histidine has been researched along with Amelogenesis Imperfecta in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Hu, JC; Hu, Y; Kasimoglu, Y; Kim, JW; Koruyucu, M; Liang, T; Saunders, TL; Seymen, F; Simmer, JP; Smith, C; Wang, SK; Zhang, C; Zhang, H | 1 |
Choi, SJ; Firatli, E; Hart, PS; Hart, TC; Ozdemir, D; Ozdemir-Karatas, M; Piesco, N; Ryu, OH | 1 |
Aldred, MJ; Crawford, PJ; Hart, PS; Hart, TC; Wright, JT; Wright, NJ | 1 |
3 other study(ies) available for histidine and Amelogenesis Imperfecta
Article | Year |
---|---|
Enamel defects in Acp4
Topics: Acid Phosphatase; Ameloblasts; Amelogenesis; Amelogenesis Imperfecta; Animals; Dental Enamel Proteins; Histidine; Humans; Mice; Mutation | 2022 |
MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.
Topics: Adenine; Amelogenesis Imperfecta; Binding Sites; Conserved Sequence; Dental Enamel Proteins; Female; Gene Expression Regulation, Enzymologic; Gene Frequency; Genes, Recessive; Genetic Heterogeneity; Glutamine; Histidine; Humans; Kallikreins; Male; Matrix Metalloproteinase 20; Matrix Metalloproteinases; Mutation; Mutation, Missense; Pedigree; Thymine | 2005 |
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.
Topics: Amelogenesis Imperfecta; Amelogenin; Amino Acid Sequence; Amino Acid Substitution; Codon, Nonsense; Dental Enamel Proteins; DNA Mutational Analysis; Female; Frameshift Mutation; Genetic Linkage; Genotype; Histidine; Humans; Leucine; Male; Mutation, Missense; Pedigree; Phenotype; Protein Structure, Tertiary; Sex Chromosome Aberrations; X Chromosome | 2002 |