp. 730-737
-
-
Lee, J.H.1
Barich, F.2
Karnell, L.H.3
-
12
-
-
0034790472
-
Proportion of heritable paraganglioma cases and associated clinical characteristics
-
Drovdlic CM, Myers EN, Peters JA, et al. Proportion of heritable paraganglioma cases and associated clinical characteristics. Laryngoscope 111:1822-1827, 2001.
-
(2001)
Laryngoscope
, vol.111
, pp. 1822-1827
-
-
Drovdlic, C.M.1
Myers, E.N.2
Peters, J.A.3
-
13
-
-
18344381765
-
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas
-
Baysal BE, Willett-Brozick JE, Lawrence EC, et al. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. J Med Genet 39:178-183, 2002.
-
(2002)
J Med Genet
, vol.39
, pp. 178-183
-
-
Baysal, B.E.1
Willett-Brozick, J.E.2
Lawrence, E.C.3
-
14
-
-
0035992265
-
Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma
-
Dannenberg H, Dinjens WN, Abbou M, et al. Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma. Clin Cancer Res 8:2061-2066, 2002.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 2061-2066
-
-
Dannenberg, H.1
Dinjens, W.N.2
Abbou, M.3
-
15
-
-
0034998621
-
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
-
Taschner PE, Jansen JC, Baysal BE, et al. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. Genes Chromosomes Cancer 31:274-281, 2001.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 274-281
-
-
Taschner, P.E.1
Jansen, J.C.2
Baysal, B.E.3
-
17
-
-
0017839528
-
Cyanotic heart disease: "low altitude" risk for carotid body tumor?
-
Nissenblatt MJ. Cyanotic heart disease: "low altitude" risk for carotid body tumor? Johns Hopkins Med J 142:18-22, 1978.
-
(1978)
Johns Hopkins Med J
, vol.142
, pp. 18-22
-
-
Nissenblatt, M.J.1
-
18
-
-
0021885506
-
Carotid body hyperplasia in cystic fibrosis and cyanotic heart disease. A combined morphometric, ultrastructural, and biochemical study
-
Lack EE, Perez-Atayde AR, Young JB. Carotid body hyperplasia in cystic fibrosis and cyanotic heart disease. A combined morphometric, ultrastructural, and biochemical study. Am J Pathol 119:301-314, 1985.
-
(1985)
Am J Pathol
, vol.119
, pp. 301-314
-
-
Lack, E.E.1
Perez-Atayde, A.R.2
Young, J.B.3
-
19
-
-
0004007167
-
-
Cambridge, UK: Cambridge University Press
-
Le Douarin NM. The neural crest. Cambridge, UK: Cambridge University Press, 1982.
-
(1982)
The Neural Crest
-
-
Le Douarin, N.M.1
-
20
-
-
3142565896
-
Paraganglia and the adrenal medulla
-
LiVolsi VA, Asa SL, eds. Philadelphia: Churchill Livingstone
-
Komminoth P, de Krijger RR, Tischler AS. Paraganglia and the adrenal medulla. In: LiVolsi VA, Asa SL, eds. Endocrine pathology, Philadelphia: Churchill Livingstone, 2002, pp. 149-169.
-
(2002)
Endocrine Pathology
, pp. 149-169
-
-
Komminoth, P.1
De Krijger, R.R.2
Tischler, A.S.3
-
21
-
-
0035731004
-
Differential diagnosis of pheochromocytomas and paragangliomas
-
McNichol AM. Differential diagnosis of pheochromocytomas and paragangliomas. Endocr Pathol 12:407-415, 2001.
-
(2001)
Endocr Pathol
, vol.12
, pp. 407-415
-
-
McNichol, A.M.1
-
22
-
-
0031863474
-
Cytokeratin expression in adrenal phaeochromocytomas and extra-adrenal paragangliomas
-
Chetty R, Pillay P, Jaichand V. Cytokeratin expression in adrenal phaeochromocytomas and extra-adrenal paragangliomas. J Clin Pathol 51:477-478, 1998.
-
(1998)
J Clin Pathol
, vol.51
, pp. 477-478
-
-
Chetty, R.1
Pillay, P.2
Jaichand, V.3
-
23
-
-
0027224018
-
A comparative immunohistochemical study of phaeochromocytomas and paragangliomas
-
Fraga M, Garcia-Caballero T, Antunez J, Couce M, Beiras A, Forteza J. A comparative immunohistochemical study of phaeochromocytomas and paragangliomas. Histol Histopathol 8:429-436, 1993.
-
(1993)
Histol Histopathol
, vol.8
, pp. 429-436
-
-
Fraga, M.1
Garcia-Caballero, T.2
Antunez, J.3
Couce, M.4
Beiras, A.5
Forteza, J.6
-
24
-
-
0016216220
-
Concurrence of carotid body tumor and pheochromocytoma
-
Sato T, Saito H, Yoshinaga K, Shibota Y, Sasano N. Concurrence of carotid body tumor and pheochromocytoma. Cancer 34:1787-1795, 1974.
-
(1974)
Cancer
, vol.34
, pp. 1787-1795
-
-
Sato, T.1
Saito, H.2
Yoshinaga, K.3
Shibota, Y.4
Sasano, N.5
-
25
-
-
0025732181
-
A report of familial carotid body tumors and multiple extra-adrenal pheochromocytomas
-
Jensen JC, Choyke PL, Rosenfeld M, et al. A report of familial carotid body tumors and multiple extra-adrenal pheochromocytomas. J Urol 145:1040-1042, 1991.
-
(1991)
J Urol
, vol.145
, pp. 1040-1042
-
-
Jensen, J.C.1
Choyke, P.L.2
Rosenfeld, M.3
-
26
-
-
0036712593
-
Hereditary paraganglioma targets diverse paraganglia
-
Baysal BE. Hereditary paraganglioma targets diverse paraganglia. J Med Genet 39:617-622, 2002.
-
(2002)
J Med Genet
, vol.39
, pp. 617-622
-
-
Baysal, B.E.1
-
27
-
-
0031949785
-
Carney's triad
-
de Jong E, Mulder W, Nooitgedacht E, Taat CW, Bras J. Carney's triad. Eur J Surg Oncol 24:147-149, 1998.
-
(1998)
Eur J Surg Oncol
, vol.24
, pp. 147-149
-
-
De Jong, E.1
Mulder, W.2
Nooitgedacht, E.3
Taat, C.W.4
Bras, J.5
-
29
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JB, Healey CS, et al. Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363:458-460, 1993.
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.2
Healey, C.S.3
-
30
-
-
0029851837
-
Expression of the RET proto-oncogene in normal human tissues, pheochromocytomas, and other tumors of neural crest origin
-
Takaya K, Yoshimasa T, Arai H, et al. Expression of the RET proto-oncogene in normal human tissues, pheochromocytomas, and other tumors of neural crest origin. J Mol Med 74:617-621, 1996.
-
(1996)
J Mol Med
, vol.74
, pp. 617-621
-
-
Takaya, K.1
Yoshimasa, T.2
Arai, H.3
-
31
-
-
0028227510
-
Expression of the ret proto-oncogene product in human normal and neoplastic tissues of neural crest origin
-
Nakamura T, Ishizaka Y, Nagao M, Hara M, Ishikawa T. Expression of the ret proto-oncogene product in human normal and neoplastic tissues of neural crest origin. J Pathol 172:255-260, 1994.
-
(1994)
J Pathol
, vol.172
, pp. 255-260
-
-
Nakamura, T.1
Ishizaka, Y.2
Nagao, M.3
Hara, M.4
Ishikawa, T.5
-
32
-
-
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, Pachnis V. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367:380-383, 1994.
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
Costantini, F.4
Pachnis, V.5
-
33
-
-
0034849573
-
The GDNF/RET signaling pathway and human diseases
-
Takahashi M. The GDNF/RET signaling pathway and human diseases. Cytokine Growth Factor Rev 12:361-373, 2001.
-
(2001)
Cytokine Growth Factor Rev
, vol.12
, pp. 361-373
-
-
Takahashi, M.1
-
34
-
-
0029038604
-
The RET protooncogene in sporadic pheochromocytomas: Frequent MEN 2-like mutations and new molecular defects
-
Beldjord C, Desclaux-Arramond F, Raffin-Sanson M, et al. The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects. J Clin Endocrinol Metab 80:2063-2068, 1995.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 2063-2068
-
-
Beldjord, C.1
Desclaux-Arramond, F.2
Raffin-Sanson, M.3
-
35
-
-
0028788184
-
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas
-
Eng C, Crossey PA, Mulligan LM, et al. Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas. J Med Genet 32: 934-937, 1995.
-
(1995)
J Med Genet
, vol.32
, pp. 934-937
-
-
Eng, C.1
Crossey, P.A.2
Mulligan, L.M.3
-
36
-
-
0030804006
-
Genetic predisposition to phaeochromocytoma: Analysis of candidate genes GDNF, RET and VHL
-
Woodward ER, Eng C, McMahon R, Voutilainen R, et al. Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL. Hum Mol Genet 6:1051-1056, 1997.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1051-1056
-
-
Woodward, E.R.1
Eng, C.2
McMahon, R.3
Voutilainen, R.4
-
37
-
-
0030897626
-
Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomas
-
Rodien P, Jeunemaitre X, Dumont C, Beldjord C, Plouin PF. Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomas. Horm Res 47:263-268, 1997.
-
(1997)
Horm Res
, vol.47
, pp. 263-268
-
-
Rodien, P.1
Jeunemaitre, X.2
Dumont, C.3
Beldjord, C.4
Plouin, P.F.5
-
38
-
-
9844261174
-
Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumors
-
Marsh DJ, Zheng Z, Arnold A, et al. Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumors. J Clin Endocrinol Metab 82:3025-3028, 1997.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3025-3028
-
-
Marsh, D.J.1
Zheng, Z.2
Arnold, A.3
-
39
-
-
0028812287
-
Mutations in the RET protooncogene in sporadic pheochromocytomas
-
Lindor NM, Honchel R, Khosla S, Thibodeau SN. Mutations in the RET protooncogene in sporadic pheochromocytomas. J Clin Endocrinol Metab 80:627-629, 1995.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 627-629
-
-
Lindor, N.M.1
Honchel, R.2
Khosla, S.3
Thibodeau, S.N.4
-
40
-
-
0029934463
-
RET proto-oncogene point mutations in sporadic neuroendocrine tumors
-
Komminoth P, Roth J, Muletta-Feurer S, Saremaslani P, Seelentag WK, Heitz PU. RET proto-oncogene point mutations in sporadic neuroendocrine tumors. J Clin Endocrinol Metab 81:2041-2046, 1996.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 2041-2046
-
-
Komminoth, P.1
Roth, J.2
Muletta-Feurer, S.3
Saremaslani, P.4
Seelentag, W.K.5
Heitz, P.U.6
-
41
-
-
0031032905
-
Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas
-
Dahia PL, Toledo SP, Mulligan LM, Maher ER, Grossman AB, Eng C. Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas. Cancer Res 57:310-313, 1997.
-
(1997)
Cancer Res
, vol.57
, pp. 310-313
-
-
Dahia, P.L.1
Toledo, S.P.2
Mulligan, L.M.3
Maher, E.R.4
Grossman, A.B.5
Eng, C.6
-
42
-
-
3543053366
-
Prognostic value of RET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas
-
van der Harst E, de Krijger RR, Bruining HA, et al. Prognostic value of RET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas. Int J Cancer 79:537-540, 1998.
-
(1998)
Int J Cancer
, vol.79
, pp. 537-540
-
-
Van Der Harst, E.1
De Krijger, R.R.2
Bruining, H.A.3
-
43
-
-
0029050524
-
Tumor-specific mutations in the tyrosine kinase domain of the RET proto-oncogene in pheochromocytomas of sporadic type
-
Yoshimoto K, Tanaka C, Hamaguchi S, et al. Tumor-specific mutations in the tyrosine kinase domain of the RET proto-oncogene in pheochromocytomas of sporadic type. Endocr J 42:265-270, 1995.
-
(1995)
Endocr J
, vol.42
, pp. 265-270
-
-
Yoshimoto, K.1
Tanaka, C.2
Hamaguchi, S.3
-
44
-
-
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 DP, Mulligan LM, et al. Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours. Hum Mol Genet 3:237-241, 1994.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 237-241
-
-
Eng, C.1
Smith, D.P.2
Mulligan, L.M.3
-
45
-
-
0005765990
-
High levels of tyrosine phosphorylated proto-ret in sporadic phenochromocytomas
-
Le Hir H, Colucci-D'Amato LG, Charlet-Berguerand N, et al. High levels of tyrosine phosphorylated proto-ret in sporadic phenochromocytomas. Cancer Res 60: 1365-1370, 2000.
-
(2000)
Cancer Res
, vol.60
, pp. 1365-1370
-
-
Le Hir, H.1
Colucci-D'Amato, L.G.2
Charlet-Berguerand, N.3
-
46
-
-
0034297287
-
Expression analysis of RET and the GDNF/GFRalpha-1 and NTN/GFRalpha-2 ligand complexes in pheochromocytomas and paragangliomas
-
Edstrom E, Frisk T, Farnebo F, Hoog A, Backdahl M, Larsson C. Expression analysis of RET and the GDNF/GFRalpha-1 and NTN/GFRalpha-2 ligand complexes in pheochromocytomas and paragangliomas. Int J Mol Med 6:469-474, 2000.
-
(2000)
Int J Mol Med
, vol.6
, pp. 469-474
-
-
Edstrom, E.1
Frisk, T.2
Farnebo, F.3
Hoog, A.4
Backdahl, M.5
Larsson, C.6
-
47
-
-
0029018244
-
Expression of the ret proto-oncogene in phaeochromocytoma. An in situ hybridization and northern blot study
-
. Matias-Guiu X, Colomer A, Mato E, et al. Expression of the ret proto-oncogene in phaeochromocytoma. An in situ hybridization and northern blot study. J Pathol 176:63-68, 1995.
-
(1995)
J Pathol
, vol.176
, pp. 63-68
-
-
Matias-Guiu, X.1
Colomer, A.2
Mato, E.3
-
48
-
-
0033921316
-
RET is expressed but not mutated in extra-adrenal paragangliomas
-
de Krijger RR, van der Harst E, Muletta-Feurer S, et al. RET is expressed but not mutated in extra-adrenal paragangliomas. J Pathol 191:264-268, 2000.
-
(2000)
J Pathol
, vol.191
, pp. 264-268
-
-
De Krijger, R.R.1
Van Der Harst, E.2
Muletta-Feurer, S.3
-
49
-
-
0035683789
-
Von Hippel-Lindau disease: Gene to bedside
-
Sims KB. Von Hippel-Lindau disease: gene to bedside. Curr Opin Neurol 14:695-703, 2001.
-
(2001)
Curr Opin Neurol
, vol.14
, pp. 695-703
-
-
Sims, K.B.1
-
50
-
-
7844234770
-
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene
-
Stolle C, Glenn G, Zbar B, et al. Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene. Hum Mutat 12:417-423, 1998.
-
(1998)
Hum Mutat
, vol.12
, pp. 417-423
-
-
Stolle, C.1
Glenn, G.2
Zbar, B.3
-
51
-
-
2642668463
-
Germline mutations in the vhl gene in patients presenting with phaeochromocytomas
-
van der Harst E, de Krijger RR, Dinjens WN, et al. Germline mutations in the vhl gene in patients presenting with phaeochromocytomas. Int J Cancer 77:337-340, 1998.
-
(1998)
Int J Cancer
, vol.77
, pp. 337-340
-
-
Van Der Harst, E.1
De Krijger, R.R.2
Dinjens, W.N.3
-
52
-
-
0031298741
-
Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes
-
Oxf
-
Bar M, Friedman E, Jakobovitz O, et al. Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes. Clin Endocrinol (Oxf) 47:707-712, 1997.
-
(1997)
Clin Endocrinol
, vol.47
, pp. 707-712
-
-
Bar, M.1
Friedman, E.2
Jakobovitz, O.3
-
53
-
-
0030781576
-
Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret proto-oncogene
-
Brauch H, Hoeppner W, Jahnig H, et al. Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret proto-oncogene. J Clin Endocrinol Metab 82:4101-4104, 1997.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 4101-4104
-
-
Brauch, H.1
Hoeppner, W.2
Jahnig, H.3
-
54
-
-
16144365122
-
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan
-
Zbar B, Kishida T, Chen F, et al. Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Hum Mutat 8:348-357, 1996.
-
(1996)
Hum Mutat
, vol.8
, pp. 348-357
-
-
Zbar, B.1
Kishida, T.2
Chen, F.3
-
55
-
-
0028981766
-
Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype
-
Chen F, Kishida T, Yao M, et al. Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype. Hum Mutat 5:66-75, 1995.
-
(1995)
Hum Mutat
, vol.5
, pp. 66-75
-
-
Chen, F.1
Kishida, T.2
Yao, M.3
-
56
-
-
0030064811
-
Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau gene
-
Gross DJ, Avishai N, Meiner V, Filon D, Zbar B, Abeliovich D. Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau gene. J Clin Endocrinol Metab 81:147-149, 1996.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 147-149
-
-
Gross, D.J.1
Avishai, N.2
Meiner, V.3
Filon, D.4
Zbar, B.5
Abeliovich, D.6
-
57
-
-
0037431550
-
Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas
-
Dannenberg H, De Krijger RR, Van Der Harst E, et al. Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas. Int J Cancer 105:190-195, 2003.
-
(2003)
Int J Cancer
, vol.105
, pp. 190-195
-
-
Dannenberg, H.1
De Krijger, R.R.2
Van Der Harst, E.3
-
58
-
-
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
-
Hofstra RM, Stelwagen T, Stulp RP, et al. 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. J Clin Endocrinol Metab 81:2881-2884, 1996.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 2881-2884
-
-
Hofstra, R.M.1
Stelwagen, T.2
Stulp, R.P.3
-
59
-
-
0034485464
-
Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas
-
Bender BU, Gutsche M, Glasker S, et al. Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas. J Clin Endocrinol Metab 85:4568-4574, 2000.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 4568-4574
-
-
Bender, B.U.1
Gutsche, M.2
Glasker, S.3
-
60
-
-
0029772338
-
Expression pattern of the von Hippel-Lindau protein in human tissues
-
Los M, Jansen GH, Kaelin WG, Lips CJ, Blijham GH, Voest EE. Expression pattern of the von Hippel-Lindau protein in human tissues. Lab Invest 75:231-238, 1996.
-
(1996)
Lab Invest
, vol.75
, pp. 231-238
-
-
Los, M.1
Jansen, G.H.2
Kaelin, W.G.3
Lips, C.J.4
Blijham, G.H.5
Voest, E.E.6
-
61
-
-
0028072991
-
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma
-
Herman JG, Latif F, Weng Y, et al. Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma. Proc Natl Acad Sci USA 91:9700-9704, 1994.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 9700-9704
-
-
Herman, J.G.1
Latif, F.2
Weng, Y.3
-
62
-
-
0031776704
-
Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: Evidence for a VHL-independent pathway in clear cell renal tumourigenesis
-
Clifford SC, Prowse AH, Affara NA, Buys CH, Maher ER. Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis. Genes Chromosomes Cancer 22:200-209, 1998.
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 200-209
-
-
Clifford, S.C.1
Prowse, A.H.2
Affara, N.A.3
Buys, C.H.4
Maher, E.R.5
-
63
-
-
0035253381
-
The von Hippel-Lindau tumor suppressor protein
-
Ivan M, Kaelin WG, Jr. The von Hippel-Lindau tumor suppressor protein. Curr Opin Genet Dev 11:27-34, 2001.
-
(2001)
Curr Opin Genet Dev
, vol.11
, pp. 27-34
-
-
Ivan, M.1
Kaelin Jr., W.G.2
-
64
-
-
0027954044
-
Mutations of the VHL tumour suppressor gene in renal carcinoma
-
Gnarra JR, Tory K, Weng Y, et al. Mutations of the VHL tumour suppressor gene in renal carcinoma. Nat Genet 7:85-90, 1994.
-
(1994)
Nat Genet
, vol.7
, pp. 85-90
-
-
Gnarra, J.R.1
Tory, K.2
Weng, Y.3
-
65
-
-
0037093238
-
Expression of hypoxia-inducible factors in human renal cancer: Relationship to angiogenesis and to the von Hippel-Lindau gene mutation
-
Turner KJ, Moore JW, Jones A, et al. Expression of hypoxia-inducible factors in human renal cancer: relationship to angiogenesis and to the von Hippel-Lindau gene mutation. Cancer Res 62:2957-2961, 2002.
-
(2002)
Cancer Res
, vol.62
, pp. 2957-2961
-
-
Turner, K.J.1
Moore, J.W.2
Jones, A.3
-
66
-
-
0035339044
-
Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease
-
Clifford SC, Cockman ME, Smallwood AC, et al. Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease. Hum Mol Genet 10:1029-1038, 2001.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1029-1038
-
-
Clifford, S.C.1
Cockman, M.E.2
Smallwood, A.C.3
-
67
-
-
0035336706
-
Von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF
-
Hoffman MA, Ohh M, Yang H, Klco JM, Ivan M, Kaelin WG, Jr. von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF. Hum Mol Genet 10:1019-1027, 2001.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1019-1027
-
-
Hoffman, M.A.1
Ohh, M.2
Yang, H.3
Klco, J.M.4
Ivan, M.5
Kaelin Jr., W.G.6
-
68
-
-
0036645091
-
Identification of cyclin D1 and other novel targets for the von Hippel-Lindau tumor suppressor gene by expression array analysis and investigation of cyclin D1 genotype as a modifier in von Hippel-Lindau disease
-
Zatyka M, da Silva NF, Clifford SC, et al. Identification of cyclin D1 and other novel targets for the von Hippel-Lindau tumor suppressor gene by expression array analysis and investigation of cyclin D1 genotype as a modifier in von Hippel-Lindau disease. Cancer Res 62:3803-3811, 2002.
-
(2002)
Cancer Res
, vol.62
, pp. 3803-3811
-
-
Zatyka, M.1
Da Silva, N.F.2
Clifford, S.C.3
-
69
-
-
0037223823
-
Regulation of microtubule stability by the von Hippel-Lindau tumour suppressor protein pVHL
-
Hergovich A, Lisztwan J, Barry R, Ballschmieter P, Krek W. Regulation of microtubule stability by the von Hippel-Lindau tumour suppressor protein pVHL. Nat Cell Biol 5:64-70, 2003.
-
(2003)
Nat Cell Biol
, vol.5
, pp. 64-70
-
-
Hergovich, A.1
Lisztwan, J.2
Barry, R.3
Ballschmieter, P.4
Krek, W.5
-
70
-
-
0035181031
-
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer
-
Airewele GE, Sigurdson AJ, Wiley KJ, et al. Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer. Genet Epidemiol 20:75-86, 2001.
-
(2001)
Genet Epidemiol
, vol.20
, pp. 75-86
-
-
Airewele, G.E.1
Sigurdson, A.J.2
Wiley, K.J.3
-
71
-
-
0030966414
-
Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1,728 patients
-
Friedman JM, Birch PH. Type 1 neurofibromatosis: a descriptive analysis of the disorder in 1,728 patients. Am J Med Genet 70:138-143, 1997.
-
(1997)
Am J Med Genet
, vol.70
, pp. 138-143
-
-
Friedman, J.M.1
Birch, P.H.2
-
72
-
-
0030960182
-
Malignant and benign tumors in patients with neurofibromatosis type 1 in a defined Swedish population
-
Zoller ME, Rembeck B, Oden A, Samuelsson M, Angervall L. Malignant and benign tumors in patients with neurofibromatosis type 1 in a defined Swedish population. Cancer 79:2125-2131, 1997.
-
(1997)
Cancer
, vol.79
, pp. 2125-2131
-
-
Zoller, M.E.1
Rembeck, B.2
Oden, A.3
Samuelsson, M.4
Angervall, L.5
-
73
-
-
0032825694
-
von Recklinghausen's disease and pheochromocytomas
-
Walther MM, Herring J, Enquist E, Keiser HR, Linehan WM. von Recklinghausen's disease and pheochromocytomas. J Urol 162:1582-1586, 1999.
-
(1999)
J Urol
, vol.162
, pp. 1582-1586
-
-
Walther, M.M.1
Herring, J.2
Enquist, E.3
Keiser, H.R.4
Linehan, W.M.5
-
74
-
-
0029065934
-
Loss of neurofibromatosis type I (NF1) gene expression in pheochromocytomas from patients without NF1
-
Gutmann DH, Geist RT, Rose K, Wallin G, Moley JE Loss of neurofibromatosis type I (NF1) gene expression in pheochromocytomas from patients without NF1. Genes Chromosomes Cancer 13:104-109, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.13
, pp. 104-109
-
-
Gutmann, D.H.1
Geist, R.T.2
Rose, K.3
Wallin, G.4
Moley, J.E.5
-
75
-
-
0026655421
-
Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis
-
Xu W, Mulligan LM, Ponder MA, et al. Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis. Genes Chromosomes Cancer 4:337-342, 1992.
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 337-342
-
-
Xu, W.1
Mulligan, L.M.2
Ponder, M.A.3
-
76
-
-
0034602950
-
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
-
Baysal BE, Ferrell RE, Willett-Brozick JE, et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 287:848-851, 2000.
-
(2000)
Science
, vol.287
, pp. 848-851
-
-
Baysal, B.E.1
Ferrell, R.E.2
Willett-Brozick, J.E.3
-
77
-
-
0034803010
-
Phenotypic dichotomy in mitochondrial complex II genetic disorders
-
Baysal BE, Rubinstein WS, Taschner PE. Phenotypic dichotomy in mitochondrial complex II genetic disorders. J Mol Med 79:495-503, 2001.
-
(2001)
J Mol Med
, vol.79
, pp. 495-503
-
-
Baysal, B.E.1
Rubinstein, W.S.2
Taschner, P.E.3
-
78
-
-
0034964421
-
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
-
Astuti D, Latif F, Dallol A, et al. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 69:49-54, 2001.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 49-54
-
-
Astuti, D.1
Latif, F.2
Dallol, A.3
-
79
-
-
0037422207
-
Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
-
Benn DE, Croxson MS, Tucker K, et al. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Oncogene 22:1358-1364, 2003.
-
(2003)
Oncogene
, vol.22
, pp. 1358-1364
-
-
Benn, D.E.1
Croxson, M.S.2
Tucker, K.3
-
80
-
-
0036777993
-
SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation
-
Cascon A, Cebrian A, Ruiz-Llorente S, Telleria D, Benitez J, Robledo M. SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation. J Med Genet 39:E64, 2002.
-
(2002)
J Med Genet
, vol.39
-
-
Cascon, A.1
Cebrian, A.2
Ruiz-Llorente, S.3
Telleria, D.4
Benitez, J.5
Robledo, M.6
-
81
-
-
0035857957
-
Germline SDHD mutation in familial phaeochromocytoma
-
Astuti D, Douglas F, Lennard TW, et al. Germline SDHD mutation in familial phaeochromocytoma. Lancet 357:1181-1182, 2001.
-
(2001)
Lancet
, vol.357
, pp. 1181-1182
-
-
Astuti, D.1
Douglas, F.2
Lennard, T.W.3
-
82
-
-
0035991632
-
Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma
-
Gascon A, Ruiz-Llorente S, Cebrian A, et al. Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma. Eur J Hum Genet 10:457-461, 2002.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 457-461
-
-
Gascon, A.1
Ruiz-Llorente, S.2
Cebrian, A.3
-
83
-
-
0037805259
-
Hereditary phaeochromocytomas and paragangliomas: A study of five susceptibility genes
-
Bauters C, Vantyghem MC, Leteurtre E, et al. Hereditary phaeochromocytomas and paragangliomas: a study of five susceptibility genes. J Med Genet 40:E75, 2003.
-
(2003)
J Med Genet
, vol.40
-
-
Bauters, C.1
Vantyghem, M.C.2
Leteurtre, E.3
-
84
-
-
0037594892
-
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC
-
Niemann S, Muller U, Engelhardt D, Lohse P. Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. Hum Genet 113:92-94, 2003.
-
(2003)
Hum Genet
, vol.113
, pp. 92-94
-
-
Niemann, S.1
Muller, U.2
Engelhardt, D.3
Lohse, P.4
-
85
-
-
0033767445
-
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
-
Niemann S, Muller U. Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat Genet 26:268-270, 2000.
-
(2000)
Nat Genet
, vol.26
, pp. 268-270
-
-
Niemann, S.1
Muller, U.2
-
86
-
-
0141704510
-
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas
-
Gimenez-Roqueplo AP, Favier J, Rustin P, et al. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. Cancer Res 63:5615-5621, 2003.
-
(2003)
Cancer Res
, vol.63
, pp. 5615-5621
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
-
87
-
-
0034671551
-
Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
-
Gimm O, Armanios M, Dziema H, Neumann HP, Eng C. Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res 60:6822-6825, 2000.
-
(2000)
Cancer Res
, vol.60
, pp. 6822-6825
-
-
Gimm, O.1
Armanios, M.2
Dziema, H.3
Neumann, H.P.4
Eng, C.5
-
88
-
-
0034977649
-
Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas
-
Aguiar RC, Cox G, Pomeroy SL, Dahia PL. Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas. J Clin Endocrinol Metab 86:2890-2894, 2001.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 2890-2894
-
-
Aguiar, R.C.1
Cox, G.2
Pomeroy, S.L.3
Dahia, P.L.4
-
89
-
-
18444375876
-
Alterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas
-
Kytola S, Nord B, Elder EE, et al. Alterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas. Genes Chromosomes Cancer 34:325-332, 2002.
-
(2002)
Genes Chromosomes Cancer
, vol.34
, pp. 325-332
-
-
Kytola, S.1
Nord, B.2
Elder, E.E.3
-
90
-
-
0037168186
-
Absence of somatic SDHD mutations in sporadic neuroendocrine tumors and detection of two germline variants in paraganglioma patients
-
Perren A, Barghorn A, Schmid S, et al. Absence of somatic SDHD mutations in sporadic neuroendocrine tumors and detection of two germline variants in paraganglioma patients. Oncogene 21:7605-7608, 2002.
-
(2002)
Oncogene
, vol.21
, pp. 7605-7608
-
-
Perren, A.1
Barghorn, A.2
Schmid, S.3
-
91
-
-
0033983147
-
Progress in understanding structure-function relationships in respiratory chain complex II
-
Ackrell BA. Progress in understanding structure-function relationships in respiratory chain complex II. FEBS Lett 466:1-5, 2000.
-
(2000)
FEBS Lett
, vol.466
, pp. 1-5
-
-
Ackrell, B.A.1
-
92
-
-
0037474155
-
Structural biology. Complex II is complex too
-
Hederstedt L. Structural biology. Complex II is complex too. Science 299:671-672, 2003.
-
(2003)
Science
, vol.299
, pp. 671-672
-
-
Hederstedt, L.1
-
93
-
-
0036774422
-
Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma
-
Gimenez-Roqueplo AP, Favier J, Rustin P, et al. Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma. J Clin Endocrinol Metab 87:4771-4774, 2002.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 4771-4774
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
-
94
-
-
0035213138
-
The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway
-
Gimenez-Roqueplo AP, Favier J, Rustin P, et al. The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway. Am J Hum Genet 69:1186-1197, 2001.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1186-1197
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
-
95
-
-
2642602091
-
Carotid body tumors in inhabitants of altitudes higher than 2000 meters above sea level
-
Rodriguez-Cuevas S, Lopez-Garza J, Labastida-Almendaro S. Carotid body tumors in inhabitants of altitudes higher than 2000 meters above sea level. Head Neck 20:374-378, 1998.
-
(1998)
Head Neck
, vol.20
, pp. 374-378
-
-
Rodriguez-Cuevas, S.1
Lopez-Garza, J.2
Labastida-Almendaro, S.3
-
96
-
-
0026530617
-
Pheochromocytomas and C-cell thyroid neoplasms in transgenic c-mos mice: A model for the human multiple endocrine neoplasia type 2 syndrome
-
Schulz N, Propst F, Rosenberg MP, et al. Pheochromocytomas and C-cell thyroid neoplasms in transgenic c-mos mice: a model for the human multiple endocrine neoplasia type 2 syndrome. Cancer Res 52:450-455, 1992.
-
(1992)
Cancer Res
, vol.52
, pp. 450-455
-
-
Schulz, N.1
Propst, F.2
Rosenberg, M.P.3
-
97
-
-
0030035352
-
Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytoma
-
Eng C, Foster KA, Healey CS, et al. Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytoma. Br J Cancer 74:339-341, 1996.
-
(1996)
Br J Cancer
, vol.74
, pp. 339-341
-
-
Eng, C.1
Foster, K.A.2
Healey, C.S.3
-
98
-
-
0035829657
-
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours
-
Astuti D, Agathanggelou A, Honorio S, et al. RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours. Oncogene 20:7573-7577, 2001.
-
(2001)
Oncogene
, vol.20
, pp. 7573-7577
-
-
Astuti, D.1
Agathanggelou, A.2
Honorio, S.3
-
99
-
-
0029931446
-
Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas
-
Oxf
-
Aguiar RC, Dahia PL, Sill H, Toledo SP, Goldman JM, Cross NC. Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas. Clin Endocrinol (Oxf) 45:93-96, 1996.
-
(1996)
Clin Endocrinol
, vol.45
, pp. 93-96
-
-
Aguiar, R.C.1
Dahia, P.L.2
Sill, H.3
Toledo, S.P.4
Goldman, J.M.5
Cross, N.C.6
-
100
-
-
0032756819
-
Screening for MEN1 mutations in patients with atypical endocrine neoplasia
-
Dackiw AP, Cote GJ, Fleming JB, et al. Screening for MEN1 mutations in patients with atypical endocrine neoplasia. Surgery 126:1097-1103; discussion 1103-1094, 1999.
-
(1999)
Surgery
, vol.126
, pp. 1097-1103
-
-
Dackiw, A.P.1
Cote, G.J.2
Fleming, J.B.3
-
101
-
-
0034671246
-
Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p
-
Benn DE, Dwight T, Richardson AL, et al. Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p. Cancer Res 60:7048-7051, 2000.
-
(2000)
Cancer Res
, vol.60
, pp. 7048-7051
-
-
Benn, D.E.1
Dwight, T.2
Richardson, A.L.3
-
102
-
-
0023228919
-
Deletion of genes on chromosome 1 in endocrine neoplasia
-
Mathew CG, Smith BA, Thorpe K, et al. Deletion of genes on chromosome 1 in endocrine neoplasia. Nature 328:524-526, 1987.
-
(1987)
Nature
, vol.328
, pp. 524-526
-
-
Mathew, C.G.1
Smith, B.A.2
Thorpe, K.3
-
103
-
-
0024561222
-
Loss of heterozygosity on chromosomes 1p and 11p in sporadic pheochromocytoma
-
Tsutsumi M, Yokota J, Kakizoe T, Koiso K, Sugimura T, Terada M. Loss of heterozygosity on chromosomes 1p and 11p in sporadic pheochromocytoma. J Natl Cancer Inst 81:367-370, 1989.
-
(1989)
J Natl Cancer Inst
, vol.81
, pp. 367-370
-
-
Tsutsumi, M.1
Yokota, J.2
Kakizoe, T.3
Koiso, K.4
Sugimura, T.5
Terada, M.6
-
104
-
-
0025865768
-
Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas
-
Khosla S, Patel VM, Hay ID, et al. Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas. J Clin Invest 87:1691-1699, 1991.
-
(1991)
J Clin Invest
, vol.87
, pp. 1691-1699
-
-
Khosla, S.1
Patel, V.M.2
Hay, I.D.3
-
105
-
-
0026548844
-
Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes
-
Moley JF, Brother MB, Fong CT, et al. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes. Cancer Res 52:770-774, 1992.
-
(1992)
Cancer Res
, vol.52
, pp. 770-774
-
-
Moley, J.F.1
Brother, M.B.2
Fong, C.T.3
-
106
-
-
0027155194
-
Deletion mapping of chromosome 1p and 22q in pheochromocytoma
-
Shin E, Fujita S, Takami K, et al. Deletion mapping of chromosome 1p and 22q in pheochromocytoma. Jpn J Cancer Res 84:402-408, 1993.
-
(1993)
Jpn J Cancer Res
, vol.84
, pp. 402-408
-
-
Shin, E.1
Fujita, S.2
Takami, K.3
-
107
-
-
0030907932
-
Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma
-
Vargas MP, Zhuang Z, Wang C, Vortmeyer A, Linehan WM, Merino MJ. Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma. Hum Pathol 28:411-415, 1997.
-
(1997)
Hum Pathol
, vol.28
, pp. 411-415
-
-
Vargas, M.P.1
Zhuang, Z.2
Wang, C.3
Vortmeyer, A.4
Linehan, W.M.5
Merino, M.J.6
-
108
-
-
0030963645
-
Absence of TP53 alterations in pheochromocytomas and medullary thyroid carcinomas
-
Herfarth KK, Wick MR, Marshall HN, Gartner E, Lum S, Moley JF. Absence of TP53 alterations in pheochromocytomas and medullary thyroid carcinomas. Genes Chromosomes Cancer 20:24-29, 1997.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 24-29
-
-
Herfarth, K.K.1
Wick, M.R.2
Marshall, H.N.3
Gartner, E.4
Lum, S.5
Moley, J.F.6
-
109
-
-
0026677578
-
Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma
-
Tanaka N, Nishisho I, Yamamoto M, et al. Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma. Genes Chromosomes Cancer 5:399-403, 1992.
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 399-403
-
-
Tanaka, N.1
Nishisho, I.2
Yamamoto, M.3
-
110
-
-
0024391266
-
Specific genetic change in tumors associated with von Hippel-Lindau disease
-
Tory K, Brauch H, Linehan M, et al. Specific genetic change in tumors associated with von Hippel-Lindau disease. J Natl Cancer Inst 81:1097-1101, 1989.
-
(1989)
J Natl Cancer Inst
, vol.81
, pp. 1097-1101
-
-
Tory, K.1
Brauch, H.2
Linehan, M.3
-
111
-
-
0025284307
-
Deletion mapping on the distal third region of chromosome 1p in multiple endocrine neoplasia type IIA
-
Yang KP, Nguyen CV, Castillo SG, Samaan NA. Deletion mapping on the distal third region of chromosome 1p in multiple endocrine neoplasia type IIA. Anticancer Res 10:527-533, 1990.
-
(1990)
Anticancer Res
, vol.10
, pp. 527-533
-
-
Yang, K.P.1
Nguyen, C.V.2
Castillo, S.G.3
Samaan, N.A.4
-
112
-
-
0027937412
-
Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL
-
Devilee P, van Schothorst EM, Bardoel AF, et al. Allelotype of head and neck paragangliomas: allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL. Genes Chromosomes Cancer 11:71-78, 1994.
-
(1994)
Genes Chromosomes Cancer
, vol.11
, pp. 71-78
-
-
Devilee, P.1
Van Schothorst, E.M.2
Bardoel, A.F.3
-
113
-
-
13144307064
-
Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction
-
van Schothorst EM, Beekman M, Torremans P, et al. Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction. Hum Pathol 29:1045-1049, 1998.
-
(1998)
Hum Pathol
, vol.29
, pp. 1045-1049
-
-
Van Schothorst, E.M.1
Beekman, M.2
Torremans, P.3
-
114
-
-
9344224009
-
Oncogene expression in carotid body tumors
-
Wang DG, Barros D'Sa AA, Johnston CF, Buchanan KD. Oncogene expression in carotid body tumors. Cancer 77:2581-2587, 1996.
-
(1996)
Cancer
, vol.77
, pp. 2581-2587
-
-
Wang, D.G.1
Barros D'Sa, A.A.2
Johnston, C.F.3
Buchanan, K.D.4
-
115
-
-
0030806170
-
Expression of apoptosis-suppressing gene bcl-2 in human carotid body tumours
-
Wang DG, Johnston CF, Barros D'Sa AA, Buchanan KD. Expression of apoptosis-suppressing gene bcl-2 in human carotid body tumours. J Pathol 183:218-221, 1997.
-
(1997)
J Pathol
, vol.183
, pp. 218-221
-
-
Wang, D.G.1
Johnston, C.F.2
Barros D'Sa, A.A.3
Buchanan, K.D.4
-
116
-
-
0031881347
-
Expression of insulin-like growth factor (IGF)-II in human prostate, breast, bladder, and paraganglioma tumors
-
Li SL, Goko H, Xu ZD, et al. Expression of insulin-like growth factor (IGF)-II in human prostate, breast, bladder, and paraganglioma tumors. Cell Tissue Res 291:469-479, 1998.
-
(1998)
Cell Tissue Res
, vol.291
, pp. 469-479
-
-
Li, S.L.1
Goko, H.2
Xu, Z.D.3
-
117
-
-
0033967276
-
Expression of angiogenic growth factors in paragangliomas
-
Jyung RW, LeClair EE, Bernat RA, et al. Expression of angiogenic growth factors in paragangliomas. Laryngoscope 110:161-167, 2000.
-
(2000)
Laryngoscope
, vol.110
, pp. 161-167
-
-
Jyung, R.W.1
LeClair, E.E.2
Bernat, R.A.3
-
118
-
-
0141519103
-
p53 alterations and their relationship to SDHD mutations in parasympathetic paragangliomas
-
van Nederveen FH, Dannenberg H, Sleddens HF, de Krijger RR, Dinjens WN. p53 alterations and their relationship to SDHD mutations in parasympathetic paragangliomas. Mod Pathol 16:849-856, 2003.
-
(2003)
Mod Pathol
, vol.16
, pp. 849-856
-
-
Van Nederveen, F.H.1
Dannenberg, H.2
Sleddens, H.F.3
De Krijger, R.R.4
Dinjens, W.N.5
-
119
-
-
0028144321
-
Mutations of the p53 gene in human functional adrenal neoplasms
-
Lin SR, Lee YJ, Tsai JH. Mutations of the p53 gene in human functional adrenal neoplasms. J Clin Endocrinol Metab 78:483-491, 1994.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 483-491
-
-
Lin, S.R.1
Lee, Y.J.2
Tsai, J.H.3
-
120
-
-
0028789492
-
Molecular and immunohistochemical analysis of P53 in phaeochromocytoma
-
Dahia PL, Aguiar RC, Tsanaclis AM, et al. Molecular and immunohistochemical analysis of P53 in phaeochromocytoma. Br J Cancer 72:1211-1213, 1995.
-
(1995)
Br J Cancer
, vol.72
, pp. 1211-1213
-
-
Dahia, P.L.1
Aguiar, R.C.2
Tsanaclis, A.M.3
-
121
-
-
0029798017
-
p53 mutations in adrenal tumors: Caucasian patients do not show the exon 4 "hot spot" found in Taiwan
-
Reincke M, Wachenfeld C, Mora P, et al. p53 mutations in adrenal tumors: Caucasian patients do not show the exon 4 "hot spot" found in Taiwan. J Clin Endocrinol Metab 81:3636-3638, 1996.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 3636-3638
-
-
Reincke, M.1
Wachenfeld, C.2
Mora, P.3
-
122
-
-
0031796242
-
The relatively high frequency of p53 gene mutations in multiple and malignant phaeochromocytomas
-
Yoshimoto T, Naruse M, Zeng Z, et al. The relatively high frequency of p53 gene mutations in multiple and malignant phaeochromocytomas. J Endocrinol 159:247-255, 1998.
-
(1998)
J Endocrinol
, vol.159
, pp. 247-255
-
-
Yoshimoto, T.1
Naruse, M.2
Zeng, Z.3
-
123
-
-
0034983617
-
The clinicopathological features and importance of p53, Rb, and mdm2 expression in phaeochromocytomas and paragangliomas
-
Lam KY, Lo CY, Wat NM, Luk JM, Lam KS. The clinicopathological features and importance of p53, Rb, and mdm2 expression in phaeochromocytomas and paragangliomas. J Clin Pathol 54:443-448, 2001.
-
(2001)
J Clin Pathol
, vol.54
, pp. 443-448
-
-
Lam, K.Y.1
Lo, C.Y.2
Wat, N.M.3
Luk, J.M.4
Lam, K.S.5
-
124
-
-
0027066835
-
Inactivation of the p53 gene is not required for tumorigenesis of medullary thyroid carcinoma or pheochromocytoma
-
Yana I, Nakamura T, Shin E, et al. Inactivation of the p53 gene is not required for tumorigenesis of medullary thyroid carcinoma or pheochromocytoma. Jpn J Cancer Res 83:1113-1116, 1992.
-
(1992)
Jpn J Cancer Res
, vol.83
, pp. 1113-1116
-
-
Yana, I.1
Nakamura, T.2
Shin, E.3
-
125
-
-
0032892353
-
Prognostic value of p53, bcl-2, and c-erbB-2 protein expression in phaeochromocytomas
-
de Krijger RR, van der Harst E, van der Ham F, et al. Prognostic value of p53, bcl-2, and c-erbB-2 protein expression in phaeochromocytomas. J Pathol 188:51-55, 1999.
-
(1999)
J Pathol
, vol.188
, pp. 51-55
-
-
De Krijger, R.R.1
Van Der Harst, E.2
Van Der Ham, F.3
-
126
-
-
0033693614
-
Prognostic value of immunohistochemical expression of topoisomerase alpha II, MIB-1, p53, E-cadherin, retinoblastoma gene protein product, and HER-2/neu in adrenal and extra-adrenal pheochromocytomas
-
Gupta D, Shidham V, Holden J, Layfield L. Prognostic value of immunohistochemical expression of topoisomerase alpha II, MIB-1, p53, E-cadherin, retinoblastoma gene protein product, and HER-2/neu in adrenal and extra-adrenal pheochromocytomas. Appl Immunohistochem Mol Morphol 8:267-274, 2000.
-
(2000)
Appl Immunohistochem Mol Morphol
, vol.8
, pp. 267-274
-
-
Gupta, D.1
Shidham, V.2
Holden, J.3
Layfield, L.4
-
127
-
-
0032436005
-
p53 protein and its messenger ribonucleic acid in human adrenal tumors
-
Adleff V, Racz K, Toth M, Varga I, Bezzegh A, Glaz E. p53 protein and its messenger ribonucleic acid in human adrenal tumors. J Endocrinol Invest 21:753-757, 1998.
-
(1998)
J Endocrinol Invest
, vol.21
, pp. 753-757
-
-
Adleff, V.1
Racz, K.2
Toth, M.3
Varga, I.4
Bezzegh, A.5
Glaz, E.6
-
128
-
-
0027978199
-
Paraganglioma of the lung - Developed after exposure to nuclear radiation by the Tschernobyl atomic reactor accident?
-
Hagemeyer O, Gabius HJ, Kayser K. Paraganglioma of the lung - developed after exposure to nuclear radiation by the Tschernobyl atomic reactor accident? Respiration 61:236-239, 1994.
-
(1994)
Respiration
, vol.61
, pp. 236-239
-
-
Hagemeyer, O.1
Gabius, H.J.2
Kayser, K.3
-
129
-
-
0034651603
-
Paraganglioma of the urinary bladder: Can biologic potential be predicted?
-
Cheng L, Leibovich BC, Cheville JC, et al. Paraganglioma of the urinary bladder: can biologic potential be predicted? Cancer 88:844-852, 2000.
-
(2000)
Cancer
, vol.88
, pp. 844-852
-
-
Cheng, L.1
Leibovich, B.C.2
Cheville, J.C.3
-
130
-
-
0028915393
-
Overexpression of the tumour suppressor gene p53 is not implicated in neuroendocrine tumour carcinogenesis
-
Wang DG, Johnston CF, Anderson N, Sloan JM, Buchanan KD. Overexpression of the tumour suppressor gene p53 is not implicated in neuroendocrine tumour carcinogenesis. J Pathol 175:397-401, 1995.
-
(1995)
J Pathol
, vol.175
, pp. 397-401
-
-
Wang, D.G.1
Johnston, C.F.2
Anderson, N.3
Sloan, J.M.4
Buchanan, K.D.5
-
131
-
-
0033084198
-
p53 and p16INK4A mutations during the progression of glomus tumor
-
Guran S, Tali ET. p53 and p16INK4A mutations during the progression of glomus tumor. Pathol Oncol Res 5:41-45, 1999.
-
(1999)
Pathol Oncol Res
, vol.5
, pp. 41-45
-
-
Guran, S.1
Tali, E.T.2
-
132
-
-
0027322205
-
Absent ras gene mutations in human adrenal cortical neoplasms and pheochromocytomas
-
Moul JW, Bishoff JT, Theune SM, Chang EH. Absent ras gene mutations in human adrenal cortical neoplasms and pheochromocytomas. J Urol 149:1389-1394, 1993.
-
(1993)
J Urol
, vol.149
, pp. 1389-1394
-
-
Moul, J.W.1
Bishoff, J.T.2
Theune, S.M.3
Chang, E.H.4
-
133
-
-
0025857633
-
Low frequency of ras gene mutations in neuroblastomas, pheochromocytomas, and medullary thyroid cancers
-
Moley JF, Brother MB, Wells SA, Spengler BA, Biedler JL, Brodeur GM. Low frequency of ras gene mutations in neuroblastomas, pheochromocytomas, and medullary thyroid cancers. Cancer Res 51:1596-1599, 1991.
-
(1991)
Cancer Res
, vol.51
, pp. 1596-1599
-
-
Moley, J.F.1
Brother, M.B.2
Wells, S.A.3
Spengler, B.A.4
Biedler, J.L.5
Brodeur, G.M.6
-
134
-
-
0031950982
-
Mutations of K-ras oncogene in human adrenal tumours in Taiwan
-
Lin SR, Tsai JH, Yang YC, Lee SC. Mutations of K-ras oncogene in human adrenal tumours in Taiwan. Br J Cancer 77:1060-1065, 1998.
-
(1998)
Br J Cancer
, vol.77
, pp. 1060-1065
-
-
Lin, S.R.1
Tsai, J.H.2
Yang, Y.C.3
Lee, S.C.4
-
135
-
-
0036781812
-
c-MYC: More than just a matter of life and death
-
Pelengaris S, Khan M, Evan G. c-MYC: more than just a matter of life and death. Nat Rev Cancer 2:764-776, 2002.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 764-776
-
-
Pelengaris, S.1
Khan, M.2
Evan, G.3
-
136
-
-
0031154139
-
Expression of the apoptosis-suppressing gene BCL-2 in pheochromocytoma is associated with the expression of C-MYC
-
Wang DG, Johnston CF, Marley JJ, et al. Expression of the apoptosis-suppressing gene BCL-2 in pheochromocytoma is associated with the expression of C-MYC. J Clin Endocrinol Metab 82:1949-1952, 1997.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 1949-1952
-
-
Wang, D.G.1
Johnston, C.F.2
Marley, J.J.3
-
137
-
-
0031057207
-
Expression patterns of the c-myc gene in adrenocortical tumors and pheochromocytomas
-
Liu J, Voutilainen R, Kahri AI, Heikkila P. Expression patterns of the c-myc gene in adrenocortical tumors and pheochromocytomas. J Endocrinol 152:175-181, 1997.
-
(1997)
J Endocrinol
, vol.152
, pp. 175-181
-
-
Liu, J.1
Voutilainen, R.2
Kahri, A.I.3
Heikkila, P.4
-
138
-
-
0025019768
-
Expression of c-fos and c-myc proto-oncogenes in human adrenal pheochromocytomas
-
Goto K, Ogo A, Yanase T, Haji M, Ohashi M, Nawata H. Expression of c-fos and c-myc proto-oncogenes in human adrenal pheochromocytomas. J Clin Endocrinol Metab 70:353-357, 1990.
-
(1990)
J Clin Endocrinol Metab
, vol.70
, pp. 353-357
-
-
Goto, K.1
Ogo, A.2
Yanase, T.3
Haji, M.4
Ohashi, M.5
Nawata, H.6
-
139
-
-
0027014452
-
Oncogene and growth factor expression in MEN 2 and related tumors
-
Moley JF, Wallin GK, Brother MB, Kim M, Wells SA, Jr, Brodeur GM. Oncogene and growth factor expression in MEN 2 and related tumors. Henry Ford Hosp Med J 40:284-288, 1992.
-
(1992)
Henry Ford Hosp Med J
, vol.40
, pp. 284-288
-
-
Moley, J.F.1
Wallin, G.K.2
Brother, M.B.3
Kim, M.4
Wells Jr., S.A.5
Brodeur, G.M.6
-
140
-
-
0013288537
-
Enhanced expression of the human gene N-myc consequent to amplification of DNA may contribute to malignant progression of neuroblastoma
-
Schwab M, Ellison J, Busch M, et al. Enhanced expression of the human gene N-myc consequent to amplification of DNA may contribute to malignant progression of neuroblastoma. Proc Natl Acad Sci USA 81:4940-4944, 1984.
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 4940-4944
-
-
Schwab, M.1
Ellison, J.2
Busch, M.3
-
141
-
-
0022388606
-
Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas
-
Seeger RC, Brodeur GM, Sather H, et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med 313:1111-1116, 1985.
-
(1985)
N Engl J Med
, vol.313
, pp. 1111-1116
-
-
Seeger, R.C.1
Brodeur, G.M.2
Sather, H.3
-
142
-
-
0037341420
-
KI-67 and hTERT expression can aid in the distinction between malignant and benign pheochromocytoma and paraganglioma
-
Elder EE, Xu D, Hoog A, et al. KI-67 AND hTERT expression can aid in the distinction between malignant and benign pheochromocytoma and paraganglioma. Mod Pathol 16:246-255, 2003.
-
(2003)
Mod Pathol
, vol.16
, pp. 246-255
-
-
Elder, E.E.1
Xu, D.2
Hoog, A.3
-
143
-
-
0031839547
-
Telomerase activity as an indicator of potentially malignant adrenal tumors
-
Hirano Y, Fujita K, Suzuki K, Ushiyama T, Ohtawara Y, Tsuda F. Telomerase activity as an indicator of potentially malignant adrenal tumors. Cancer 83:772-776, 1998.
-
(1998)
Cancer
, vol.83
, pp. 772-776
-
-
Hirano, Y.1
Fujita, K.2
Suzuki, K.3
Ushiyama, T.4
Ohtawara, Y.5
Tsuda, F.6
-
145
-
-
0031941920
-
Elevated levels of telomerase activity in malignant pheochromocytoma
-
Kubota Y, Nakada T, Sasagawa I, Yanai H, Itoh K. Elevated levels of telomerase activity in malignant pheochromocytoma. Cancer 82:176-179, 1998.
-
(1998)
Cancer
, vol.82
, pp. 176-179
-
-
Kubota, Y.1
Nakada, T.2
Sasagawa, I.3
Yanai, H.4
Itoh, K.5
-
146
-
-
18244403801
-
Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome
-
Lui WO, Chen J, Glasker S, et al. Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome. Oncogene 21:1117-1122, 2002.
-
(2002)
Oncogene
, vol.21
, pp. 1117-1122
-
-
Lui, W.O.1
Chen, J.2
Glasker, S.3
-
147
-
-
0034965261
-
Differential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridization
-
Dannenberg H, de Krijger RR, Zhao J, et al. Differential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridization. Am J Pathol 158: 1937-1942, 2001.
-
(2001)
Am J Pathol
, vol.158
, pp. 1937-1942
-
-
Dannenberg, H.1
De Krijger, R.R.2
Zhao, J.3
-
148
-
-
0033888975
-
Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas
-
Dannenberg H, Speel EJ, Zhao J, et al. Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas. Am J Pathol 157:353-359, 2000.
-
(2000)
Am J Pathol
, vol.157
, pp. 353-359
-
-
Dannenberg, H.1
Speel, E.J.2
Zhao, J.3
-
149
-
-
0033888981
-
Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology
-
Edstrom E, Mahlamaki E, Nord B, et al. Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology. Am J Pathol 156:651-659, 2000.
-
(2000)
Am J Pathol
, vol.156
, pp. 651-659
-
-
Edstrom, E.1
Mahlamaki, E.2
Nord, B.3
-
150
-
-
0038488950
-
A multigenic program mediating breast cancer metastasis to bone
-
Kang Y, Siegel PM, Shu W, et al. A multigenic program mediating breast cancer metastasis to bone. Cancer Cell 3:537-549, 2003.
-
(2003)
Cancer Cell
, vol.3
, pp. 537-549
-
-
Kang, Y.1
Siegel, P.M.2
Shu, W.3
-
151
-
-
0037229767
-
Cancer's deadly signature
-
Liotta LA, Kohn EC. Cancer's deadly signature. Nat Genet 33:10-11, 2003.
-
(2003)
Nat Genet
, vol.33
, pp. 10-11
-
-
Liotta, L.A.1
Kohn, E.C.2
-
152
-
-
18244409687
-
Gene expression profiling predicts clinical outcome of breast cancer
-
van 't Veer LJ, Dai H, van de Vijver MJ, et al. Gene expression profiling predicts clinical outcome of breast cancer. Nature 415:530-536, 2002.
-
(2002)
Nature
, vol.415
, pp. 530-536
-
-
Van 't Veer, L.J.1
Dai, H.2
Van De Vijver, M.J.3
-
153
-
-
0034614637
-
The hallmarks of cancer
-
Hanahan D, Weinberg RA. The hallmarks of cancer. Cell 100:57-70, 2000.
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
154
-
-
0023235756
-
Flow cytometric determination of nuclear DNA content in benign adrenal pheochromocytomas
-
Amberson JB, Vaughan ED, Jr, Gray GF, Naus GJ. Flow cytometric determination of nuclear DNA content in benign adrenal pheochromocytomas. Urology 30:102-104, 1987.
-
(1987)
Urology
, vol.30
, pp. 102-104
-
-
Amberson, J.B.1
Vaughan Jr., E.D.2
Gray, G.F.3
Naus, G.J.4
-
155
-
-
0022861185
-
Pheochromocytoma: Nuclear deoxyribonucleic acid patterns studied by flow cytometry
-
Hosaka Y, Rainwater LM, Grant CS, Farrow GM, van Heerden JA, Lieber MM. Pheochromocytoma: nuclear deoxyribonucleic acid patterns studied by flow cytometry. Surgery 100:1003-1010, 1986.
-
(1986)
Surgery
, vol.100
, pp. 1003-1010
-
-
Hosaka, Y.1
Rainwater, L.M.2
Grant, C.S.3
Farrow, G.M.4
Van Heerden, J.A.5
Lieber, M.M.6
-
156
-
-
0028023467
-
Deoxyribonucleic acid flow cytometric study in pheochromocytomas and its correlation with clinical parameters
-
Lai MK, Sun CF, Chen CS, Huang CC, Chu SH, Chuang CK. Deoxyribonucleic acid flow cytometric study in pheochromocytomas and its correlation with clinical parameters. Urology 44:185-188, 1994.
-
(1994)
Urology
, vol.44
, pp. 185-188
-
-
Lai, M.K.1
Sun, C.F.2
Chen, C.S.3
Huang, C.C.4
Chu, S.H.5
Chuang, C.K.6
-
157
-
-
0036319408
-
The value of plasma markers for the clinical behaviour of phaeochromocytomas
-
van der Harst E, de Herder WW, de Krijger RR, et al. The value of plasma markers for the clinical behaviour of phaeochromocytomas. Eur J Endocrinol 147:85-94, 2002.
-
(2002)
Eur J Endocrinol
, vol.147
, pp. 85-94
-
-
Van Der Harst, E.1
De Herder, W.W.2
De Krijger, R.R.3
-
158
-
-
0031938425
-
CD44 expression in normal adrenal tissue and adrenal tumours
-
Barshack I, Goldberg I, Nass D, Olchovsky D, Kopolovic J. CD44 expression in normal adrenal tissue and adrenal tumours. J Clin Pathol 51:52-54, 1998.
-
(1998)
J Clin Pathol
, vol.51
, pp. 52-54
-
-
Barshack, I.1
Goldberg, I.2
Nass, D.3
Olchovsky, D.4
Kopolovic, J.5
-
159
-
-
0030450973
-
Expression of interleukin-1 in human pheochromocytoma
-
Bornstein SR, Ehrhart-Bornstein M, Gonzalez-Hernandez J, Schroder S, Scherbaum WA. Expression of interleukin-1 in human pheochromocytoma. J Endocrinol Invest 19:693-698, 1996.
-
(1996)
J Endocrinol Invest
, vol.19
, pp. 693-698
-
-
Bornstein, S.R.1
Ehrhart-Bornstein, M.2
Gonzalez-Hernandez, J.3
Schroder, S.4
Scherbaum, W.A.5
-
160
-
-
0033570066
-
Predicting metastasis of pheochromocytomas using DNA flow cytometry and immunohistochemical markers of cell proliferation: A positive correlation between MIB-1 staining and malignant tumor behavior
-
Brown HM, Komorowski RA, Wilson SD, Demeure MJ, Zhu YR. Predicting metastasis of pheochromocytomas using DNA flow cytometry and immunohistochemical markers of cell proliferation: A positive correlation between MIB-1 staining and malignant tumor behavior. Cancer 86:1583-1589, 1999.
-
(1999)
Cancer
, vol.86
, pp. 1583-1589
-
-
Brown, H.M.1
Komorowski, R.A.2
Wilson, S.D.3
Demeure, M.J.4
Zhu, Y.R.5
-
161
-
-
0030747689
-
Expression and prognostic value of c-erbB-2 oncogene product in human phaeochromocytomas
-
Castilla-Guerra L, Moreno AM, Fernandez-Moreno MC, Utrilla JC, Fernandez E, Galera-Davison H. Expression and prognostic value of c-erbB-2 oncogene product in human phaeochromocytomas. Histopathology 31:144-149, 1997.
-
(1997)
Histopathology
, vol.31
, pp. 144-149
-
-
Castilla-Guerra, L.1
Moreno, A.M.2
Fernandez-Moreno, M.C.3
Utrilla, J.C.4
Fernandez, E.5
Galera-Davison, H.6
-
162
-
-
0031948355
-
Prognostic markers in pheochromocytoma
-
Clarke MR, Weyant RJ, Watson CG, Carty SE. Prognostic markers in pheochromocytoma. Hum Pathol 29:522-526, 1998.
-
(1998)
Hum Pathol
, vol.29
, pp. 522-526
-
-
Clarke, M.R.1
Weyant, R.J.2
Watson, C.G.3
Carty, S.E.4
-
163
-
-
12244302219
-
Transcription profiling of benign and malignant adrenal tumors by cDNA macroarray analysis
-
De Fraipont F, Le Moigne G, Defaye G, et al. Transcription profiling of benign and malignant adrenal tumors by cDNA macroarray analysis. Endocr Res 28:785-786, 2002.
-
(2002)
Endocr Res
, vol.28
, pp. 785-786
-
-
De Fraipont, F.1
Le Moigne, G.2
Defaye, G.3
-
164
-
-
0036792605
-
Angiogenesis and vascular architecture in pheochromocytomas: Distinctive traits in malignant tumors
-
Favier J, Plouin PF, Corvol P, Case JM. Angiogenesis and vascular architecture in pheochromocytomas: distinctive traits in malignant tumors. Am J Pathol 161:1235-1246, 2002.
-
(2002)
Am J Pathol
, vol.161
, pp. 1235-1246
-
-
Favier, J.1
Plouin, P.F.2
Corvol, P.3
Case, J.M.4
-
165
-
-
0033085752
-
BCL-2 expression and inhibin-A in adrenal neoplasms: A comparative study
-
Fogt F, Zimmerman RL, Mulligan N, et al. BCL-2 expression and inhibin-A in adrenal neoplasms: a comparative study. Int J Mol Med 3:271-274, 1999.
-
(1999)
Int J Mol Med
, vol.3
, pp. 271-274
-
-
Fogt, F.1
Zimmerman, R.L.2
Mulligan, N.3
-
166
-
-
0026070779
-
Immunohistochemical characterization of HLA-DR-antigen positive dendritic cells in phaeochromocytomas and paragangliomas as a prognostic marker
-
Furihata M, Ohtsuki Y. Immunohistochemical characterization of HLA-DR-antigen positive dendritic cells in phaeochromocytomas and paragangliomas as a prognostic marker. Virchows Arch A Pathol Anat Histopathol 418:33-39, 1991.
-
(1991)
Virchows Arch a Pathol Anat Histopathol
, vol.418
, pp. 33-39
-
-
Furihata, M.1
Ohtsuki, Y.2
-
167
-
-
0034985403
-
Clinical differences between benign and malignant pheochromocytomas
-
Glodny B, Winde G, Herwig R, et al. Clinical differences between benign and malignant pheochromocytomas. Endocr J 48:151-159, 2001.
-
(2001)
Endocr J
, vol.48
, pp. 151-159
-
-
Glodny, B.1
Winde, G.2
Herwig, R.3
-
168
-
-
0025133121
-
Neuropeptide Y and neuron-specific enolase levels in benign and malignant pheochro-mocytomas
-
Grouzmann E, Gicquel C, Plouin PF, Schlumberger M, Comoy E, Bohuon C. Neuropeptide Y and neuron-specific enolase levels in benign and malignant pheochro-mocytomas. Cancer 66:1833-1835, 1990.
-
(1990)
Cancer
, vol.66
, pp. 1833-1835
-
-
Grouzmann, E.1
Gicquel, C.2
Plouin, P.F.3
Schlumberger, M.4
Comoy, E.5
Bohuon, C.6
-
169
-
-
0027531696
-
Morphometric analysis of benign and malignant adrenal pheochromocytomas
-
Hoffman K, Gil J, Barba J, et al. Morphometric analysis of benign and malignant adrenal pheochromocytomas. Arch Pathol Lab Med 117:244-247, 1993.
-
(1993)
Arch Pathol Lab Med
, vol.117
, pp. 244-247
-
-
Hoffman, K.1
Gil, J.2
Barba, J.3
-
170
-
-
0035215661
-
Dopamine and dopa urinary excretion in patients with pheochromocytoma - Diagnostic implications
-
Januszewicz W, Wocial B, Januszewicz A, Gryglas P, Prejbisz A. Dopamine and dopa urinary excretion in patients with pheochromocytoma - diagnostic implications. Blood Press 10:212-216, 2001.
-
(2001)
Blood Press
, vol.10
, pp. 212-216
-
-
Januszewicz, W.1
Wocial, B.2
Januszewicz, A.3
Gryglas, P.4
Prejbisz, A.5
-
171
-
-
0036020542
-
N-cadherin expression in adrenal tumors: Upregulation in malignant pheochromocytoma and downregulation in adrenocortical carcinoma
-
Khorram-Manesh A, Ahlman H, Jansson S, Nilsson O. N-cadherin expression in adrenal tumors: upregulation in malignant pheochromocytoma and downregulation in adrenocortical carcinoma. Endocr Pathol 13:99-110, 2002.
-
(2002)
Endocr Pathol
, vol.13
, pp. 99-110
-
-
Khorram-Manesh, A.1
Ahlman, H.2
Jansson, S.3
Nilsson, O.4
-
172
-
-
0031959446
-
Telomerase activity in adrenal cortical tumors and pheochromocytomas with reference to clinicopathologic features
-
Kinoshita H, Ogawa O, Mishina M, et al. Telomerase activity in adrenal cortical tumors and pheochromocytomas with reference to clinicopathologic features. Urol Res 26:29-32, 1998.
-
(1998)
Urol Res
, vol.26
, pp. 29-32
-
-
Kinoshita, H.1
Ogawa, O.2
Mishina, M.3
-
173
-
-
0036207949
-
Survivin: A novel neuroendocrine marker for pheochromocytoma
-
Koch CA, Vortmeyer AO, Diallo R, et al. Survivin: a novel neuroendocrine marker for pheochromocytoma. Eur J Endocrinol 146:381-388, 2002.
-
(2002)
Eur J Endocrinol
, vol.146
, pp. 381-388
-
-
Koch, C.A.1
Vortmeyer, A.O.2
Diallo, R.3
-
174
-
-
0035287650
-
Usefulness of VEGF, MMP-2, MMP-3 and TIMP-2 serum level evaluation in patients with adrenal tumours
-
Kolomecki K, Stepien H, Bartos M, Kuzdak K. Usefulness of VEGF, MMP-2, MMP-3 and TIMP-2 serum level evaluation in patients with adrenal tumours. Endocr Regul 35:9-16, 2001.
-
(2001)
Endocr Regul
, vol.35
, pp. 9-16
-
-
Kolomecki, K.1
Stepien, H.2
Bartos, M.3
Kuzdak, K.4
-
175
-
-
0036020549
-
Prediction of malignant behavior of pheochromocytomas and paragangliomas using immunohistochemical techniques
-
Kumaki N, Kajiwara H, Kameyama K, et al. Prediction of malignant behavior of pheochromocytomas and paragangliomas using immunohistochemical techniques. Endocr Pathol 13:149-156, 2002.
-
(2002)
Endocr Pathol
, vol.13
, pp. 149-156
-
-
Kumaki, N.1
Kajiwara, H.2
Kameyama, K.3
-
176
-
-
0029905006
-
Tumor angiogenesis in pheochromocytomas and paragangliomas
-
Liu Q, Djuricin G, Staren ED, et al. Tumor angiogenesis in pheochromocytomas and paragangliomas. Surgery 120:938-942; discussion 942-933, 1996.
-
(1996)
Surgery
, vol.120
, pp. 938-942
-
-
Liu, Q.1
Djuricin, G.2
Staren, E.D.3
-
177
-
-
0031055993
-
Leu-M1 immunoreactiviry and phaeochromocytoma
-
Masmiquel L, Castro-Forns M, de Torres I, Garcia A, Vidal MT, Simo R. Leu-M1 immunoreactiviry and phaeochromocytoma. J Clin Pathol 50:168-170, 1997.
-
(1997)
J Clin Pathol
, vol.50
, pp. 168-170
-
-
Masmiquel, L.1
Castro-Forns, M.2
De Torres, I.3
Garcia, A.4
Vidal, M.T.5
Simo, R.6
-
178
-
-
0033120654
-
Expression of neuropeptides and other neuroendocrine markers in human phaeochromocytomas
-
Moreno AM, Castilla-Guerra L, Martinez-Torres MC, Torres-Olivera F, Fernandez E, Galera-Davidson H. Expression of neuropeptides and other neuroendocrine markers in human phaeochromocytomas. Neuropeptides 33:159-163, 1999.
-
(1999)
Neuropeptides
, vol.33
, pp. 159-163
-
-
Moreno, A.M.1
Castilla-Guerra, L.2
Martinez-Torres, M.C.3
Torres-Olivera, F.4
Fernandez, E.5
Galera-Davidson, H.6
-
179
-
-
0033398161
-
Immunohistochemical estimations of growth activity to predict biological behavior of pheochromocytomas
-
Nagura S, Katoh R, Kawaoi A, Kobayashi M, Obara T, Omata K. Immunohistochemical estimations of growth activity to predict biological behavior of pheochromocytomas. Mod Pathol 12:1107-1111, 1999.
-
(1999)
Mod Pathol
, vol.12
, pp. 1107-1111
-
-
Nagura, S.1
Katoh, R.2
Kawaoi, A.3
Kobayashi, M.4
Obara, T.5
Omata, K.6
-
180
-
-
0029066832
-
Remarkably suppressed manganese superoxide dismutase activity in malignant pheochromocytoma
-
Nakada T, Kubota Y, Sasagawa I, Yagisawa T, Watanabe M, Ishigooka M. Remarkably suppressed manganese superoxide dismutase activity in malignant pheochromocytoma. J Urol 153:1787-1790, 1995.
-
(1995)
J Urol
, vol.153
, pp. 1787-1790
-
-
Nakada, T.1
Kubota, Y.2
Sasagawa, I.3
Yagisawa, T.4
Watanabe, M.5
Ishigooka, M.6
-
181
-
-
0035075864
-
Tumour angiogenesis and Ki-67 expression in phaeochromocytoma
-
Ohji H, Sasagawa I, Iciyanagi O, Suzuki Y, Nakada T. Tumour angiogenesis and Ki-67 expression in phaeochromocytoma. BJU Int 87:381-385, 2001.
-
(2001)
BJU Int
, vol.87
, pp. 381-385
-
-
Ohji, H.1
Sasagawa, I.2
Iciyanagi, O.3
Suzuki, Y.4
Nakada, T.5
-
182
-
-
0036436752
-
Differential heparanase-1 expression in malignant and benign pheochromocytomas
-
Quiros RM, Kim AW, Maxhimer J, Gattuso P, Xu X, Prinz RA. Differential heparanase-1 expression in malignant and benign pheochromocytomas. J Surg Res 108:44-50, 2002.
-
(2002)
J Surg Res
, vol.108
, pp. 44-50
-
-
Quiros, R.M.1
Kim, A.W.2
Maxhimer, J.3
Gattuso, P.4
Xu, X.5
Prinz, R.A.6
-
183
-
-
0036024692
-
Expression of HER-2/neu receptor protein in adrenal tumors
-
Saeger W, Fassnacht M, Reincke M, Allolio B. Expression of HER-2/neu receptor protein in adrenal tumors. Pathol Res Pract 198:445-448, 2002.
-
(2002)
Pathol Res Pract
, vol.198
, pp. 445-448
-
-
Saeger, W.1
Fassnacht, M.2
Reincke, M.3
Allolio, B.4
-
184
-
-
0034744030
-
Inhibin/activin betaB-subunit expression in pheochromocytomas favors benign diagnosis
-
Salmenkivi K, Arola J, Voutilainen R, et al. Inhibin/activin betaB-subunit expression in pheochromocytomas favors benign diagnosis. J Clin Endocrinol Metab 86:2231-2235, 2001.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 2231-2235
-
-
Salmenkivi, K.1
Arola, J.2
Voutilainen, R.3
-
185
-
-
0034754143
-
Increased expression of tenascin in pheochromocytomas correlates with malignancy
-
Salmenkivi K, Haglund C, Arola J, Heikkila P. Increased expression of tenascin in pheochromocytomas correlates with malignancy. Am J Surg Pathol 25:1419-1423, 2001.
-
(2001)
Am J Surg Pathol
, vol.25
, pp. 1419-1423
-
-
Salmenkivi, K.1
Haglund, C.2
Arola, J.3
Heikkila, P.4
-
186
-
-
0035176827
-
Increased expression of cyclooxygenase-2 in malignant pheochromocytomas
-
Salmenkivi K, Haglund C, Ristimaki A, Arola J, Heikkila P. Increased expression of cyclooxygenase-2 in malignant pheochromocytomas. J Clin Endocrinol Metab 86:5615-5619, 2001.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 5615-5619
-
-
Salmenkivi, K.1
Haglund, C.2
Ristimaki, A.3
Arola, J.4
Heikkila, P.5
-
187
-
-
0026439376
-
Malignant pheochromocytoma: Clinical, biological, histologic and therapeutic data in a series of 20 patients with distant metastases
-
Schlumberger M, Gicquel C, Lumbroso J, et al. Malignant pheochromocytoma: clinical, biological, histologic and therapeutic data in a series of 20 patients with distant metastases. J Endocrinol Invest 15:631-642, 1992.
-
(1992)
J Endocrinol Invest
, vol.15
, pp. 631-642
-
-
Schlumberger, M.1
Gicquel, C.2
Lumbroso, J.3
-
188
-
-
0030799420
-
Features of malignancy in a benign pheochromocytoma
-
Stumvoll M, Fritsche A, Pickert A, Overkamp D. Features of malignancy in a benign pheochromocytoma. Horm Res 48:135-136, 1997.
-
(1997)
Horm Res
, vol.48
, pp. 135-136
-
-
Stumvoll, M.1
Fritsche, A.2
Pickert, A.3
Overkamp, D.4
-
189
-
-
0033730230
-
Catecholamine secretion and ploidy in phaeochromocytoma
-
Tormey WP, Fitzgerald RJ, Thomas G, Kay EW, Leader MB. Catecholamine secretion and ploidy in phaeochromocytoma. Int J Clin Pract 54:520-523, 2000.
-
(2000)
Int J Clin Pract
, vol.54
, pp. 520-523
-
-
Tormey, W.P.1
Fitzgerald, R.J.2
Thomas, G.3
Kay, E.W.4
Leader, M.B.5
-
190
-
-
0025805052
-
S100 protein-positive sustentacular cells in malignant and locally aggressive adrenal pheochromocytomas
-
Unger P, Hoffman K, Pertsemlidis D, Thung S, Wolfe D, Kaneko M. S100 protein-positive sustentacular cells in malignant and locally aggressive adrenal pheochromocytomas. Arch Pathol Lab Med 115:484-487, 1991.
-
(1991)
Arch Pathol Lab Med
, vol.115
, pp. 484-487
-
-
Unger, P.1
Hoffman, K.2
Pertsemlidis, D.3
Thung, S.4
Wolfe, D.5
Kaneko, M.6
-
191
-
-
0034040882
-
Proliferative index in phaeochromocytomas: Does it predict the occurrence of metastases?
-
van der Harst E, Bruining HA, Jaap Bonjer H, et al. Proliferative index in phaeochromocytomas: does it predict the occurrence of metastases? J Pathol 191:175-180, 2000.
-
(2000)
J Pathol
, vol.191
, pp. 175-180
-
-
Van Der Harst, E.1
Bruining, H.A.2
Jaap Bonjer, H.3
-
192
-
-
0028307836
-
Tumour predisposition in mice heterozygous for a targeted mutation in Nf1
-
Jacks T, Shih TS, Schmitt EM, Bronson RT, Bernards A, Weinberg RA. Tumour predisposition in mice heterozygous for a targeted mutation in Nf1. Nat Genet 7:353-361, 1994.
-
(1994)
Nat Genet
, vol.7
, pp. 353-361
-
-
Jacks, T.1
Shih, T.S.2
Schmitt, E.M.3
Bronson, R.T.4
Bernards, A.5
Weinberg, R.A.6
-
193
-
-
0034651526
-
C-cell hyperplasia, pheochromocytoma and sympathoadrenal malformation in a mouse model of multiple endocrine neoplasia type 2B
-
Smith-Hicks CL, Sizer KC, Powers JF, Tischler AS, Costantini F. C-cell hyperplasia, pheochromocytoma and sympathoadrenal malformation in a mouse model of multiple endocrine neoplasia type 2B. Embo J 19:612-622, 2000.
-
(2000)
Embo J
, vol.19
, pp. 612-622
-
-
Smith-Hicks, C.L.1
Sizer, K.C.2
Powers, J.F.3
Tischler, A.S.4
Costantini, F.5
-
194
-
-
0034665364
-
Tissue-specific carcinogenesis in transgenic mice expressing the RET proto-oncogene with a multiple endocrine neoplasia type 2A mutation
-
Kawai K, Iwashita T, Murakami H, et al. Tissue-specific carcinogenesis in transgenic mice expressing the RET proto-oncogene with a multiple endocrine neoplasia type 2A mutation. Cancer Res 60:5254-5260, 2000.
-
(2000)
Cancer Res
, vol.60
, pp. 5254-5260
-
-
Kawai, K.1
Iwashita, T.2
Murakami, H.3
-
195
-
-
0035970092
-
A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors
-
Crabtree JS, Scacheri PC, Ward JM, et al. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors. Proc Natl Acad Sci USA 98:1118-1123, 2001.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 1118-1123
-
-
Crabtree, J.S.1
Scacheri, P.C.2
Ward, J.M.3
-
196
-
-
0033616597
-
RB-mediated suppression of spontaneous multiple neuroendocrine neoplasia and lung metastases in Rb+/- Mice
-
Nikitin AY, Juarez-Perez MI, Li S, Huang L, Lee WH. RB-mediated suppression of spontaneous multiple neuroendocrine neoplasia and lung metastases in Rb+/- mice. Proc Natl Acad Sci USA 96:3916-3921, 1999.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 3916-3921
-
-
Nikitin, A.Y.1
Juarez-Perez, M.I.2
Li, S.3
Huang, L.4
Lee, W.H.5
-
197
-
-
0036351277
-
High-level expression of receptor tyrosine kinase ret and responsiveness to ret-activating ligands in pheochromocytoma cell lines from neurofibromatosis knockout mice
-
Powers JF, Schelling K, Brachold JM, et al. High-level expression of receptor tyrosine kinase ret and responsiveness to ret-activating ligands in pheochromocytoma cell lines from neurofibromatosis knockout mice. Mol Cell Neurosci 20:382-389, 2002.
-
(2002)
Mol Cell Neurosci
, vol.20
, pp. 382-389
-
-
Powers, J.F.1
Schelling, K.2
Brachold, J.M.3
-
198
-
-
0037022364
-
Genetic analysis of Pten and Ink4a/Arf interactions in the suppression of tumorigenesis in mice
-
You MJ, Castrillon DH, Bastian BC, et al. Genetic analysis of Pten and Ink4a/Arf interactions in the suppression of tumorigenesis in mice. Proc Natl Acad Sci USA 99:1455-1460, 2002.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 1455-1460
-
-
You, M.J.1
Castrillon, D.H.2
Bastian, B.C.3
-
199
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D, Segraves R, Sudar D, et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20:207-211, 1998.
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
-
200
-
-
0037468269
-
Genomewide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays
-
Clark J, Edwards S, Feber A, et al. Genomewide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays. Oncogene 22: 1247-1252, 2003.
-
(2003)
Oncogene
, vol.22
, pp. 1247-1252
-
-
Clark, J.1
Edwards, S.2
Feber, A.3
-
201
-
-
0036218046
-
Genome-wide detection of chromosomal imbalances in tumors using BAG microarrays
-
Cai WW, Mao JH, Chow CW, Damani S, Balmain A, Bradley A. Genome-wide detection of chromosomal imbalances in tumors using BAG microarrays. Nat Biotechnol 20:393-396, 2002.
-
(2002)
Nat Biotechnol
, vol.20
, pp. 393-396
-
-
Cai, W.W.1
Mao, J.H.2
Chow, C.W.3
Damani, S.4
Balmain, A.5
Bradley, A.6
-
202
-
-
0037738895
-
Profiling breast cancer by array CGH
-
Albertson DG. Profiling breast cancer by array CGH. Breast Cancer Res Treat 78:289-298, 2003.
-
(2003)
Breast Cancer Res Treat
, vol.78
, pp. 289-298
-
-
Albertson, D.G.1
-
203
-
-
0036831826
-
The pathogenesis of pituitary tumours
-
Asa SL, Ezzat S. The pathogenesis of pituitary tumours. Nat Rev Cancer 2:836-849, 2002.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 836-849
-
-
Asa, S.L.1
Ezzat, S.2
|