-
1
-
-
0036841566
-
Hyperparathyroidism in hereditary syndromes: Special expressions and special managements
-
Marx SJ, Simonds WF, Agarwal SK, et al. Hyperparathyroidism in hereditary syndromes: special expressions and special managements. J Bone Miner Res 2002;17(suppl 2):N37-N43.
-
(2002)
J Bone Miner Res
, vol.17
, Issue.SUPPL. 2
-
-
Marx, S.J.1
Simonds, W.F.2
Agarwal, S.K.3
-
2
-
-
0025642521
-
Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: A clinically and genetically distinct syndrome
-
Jackson CE, Norum RA, Boyd SB, et al. Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome. Surgery 1990;108:1006-13.
-
(1990)
Surgery
, vol.108
, pp. 1006-1013
-
-
Jackson, C.E.1
Norum, R.A.2
Boyd, S.B.3
-
3
-
-
19944434120
-
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome
-
Bradley KJ, Hobbs MR, Buley ID, et al. Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. J Intern Med 2005;257:18-26.
-
(2005)
J Intern Med
, vol.257
, pp. 18-26
-
-
Bradley, K.J.1
Hobbs, M.R.2
Buley, I.D.3
-
4
-
-
0028958106
-
Hereditary hyperparathyroidism-jaw tumor syndrome: The endocrine tumor gene HRPT2 maps to chromosome Iq21-q31
-
Szabo J, Heath B, Hill VM, et al. Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome Iq21-q31. Am J Hum Genet 1995;56:944-50.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 944-950
-
-
Szabo, J.1
Heath, B.2
Hill, V.M.3
-
5
-
-
18744385803
-
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
-
Carpten JD, Robbins CM, Villablanca A, et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 2002;32:676-80.
-
(2002)
Nat Genet
, vol.32
, pp. 676-680
-
-
Carpten, J.D.1
Robbins, C.M.2
Villablanca, A.3
-
6
-
-
0041328511
-
-
Howell VM, Haven CJ, Kahnoski K, et al. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J Med Genet 2003;40:657-63. [Erratum in J Med Genet 2004;41:20.]
-
Howell VM, Haven CJ, Kahnoski K, et al. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J Med Genet 2003;40:657-63. [Erratum in J Med Genet 2004;41:20.]
-
-
-
-
7
-
-
0142213734
-
Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma
-
Shattuck TM, Valimaki S, Obara T, et al. Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. N Engl J Med 2003;349:1722-9.
-
(2003)
N Engl J Med
, vol.349
, pp. 1722-1729
-
-
Shattuck, T.M.1
Valimaki, S.2
Obara, T.3
-
8
-
-
0029843950
-
Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands
-
Herman JG, Graff JR, Myohanen S, Nelkin BD, Baylin SB. Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands. Proc Natl Acad Sci U S A 1996;93:9821-6.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 9821-9826
-
-
Herman, J.G.1
Graff, J.R.2
Myohanen, S.3
Nelkin, B.D.4
Baylin, S.B.5
-
9
-
-
0033816924
-
Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer
-
Grady WM, Willis J, Guilford PJ, et al. Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer. Nat Genet 2000;26:16-7.
-
(2000)
Nat Genet
, vol.26
, pp. 16-17
-
-
Grady, W.M.1
Willis, J.2
Guilford, P.J.3
-
10
-
-
0035452392
-
The E-cadherin gene is silenced by CpG methylation in human oral squamous cell carcinomas
-
Nakayama S, Sasaki A, Mese H, Alcalde RE, Tsuji T, Matsumura T. The E-cadherin gene is silenced by CpG methylation in human oral squamous cell carcinomas. Int J Cancer 2001;93:667-73.
-
(2001)
Int J Cancer
, vol.93
, pp. 667-673
-
-
Nakayama, S.1
Sasaki, A.2
Mese, H.3
Alcalde, R.E.4
Tsuji, T.5
Matsumura, T.6
-
11
-
-
0041672342
-
Aberrant methylation and silencing of ARHI, an imprinted tumor suppressor gene in which the function is lost in breast cancers
-
Yuan J, Luo RZ, Fujii S, et al. Aberrant methylation and silencing of ARHI, an imprinted tumor suppressor gene in which the function is lost in breast cancers. Cancer Res 2003;63:4174-80.
-
(2003)
Cancer Res
, vol.63
, pp. 4174-4180
-
-
Yuan, J.1
Luo, R.Z.2
Fujii, S.3
-
12
-
-
33751505540
-
DNA methylation profiling of human chromosomes 6, 20 and 22
-
Eckhardt F, Lewin J, Cortese R, et al. DNA methylation profiling of human chromosomes 6, 20 and 22. Nat Genet 2006;38:1378-85.
-
(2006)
Nat Genet
, vol.38
, pp. 1378-1385
-
-
Eckhardt, F.1
Lewin, J.2
Cortese, R.3
-
13
-
-
0036141731
-
Familial isolated hyperparathyroidism: Clinical and genetic characteristics of 36 kindreds
-
Simonds WF, James-Newton LA, Agarwal SK, et al. Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds. Medicine (Baltimore) 2002;81:1-26.
-
(2002)
Medicine (Baltimore)
, vol.81
, pp. 1-26
-
-
Simonds, W.F.1
James-Newton, L.A.2
Agarwal, S.K.3
-
14
-
-
0036228986
-
Genetic analysis of the MEN1 gene and HRPT2 locus in two Italian kindreds with familial isolated hyperparathyroidism
-
Cetani F, Pardi E, Giovannetti A, et al. Genetic analysis of the MEN1 gene and HRPT2 locus in two Italian kindreds with familial isolated hyperparathyroidism. Clin Endocrinol (Oxf) 2002;56:457-64.
-
(2002)
Clin Endocrinol (Oxf)
, vol.56
, pp. 457-464
-
-
Cetani, F.1
Pardi, E.2
Giovannetti, A.3
-
16
-
-
0036720037
-
Consistent decrease in telomere length in parathyroid tumors but alteration in telomerase activity limited to malignancies: Preliminary report
-
Kammori M, Nakamura K, Kanauchi H, et al. Consistent decrease in telomere length in parathyroid tumors but alteration in telomerase activity limited to malignancies: preliminary report. World J Surg 2002;26:1083-7.
-
(2002)
World J Surg
, vol.26
, pp. 1083-1087
-
-
Kammori, M.1
Nakamura, K.2
Kanauchi, H.3
-
18
-
-
0015590315
-
Parathyroid carcinoma. A study of 70 cases
-
Schantz A, Castleman B. Parathyroid carcinoma. A study of 70 cases. Cancer 1973;31:600-5.
-
(1973)
Cancer
, vol.31
, pp. 600-605
-
-
Schantz, A.1
Castleman, B.2
-
19
-
-
0033179565
-
Two hundred eighty-six cases of parathyroid carcinoma treated in the US between 1985-1995: A National Cancer Data Base Report. The American College of Surgeons Commission on Cancer and the American Cancer Society
-
Hundahl SA, Fleming ID, Fremgen AM, Menck HR. Two hundred eighty-six cases of parathyroid carcinoma treated in the US between 1985-1995: a National Cancer Data Base Report. The American College of Surgeons Commission on Cancer and the American Cancer Society. Cancer 1999;86:538-44.
-
(1999)
Cancer
, vol.86
, pp. 538-544
-
-
Hundahl, S.A.1
Fleming, I.D.2
Fremgen, A.M.3
Menck, H.R.4
-
20
-
-
5144220874
-
Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma
-
Tan MH, Morrison C, Wang P, et al. Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma. Clin Cancer Res 2004;10:6629-37.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 6629-6637
-
-
Tan, M.H.1
Morrison, C.2
Wang, P.3
-
21
-
-
0036753290
-
-
Fraga MF, Esteller M. DNA methylation: a profile of methods and applications. Biotechniques 2002;33:632, 634, 636-49.
-
Fraga MF, Esteller M. DNA methylation: a profile of methods and applications. Biotechniques 2002;33:632, 634, 636-49.
-
-
-
|