glycine has been researched along with Xeroderma Pigmentosum in 2 studies
Xeroderma Pigmentosum: A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Khan, SG | 1 |
Levy, HL | 1 |
Legerski, R | 1 |
Quackenbush, E | 1 |
Reardon, JT | 1 |
Emmert, S | 1 |
Sancar, A | 1 |
Li, L | 1 |
Schneider, TD | 1 |
Cleaver, JE | 1 |
Kraemer, KH | 1 |
O'Driscoll, M | 1 |
Macpherson, P | 1 |
Xu, YZ | 1 |
Karran, P | 1 |
2 other studies available for glycine and Xeroderma Pigmentosum
Article | Year |
---|---|
Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia.
Topics: Alternative Splicing; Autistic Disorder; Blotting, Northern; Child, Preschool; Chromosomes, Human, P | 1998 |
The cytotoxicity of DNA carboxymethylation and methylation by the model carboxymethylating agent azaserine in human cells.
Topics: Adenine; Alkylating Agents; Azaserine; Azo Compounds; Burkitt Lymphoma; Carcinogens; DNA Adducts; DN | 1999 |