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 |