dermatan sulfate has been researched along with Abnormalities, Multiple in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Cerón, M; Jiménez-Mariscal, JL; Peña-Gomar, I; Reyes-López, CA; Rosas-Trigueros, J | 1 |
| Baenziger, JU; Dündar, M; Janecke, AR; Müller, T | 1 |
| Beck, M; Glössl, J; Kresse, H; Rüter, R | 1 |
3 other study(ies) available for dermatan sulfate and Abnormalities, Multiple
| Article | Year |
|---|---|
c.1898C>G/p.Ser633Trp Mutation in Alpha-L-Iduronidase: Clinical and Structural Implications.
Topics: Abnormalities, Multiple; Catalytic Domain; Crystallography, X-Ray; Dermatan Sulfate; Enzyme Replacement Therapy; Gene Expression; Heparitin Sulfate; Humans; Iduronidase; Infant; Male; Molecular Dynamics Simulation; Mucopolysaccharidosis I; Point Mutation; Principal Component Analysis; Protein Binding; Protein Conformation, alpha-Helical; Protein Conformation, beta-Strand; Protein Interaction Domains and Motifs; Substrate Specificity | 2021 |
Loss of dermatan-4-sulfotransferase 1 (D4ST1/CHST14) function represents the first dermatan sulfate biosynthesis defect, "dermatan sulfate-deficient adducted thumb-clubfoot syndrome".
Topics: Abnormalities, Multiple; Clubfoot; Dermatan Sulfate; Ehlers-Danlos Syndrome; Eye Abnormalities; Frameshift Mutation; Humans; Joint Instability; Skin Abnormalities; Sulfotransferases; Thumb | 2011 |
Abnormal proteodermatan sulfate in three patients with Coffin-Lowry syndrome.
Topics: Abnormalities, Multiple; Adult; Bone and Bones; Cells, Cultured; Child, Preschool; Chondroitin; Dermatan Sulfate; Fibroblasts; Glucuronates; Glucuronic Acid; Humans; Iduronic Acid; Intellectual Disability; Male; Proteoglycans; Sex Factors; Skin; Skin Diseases; Syndrome | 1983 |