Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2016 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

2 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "UV-sensitive syndrome 1"
Page 1
Transcription coupled DNA repair protein UVSSA binds to DNA and RNA: Mapping of nucleic acid interaction sites on human UVSSA.
Mistry H, Gupta GD. Mistry H, et al. Arch Biochem Biophys. 2023 Feb;735:109515. doi: 10.1016/j.abb.2023.109515. Epub 2023 Jan 6. Arch Biochem Biophys. 2023. PMID: 36623745
Mutations in UVSSA render the cells TCR-deficient and have been linked to UV-sensitive syndrome. Human UVSSA is a 709-residue long protein with two short conserved domains; an N-terminal (residues 1-150) and a C-terminal (residues 495-605) domain, whil …
Mutations in UVSSA render the cells TCR-deficient and have been linked to UV-sensitive syndrome. Human UVSSA is a 709-r …
Stabilization of Ultraviolet (UV)-stimulated Scaffold Protein A by Interaction with Ubiquitin-specific Peptidase 7 Is Essential for Transcription-coupled Nucleotide Excision Repair.
Higa M, Zhang X, Tanaka K, Saijo M. Higa M, et al. J Biol Chem. 2016 Jun 24;291(26):13771-9. doi: 10.1074/jbc.M116.724658. Epub 2016 Apr 28. J Biol Chem. 2016. PMID: 27129218 Free PMC article.
UV-sensitive syndrome is an autosomal recessive disorder characterized by hypersensitivity to UV light and deficiency in transcription-coupled nucleotide excision repair (TC-NER), a subpathway of nucleotide excision repair that rapidly removes transcription-b …
UV-sensitive syndrome is an autosomal recessive disorder characterized by hypersensitivity to UV light and deficiency i …