tryptophan and Anodontia

tryptophan has been researched along with Anodontia in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Higashi, Y; Jezewski, PA; Kimura, M; Machida, J; Miyachi, H; Nakayama, A; Shibata, A; Shimozato, K; Tatematsu, T; Tokita, Y; Yamaguchi, S1
Bailleul-Forestier, I; Bennaceur, S; de Roux, N; Gros, C; Leger, J; Zenaty, D1
Hoshino, A; Kaewkhampa, A; Kantaputra, PN; Lees, M; Masrour, N; McEntagart, M; Moore, GE; Paramee, M; Pauws, E; Stanier, P1

Other Studies

3 other study(ies) available for tryptophan and Anodontia

ArticleYear
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
    European journal of oral sciences, 2014, Volume: 122, Issue:1

    Topics: Adenine; Anodontia; Axin Protein; Cell Culture Techniques; Cell Nucleus; Chromosome Segregation; Codon, Nonsense; Codon, Terminator; Dinucleotide Repeats; Exons; Female; Genes, Homeobox; Guanine; HEK293 Cells; Humans; Male; Middle Aged; MSX1 Transcription Factor; PAX9 Transcription Factor; Tryptophan; Young Adult

2014
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.
    International journal of paediatric dentistry, 2010, Volume: 20, Issue:4

    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.
    Journal of dental research, 2011, Volume: 90, Issue:4

    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