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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

262 related items for PubMed ID: 21040462

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. [Inter- and intrafamilial expression of cleidocranial dysostosis].
    Golan I, Baumert U, Pragier R, Aknin JJ, Rodde J, Müssig D.
    Orthod Fr; 2003 Mar 15; 74(1):7-13. PubMed ID: 15301373
    [Abstract] [Full Text] [Related]

  • 23. Molecular Genetics of Cleidocranial Dysplasia.
    Motaei J, Salmaninejad A, Jamali E, Khorsand I, Ahmadvand M, Shabani S, Karimi F, Nazari MS, Ketabchi G, Naqipour F.
    Fetal Pediatr Pathol; 2021 Oct 15; 40(5):442-454. PubMed ID: 31984822
    [Abstract] [Full Text] [Related]

  • 24. [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 15; 48(11):834-8. PubMed ID: 21215027
    [Abstract] [Full Text] [Related]

  • 25. 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 Nov 15; 30(2):184-93. PubMed ID: 12732182
    [Abstract] [Full Text] [Related]

  • 26. 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 15; 40(4):434-7. PubMed ID: 21115325
    [Abstract] [Full Text] [Related]

  • 27. 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 15; 94(7):936-44. PubMed ID: 25818585
    [Abstract] [Full Text] [Related]

  • 28. The effect of the cleidocranial dysplasia-related novel 1116_1119insC mutation in the RUNX2 gene on the biological function of mesenchymal cells.
    Ding B, Li C, Xuan K, Liu N, Tang L, Liu Y, Guo W, Liu W, Jin Y.
    Eur J Med Genet; 2013 Apr 15; 56(4):180-7. PubMed ID: 23376464
    [Abstract] [Full Text] [Related]

  • 29. Classical cleidocranial dysplasia in an adult, due to a novel frameshift pathogenic variant in RUNX2.
    Hebbar M, Girisha KM, Shukla A.
    BMJ Case Rep; 2016 May 13; 2016():. PubMed ID: 27177937
    [Abstract] [Full Text] [Related]

  • 30. Identification of a novel frameshift mutation (383insT) in the RUNX2 (PEBP2 alpha/CBFA1/AML3) gene in a Japanese patient with cleidocranial dysplasia.
    Goseki-Sone M, Orimo H, Watanabe A, Hamatani R, Yokozeki M, Ohyama K, Kuroda T, Watanabe H, Miyazaki H, Shimada T, Oida S.
    J Bone Miner Metab; 2001 May 13; 19(4):263-6. PubMed ID: 11448020
    [Abstract] [Full Text] [Related]

  • 31. Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report.
    Inchingolo AD, Patano A, Coloccia G, Ceci S, Inchingolo AM, Marinelli G, Malcangi G, Montenegro V, Laudadio C, Palmieri G, Bordea IR, Ponzi E, Orsini P, Ficarella R, Scarano A, Lorusso F, Dipalma G, Corsalini M, Gentile M, Venere DD, Inchingolo F.
    Medicina (Kaunas); 2021 Dec 10; 57(12):. PubMed ID: 34946295
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review.
    Ma D, Wang X, Guo J, Zhang J, Cai T.
    Medicine (Baltimore); 2018 Aug 10; 97(32):e11328. PubMed ID: 30095610
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Intrafamilial variability in cleidocranial dysplasia: a three generation family.
    Chitayat D, Hodgkinson KA, Azouz EM.
    Am J Med Genet; 1992 Feb 01; 42(3):298-303. PubMed ID: 1536165
    [Abstract] [Full Text] [Related]

  • 39. Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia.
    Quack I, Vonderstrass B, Stock M, Aylsworth AS, Becker A, Brueton L, Lee PJ, Majewski F, Mulliken JB, Suri M, Zenker M, Mundlos S, Otto F.
    Am J Hum Genet; 1999 Nov 01; 65(5):1268-78. PubMed ID: 10521292
    [Abstract] [Full Text] [Related]

  • 40. Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia.
    Bergwitz C, Prochnau A, Mayr B, Kramer FJ, Rittierodt M, Berten HL, Hausamen JE, Brabant G.
    J Inherit Metab Dis; 2001 Nov 01; 24(6):648-56. PubMed ID: 11768584
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 14.