arginine has been researched along with Anodontia in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 4 (80.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hyun, HK; Kim, JW; Ko, J; Lee, KE; Lee, SH; Shin, TJ | 1 |
| Biedziak, B; Jagodziński, PP; Matuszewska-Trojan, S; Mostowska, A; Zadurska, M | 1 |
| Bailleul-Forestier, I; Bennaceur, S; de Roux, N; Gros, C; Leger, J; Zenaty, D | 1 |
| Hoshino, A; Kaewkhampa, A; Kantaputra, PN; Lees, M; Masrour, N; McEntagart, M; Moore, GE; Paramee, M; Pauws, E; Stanier, P | 1 |
| Adeyemo, WL; Erginel-Unaltuna, N; Ewers, R; Frei, K; Item, CB; Sinko, K; Thurnher, D; Turhani, D; Watzinger, F; Wittwer, G; Yerit, K | 1 |
5 other study(ies) available for arginine and Anodontia
| Article | Year |
|---|---|
Oligodontia and curly hair occur with ectodysplasin-a mutations.
Topics: Anodontia; Arginine; Child; Child, Preschool; Codon; Conserved Sequence; Ectodysplasins; Exome; Gene Frequency; Genetic Diseases, X-Linked; Genetic Variation; Guanine; Hair; Humans; Leucine; Male; Mutation, Missense; Pedigree; Phenylalanine; Signal Transduction; Thymine; Valine | 2014 |
WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
Topics: Adolescent; Adult; Anodontia; Arginine; Base Sequence; Child; Cohort Studies; Conserved Sequence; Cysteine; Female; Genetic Variation; Genotype; Humans; Incisor; Isoleucine; Leucine; Male; MSX1 Transcription Factor; Mutation; Open Reading Frames; PAX9 Transcription Factor; Phenylalanine; Polymorphism, Genetic; Tooth Abnormalities; Wnt Proteins; Young Adult | 2015 |
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.
Topics: Adenine; Adolescent; Adult; Anodontia; Arginine; Bicuspid; Child, Preschool; Cleft Palate; Cysteine; Cytosine; Female; Glutamine; Glycine; Guanine; Humans; Incisor; Kallmann Syndrome; Male; Middle Aged; Molar; Mutation; Receptor, Fibroblast Growth Factor, Type 1; Sequence Deletion; Tooth Abnormalities; Tooth Root; Tooth, Deciduous; Tryptophan; Young Adult | 2010 |
Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.
Topics: Adolescent; Anodontia; Arginine; Child; Child, Preschool; Cleft Lip; Cleft Palate; Cohort Studies; Conserved Sequence; DNA-Binding Proteins; Exons; Female; Genetic Variation; Glutamine; Humans; Labial Frenum; Leucine; Male; Mutation, Missense; Phenotype; Polymorphism, Genetic; Proline; Promoter Regions, Genetic; Serine; T-Box Domain Proteins; Tongue Diseases; Transcription, Genetic; Tryptophan; Tyrosine | 2011 |
Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
Topics: 5' Untranslated Regions; Abnormalities, Multiple; Anodontia; Arginine; Base Sequence; Cleft Lip; Cleft Palate; DNA; DNA Primers; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Exons; Family Health; Female; Genes, Dominant; Glycine; Heterozygote; Humans; Interferon Regulatory Factors; Male; Molecular Sequence Data; Mouth Abnormalities; Mutation; Pedigree; Penetrance; Phenotype; Promoter Regions, Genetic; Protein Structure, Tertiary; Sequence Analysis, DNA; Syndrome; Transcription Factors; Turkey | 2005 |