glutamine has been researched along with Anodontia 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 | 0 (0.00) | 29.6817 |
| 2010's | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Annilo, T; Eelmets, M; Gerst-Talas, U; Gilissen, C; Hoischen, A; Jagomägi, T; Kals, M; Krjutškov, K; Mägi, R; Metspalu, A; Nikopensius, T; Remm, M; Saag, 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 |
3 other study(ies) available for glutamine and Anodontia
| Article | Year |
|---|---|
Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).
Topics: Alleles; Anodontia; Chromosome Mapping; Codon, Nonsense; Conserved Sequence; Ectodysplasins; Exome; Female; Gene Expression; Genetic Variation; Glutamine; Guanine; Heterozygote; Humans; INDEL Mutation; Male; Odontogenesis; Phenotype; Polymorphism, Single Nucleotide; Receptors, Ectodysplasin; Sequence Analysis; Sequence Analysis, Protein; Signal Transduction; Structural Homology, Protein; Thymine; Tumor Necrosis Factors; X Chromosome Inactivation | 2013 |
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 |