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Volumn 46, Issue 3, 2008, Pages 229-230

Mutations in SH3BP2, the cherubism gene, were not detected in central or peripheral giant cell tumours of the jaw

Author keywords

Cherubism; Giant cell granuloma of jaw; Mutation; SH3BP2

Indexed keywords

PARAFFIN;

EID: 40149085868     PISSN: 02664356     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bjoms.2007.04.014     Document Type: Article
Times cited : (34)

References (9)
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    • de Lange J, van Maarle MC, van den Akker HP, Redeker EJ., DNA analysis of the SH3BP2 gene in patients with aggressive central giant cell granuloma. Br J Oral Maxillofac Surg; Epub ahead of print, in press.
  • 3
    • 0034320064 scopus 로고    scopus 로고
    • Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism
    • J. Mangion S. Edkins A.N. Goss M.R. Stratton A.M. Flanagan Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism J Med Genet 37 2000 E37
    • (2000) J Med Genet , vol.37 , pp. E37
    • Mangion, J.1    Edkins, S.2    Goss, A.N.3    Stratton, M.R.4    Flanagan, A.M.5
  • 6
    • 18344370436 scopus 로고    scopus 로고
    • PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogenetity
    • M. Tartaglia K. Kalidas A. Shaw X. Song D.L. Musat I. van der Burgt PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogenetity Am J Hum Genet 70 2002 1555 1563
    • (2002) Am J Hum Genet , vol.70 , pp. 1555-1563
    • Tartaglia, M.1    Kalidas, K.2    Shaw, A.3    Song, X.4    Musat, D.L.5    van der Burgt, I.6
  • 7
    • 85120093567 scopus 로고    scopus 로고
    • van Capelle CI, Hogeman PH, van der Sijs-Bos CJ, Heggelman BG, Idowu B, Slootweg PJ, et al., Neurofibromatosis presenting with a cherubism phenotype. Eur J Pediatr; Epub ahead of print, in press.
  • 8
    • 22244487321 scopus 로고    scopus 로고
    • Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism
    • T. Jafarov N. Ferimazova E. Reichenberger Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism Clin Genet 68 2005 190 191
    • (2005) Clin Genet , vol.68 , pp. 190-191
    • Jafarov, T.1    Ferimazova, N.2    Reichenberger, E.3
  • 9
    • 33845988776 scopus 로고    scopus 로고
    • Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 “cherubism” mice
    • Y. Ueki C.Y. Lin M. Senoo T. Ebihara N. Agata M. Onji Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 “cherubism” mice Cell 128 2007 71 83
    • (2007) Cell , vol.128 , pp. 71-83
    • Ueki, Y.1    Lin, C.Y.2    Senoo, M.3    Ebihara, T.4    Agata, N.5    Onji, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.