BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 16836910)

  • 21. SH3BP2-encoding exons involved in cherubism are not associated with central giant cell granuloma.
    Teixeira RC; Horz HP; Damante JH; Garlet GP; Santos CF; Nogueira RL; Cavalcante RB; Conrads G
    Int J Oral Maxillofac Surg; 2011 Aug; 40(8):851-5. PubMed ID: 21680150
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Cherubism].
    Brix M; Peters H; Lebeau J
    Rev Stomatol Chir Maxillofac; 2009 Nov; 110(5):293-8. PubMed ID: 19836038
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Clinical and genetic analysis of patients with cherubism.
    Machado RA; Pontes H; Pires FR; Silveira HM; Bufalino A; Carlos R; Tuji FM; Alves D; Santos-Silva AR; Lopes MA; Capistrano HM; Coletta RD; Fonseca FP
    Oral Dis; 2017 Nov; 23(8):1109-1115. PubMed ID: 28644570
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Study on TR beta gene mutation in a thyroid hormone resistance syndrome family].
    Liu JF; Shi BY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):423-6. PubMed ID: 16883531
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. [SH3BP2 heterozygous mutation amplifies macrophage inflammatory responses to infection in a mouse model of cherubism].
    Deckert M; Prod'Homme V
    Med Sci (Paris); 2015; 31(6-7):589-91. PubMed ID: 26152156
    [No Abstract]   [Full Text] [Related]  

  • 28. Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Law LK; Tang NL; Hui J; Fung SL; Ruiter J; Wanders RJ; Fok TF; Lam CW
    Clin Chim Acta; 2009 Jun; 404(2):95-9. PubMed ID: 19265687
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two new mutations in the keratin 4 gene causing oral white sponge nevus in Chinese family.
    Zhang JM; Yang ZW; Chen RY; Gao P; Zhang YR; Zhang LF
    Oral Dis; 2009 Jan; 15(1):100-5. PubMed ID: 18992023
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Jawing about TNF: new hope for cherubism.
    Novack DV; Faccio R
    Cell; 2007 Jan; 128(1):15-7. PubMed ID: 17218248
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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]  

  • 32. [Mutations in the ED1 gene in families with X-linked hypohidrotic ectodermal dysplasia].
    Fan HL; Ye XQ; Shi B; Zhang YL; Bian Z
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2007 May; 42(5):272-5. PubMed ID: 17686277
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Approaches to detect the gene mutations in autosomal recessive Alport's syndrome: analysis of a family].
    Hou P; Lü JC; Chen YQ; Ding JX; Li GT; Zhang H
    Zhonghua Yi Xue Za Zhi; 2008 Feb; 88(8):573-5. PubMed ID: 18649777
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Pro416Arg cherubism mutation in Sh3bp2 knock-in mice affects osteoblasts and alters bone mineral and matrix properties.
    Wang CJ; Chen IP; Koczon-Jaremko B; Boskey AL; Ueki Y; Kuhn L; Reichenberger EJ
    Bone; 2010 May; 46(5):1306-15. PubMed ID: 20117257
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.
    Tian X; Fujiki K; Zhang Y; Murakami A; Li Q; Kanai A; Wang W; Hao Y; Ma Z
    Am J Ophthalmol; 2007 Sep; 144(3):473-5. PubMed ID: 17765440
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Analysis of ARSA mutations in a Chinese family with metachromatic leukodystrophy].
    Wang JM; Jiang YW; Shi HP; Zhang WM; Pan H; Bao XH; Wu Y; Qin J; Wu XR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):378-82. PubMed ID: 16883521
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cherubism - new hypotheses on pathogenesis and therapeutic consequences.
    Hyckel P; Berndt A; Schleier P; Clement JH; Beensen V; Peters H; Kosmehl H
    J Craniomaxillofac Surg; 2005 Feb; 33(1):61-8. PubMed ID: 15694152
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Identification of two novel mutations of human blood coagulation factor V gene in a Chinese family with congenital factor V deficiency].
    Zheng WD; Liu YH; Liu HF; Chen ZH; Wang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Oct; 23(5):515-8. PubMed ID: 17029198
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.