Page last updated: 2024-10-16

adenine and Dentin Dysplasia

adenine has been researched along with Dentin Dysplasia in 3 studies

Dentin Dysplasia: An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)

Research Excerpts

ExcerptRelevanceReference
"Hypophosphatasia is caused by mutations of the tissue-non-specific alkaline phosphatase (TNSALP) gene with deficiency of dentin structure."1.36Genetic etiology and dental pulp cell deficiency of hypophosphatasia. ( Gan, Y; Ge, L; Lei, H; Li, J; Liu, H; Zhu, T, 2010)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Liu, H1
Li, J1
Lei, H1
Zhu, T1
Gan, Y1
Ge, L1
Lee, SK2
Lee, KE2
Hwang, YH1
Kida, M1
Tsutsumi, T1
Ariga, T1
Park, JC1
Kim, JW2
Jung, SE1
Lee, Zh1

Other Studies

3 other studies available for adenine and Dentin Dysplasia

ArticleYear
Genetic etiology and dental pulp cell deficiency of hypophosphatasia.
    Journal of dental research, 2010, Volume: 89, Issue:12

    Topics: Adenine; Alkaline Phosphatase; Cells, Cultured; Child; Child, Preschool; Dental Cementum; Dental Ena

2010
Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.
    Oral diseases, 2011, Volume: 17, Issue:3

    Topics: Adenine; Amelogenesis; Aspartic Acid; Child; Dental Enamel Hypoplasia; Dentin Dysplasia; Dentinogene

2011
Functional splicing assay of DSPP mutations in hereditary dentin defects.
    Oral diseases, 2011, Volume: 17, Issue:7

    Topics: Adenine; Codon, Nonsense; Conserved Sequence; Cytosine; Dentin Dysplasia; Dentinogenesis Imperfecta;

2011