Compounds > valine

valine and Capdepont Teeth

valine has been researched along with Capdepont Teeth in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hahn, SH; Jeon, D; Jung, YJ; Kim, JW; Lee, G; Lee, H; Lee, KE; Lee, SH; Lee, SK; Shin, CU1
Ariga, T; Ikeda, H; Kida, M; Shindoh, M; Tsutsumi, T1
Ariga, T; Hwang, YH; Kida, M; Kim, JW; Lee, KE; Lee, SK; Park, JC; Tsutsumi, T1
Jung, SE; Kim, JW; Lee, KE; Lee, SK; Lee, Zh1

Other Studies

4 other study(ies) available for valine and Capdepont Teeth

ArticleYear
A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II.
    Journal of dental research, 2009, Volume: 88, Issue:1

    Topics: Adenosine; Aspartic Acid; Child, Preschool; Dental Pulp Cavity; Dental Pulp Exposure; Dentinogenesis Imperfecta; Exons; Extracellular Matrix Proteins; Female; Genes, Dominant; Humans; Introns; Male; Mutation; Pedigree; Phosphoproteins; Sialoglycoproteins; Thymine; Tooth, Deciduous; Valine

2009
De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family.
    European journal of oral sciences, 2009, Volume: 117, Issue:6

    Topics: Adenosine; Adult; Alleles; Amino Acid Sequence; Aspartic Acid; Child, Preschool; Codon; Conserved Sequence; Dentinogenesis Imperfecta; Exons; Extracellular Matrix Proteins; Genes, Dominant; Humans; Japan; Male; Mutation, Missense; Nucleotides; Pedigree; Phosphoproteins; Sialoglycoproteins; Thymine; Valine

2009
Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.
    Oral diseases, 2011, Volume: 17, Issue:3

    Topics: Adenine; Amelogenesis; Aspartic Acid; Child; Dental Enamel Hypoplasia; Dentin Dysplasia; Dentinogenesis Imperfecta; Exons; Extracellular Matrix Proteins; Female; Genotype; Haplotypes; Humans; Mutation; Pedigree; Phenotype; Phosphoproteins; Sialoglycoproteins; Thymine; Tooth Crown; Valine

2011
Functional splicing assay of DSPP mutations in hereditary dentin defects.
    Oral diseases, 2011, Volume: 17, Issue:7

    Topics: Adenine; Codon, Nonsense; Conserved Sequence; Cytosine; Dentin Dysplasia; Dentinogenesis Imperfecta; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Genotype; Guanine; Humans; Isoleucine; Mutagenesis; Mutation; Mutation, Missense; Phenotype; Phosphoproteins; Polymerase Chain Reaction; Proline; RNA Splice Sites; RNA Splicing; Sialoglycoproteins; Thymine; Valine

2011