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Volumn 36, Issue 4, 2007, Pages 365-369

A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone

Author keywords

[No Author keywords available]

Indexed keywords

PARAFIBROMIN; TECHNETIUM 99M; TUMOR SUPPRESSOR PROTEIN; UNCLASSIFIED DRUG;

EID: 33847053143     PISSN: 09015027     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijom.2006.08.007     Document Type: Article
Times cited : (25)

References (20)
  • 9
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    • Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome
    • Jackson C.E., Norum R.A., Boyd S.B., Talpos G.B., Wilson S.D., Taggart R.T., and Mallette L.E. Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome. Surgery 108 (1990) 1006-1013
    • (1990) Surgery , vol.108 , pp. 1006-1013
    • Jackson, C.E.1    Norum, R.A.2    Boyd, S.B.3    Talpos, G.B.4    Wilson, S.D.5    Taggart, R.T.6    Mallette, L.E.7
  • 10
    • 0034700450 scopus 로고    scopus 로고
    • Hyperparathyroidism and hypoparathyroid disorders
    • Marx S.J. Hyperparathyroidism and hypoparathyroid disorders. N Engl J Med 343 (2000) 1863-1875
    • (2000) N Engl J Med , vol.343 , pp. 1863-1875
    • Marx, S.J.1
  • 15
    • 0842291514 scopus 로고    scopus 로고
    • Familial isolated hyperparathyroidism is rarely caused by germ-line mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome
    • Simonds W.F., Robbins C.M., Agarwal S.K., Hendy G.N., Carpten J.D., and Marx S.J. Familial isolated hyperparathyroidism is rarely caused by germ-line mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 89 (2004) 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
  • 16
    • 33746417234 scopus 로고    scopus 로고
    • Pathology and genetics of the head and neck tumours
    • Barnes L., Eveson J.W., Reichart P., and Sidransky D. (Eds), IARC Press, Lyon
    • Slootweg P.J., and EI Mofty S.K. Pathology and genetics of the head and neck tumours. In: Barnes L., Eveson J.W., Reichart P., and Sidransky D. (Eds). World Health Organization Classification of Tumours (2005), IARC Press, Lyon 319-320
    • (2005) World Health Organization Classification of Tumours , pp. 319-320
    • Slootweg, P.J.1    EI Mofty, S.K.2
  • 19
    • 14644397229 scopus 로고    scopus 로고
    • Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression
    • Woodard G.E., Lin L., Zhang J.H., Agarwal S.K., Mark S.J., and Simonds W.F. Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression. Oncogene 24 (2005) 1272-1276
    • (2005) Oncogene , vol.24 , pp. 1272-1276
    • Woodard, G.E.1    Lin, L.2    Zhang, J.H.3    Agarwal, S.K.4    Mark, S.J.5    Simonds, W.F.6
  • 20
    • 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., and Krek W. The HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II. Mol Cell Biol 25 (2005) 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.