-
1
-
-
0022912449
-
Histopathology and classification of renal cell tumors (adenomas, oncocytomas and carcinomas). The basic cytological and histopathological elements and their use for diagnostics
-
Thoenes W, Storkel S, Rumpelt HJ. Histopathology and classification of renal cell tumors (adenomas, oncocytomas and carcinomas). The basic cytological and histopathological elements and their use for diagnostics. Path Res Pract. 1986;181(2):125-143.
-
(1986)
Path Res Pract
, vol.181
, Issue.2
, pp. 125-143
-
-
Thoenes, W.1
Storkel, S.2
Rumpelt, H.J.3
-
2
-
-
9744268261
-
-
Maher ER. Von Hippel-Lindau disease. Curr Mol Med. 2004;4(8):833-842.
-
Maher ER. Von Hippel-Lindau disease. Curr Mol Med. 2004;4(8):833-842.
-
-
-
-
3
-
-
2342583527
-
Searching for the hereditary causes of renal-cell carcinoma
-
Pavlovich CP, Schmidt LS. Searching for the hereditary causes of renal-cell carcinoma. Nat Rev Cancer. 2004;4(5):381-393.
-
(2004)
Nat Rev Cancer
, vol.4
, Issue.5
, pp. 381-393
-
-
Pavlovich, C.P.1
Schmidt, L.S.2
-
4
-
-
33846876103
-
Identification of the genes for kidney cancer: Opportunity for disease-specific targeted therapeutics
-
Linehan WM, Pinto PA, Srinivasan R, et al. Identification of the genes for kidney cancer: opportunity for disease-specific targeted therapeutics. Clin Cancer Res. 2007;13:671s-679s.
-
(2007)
Clin Cancer Res
, vol.13
-
-
Linehan, W.M.1
Pinto, P.A.2
Srinivasan, R.3
-
5
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumour suppressor gene
-
Latif F, Tory K, Gnarra J, et al. Identification of the von Hippel-Lindau disease tumour suppressor gene. Science. 1993;260(5112):1317-1320.
-
(1993)
Science
, vol.260
, Issue.5112
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
-
6
-
-
17344381429
-
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas
-
Schmidt L, Duh F-M, Chen F, et al. Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Nat Genet. 1997;16(1):68-73.
-
(1997)
Nat Genet
, vol.16
, Issue.1
, pp. 68-73
-
-
Schmidt, L.1
Duh, F.-M.2
Chen, F.3
-
7
-
-
0000939691
-
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the BirtHogg-Dubé syndrome
-
Nickerson ML, Warren MB, Toro JR, et al. Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the BirtHogg-Dubé syndrome. Cancer Cell. 2002;2(2):157-164.
-
(2002)
Cancer Cell
, vol.2
, Issue.2
, pp. 157-164
-
-
Nickerson, M.L.1
Warren, M.B.2
Toro, J.R.3
-
8
-
-
0030992453
-
Familial non-VHL non-papillary clear-cell renal cancer
-
Teh B, Giraud S, Sari F, et al. Familial non-VHL non-papillary clear-cell renal cancer. Lancet. 1997;349(9055):848-849.
-
(1997)
Lancet
, vol.349
, Issue.9055
, pp. 848-849
-
-
Teh, B.1
Giraud, S.2
Sari, F.3
-
9
-
-
0034026499
-
Familial clear cell renal cell carcinoma (FCRC): Clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes
-
Woodward ER, Clifford SC, Astuti D, et al. Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes. J Med Genet. 2000;37(5):348-353.
-
(2000)
J Med Genet
, vol.37
, Issue.5
, pp. 348-353
-
-
Woodward, E.R.1
Clifford, S.C.2
Astuti, D.3
-
10
-
-
18544365990
-
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
-
Tomlinson IP, Alam NA, Rowan AJ, et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet. 2002;30(4):406-410.
-
(2002)
Nat Genet
, vol.30
, Issue.4
, pp. 406-410
-
-
Tomlinson, I.P.1
Alam, N.A.2
Rowan, A.J.3
-
11
-
-
33745234207
-
Increased risk of cancer in patients with fumarate hydratase germline mutation
-
Lehtonen HJ, Kiuru M, Ylisaukko-Oja SK, et al. Increased risk of cancer in patients with fumarate hydratase germline mutation. J Med Genet. 2006;43(6):523-526.
-
(2006)
J Med Genet
, vol.43
, Issue.6
, pp. 523-526
-
-
Lehtonen, H.J.1
Kiuru, M.2
Ylisaukko-Oja, S.K.3
-
12
-
-
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. 2000;287(5454):848-851.
-
(2000)
Science
, vol.287
, Issue.5454
, pp. 848-851
-
-
Baysal, B.E.1
Ferrell, R.E.2
Willett-Brozick, J.E.3
-
13
-
-
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. 2000;26(3):268-270.
-
(2000)
Nat Genet
, vol.26
, Issue.3
, pp. 268-270
-
-
Niemann, S.1
Muller, U.2
-
14
-
-
0035857957
-
Germline SDHD mutation in familial phaeochromocytoma
-
Astuti D, Douglas F, Lennard TW, et al. Germline SDHD mutation in familial phaeochromocytoma. Lancet. 2001;357:1181-1182.
-
(2001)
Lancet
, vol.357
, pp. 1181-1182
-
-
Astuti, D.1
Douglas, F.2
Lennard, T.W.3
-
15
-
-
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. 2001;69(1):49-54.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.1
, pp. 49-54
-
-
Astuti, D.1
Latif, F.2
Dallol, A.3
-
16
-
-
9144249602
-
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma
-
Vanharanta S, Buchta M, McWhinney SR, et al. Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. Am J Hum Genet. 2004;74(1):153-159.
-
(2004)
Am J Hum Genet
, vol.74
, Issue.1
, pp. 153-159
-
-
Vanharanta, S.1
Buchta, M.2
McWhinney, S.R.3
-
17
-
-
37349074531
-
Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD
-
Pasini B, McWhinney SR, Bei T, et al. Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. Eur J Hum Genet. 2008;16(1):79-88.
-
(2008)
Eur J Hum Genet
, vol.16
, Issue.1
, pp. 79-88
-
-
Pasini, B.1
McWhinney, S.R.2
Bei, T.3
-
18
-
-
3142626559
-
-
Morris MR, Maina E, Morgan NV, et al. Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma. J Clin Pathol. 2004;57(7):706-711.
-
Morris MR, Maina E, Morgan NV, et al. Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma. J Clin Pathol. 2004;57(7):706-711.
-
-
-
-
19
-
-
33644822473
-
Clinical presentation and penetrance of pheochromocytoma/ paraganglioma syndromes
-
Benn DE, Gimenez AP, Reilly JR, et al. Clinical presentation and penetrance of pheochromocytoma/ paraganglioma syndromes. J Clin Endocrinol Metab. 2006;91(3):827-836.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, Issue.3
, pp. 827-836
-
-
Benn, D.E.1
Gimenez, A.P.2
Reilly, J.R.3
-
20
-
-
31344478803
-
Mutation analysis of SDHB and SDHC. novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
-
Bayley JP, van Minderhout I, Weiss MM, et al. Mutation analysis of SDHB and SDHC. novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. BMC Med Genet. 2006;7(1):1-10.
-
(2006)
BMC Med Genet
, vol.7
, Issue.1
, pp. 1-10
-
-
Bayley, J.P.1
van Minderhout, I.2
Weiss, M.M.3
-
21
-
-
0036774422
-
Functional consequences of a SDHB gene mutation in an apparently spordaric pheochromocytoma
-
Gimenez-Roqueplo AP, Favier J, Rustin P, et al. Functional consequences of a SDHB gene mutation in an apparently spordaric pheochromocytoma. J Clin Endocrinol Metab. 2002;87(10):4771-4774.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, Issue.10
, pp. 4771-4774
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
-
22
-
-
4143105824
-
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations
-
Neumann HP, Pawlu C, Peczkowska M, et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA. 2004;292(8):943-951.
-
(2004)
JAMA
, vol.292
, Issue.8
, pp. 943-951
-
-
Neumann, H.P.1
Pawlu, C.2
Peczkowska, M.3
-
23
-
-
51649101534
-
-
Srirangalingam U, Walker L, Khoo B, et al. Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B gene mutation carriers [published online ahead of print April 14, 2008]. Clin Endocrinol. doi:10.1111/j.1365-2265.2008.03274.x.
-
Srirangalingam U, Walker L, Khoo B, et al. Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B gene mutation carriers [published online ahead of print April 14, 2008]. Clin Endocrinol. doi:10.1111/j.1365-2265.2008.03274.x.
-
-
-
-
24
-
-
33751530026
-
Expression of HIF-1alpha, HIF-2alpha (EPAS1), and their target genes in paraganglioma and pheochromocytoma with VHL and SDH mutations
-
Pollard PJ, El-Bahrawy M, Poulsom R, et al. Expression of HIF-1alpha, HIF-2alpha (EPAS1), and their target genes in paraganglioma and pheochromocytoma with VHL and SDH mutations. J Clin Endocrinol Metab. 2006;91(11):4593-4598.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, Issue.11
, pp. 4593-4598
-
-
Pollard, P.J.1
El-Bahrawy, M.2
Poulsom, R.3
-
25
-
-
23644436667
-
Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: Developmental culling and cancer
-
Lee S, Nakamura E, Yang H, et al. Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer. Cancer Cell. 2005;8(2):155-167.
-
(2005)
Cancer Cell
, vol.8
, Issue.2
, pp. 155-167
-
-
Lee, S.1
Nakamura, E.2
Yang, H.3
-
26
-
-
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. 2001;10(10):1029-1038.
-
(2001)
Hum Mol Genet
, vol.10
, Issue.10
, pp. 1029-1038
-
-
Clifford, S.C.1
Cockman, M.E.2
Smallwood, A.C.3
-
27
-
-
34547174217
-
Hypoxia-inducible factor linked to differential kidney cancer risk seen with type 2A and type 2B VHL mutations
-
Li L, Zhang L, Zhang X, et al. Hypoxia-inducible factor linked to differential kidney cancer risk seen with type 2A and type 2B VHL mutations. Mol Cell Biol. 2007;27(15):5381-5392.
-
(2007)
Mol Cell Biol
, vol.27
, Issue.15
, pp. 5381-5392
-
-
Li, L.1
Zhang, L.2
Zhang, X.3
-
28
-
-
2342597973
-
Inhibition of HIF2alpha is sufficient to suppress pVHL-defective tumor growth
-
Kondo K, Kim WY, Lechpammer M, et al. Inhibition of HIF2alpha is sufficient to suppress pVHL-defective tumor growth. PLoS Biol. 2003;1(3):E83.
-
(2003)
PLoS Biol
, vol.1
, Issue.3
-
-
Kondo, K.1
Kim, W.Y.2
Lechpammer, M.3
|