cysteine and Abnormalities, Teeth

cysteine 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
Biedziak, B; JagodziƄski, PP; Matuszewska-Trojan, S; Mostowska, A; Zadurska, M1
Cai, T; Dong, M; Duan, X; Gao, S; He, L; Hu, K; Li, Q; Mao, T; Shi, S; Wang, L; Xia, D; Xue, Y1
Bailleul-Forestier, I; Bennaceur, S; de Roux, N; Gros, C; Leger, J; Zenaty, D1

Other Studies

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

ArticleYear
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
Dental Abnormalities Caused by Novel Compound Heterozygous CTSK Mutations.
    Journal of dental research, 2015, Volume: 94, Issue:5

    Topics: Adenine; Adult; Alleles; Alveolar Process; Amino Acid Sequence; Animals; Cathepsin K; Chlorocebus aethiops; Codon, Terminator; Conserved Sequence; COS Cells; Cysteine; Dental Cementum; Guanine; Heterozygote; Humans; Male; Models, Genetic; Mutation, Missense; Pedigree; Phenol; Pycnodysostosis; Radiography, Panoramic; Tooth Abnormalities; Tryptophan; Tyrosine; X-Ray Microtomography

2015
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