Page last updated: 2024-10-18

glycine and Xeroderma Pigmentosum

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.

Research

Studies (2)

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

Authors

AuthorsStudies
Khan, SG1
Levy, HL1
Legerski, R1
Quackenbush, E1
Reardon, JT1
Emmert, S1
Sancar, A1
Li, L1
Schneider, TD1
Cleaver, JE1
Kraemer, KH1
O'Driscoll, M1
Macpherson, P1
Xu, YZ1
Karran, P1

Other Studies

2 other studies available for glycine and Xeroderma Pigmentosum

ArticleYear
Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia.
    The Journal of investigative dermatology, 1998, Volume: 111, Issue:5

    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.
    Carcinogenesis, 1999, Volume: 20, Issue:9

    Topics: Adenine; Alkylating Agents; Azaserine; Azo Compounds; Burkitt Lymphoma; Carcinogens; DNA Adducts; DN

1999