BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 15121283)

  • 1. Re: Silva EC, Souza PEA, Barreto DC, Dias RP, Gomez RS, An extreme case of cherubism (Br J Oral Maxillofac Surg 2002;40:45-8).
    Karaca I; Ugar DA
    Br J Oral Maxillofac Surg; 2004 Jun; 42(3):274; author reply 274. PubMed ID: 15121283
    [No Abstract]   [Full Text] [Related]  

  • 2. SOS1: a new player in the Noonan-like/multiple giant cell lesion syndrome.
    Hanna N; Parfait B; Talaat IM; Vidaud M; Elsedfy HH
    Clin Genet; 2009 Jun; 75(6):568-71. PubMed ID: 19438935
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Cherubism in a patient with Noonan syndrome: report of a case.
    Levine B; Skope L; Parker R
    J Oral Maxillofac Surg; 1991 Sep; 49(9):1014-8. PubMed ID: 1886012
    [No Abstract]   [Full Text] [Related]  

  • 5. A missense mutation in the SH3BP2 gene on chromosome 4p16.3 found in a case of nonfamilial cherubism.
    Imai Y; Kanno K; Moriya T; Kayano S; Seino H; Matsubara Y; Yamada A
    Cleft Palate Craniofac J; 2003 Nov; 40(6):632-8. PubMed ID: 14577811
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Noonan syndrome/cherubism association.
    Dunlap C; Neville B; Vickers RA; O'Neil D; Barker B
    Oral Surg Oral Med Oral Pathol; 1989 Jun; 67(6):698-705. PubMed ID: 2740093
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism.
    Ueki Y; Tiziani V; Santanna C; Fukai N; Maulik C; Garfinkle J; Ninomiya C; doAmaral C; Peters H; Habal M; Rhee-Morris L; Doss JB; Kreiborg S; Olsen BR; Reichenberger E
    Nat Genet; 2001 Jun; 28(2):125-6. PubMed ID: 11381256
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Noonan syndrome with giant cell lesions.
    de Lange J; van der Akker HP
    Int J Paediatr Dent; 2006 Jan; 16(1):69. PubMed ID: 16364097
    [No Abstract]   [Full Text] [Related]  

  • 9. Fibrous dysplasia of the maxilla.
    Gadodia A; Seith A
    J Pediatr Surg; 2010 Apr; 45(4):848; author reply 848. PubMed ID: 20385301
    [No Abstract]   [Full Text] [Related]  

  • 10. Noonan-like/multiple giant cell lesion syndrome: report of a case and review of the literature.
    Wolvius EB; de Lange J; Smeets EE; van der Wal KG; van den Akker HP
    J Oral Maxillofac Surg; 2006 Aug; 64(8):1289-92. PubMed ID: 16860226
    [No Abstract]   [Full Text] [Related]  

  • 11. A novel mutation of the SH3BP2 gene in an aggressive case of cherubism.
    Carvalho VM; Perdigão PF; Pimenta FJ; de Souza PE; Gomez RS; De Marco L
    Oral Oncol; 2008 Feb; 44(2):153-5. PubMed ID: 17368082
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism.
    Jafarov T; Ferimazova N; Reichenberger E
    Clin Genet; 2005 Aug; 68(2):190-1. PubMed ID: 15996221
    [No Abstract]   [Full Text] [Related]  

  • 13. Cherubism Study Results May Apply to Common Inflammatory Bone Diseases.
    Dent Today; 2015 May; 34(5):54. PubMed ID: 26473261
    [No Abstract]   [Full Text] [Related]  

  • 14. [Gene mutation and expression of SH-3BP-2 in cherubism].
    Li YW; Meng XM; Yu SF; Gao P
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2009 Apr; 44(4):227-31. PubMed ID: 19576004
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Mutation detection in SH3BP2 gene in a cherubism family].
    Li CY; Yu SF
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2006 Jun; 41(6):368-71. PubMed ID: 16836910
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic aspects of cherubism].
    Brix M; Peters H; Ranfaing E; Ricbourg B
    Rev Stomatol Chir Maxillofac; 2006 Apr; 107(2):105-8. PubMed ID: 16738517
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel nucleotide mutation leading to a recurrent amino acid alteration in SH3BP2 in a patient with cherubism.
    Sangu N; Shimosato T; Inoda H; Shimada S; Shimojima K; Ando T; Yamamoto T
    Congenit Anom (Kyoto); 2013 Dec; 53(4):166-9. PubMed ID: 24712477
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of a Norwegian cherubism cohort; molecular genetic findings, oral manifestations and quality of life.
    Prescott T; Redfors M; Rustad CF; Eiklid KL; Geirdal AØ; Storhaug K; Jensen JL
    Eur J Med Genet; 2013 Mar; 56(3):131-7. PubMed ID: 23298620
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new mutation in the SH3BP2 gene showing reduced penetrance in a family affected with cherubism.
    de Lange J; van Maarle MC; van den Akker HP; Redeker EJ
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 Mar; 103(3):378-81. PubMed ID: 17321449
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.