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Journal Abstract Search

276 related items for PubMed ID: 16270353

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. The cleidocranial dysplasia-related R131G mutation in the Runt-related transcription factor RUNX2 disrupts binding to DNA but not CBF-beta.
    Han MS, Kim HJ, Wee HJ, Lim KE, Park NR, Bae SC, van Wijnen AJ, Stein JL, Lian JB, Stein GS, Choi JY.
    J Cell Biochem; 2010 May; 110(1):97-103. PubMed ID: 20225274
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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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  • 6. 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 Jul 01; 12(7):e0181653. PubMed ID: 28738062
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  • 7. A novel RUNX2 mutation in cleidocranial dysplasia patients.
    Xuan D, Li S, Zhang X, Lin L, Wang C, Zhang J.
    Biochem Genet; 2008 Dec 01; 46(11-12):702-7. PubMed ID: 18777095
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  • 8. A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia.
    Zeng L, Wei J, Zhao N, Sun S, Wang Y, Feng H.
    Arch Oral Biol; 2018 Dec 01; 96():243-248. PubMed ID: 29089101
    [Abstract] [Full Text] [Related]

  • 9. 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 Dec 01; 37(2):115-20. PubMed ID: 17522365
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  • 10. PEBP2alphaA/CBFA1 mutations in Japanese cleidocranial dysplasia patients.
    Zhang YW, Yasui N, Kakazu N, Abe T, Takada K, Imai S, Sato M, Nomura S, Ochi T, Okuzumi S, Nogami H, Nagai T, Ohashi H, Ito Y.
    Gene; 2000 Feb 22; 244(1-2):21-8. PubMed ID: 10689183
    [Abstract] [Full Text] [Related]

  • 11. 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 22; 119(1):1152-1162. PubMed ID: 28703881
    [Abstract] [Full Text] [Related]

  • 12. 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 22; 96(5):429-438. PubMed ID: 31347140
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  • 13. 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 20; 130(2):165-170. PubMed ID: 28091408
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  • 15. 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 20; 37(5):772-776. PubMed ID: 29058294
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  • 16. 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 20; 121(3 Pt 1):142-7. PubMed ID: 23659235
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  • 19. 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 15; 111(6):1473-81. PubMed ID: 20872798
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