aspartic acid has been researched along with Dentin Dysplasia in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fisher, LW; Hart, PS; Hart, TC; McKnight, DA; Simmer, JP | 1 |
| Ariga, T; Hwang, YH; Kida, M; Kim, JW; Lee, KE; Lee, SK; Park, JC; Tsutsumi, T | 1 |
2 other study(ies) available for aspartic acid and Dentin Dysplasia
| Article | Year |
|---|---|
Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta.
Topics: 3' Untranslated Regions; Amino Acid Sequence; Aspartic Acid; Base Pairing; Chromosomes, Human, Pair 4; Dentin Dysplasia; Dentinogenesis Imperfecta; Exons; Extracellular Matrix Proteins; Frameshift Mutation; Haplotypes; Heterozygote; Homozygote; Humans; Pedigree; Phenotype; Phosphoproteins; Promoter Regions, Genetic; Repetitive Sequences, Nucleic Acid; Sequence Analysis, Protein; Sequence Deletion; Serine; Sialoglycoproteins | 2008 |
Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.
Topics: Adenine; Amelogenesis; Aspartic Acid; Child; Dental Enamel Hypoplasia; Dentin Dysplasia; Dentinogenesis Imperfecta; Exons; Extracellular Matrix Proteins; Female; Genotype; Haplotypes; Humans; Mutation; Pedigree; Phenotype; Phosphoproteins; Sialoglycoproteins; Thymine; Tooth Crown; Valine | 2011 |