phosphoglycolate has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 3 studies
phosphoglycolate: RN given refers to parent acid
2-phosphoglycolic acid : The O-phospho derivative of glycolic acid.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akopiants, K | 2 |
| Mohapatra, S | 1 |
| Menon, V | 1 |
| Zhou, T | 2 |
| Valerie, K | 3 |
| Povirk, LF | 3 |
| Hawkins, AJ | 1 |
| Subler, MA | 1 |
| Wiley, JL | 1 |
| Taylor, SM | 1 |
| Rice, AC | 1 |
| Windle, JJ | 1 |
| Lee, JW | 1 |
| Tatavarthi, H | 1 |
| Lupski, JR | 1 |
3 other studies available for phosphoglycolate and Autosomal Dominant Cerebellar Ataxia, Type II
| Article | Year |
|---|---|
Tracking the processing of damaged DNA double-strand break ends by ligation-mediated PCR: increased persistence of 3'-phosphoglycolate termini in SCAN1 cells.
Topics: Cell Line, Transformed; DNA; DNA Breaks, Double-Stranded; DNA-Activated Protein Kinase; Glycolates; | 2014 |
In vitro complementation of Tdp1 deficiency indicates a stabilized enzyme-DNA adduct from tyrosyl but not glycolate lesions as a consequence of the SCAN1 mutation.
Topics: Animals; Blotting, Southern; Blotting, Western; Catalysis; DNA Adducts; DNA Breaks, Double-Stranded; | 2009 |
Deficiency in 3'-phosphoglycolate processing in human cells with a hereditary mutation in tyrosyl-DNA phosphodiesterase (TDP1).
Topics: Cell Line; DNA Damage; Glycolates; Humans; Mutation; Phosphoric Diester Hydrolases; Phosphorylation; | 2005 |