aminoquinuride has been researched along with Bessel-Hagen Disease in 2 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Billings, PC; Mundy, C; Pacifici, M; Takano, H; Yang, E | 1 |
| Billings, PC; Huegel, J; Koyama, E; Mundy, C; Nygren, P; Pacifici, M; Sgariglia, F; Yamaguchi, Y | 1 |
2 other study(ies) available for aminoquinuride and Bessel-Hagen Disease
| Article | Year |
|---|---|
Heparan sulfate antagonism alters bone morphogenetic protein signaling and receptor dynamics, suggesting a mechanism in hereditary multiple exostoses.
Topics: Animals; Bone Morphogenetic Protein 2; Bone Morphogenetic Protein Receptors, Type II; Cells, Cultured; Chondrogenesis; Exostoses, Multiple Hereditary; Gene Expression Regulation; Heparitin Sulfate; Humans; Mice; Mice, Inbred C3H; Phosphorylation; Signal Transduction; Urea | 2018 |
Perichondrium phenotype and border function are regulated by Ext1 and heparan sulfate in developing long bones: a mechanism likely deranged in Hereditary Multiple Exostoses.
Topics: Animals; Bone and Bones; Bone Morphogenetic Protein 2; Cartilage; Chondrogenesis; Choristoma; Embryo, Mammalian; Exostoses, Multiple Hereditary; Gene Deletion; Gene Expression Regulation, Developmental; Heparitin Sulfate; Humans; Kinetics; Mice; Models, Biological; N-Acetylglucosaminyltransferases; Phenotype; Protein Binding; Signal Transduction; Urea | 2013 |