BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

70 related articles for article (PubMed ID: 24554542)

  • 1. Identification of genetic risk factors for maxillary lateral incisor agenesis.
    Alves-Ferreira M; Pinho T; Sousa A; Sequeiros J; Lemos C; Alonso I
    J Dent Res; 2014 May; 93(5):452-8. PubMed ID: 24554542
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review.
    Tallón-Walton V; Manzanares-Céspedes MC; Carvalho-Lobato P; Valdivia-Gandur I; Arte S; Nieminen P
    Med Oral Patol Oral Cir Bucal; 2014 May; 19(3):e248-54. PubMed ID: 24316698
    [TBL] [Abstract][Full Text] [Related]  

  • 3. "Examining the link between tooth agenesis and papillary thyroid cancer: is there a risk factor?" Observational study.
    Matošić Ž; Šimunović L; Jukić T; Granić R; Meštrović S
    Prog Orthod; 2024 Mar; 25(1):12. PubMed ID: 38523193
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Gene Network Underlying Hypodontia.
    Yin W; Bian Z
    J Dent Res; 2015 Jul; 94(7):878-85. PubMed ID: 25910507
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenitally missing maxillary lateral incisors: update on the functional and esthetic parameters of patients treated with implants or space closure and teeth recontouring.
    Pini NI; Marchi LM; Pascotto RC
    Open Dent J; 2014; 8():289-94. PubMed ID: 25646137
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis.
    Sarkar T; Bansal R; Das P
    PLoS One; 2014; 9(9):e106811. PubMed ID: 25203534
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.
    Yamaguchi S; Machida J; Kamamoto M; Kimura M; Shibata A; Tatematsu T; Miyachi H; Higashi Y; Jezewski P; Nakayama A; Shimozato K; Tokita Y
    PLoS One; 2014; 9(8):e102944. PubMed ID: 25101640
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia.
    Wong SW; Liu HC; Han D; Chang HG; Zhao HS; Wang YX; Feng HL
    Mutagenesis; 2014 Sep; 29(5):319-23. PubMed ID: 24914010
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.
    Peters H; Neubüser A; Kratochwil K; Balling R
    Genes Dev; 1998 Sep; 12(17):2735-47. PubMed ID: 9732271
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
    Vastardis H; Karimbux N; Guthua SW; Seidman JG; Seidman CE
    Nat Genet; 1996 Aug; 13(4):417-21. PubMed ID: 8696335
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypodontia: An Update on Its Etiology, Classification, and Clinical Management.
    Al-Ani AH; Antoun JS; Thomson WM; Merriman TR; Farella M
    Biomed Res Int; 2017; 2017():9378325. PubMed ID: 28401166
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Not Available].
    Dallel I; Marwen W; Ben Abdallah S; Tobji S; Ben Amor A; Canal P
    Int Orthod; 2018 Jun; 16(2):384-407. PubMed ID: 29650345
    [No Abstract]   [Full Text] [Related]  

  • 13. "Maxillary lateral incisor partial anodontia sequence": a clinical entity with epigenetic origin.
    Consolaro A; Cardoso MA; Consolaro RB
    Dental Press J Orthod; 2017; 22(6):28-34. PubMed ID: 29364376
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tooth agenesis: An overview of diagnosis, aetiology and management.
    Meade MJ; Dreyer CW
    Jpn Dent Sci Rev; 2023 Dec; 59():209-218. PubMed ID: 37645267
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The investigation of WNT6 and WNT10A single nucleotide polymorphisms as potential biomarkers for dental pulp calcification in orthodontic patients.
    Ramirez I; Kirschneck C; Corrêa Silva-Sousa A; Proff P; S Antunes L; Gabbardo MCL; Silva Barroso de Oliveira D; Sousa-Neto MD; Baratto-Filho F; Küchler EC
    PLoS One; 2023; 18(8):e0288782. PubMed ID: 37566620
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report.
    Reis PM; Faber J; Rosa JS; Bueno M; Barriviera M; Lia ÉN
    Int J Clin Pediatr Dent; 2023; 16(1):147-152. PubMed ID: 37020764
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic/Protein Association of Atopic Dermatitis and Tooth Agenesis.
    Ouyang W; Goh CE; Ng WB; Chew FT; Yap EPH; Hsu CS
    Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36982827
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic and Morphological Variation in Hypodontia of Maxillary Lateral Incisors.
    Kerekes-Máthé B; Mártha K; Bănescu C; O'Donnell MB; Brook AH
    Genes (Basel); 2023 Jan; 14(1):. PubMed ID: 36672972
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maxillary lateral incisor agenesis is associated with maxillary form: a geometric morphometric analysis.
    Nemec M; Schwarz L; Bertl MH; Bertl K; Gahleitner A; Mitteroecker P; Jonke E
    Clin Oral Investig; 2023 Mar; 27(3):1063-1070. PubMed ID: 36036293
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bidimensional system for space closure treatment of missing lateral incisors: 10 years follow-up.
    Greco M; Rosa M; Rombolà A
    J Orthod Sci; 2021; 10():24. PubMed ID: 34760817
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.