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 *

95 related articles for article (PubMed ID: 12269998)

  • 1. Common mutations and independent assortment of CCD.
    Baumert U; Golan I; Müssig D
    J Oral Pathol Med; 2002 Oct; 31(9):567-8. PubMed ID: 12269998
    [No Abstract]   [Full Text] [Related]  

  • 2. Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip.
    Yamachika E; Tsujigiwa H; Ishiwari Y; Mizukawa N; Nagai N; Sugahara T
    J Oral Pathol Med; 2001 Jul; 30(6):381-3. PubMed ID: 11459326
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the RUNX2 gene in patients with cleidocranial dysplasia.
    Otto F; Kanegane H; Mundlos S
    Hum Mutat; 2002 Mar; 19(3):209-16. PubMed ID: 11857736
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.
    Zhou G; Chen Y; Zhou L; Thirunavukkarasu K; Hecht J; Chitayat D; Gelb BD; Pirinen S; Berry SA; Greenberg CR; Karsenty G; Lee B
    Hum Mol Genet; 1999 Nov; 8(12):2311-6. PubMed ID: 10545612
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
    Mundlos S; Otto F; Mundlos C; Mulliken JB; Aylsworth AS; Albright S; Lindhout D; Cole WG; Henn W; Knoll JH; Owen MJ; Mertelsmann R; Zabel BU; Olsen BR
    Cell; 1997 May; 89(5):773-9. PubMed ID: 9182765
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of a Japanese patient with cleidocranial dysplasia possessing a mutation of CBFA1 gene.
    Sakai N; Hasegawa H; Yamazaki Y; Ui K; Tokunaga K; Hirose R; Uchinuma E; Susami T; Takato T
    J Craniofac Surg; 2002 Jan; 13(1):31-4. PubMed ID: 11886988
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
    Lee B; Thirunavukkarasu K; Zhou L; Pastore L; Baldini A; Hecht J; Geoffroy V; Ducy P; Karsenty G
    Nat Genet; 1997 Jul; 16(3):307-10. PubMed ID: 9207800
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The etiologic factor of cleidocranial dysplasia.
    Golan I; Baumert U; Muessig D
    J Allergy Clin Immunol; 2001 Sep; 108(3):469. PubMed ID: 11544473
    [No Abstract]   [Full Text] [Related]  

  • 9. [Application of genetics in dentistry].
    Ochiai S
    Nihon Shika Ishikai Zasshi; 1965 Sep; 18(6):467-74. PubMed ID: 5220198
    [No Abstract]   [Full Text] [Related]  

  • 10. Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.
    Tessa A; Salvi S; Casali C; Garavelli L; Digilio MC; Dotti MT; Di Giandomenico S; Valoppi M; Grieco GS; Comanducci G; Bianchini G; Fortini D; Federico A; Giannotti A; Santorelli FM
    Hum Mutat; 2003 Jul; 22(1):104. PubMed ID: 12815605
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia.
    Machuca-Tzili L; Monroy-Jaramillo N; González-del Angel A; Kofman-Alfaro S
    Clin Genet; 2002 May; 61(5):349-53. PubMed ID: 12081718
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia.
    Giannotti A; Tessa A; Patrono C; Florio LD; Velardo M; Dionisi-Vici C; Bertini E; Santorelli FM
    Hum Mutat; 2000 Sep; 16(3):277. PubMed ID: 10980549
    [No Abstract]   [Full Text] [Related]  

  • 13. Radiological findings and molecular genetic confirmation of cleidocranial dysplasia.
    Golan I; Baumert U; Held P; Feuerbach S; Müssig D
    Clin Radiol; 2002 Jun; 57(6):525-9. PubMed ID: 12069472
    [No Abstract]   [Full Text] [Related]  

  • 14. RUNX genes, neoplasia, and cleidocranial dysplasia.
    Cohen MM
    Am J Med Genet; 2001 Dec; 104(3):185-8. PubMed ID: 11754042
    [No Abstract]   [Full Text] [Related]  

  • 15. A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia.
    Zhang YW; Yasui N; Ito K; Huang G; Fujii M; Hanai J; Nogami H; Ochi T; Miyazono K; Ito Y
    Proc Natl Acad Sci U S A; 2000 Sep; 97(19):10549-54. PubMed ID: 10962029
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 244(1-2):21-8. PubMed ID: 10689183
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case of Japanese cleidocranial dysplasia with a CBFA1 frameshift mutation.
    Yokozeki M; Ohyama K; Tsuji M; Goseki-Sone M; Oida S; Orimo H; Moriyama K; Kuroda T
    J Craniofac Genet Dev Biol; 2000; 20(3):121-6. PubMed ID: 11321596
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development.
    Otto F; Thornell AP; Crompton T; Denzel A; Gilmour KC; Rosewell IR; Stamp GW; Beddington RS; Mundlos S; Olsen BR; Selby PB; Owen MJ
    Cell; 1997 May; 89(5):765-71. PubMed ID: 9182764
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Targeted reversion of induced pluripotent stem cells from patients with human cleidocranial dysplasia improves bone regeneration in a rat calvarial bone defect model.
    Saito A; Ooki A; Nakamura T; Onodera S; Hayashi K; Hasegawa D; Okudaira T; Watanabe K; Kato H; Onda T; Watanabe A; Kosaki K; Nishimura K; Ohtaka M; Nakanishi M; Sakamoto T; Yamaguchi A; Sueishi K; Azuma T
    Stem Cell Res Ther; 2018 Jan; 9(1):12. PubMed ID: 29357927
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 32(4):437-443. PubMed ID: 28505335
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.