erythrosine has been researched along with Chondrodysplasia Punctata in 1 studies
Fluoresceins: A family of spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one derivatives. These are used as dyes, as indicators for various metals, and as fluorescent labels in immunoassays.
Chondrodysplasia Punctata: A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC), an autosomal dominant form (Conradi-Hunermann syndrome), and a milder X-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In fibroblasts of chondrodysplasia punctata patients with defects in the peroxisomal import of proteins carrying a PTS2 sequence, import of the PTS1-peptide probe into peroxisomes appeared normal, but these peroxisomes have a pH of 6." | 2.41 | Targeted fluorescent probes in peroxisome function. ( Dansen, TB; Wanders, RJ; Wirtz, KW, 2001) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dansen, TB | 1 |
| Wanders, RJ | 1 |
| Wirtz, KW | 1 |
1 review available for erythrosine and Chondrodysplasia Punctata
| Article | Year |
|---|---|
Targeted fluorescent probes in peroxisome function.
Topics: Amino Acid Sequence; Animals; Boron Compounds; Chondrodysplasia Punctata; Drug Design; Fibroblasts; | 2001 |