These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 25119901)

  • 1. [Identification of three novel frameshift mutations in the RUNX2 gene in three sporadic Chinese cases with cleidocranial dysplasia].
    Qi Z; Yang W; Meng Y; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):415-9. PubMed ID: 25119901
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. [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]  

  • 5. Novel mutation of RUNX2 gene in a patient with cleidocranial dysplasia.
    Guo YW; Chiu CY; Liu CL; Jap TS; Lin LY
    Int J Clin Exp Pathol; 2015; 8(1):1057-62. PubMed ID: 25755819
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case.
    Qin XY; Jia PZ; Zhao HX; Li WR; Chen F; Lin JX
    Chin Med J (Engl); 2017 Jan; 130(2):165-170. PubMed ID: 28091408
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia.
    Zhang C; Zheng S; Wang Y; Zhao Y; Zhu J; Ge L
    Mutagenesis; 2010 Nov; 25(6):589-94. PubMed ID: 20702542
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia.
    Gong L; Odilov B; Han F; Liu F; Sun Y; Zhang N; Zuo X; Yang J; Wang S; Hou X; Ren J
    Genes Genomics; 2022 Jun; 44(6):683-690. PubMed ID: 35235174
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia.
    Xu W; Chen Q; Liu C; Chen J; Xiong F; Wu B
    BMC Med Genet; 2017 Feb; 18(1):13. PubMed ID: 28173761
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia.
    Zhang T; Wu J; Zhao X; Hou F; Ma T; Wang H; Zhang X; Zhang X
    Arch Oral Biol; 2019 Apr; 100():49-56. PubMed ID: 30798031
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype-phenotype correlations.
    Yoshida T; Kanegane H; Osato M; Yanagida M; Miyawaki T; Ito Y; Shigesada K
    Blood Cells Mol Dis; 2003; 30(2):184-93. PubMed ID: 12732182
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.