Compounds > phenylalanine

phenylalanine and Abnormalities, Teeth

phenylalanine has been researched along with Abnormalities, Teeth 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
Chen, IP; Dutra, EH; Reichenberger, EJ; Tadinada, A; Uribe, F; Utreja, A1
Biedziak, B; Jagodziński, PP; Matuszewska-Trojan, S; Mostowska, A; Zadurska, M1
Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V1

Other Studies

3 other study(ies) available for phenylalanine and Abnormalities, Teeth

ArticleYear
Dental Anomalies Associated with Craniometaphyseal Dysplasia.
    Journal of dental research, 2014, Volume: 93, Issue:6

    Topics: Acid Phosphatase; Animals; Bone Density; Bone Diseases, Developmental; Cephalometry; Cone-Beam Computed Tomography; Craniofacial Abnormalities; Disease Models, Animal; Gene Knock-In Techniques; Humans; Hyperostosis; Hypertelorism; Isoenzymes; Mandible; Maxilla; Mice; Mutation; Osteoclasts; Phenylalanine; Phosphate Transport Proteins; Sequence Deletion; Skull Base; Tartrate-Resistant Acid Phosphatase; Tooth Abnormalities; Tooth Movement Techniques; Vertical Dimension; X-Ray Microtomography

2014
WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
    European journal of oral sciences, 2015, Volume: 123, Issue:1

    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
Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.
    The FEBS journal, 2013, Volume: 280, Issue:6

    Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine

2013