Page last updated: 2024-08-25

aminoquinuride and Bessel-Hagen Disease

aminoquinuride has been researched along with Bessel-Hagen Disease in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Billings, PC; Mundy, C; Pacifici, M; Takano, H; Yang, E1
Billings, PC; Huegel, J; Koyama, E; Mundy, C; Nygren, P; Pacifici, M; Sgariglia, F; Yamaguchi, Y1

Other Studies

2 other study(ies) available for aminoquinuride and Bessel-Hagen Disease

ArticleYear
Heparan sulfate antagonism alters bone morphogenetic protein signaling and receptor dynamics, suggesting a mechanism in hereditary multiple exostoses.
    The Journal of biological chemistry, 2018, 05-18, Volume: 293, Issue:20

    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.
    Developmental biology, 2013, May-01, Volume: 377, Issue:1

    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