arginine has been researched along with Cleidocranial Digital Dysostosis in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ge, X; Liu, YF; Su, WQ; Wang, XJ; Wu, LZ; Zhang, Y | 1 |
| Ge, LH; Wang, YX; Zhang, CY; Zhao, YM; Zheng, SG; Zhu, JX; Zhu, X | 1 |
| Banshodani, A; Hattori, M; Kosaki, K; Kozai, K; Moriyama, K; Suda, N; Tanimoto, K | 1 |
| Bertini, E; Dionisi-Vici, C; Florio, LD; Giannotti, A; Patrono, C; Santorelli, FM; Tessa, A; Velardo, M | 1 |
| Hasegawa, H; Hirose, R; Sakai, N; Susami, T; Takato, T; Tokunaga, K; Uchinuma, E; Ui, K; Yamazaki, Y | 1 |
5 other study(ies) available for arginine and Cleidocranial Digital Dysostosis
| Article | Year |
|---|---|
Role of the RUNX2 p.R225Q mutation in cleidocranial dysplasia: a rare presentation and an analysis of the RUNX2 protein structure.
Topics: Adult; Arginine; Asian People; Binding Sites; Child; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Female; Glutamine; Humans; Male; Middle Aged; Models, Molecular; Mutation, Missense; Pedigree | 2014 |
Novel RUNX2 mutations in Chinese individuals with cleidocranial dysplasia.
Topics: Arginine; Cell Line; China; Cleidocranial Dysplasia; Codon; Codon, Terminator; Core Binding Factor Alpha 1 Subunit; Cytosine; Exons; Frameshift Mutation; Genes, Reporter; Humans; Isoleucine; Leucine; Mutation, Missense; Osteocalcin; Pedigree; Promoter Regions, Genetic; Sequence Deletion; Threonine; Thymine; Transcriptional Activation; Transfection | 2009 |
Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
Topics: Adenine; Adolescent; Adult; Arginine; Child; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Diseases in Twins; DNA Copy Number Variations; Epigenesis, Genetic; Female; Frameshift Mutation; Genetic Heterogeneity; Genetic Variation; Genotype; Glutamine; Humans; Male; Middle Aged; Mutagenesis, Insertional; Mutation; Mutation, Missense; Point Mutation; Proline; Serine; Thymine; Tooth, Supernumerary; Twins, Monozygotic | 2010 |
A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia.
Topics: Amino Acid Substitution; Arginine; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Humans; Italy; Mutation, Missense; Neoplasm Proteins; Transcription Factors; Tryptophan | 2000 |
A case of a Japanese patient with cleidocranial dysplasia possessing a mutation of CBFA1 gene.
Topics: Aged; Amino Acid Substitution; Arginine; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Core Binding Factors; DNA Mutational Analysis; Humans; Japan; Male; Mutation, Missense; Neoplasm Proteins; Transcription Factors; Tryptophan | 2002 |