BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 19515746)

  • 1. RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
    Li Y; Pan W; Xu W; He N; Chen X; Liu H; Darryl Quarles L; Zhou H; Xiao Z
    Mutagenesis; 2009 Sep; 24(5):425-31. PubMed ID: 19515746
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel small deletion mutation in RUNX2 gene in one Chinese family with cleidocranial dysplasia.
    Chen T; Hou J; Hu LL; Gao J; Wu BL
    Int J Clin Exp Pathol; 2014; 7(5):2490-5. PubMed ID: 24966961
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the RUNX2 gene in Chinese patients with cleidocranial dysplasia.
    Xuan D; Li S; Zhang X; Hu F; Lin L; Wang C; Zhang J
    Ann Clin Lab Sci; 2008; 38(1):15-24. PubMed ID: 18316777
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of novel RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
    Zhang X; Liu Y; Wang X; Sun X; Zhang C; Zheng S
    PLoS One; 2017; 12(7):e0181653. PubMed ID: 28738062
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia.
    Fang CY; Xue JJ; Tan L; Jiang CH; Gao QP; Liang DS; Wu LQ
    Genet Mol Res; 2011 Dec; 10(4):3539-44. PubMed ID: 22194205
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia.
    Wang GX; Sun RP; Song FL
    Genet Mol Res; 2010 Jan; 9(1):41-7. PubMed ID: 20082269
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel RUNX2 frameshift mutations in Chinese patients with cleidocranial dysplasia.
    Huang Y; Song Y; Zhang C; Chen G; Wang S; Bian Z
    Eur J Oral Sci; 2013 Jun; 121(3 Pt 1):142-7. PubMed ID: 23659235
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Two novel RUNX2 gene mutations in two Chinese families with cleidocranial dysplasia].
    Gao C; Wu L; Geng XJ; Song LJ; Luo Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):140-3. PubMed ID: 20376792
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype.
    Kim HJ; Nam SH; Kim HJ; Park HS; Ryoo HM; Kim SY; Cho TJ; Kim SG; Bae SC; Kim IS; Stein JL; van Wijnen AJ; Stein GS; Lian JB; Choi JY
    J Cell Physiol; 2006 Apr; 207(1):114-22. PubMed ID: 16270353
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia.
    Zeng L; Wei J; Han D; Liu H; Liu Y; Zhao N; Sun S; Wang Y; Feng H
    Mutagenesis; 2017 Jul; 32(4):437-443. PubMed ID: 28505335
    [TBL] [Abstract][Full Text] [Related]  

  • 11. RUNX2 mutations in cleidocranial dysplasia.
    Lee KE; Seymen F; Ko J; Yildirim M; Tuna EB; Gencay K; Kim JW
    Genet Mol Res; 2013 Oct; 12(4):4567-74. PubMed ID: 24222232
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mutation analysis of the RUNX2 gene in a family with cleidocranial dysplasia].
    Jiang T; Jiang X; Zhang Y
    Hua Xi Kou Qiang Yi Xue Za Zhi; 2013 Oct; 31(5):522-5. PubMed ID: 24298808
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel RUNX2 mutations in Chinese individuals with cleidocranial dysplasia.
    Zhang CY; Zheng SG; Wang YX; Zhu JX; Zhu X; Zhao YM; Ge LH
    J Dent Res; 2009 Sep; 88(9):861-6. PubMed ID: 19767586
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation in the C-terminal region of RUNX2/CBFA1 distal to the DNA-binding runt domain in a Japanese patient with cleidocranial dysplasia.
    Kamamoto M; Machida J; Miyachi H; Ono T; Nakayama A; Shimozato K; Tokita Y
    Int J Oral Maxillofac Surg; 2011 Apr; 40(4):434-7. PubMed ID: 21115325
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel Alu-mediated microdeletion in the RUNX2 gene in a Chinese patient with cleidocranial dysplasia.
    Qian Y; Zhang Y; Wei B; Zhang M; Yang J; Leng C; Ge Z; Xu X; Sun M
    J Genet; 2018 Mar; 97(1):137-143. PubMed ID: 29666333
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effect of cleidocranial dysplasia-related novel mutation of RUNX2 on characteristics of dental pulp cells and tooth development.
    Xuan D; Sun X; Yan Y; Xie B; Xu P; Zhang J
    J Cell Biochem; 2010 Dec; 111(6):1473-81. PubMed ID: 20872798
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel gene mutation of Runx2 in cleidocranial dysplasia.
    Peng YJ; Chen QY; Fu DJ; Liu ZM; Mao TT; Li J; She WT
    J Huazhong Univ Sci Technolog Med Sci; 2017 Oct; 37(5):772-776. PubMed ID: 29058294
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Clinical and image features, and identification of pathogenic gene mutation of two cleidocranial dysplasia families].
    Wang GX; Ma LX; Xu WF; Song FL; Sun RP
    Zhonghua Er Ke Za Zhi; 2010 Nov; 48(11):834-8. PubMed ID: 21215027
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation of gene CBFA1/RUNX2 in cleidocranial dysplasia.
    Lo Muzio L; Tetè S; Mastrangelo F; Cazzolla AP; Lacaita MG; Margaglione M; Campisi G
    Ann Clin Lab Sci; 2007; 37(2):115-20. PubMed ID: 17522365
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Role of the RUNX2 p.R225Q mutation in cleidocranial dysplasia: a rare presentation and an analysis of the RUNX2 protein structure.
    Wu LZ; Su WQ; Liu YF; Ge X; Zhang Y; Wang XJ
    Genet Mol Res; 2014 Feb; 13(1):1187-94. PubMed ID: 24634175
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.