BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 33552642)

  • 1. Unusual Characteristics and Variable Expressivity in a Brazilian Family with Cherubism.
    Deconte D; Correia EPE; Haubert G; de Souza V; Correia JD; Maahs MAP; Zen PRG; Fiegenbaum M; Rosa RFM
    J Pediatr Genet; 2021 Mar; 10(1):63-69. PubMed ID: 33552642
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identical Mutation in SH3BP2 Gene Causes Clinical Phenotypes with Different Severity in Mother and Daughter - Case Report.
    Preda L; Dinca O; Bucur A; Dragomir C; Severin E
    Mol Syndromol; 2010; 1(2):87-90. PubMed ID: 21045962
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variable expressivity familial cherubism: woman transmitting cherubism without suffering the disease.
    Pérez-Sayáns M; Barros-Angueira F; Suárez-Peñaranda JÉ; García-García A
    Head Face Med; 2013 Nov; 9():33. PubMed ID: 24382142
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel c.1255G>T (p.D419Y) mutation in SH3BP2 gene causes cherubism in a Turkish family.
    Dinckan N; Guven Y; Kayserili H; Aktoren O; Uyguner OZ
    Oral Surg Oral Med Oral Pathol Oral Radiol; 2012 Nov; 114(5):e42-6. PubMed ID: 23083484
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of the SH3BP2 gene in 2 families of cherubism.
    Tuna EB; Shimizu T; Seymen F; Yildirim M; Gencay K; Maeda T
    Pediatr Dent; 2012; 34(3):198-202. PubMed ID: 22795151
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubism.
    Lo B; Faiyaz-Ul-Haque M; Kennedy S; Aviv R; Tsui LC; Teebi AS
    Am J Med Genet A; 2003 Aug; 121A(1):37-40. PubMed ID: 12900899
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A c.1244G>A (p.Arg415Gln) mutation in SH3BP2 gene causes cherubism in a Turkish family: report of a family with review of the literature.
    Sekerci AE; Balta B; Dundar M; Hu Y; Reichenberger EJ; Etoz OA; Nazlim S; Bayrakdar IS
    Med Oral Patol Oral Cir Bucal; 2014 Jul; 19(4):e340-4. PubMed ID: 24608212
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cherubism: a case report of a three-generation inheritance and literature review.
    Tsodoulos S; Ilia A; Antoniades K; Angelopoulos C
    J Oral Maxillofac Surg; 2014 Feb; 72(2):405.e1-9. PubMed ID: 24280174
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutations in the SH3BP2 gene associated with sporadic central giant cell lesions and cherubism.
    Carvalho VM; Perdigão PF; Amaral FR; de Souza PE; De Marco L; Gomez RS
    Oral Dis; 2009 Jan; 15(1):106-10. PubMed ID: 19017279
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in SH3BP2, the cherubism gene, were not detected in central or peripheral giant cell tumours of the jaw.
    Idowu BD; Thomas G; Frow R; Diss TC; Flanagan AM
    Br J Oral Maxillofac Surg; 2008 Apr; 46(3):229-230. PubMed ID: 17544554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microbe-Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice.
    Kittaka M; Yoshimoto T; Schlosser C; Kajiya M; Kurihara H; Reichenberger EJ; Ueki Y
    JBMR Plus; 2020 Jun; 4(6):e10352. PubMed ID: 32537546
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cherubism as a systemic skeletal disease: evidence from an aggressive case.
    Morice A; Joly A; Ricquebourg M; Maruani G; Durand E; Galmiche L; Amiel J; Vial Y; Cavé H; Belhous K; Piketty M; Cohen-Solal M; Berdal A; Collet C; Picard A; Coudert AE; Kadlub N
    BMC Musculoskelet Disord; 2020 Aug; 21(1):564. PubMed ID: 32825821
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SH3BP2 is rarely mutated in exon 9 in giant cell lesions outside cherubism.
    Lietman SA; Prescott NL; Hicks DG; Westra WH; Levine MA
    Clin Orthop Relat Res; 2007 Jun; 459():22-7. PubMed ID: 17545756
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cherubism misdiagnosed as giant cell tumor: a case report and review of literature.
    Jiao Y; Zhou M; Yang Y; Zhou J; Duan X
    Int J Clin Exp Med; 2015; 8(3):4656-63. PubMed ID: 26064398
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Investigation of the SH3BP2 gene mutation in cherubism.
    Lee JY; Jung YS; Kim SA; Lee SH; Ahn SG; Yoon JH
    Acta Med Okayama; 2008 Jun; 62(3):209-12. PubMed ID: 18596838
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a novel mutation of SH3BP2 in cherubism and demonstration that SH3BP2 mutations lead to increased NFAT activation.
    Lietman SA; Kalinchinko N; Deng X; Kohanski R; Levine MA
    Hum Mutat; 2006 Jul; 27(7):717-8. PubMed ID: 16786512
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Angioid streaks and optic disc drusen in cherubism: a case report.
    Mello LGM; Saraiva FP; Monteiro MLR
    Arq Bras Oftalmol; 2020; 83(6):535-537. PubMed ID: 33470282
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NFATc1 and TNFalpha expression in giant cell lesions of the jaws.
    Amaral FR; Brito JA; Perdigão PF; Carvalho VM; de Souza PE; Gomez MV; De Marco L; Gomez RS
    J Oral Pathol Med; 2010 Mar; 39(3):269-74. PubMed ID: 20002873
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinicopathologic and Molecular Characteristics of Familial Cherubism with Associated Odontogenic Tumorous Proliferations.
    Argyris PP; Gopalakrishnan R; Hu Y; Reichenberger EJ; Koutlas IG
    Head Neck Pathol; 2018 Mar; 12(1):136-144. PubMed ID: 28721660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cherubism: a case report.
    Dincă O; Severin E; Vlădan C; Bodnar DC; Bucur A
    Rom J Morphol Embryol; 2014; 55(2 Suppl):655-8. PubMed ID: 25178340
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.