Results 51 to 60 of about 732,644 (123)

Identification and characterization of MUS81 point mutations that abolish interaction with the SLX4 scaffold protein [PDF]

open access: yes, 2014
MUS81-EME1 is a conserved structure-selective endonuclease with a preference for branched DNA substrates in vitro that correspond to intermediates of DNA repair.
Rouse, John   +3 more
core   +1 more source

Hereditary colorectal cancer : assessment of genotype-phenotype correlations and analysis of rare susceptibility genes in familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC) [PDF]

open access: yes, 2008
Each year 3500 people in Switzerland are diagnosed with colorectal cancer. Approximately 20 percent of all affected patients have two or more first or second-degree relatives with colorectal cancer (at-risk family members). About five percent of these
Necker, Judith
core   +1 more source

Endonuclease-independent DNA Mismatch Repair Processes on the Lagging Strand [PDF]

open access: yes, 2018
DNA mismatch repair (MMR) pathways coordinate the excision and re-synthesis of newly-replicated DNA if a mismatched base-pair has been identified by protein MutS or MutS homologues (MSHs) after replication.
Josephs, Eric   +1 more
core  

Fluorescence-based incision assay for human XPF-ERCC1 activity identifies important elements of DNA junction recognition [PDF]

open access: yes, 2012
The structure-specific endonuclease activity of the human XPF–ERCC1 complex is essential for a number of DNA processing mechanisms that help to maintain genomic integrity.
Lally, J.   +5 more
core   +1 more source

Investigating DNA remodeling in DNA mismatch repair

open access: yes
Many DNA metabolic pathways, including DNA repair, require the transmission of signals across long stretches of DNA or between DNA molecules. Solutions to this signaling challenge involve various mechanisms: protein factors can travel between these sites,
Collingwood, Bryce William
core   +1 more source

PCNA function in the activation and strand direction of MutLα endonuclease in mismatch repair

open access: yes, 2010
MutLα (MLH1–PMS2) is a latent endonuclease that is activated in a mismatch-, MutSα-, proliferating cell nuclear antigen (PCNA)-, replication factor C (RFC)-, and ATP-dependent manner, with nuclease action directed to the heteroduplex strand that contains
Ravi R. Iyer   +5 more
core   +1 more source

Publication Only

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Synthesis and quantitative structure-activity relationship of imidazotetrazine prodrugs with activity independent of O6-methylguanine-DNA-methyltransferase, DNA mismatch repair, and p53 [PDF]

open access: yes, 2013
YesThe antitumor prodrug temozolomide is compromised by its dependence for activity on DNA mismatch repair (MMR) and the repair of the chemosensitive DNA lesion, O6-methylguanine (O6-MeG), by O6-methylguanine-DNA-methyltransferase (E.C.
Phillips, Roger M.   +9 more
core   +1 more source

The human Suv3 helicase interacts with replication protein A and flap endonuclease 1 in the nucleus [PDF]

open access: yes, 2011
The human Suv3 helicase has been shown to be a major player in mitochondrial RNA surveillance and decay. In the present study we identify two new interaction partners of hSUV3: the RPA (replication protein A0 and FEN1 (flap endonuclease).
Stępień, Piotr P.   +2 more
core   +1 more source

Investigating strand specific iterative nicking in mismatch repair

open access: yes
In eukaryotic post-replicative DNA mismatch repair, MutS homolog complexes detect mismatches and in the major eukaryotic pathway, recruit multiple copies of the Mlh1-Pms1/MLH1-PMS2 (yeast/human) complex, which nick the newly replicated DNA strand upon ...
0000-0001-5725-0463   +1 more
core   +1 more source

Home - About - Disclaimer - Privacy