adenine has been researched along with Amelogenesis Imperfecta in 9 studies
Amelogenesis Imperfecta: A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The proven candidate genes for amelogenesis imperfecta (AI) are AMELX, ENAM, MMP20, KLK4, FAM83H, and WDR72." | 1.36 | Novel WDR72 mutation and cytoplasmic localization. ( De La Garza, RJ; Gencay, K; Hu, JC; Hwang, YH; Kang, HY; Kim, JW; Lee, KE; Lee, SK; Nam, KH; Seymen, F; Simmer, JP; Tuna, EB; Yildirim, M, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 5 (55.56) | 29.6817 |
| 2010's | 3 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dashash, M | 1 |
| Bazrafshani, MR | 1 |
| Poulton, K | 1 |
| Jaber, S | 1 |
| Naeem, E | 1 |
| Blinkhorn, AS | 1 |
| Kang, HY | 2 |
| Seymen, F | 2 |
| Lee, SK | 2 |
| Yildirim, M | 2 |
| Tuna, EB | 2 |
| Patir, A | 1 |
| Lee, KE | 2 |
| Kim, JW | 2 |
| Chan, HC | 1 |
| Mai, L | 1 |
| Oikonomopoulou, A | 1 |
| Chan, HL | 1 |
| Richardson, AS | 1 |
| Wang, SK | 1 |
| Simmer, JP | 3 |
| Hu, JC | 3 |
| Gencay, K | 1 |
| Hwang, YH | 1 |
| Nam, KH | 1 |
| De La Garza, RJ | 1 |
| Ozdemir, D | 2 |
| Hart, PS | 2 |
| Ryu, OH | 2 |
| Choi, SJ | 1 |
| Ozdemir-Karatas, M | 1 |
| Firatli, E | 2 |
| Piesco, N | 1 |
| Hart, TC | 3 |
| Aren, G | 1 |
| Wright, JT | 1 |
| Daly, B | 1 |
| Simmons, D | 1 |
| Hong, S | 1 |
| Hart, SP | 1 |
| Atsawasuwan, P | 1 |
| Yamauchi, M | 1 |
| Papagerakis, P | 1 |
| Lin, HK | 1 |
| Lee, KY | 1 |
| Hu, Y | 1 |
| Bartlett, JD | 1 |
| Collier, PM | 1 |
| Sauk, JJ | 1 |
| Rosenbloom, SJ | 1 |
| Yuan, ZA | 1 |
| Gibson, CW | 1 |
9 other studies available for adenine and Amelogenesis Imperfecta
| Article | Year |
|---|---|
Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
Topics: Adenine; Amelogenesis Imperfecta; Amino Acid Sequence; Case-Control Studies; Child; Child, Preschool | 2011 |
Candidate gene strategy reveals ENAM mutations.
Topics: Adenine; Amelogenesis Imperfecta; Amino Acid Sequence; Codon, Nonsense; Dental Enamel Hypoplasia; De | 2009 |
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
Topics: Adenine; Alleles; Amelogenesis Imperfecta; Amino Acid Sequence; Calcium; Casein Kinases; Cytosine; D | 2010 |
Novel WDR72 mutation and cytoplasmic localization.
Topics: Adenine; Alleles; Amelogenesis Imperfecta; Codon, Nonsense; Cytoplasm; Dental Enamel; Exons; Genotyp | 2010 |
MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.
Topics: Adenine; Amelogenesis Imperfecta; Binding Sites; Conserved Sequence; Dental Enamel Proteins; Female; | 2005 |
Phenotype of ENAM mutations is dosage-dependent.
Topics: Adenine; Adolescent; Amelogenesis Imperfecta; Child; Codon, Nonsense; Cytosine; Dental Enamel Protei | 2005 |
Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation.
Topics: Adenine; Amelogenesis Imperfecta; Crystallization; Crystallography; Dental Enamel; Dental Enamel Pro | 2006 |
Premature stop codon in MMP20 causing amelogenesis imperfecta.
Topics: Adenine; Amelogenesis Imperfecta; Child; Codon, Nonsense; Dental Enamel; Exons; Female; Guanine; Hum | 2008 |
An amelogenin gene defect associated with human X-linked amelogenesis imperfecta.
Topics: Adenine; Ameloblasts; Amelogenesis Imperfecta; Amelogenin; Base Sequence; Cytosine; Dental Enamel; D | 1997 |