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Volumn 91, Issue 8, 2006, Pages 2827-2832

Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: Implications for cancer surveillance

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CALCIUM BLOOD LEVEL; CANCER EPIDEMIOLOGY; CLINICAL ARTICLE; CONFERENCE PAPER; CONTROLLED STUDY; ECHOGRAPHY; FRAMESHIFT MUTATION; GERM LINE GENE THERAPY; HRPT2 GENE; HUMAN; HYPERCALCEMIA; HYPERPARATHYROIDISM; INTRON; MALE; PARATHYROID TUMOR; PRIORITY JOURNAL; STOP CODON; SUPPRESSOR GENE;

EID: 33747668789     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2005-1239     Document Type: Conference Paper
Times cited : (89)

References (20)
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    • HRPT2, a tumor suppressor gene for hyperparathyroidism-jaw tumor syndrome
    • Wang PF, Tan MH, Zhang C, Morreau H, Teh BT 2005 HRPT2, a tumor suppressor gene for hyperparathyroidism-jaw tumor syndrome. Horm Metab Res 37:380-383
    • (2005) Horm Metab Res , vol.37 , pp. 380-383
    • Wang, P.F.1    Tan, M.H.2    Zhang, C.3    Morreau, H.4    Teh, B.T.5
  • 3
    • 20344391925 scopus 로고    scopus 로고
    • The HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II
    • Yart A, Gstaiger M, Wirbelauer C, Pecnik M, Anastasiou D, Hess D, Krek W 2005 The HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II. Mol Cell Biol 25:5052-5060
    • (2005) Mol Cell Biol , vol.25 , pp. 5052-5060
    • Yart, A.1    Gstaiger, M.2    Wirbelauer, C.3    Pecnik, M.4    Anastasiou, D.5    Hess, D.6    Krek, W.7
  • 5
    • 30544452321 scopus 로고    scopus 로고
    • Identification of a functional bipartite nuclear localization signal in the tumor suppressor parafibromin
    • Hahn MA, Marsh DJ 2005 Identification of a functional bipartite nuclear localization signal in the tumor suppressor parafibromin. Oncogene 24:6241-6248
    • (2005) Oncogene , vol.24 , pp. 6241-6248
    • Hahn, M.A.1    Marsh, D.J.2
  • 8
    • 0842291514 scopus 로고    scopus 로고
    • Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome
    • Simonds WF, Robbins CM, Agarwal SK, Hendy GN, Carpten JD, Marx SJ 2004 Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 89:96-102
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 96-102
    • Simonds, W.F.1    Robbins, C.M.2    Agarwal, S.K.3    Hendy, G.N.4    Carpten, J.D.5    Marx, S.J.6
  • 10
    • 1842403802 scopus 로고    scopus 로고
    • Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: Linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas
    • Teh BT, Farnebo F, Kristoffersson U, Sundelin B, Cardinal J, Axelson R, Yap A, Epstein M, Heath 3rd H, Cameron D, Larsson C 1996 Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas. J Clin Endocrinol Metab 81:4204-4211
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 4204-4211
    • Teh, B.T.1    Farnebo, F.2    Kristoffersson, U.3    Sundelin, B.4    Cardinal, J.5    Axelson, R.6    Yap, A.7    Epstein, M.8    Heath III, H.9    Cameron, D.10    Larsson, C.11
  • 20
    • 12344296364 scopus 로고    scopus 로고
    • Parathyroid surgery in familial hyperparathyroid disorders
    • Carling T, Udelsman R 2005 Parathyroid surgery in familial hyperparathyroid disorders. J Intern Med 257:27-37
    • (2005) J Intern Med , vol.257 , pp. 27-37
    • Carling, T.1    Udelsman, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.