BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 21870721)

  • 1. [Pierre Marie-Sainton cleidocranial dysplasia].
    Diaconescu S; Păduraru G; Vâscu AM; Burlea M
    Rev Med Chir Soc Med Nat Iasi; 2011; 115(2):341-8. PubMed ID: 21870721
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation.
    Suda N; Hamada T; Hattori M; Torii C; Kosaki K; Moriyama K
    Orthod Craniofac Res; 2007 Nov; 10(4):222-5. PubMed ID: 17973689
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. RUNX2 mutations in cleidocranial dysplasia patients.
    Ryoo HM; Kang HY; Lee SK; Lee KE; Kim JW
    Oral Dis; 2010 Jan; 16(1):55-60. PubMed ID: 19744171
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
    Suda N; Hattori M; Kosaki K; Banshodani A; Kozai K; Tanimoto K; Moriyama K
    Orthod Craniofac Res; 2010 Nov; 13(4):197-202. PubMed ID: 21040462
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Orthodontic and oral surgery therapy in cleidocranial dysplasia].
    Balaton G; Tarján I; Balaton P; Barabási Z; Gyulai Gál S; Nagy K; Vajó Z
    Fogorv Sz; 2007 Feb; 100(1):17-21. PubMed ID: 17444132
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cleidocranial dysplasia: oral features and genetic analysis of 11 patients.
    Bufalino A; Paranaíba LM; Gouvêa AF; Gueiros LA; Martelli-Júnior H; Junior JJ; Lopes MA; Graner E; De Almeida OP; Vargas PA; Coletta RD
    Oral Dis; 2012 Mar; 18(2):184-90. PubMed ID: 22023169
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Delayed tooth eruption and suppressed osteoclast number in the eruption pathway of heterozygous Runx2/Cbfa1 knockout mice.
    Yoda S; Suda N; Kitahara Y; Komori T; Ohyama K
    Arch Oral Biol; 2004 Jun; 49(6):435-42. PubMed ID: 15099800
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cleidocranial dysplasia: a case report].
    Kanda M; Kabe S; Kanki T; Sato J; Hasegawa Y
    No Shinkei Geka; 1997 Dec; 25(12):1109-13. PubMed ID: 9430147
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings.
    Visosky AM; Johnson J; Bingea B; Gurney T; Lalwani AK
    Laryngoscope; 2003 Sep; 113(9):1508-14. PubMed ID: 12972925
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. Cleidocranial dysplasia: a family report.
    Chelvan HT; Malathi N; Kailasam V; Ponnudurai A
    J Indian Soc Pedod Prev Dent; 2009; 27(4):249-52. PubMed ID: 19915277
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Syndromes. 1. Cleidocranial dysplasia].
    Freihofer HP
    Ned Tijdschr Tandheelkd; 1998 Jun; 105(6):204-5. PubMed ID: 11928139
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel RUNX2 gene mutation in an Italian family with cleidocranial dysplasia.
    Marchisella C; Rolando F; Muscarella LA; Zelante L; Bracco P; Piemontese MR
    Eur J Orthod; 2011 Oct; 33(5):498-502. PubMed ID: 21131390
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The Pierre Marie-Sainton syndrome].
    Fraysse E; Fraysse H; Dubertrand Y; Bonifassi J; Flach F; Damery C; Barnier G; Perrier d'Arc G
    Rev Stomatol Chir Maxillofac; 1985; 86(2):103-6. PubMed ID: 3858945
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Delayed Eruption In Cleidocranial Dysplasia.
    Ahmed S; Shaheen MN; Hameed F
    J Ayub Med Coll Abbottabad; 2020; 32(3):405-407. PubMed ID: 32829560
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth.
    Anthonappa RP; King NM; Mahmoud Rabie AB
    J Investig Clin Dent; 2013 May; 4(2):124-7. PubMed ID: 23188595
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Orthodontic treatment in a patient with cleidocranial dysostosis.
    Farronato G; Maspero C; Farronato D; Gioventù S
    Angle Orthod; 2009 Jan; 79(1):178-85. PubMed ID: 19123713
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations.
    Cunningham ML; Seto ML; Hing AV; Bull MJ; Hopkin RJ; Leppig KA
    Birth Defects Res A Clin Mol Teratol; 2006 Feb; 76(2):78-85. PubMed ID: 16463420
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.