thymine has been researched along with Dental Enamel Hypoplasia in 8 studies
Dental Enamel Hypoplasia: An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Our findings confirm that APECED causes enamel defects that are individually but chronologically distributed, and can alter enamel development early enough to affect deciduous teeth." | 1.35 | Clinical and microstructural aberrations of enamel of deciduous and permanent teeth in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. ( Pavlic, A; Waltimo-Sirén, J, 2009) |
| "Our findings confirm that APECED causes enamel defects that are individually but chronologically distributed, and can alter enamel development early enough to affect deciduous teeth." | 1.35 | Clinical and microstructural aberrations of enamel of deciduous and permanent teeth in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. ( Pavlic, A; Waltimo-Sirén, J, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (50.00) | 29.6817 |
| 2010's | 4 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wang, S | 1 |
| Choi, M | 1 |
| Richardson, AS | 2 |
| Reid, BM | 1 |
| Seymen, F | 3 |
| Yildirim, M | 2 |
| Tuna, E | 1 |
| Gençay, K | 2 |
| Simmer, JP | 3 |
| Hu, JC | 3 |
| Lee, KE | 3 |
| Koruyucu, M | 1 |
| Bayram, M | 1 |
| Tuna, EB | 2 |
| Lee, ZH | 1 |
| Kim, JW | 4 |
| Pavlic, A | 2 |
| Waltimo-Sirén, J | 2 |
| Kang, HY | 1 |
| Lee, SK | 2 |
| Patir, A | 1 |
| Chan, HC | 1 |
| Mai, L | 1 |
| Oikonomopoulou, A | 1 |
| Chan, HL | 1 |
| Wang, SK | 1 |
| Hwang, YH | 1 |
| Kida, M | 1 |
| Tsutsumi, T | 1 |
| Ariga, T | 1 |
| Park, JC | 1 |
| Hu, YY | 1 |
| Lin, BP | 1 |
| Boyd, C | 1 |
| Wright, JT | 1 |
| Yamada, CJ | 1 |
| Rayes, SK | 1 |
| Feigal, RJ | 1 |
8 other studies available for thymine and Dental Enamel Hypoplasia
| Article | Year |
|---|---|
STIM1 and SLC24A4 Are Critical for Enamel Maturation.
Topics: Alanine; Ameloblasts; Amelogenesis; Animals; Antiporters; Arginine; Calcium Signaling; Child; Child, | 2014 |
ENAM mutations with incomplete penetrance.
Topics: Adolescent; Amelogenesis Imperfecta; Child; Chromosome Segregation; Codon, Nonsense; Codon, Terminat | 2014 |
Clinical and microstructural aberrations of enamel of deciduous and permanent teeth in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.
Topics: Adolescent; AIRE Protein; Amelogenesis; Child; Cytosine; Dental Enamel; Dental Enamel Hypoplasia; DN | 2009 |
Candidate gene strategy reveals ENAM mutations.
Topics: Adenine; Amelogenesis Imperfecta; Amino Acid Sequence; Codon, Nonsense; Dental Enamel Hypoplasia; De | 2009 |
Clinical and microstructural aberrations of enamel of deciduous and permanent teeth in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.
Topics: Adolescent; AIRE Protein; Amelogenesis; Arginine; Asparagine; Child; Cuspid; Cytosine; Dental Enamel | 2009 |
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
Topics: Adenine; Alleles; Amelogenesis Imperfecta; Amino Acid Sequence; Calcium; Casein Kinases; Cytosine; D | 2010 |
Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.
Topics: Adenine; Amelogenesis; Aspartic Acid; Child; Dental Enamel Hypoplasia; Dentin Dysplasia; Dentinogene | 2011 |
Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Amelogenin; Child; Codon; Cytosine; Dental Enamel; Dental Enamel Hypoplasia | 2004 |