Tooth agenesis: from molecular genetics to molecular dentistry. (Q37198331)

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scientific article published on July 2008

Language	Label	Description	Also known as
English	Tooth agenesis: from molecular genetics to molecular dentistry.	scientific article published on July 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18573979%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

Europe PubMed Central

Tooth agenesis: from molecular genetics to molecular dentistry (English)

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18573979%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18573979%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Abigail S. Tucker

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18573979%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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E Matalova

1

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Europe PubMed Central

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9 January 2020

J Fleischmannova

2

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Europe PubMed Central

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9 January 2020

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publication date

1 July 2008

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9 January 2020

Journal of Dental Research

1 reference

Europe PubMed Central

PubMed publication ID

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9 January 2020

87

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9 January 2020

7

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9 January 2020

617-623

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9 January 2020

Implants for life? A critical review of implant-supported restorations

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The impact of tissue engineering on dentistry

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Mouse models of tooth abnormalities

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Gene defect in ectodermal dysplasia implicates a death domain adapter in development

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Tissue engineering of tooth crown, root, and periodontium.

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A nonsense mutation in MSX1 causes Witkop syndrome

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Genes affecting tooth morphogenesis.

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Implant surfaces and interface processes

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X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

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Novel MSX1 frameshift causes autosomal-dominant oligodontia

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Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

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Anomalies of tooth formation in hypohidrotic ectodermal dysplasia.

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The role of MSX1 in human tooth agenesis

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Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

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Function of Rieger syndrome gene in left-right asymmetry and craniofacial development

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Craniofacial tissue engineering by stem cells

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Long-term effects of chemotherapy on dental status in children treated for nephroblastoma

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Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans

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Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

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Biomolecular modification of implant surfaces

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Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis

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Mouse Otlx2/RIEG expression in the odontogenic epithelium precedes tooth initiation and requires mesenchyme-derived signals for its maintenance.

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Tooth regeneration: implications for the use of bioengineered organs in first-wave organ replacement

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Studies on Pax9-Msx1 protein interactions

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Stem-cell-based tissue engineering of murine teeth.

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Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development

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The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations

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Antibiotic prophylaxis and postoperative complications after tooth extraction and implant placement: a review of the literature

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Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region

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Mutation of PAX9 is associated with oligodontia

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In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

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MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

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Influence of inflammatory reactions vs. occlusal loading on peri-implant marginal bone level

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A human MSX1 homeodomain missense mutation causes selective tooth agenesis

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MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.

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