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Journal Abstract Search

185 related items for PubMed ID: 28703881

  • 1. A novel RUNX2 mutation in exon 8, G462X, in a patient with Cleidocranial Dysplasia.
    Jung YJ, Bae HS, Ryoo HM, Baek SH.
    J Cell Biochem; 2018 Jan; 119(1):1152-1162. PubMed ID: 28703881
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  • 4. RUNX2 mutation impairs osteogenic differentiation of dental follicle cells.
    Liu Y, Sun X, Zhang X, Wang X, Zhang C, Zheng S.
    Arch Oral Biol; 2019 Jan; 97():156-164. PubMed ID: 30391791
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  • 6. 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 01; 32(4):437-443. PubMed ID: 28505335
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  • 7. 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 07; 18(1):13. PubMed ID: 28173761
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  • 9. Functional analysis of novel RUNX2 mutations identified in patients with cleidocranial dysplasia.
    Hordyjewska-Kowalczyk E, Sowińska-Seidler A, Olech EM, Socha M, Glazar R, Kruczek A, Latos-Bieleńska A, Tylzanowski P, Jamsheer A.
    Clin Genet; 2019 Nov 07; 96(5):429-438. PubMed ID: 31347140
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  • 11. Genome sequencing identified a novel exonic microdeletion in the RUNX2 gene that causes cleidocranial dysplasia.
    Zhang J, Li YZ, Chen WQ, Yuan JY, Li Q, Meng YX, Yu YD, Guo Q.
    Clin Chim Acta; 2022 Mar 01; 528():6-12. PubMed ID: 35065050
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  • 12. Abnormal bone remodelling activity of dental follicle cells from a cleidocranial dysplasia patient.
    Liu Y, Zhang X, Sun X, Wang X, Zhang C, Zheng S.
    Oral Dis; 2018 Oct 01; 24(7):1270-1281. PubMed ID: 29787635
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  • 15. Dental Follicle Cells Participate in Tooth Eruption via the RUNX2-MiR-31-SATB2 Loop.
    Ge J, Guo S, Fu Y, Zhou P, Zhang P, Du Y, Li M, Cheng J, Jiang H.
    J Dent Res; 2015 Jul 01; 94(7):936-44. PubMed ID: 25818585
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  • 16. 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 01; 100():49-56. PubMed ID: 30798031
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  • 18. 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 01; 44(6):683-690. PubMed ID: 35235174
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  • 19. 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 Jun 01; 12(7):e0181653. PubMed ID: 28738062
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