Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Peter Kolesár"'
Publikováno v:
Biomolecules, Vol 2, Iss 3, Pp 350-375 (2012)
DNA double-strand breaks (DSBs) comprise one of the most toxic DNA lesions, as the failure to repair a single DSB has detrimental consequences on the cell. Homologous recombination (HR) constitutes an error-free repair pathway for the repair of DSBs.
Externí odkaz:
https://doaj.org/article/a03f7bd969df4ac9a7af18142fffd611
Autor:
Edit Lelkes, Jitka Jemelková, Marcela Holá, Barbora Štefanovie, Peter Kolesár, Radka Vágnerová, Eva Dvořák Tomaštíková, Ales Pecinka, Karel J. Angelis, Jan J. Paleček
Publikováno v:
The Plant Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddb00f6f5b2861053618e6b06108b985
https://doi.org/10.1111/tpj.16282
https://doi.org/10.1111/tpj.16282
Publikováno v:
Cells, Vol 13, Iss 10, p 812 (2024)
In the original publication [...]
Externí odkaz:
https://doaj.org/article/a1d25c6906144eab87e48379f23b7788
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-18 (2021)
CAPPs are putative Primase-Polymerases associated with CRISPR-Cas operons. Here, the authors show CAPPs genetic and physical association with Cas1 and Cas2, their capacity to function as DNA-dependent DNA primases and DNA polymerases, and that Cas1-C
Externí odkaz:
https://doaj.org/article/efc9c689cc494105b57df2aab55a9b23
Autor:
Peter, Kolesár, Gabriel, Minárik, Marián, Baldovic, Andrej, Ficek, László, Kovács, L'udevít, Kádasi
Publikováno v:
General physiology and biophysics. 27(4)
Cystic fibrosis (CF) is the most common lethal autosomal recessive disorder in Caucasians. Its incidence is approximately 1:2500 newborns. CF is caused by mutations in the transmembrane conductance regulator (CFTR) gene, which encodes an important ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad9de1c8b300a7b275a1c6e6b63048a6
https://pubmed.ncbi.nlm.nih.gov/19202204
https://pubmed.ncbi.nlm.nih.gov/19202204
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Abstract The SMC (Structural Maintenance of Chromosomes) complexes are composed of SMC dimers, kleisin and kleisin-interacting (HAWK or KITE) subunits. Mutual interactions of these subunits constitute the basal architecture of the SMC complexes. In a
Externí odkaz:
https://doaj.org/article/c65c459f638e40849aacc4d743d98a78
Publikováno v:
Cells, Vol 11, Iss 1, p 165 (2022)
Structural Maintenance of Chromosomes (SMC) complexes are important for many aspects of the chromosomal organization. Unlike cohesin and condensin, the SMC5/6 complex contains a variant RING domain carried by its Nse1 subunit. RING domains are charac
Externí odkaz:
https://doaj.org/article/5ff87f4fac8f4fbb81378382fce627f3
Autor:
Thomas A. Guilliam, Nigel C. Brissett, Aaron Ehlinger, Benjamin A. Keen, Peter Kolesar, Elaine M. Taylor, Laura J. Bailey, Howard D. Lindsay, Walter J. Chazin, Aidan J. Doherty
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
PrimPol is a multifunctional replicative enzyme that can bypass DNA damage, as well as reprime replication restart. Here, the authors have elucidated how PrimPol is recruited to stalled replication forks via specific interactions with RPA, which stim
Externí odkaz:
https://doaj.org/article/6c3b35c0421a4ab2b8722df6acbdcac6
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