Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Erin E Henninger"'
Autor:
Karl P Hodel, Richard de Borja, Erin E Henninger, Brittany B Campbell, Nathan Ungerleider, Nicholas Light, Tong Wu, Kimberly G LeCompte, A Yasemin Goksenin, Bruce A Bunnell, Uri Tabori, Adam Shlien, Zachary F Pursell
Publikováno v:
eLife, Vol 7 (2018)
Tumors defective for DNA polymerase (Pol) ε proofreading have the highest tumor mutation burden identified. A major unanswered question is whether loss of Pol ε proofreading by itself is sufficient to drive this mutagenesis, or whether additional f
Externí odkaz:
https://doaj.org/article/b21959d54c17454baf2f9fe1bada282c
Autor:
Erin E. Henninger, Pascale Jolivet, Prisca Berardi, Emilie Fallet, Mohcen Benmounah, Bechara Zeinoun, Gilles Charvin, Zhou Xu, Stefano Mattarocci, Maria Teresa Teixeira
Telomere maintenance relies on telomerase activity to compensate for the DNA end replication problem and on an efficient semi-conservative DNA replication machinery to traverse telomeric repetitive sequences, reputed to be hard to replicate. Here, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::386fb5637d7cdbb103ffcb48be65623f
https://doi.org/10.1101/2020.08.27.269621
https://doi.org/10.1101/2020.08.27.269621
Publikováno v:
Current Opinion in Genetics and Development
Current Opinion in Genetics and Development, Elsevier, 2020, 60, pp.99-106. ⟨10.1016/j.gde.2020.02.018⟩
Current Opinion in Genetics and Development, Elsevier, 2020, 60, pp.99-106. ⟨10.1016/j.gde.2020.02.018⟩
International audience; Telomeres are part of the system that guards genome integrity in eukaryotes, protecting linear chromosomes from fusions and degradations. The protective functions of telomeres are put at risk in physiological situations where
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f073f92e769cde117717a0f214ab56c
https://hal.archives-ouvertes.fr/hal-03015050
https://hal.archives-ouvertes.fr/hal-03015050
Autor:
Kimberly G. LeCompte, Bruce A. Bunnell, Karl P. Hodel, Richard de Borja, Adam Shlien, Erin E. Henninger, Zachary F. Pursell, A. Yasemin Göksenin, Tong Wu, Nathan Ungerleider, Nicholas Light, Uri Tabori, Brittany Campbell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c818e4daaf66e783373043a0519b44c
https://doi.org/10.7554/elife.32692.034
https://doi.org/10.7554/elife.32692.034
Autor:
Tong Wu, Richard de Borja, Brittany Campbell, A. Yasemin Göksenin, Adam Shlien, Erin E. Henninger, Zachary F. Pursell, Karl P. Hodel, Kimberly G. LeCompte, Nicholas Light, Bruce A. Bunnell, Nathan Ungerleider, Uri Tabori
Publikováno v:
eLife
eLife, eLife Sciences Publication, 2018, 7, pp.e32692. ⟨10.7554/eLife.32692⟩
eLife, Vol 7 (2018)
eLife, eLife Sciences Publication, 2018, 7, pp.e32692. ⟨10.7554/eLife.32692⟩
eLife, Vol 7 (2018)
Tumors defective for DNA polymerase (Pol) ε proofreading have the highest tumor mutation burden identified. A major unanswered question is whether loss of Pol ε proofreading by itself is sufficient to drive this mutagenesis, or whether additional f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d99f1cec74a31e230bbe621b2a8a3f4b
https://hal.sorbonne-universite.fr/hal-01737948/document
https://hal.sorbonne-universite.fr/hal-01737948/document
Autor:
Adam, Shlien, Brittany B, Campbell, Richard, de Borja, Ludmil B, Alexandrov, Daniele, Merico, David, Wedge, Peter, Van Loo, Patrick S, Tarpey, Paul, Coupland, Sam, Behjati, Aaron, Pollett, Tatiana, Lipman, Abolfazl, Heidari, Shriya, Deshmukh, Na'ama, Avitzur, Bettina, Meier, Moritz, Gerstung, Ye, Hong, Diana M, Merino, Manasa, Ramakrishna, Marc, Remke, Roland, Arnold, Gagan B, Panigrahi, Neha P, Thakkar, Karl P, Hodel, Erin E, Henninger, A Yasemin, Göksenin, Doua, Bakry, George S, Charames, Harriet, Druker, Jordan, Lerner-Ellis, Matthew, Mistry, Rina, Dvir, Ronald, Grant, Ronit, Elhasid, Roula, Farah, Glenn P, Taylor, Paul C, Nathan, Sarah, Alexander, Shay, Ben-Shachar, Simon C, Ling, Steven, Gallinger, Shlomi, Constantini, Peter, Dirks, Annie, Huang, Stephen W, Scherer, Richard G, Grundy, Carol, Durno, Melyssa, Aronson, Anton, Gartner, M Stephen, Meyn, Michael D, Taylor, Zachary F, Pursell, Christopher E, Pearson, David, Malkin, P Andrew, Futreal, Michael R, Stratton, Eric, Bouffet, Cynthia, Hawkins, Peter J, Campbell, Uri, Tabori
Publikováno v:
Nature Genetics. 47:257-262
DNA replication-associated mutations are repaired by two components: polymerase proofreading and mismatch repair. The mutation consequences of disruption to both repair components in humans are not well studied. We sequenced cancer genomes from child
Autor:
Erin E. Henninger, Zachary F. Pursell
Publikováno v:
IUBMB Life. 66:339-351
DNA Polymerase Epsilon (Pol e) is one of three DNA Polymerases (along with Pol δ and Pol α) required for nuclear DNA replication in eukaryotes. Pol e is comprised of four subunits, the largest of which is encoded by the POLE gene and contains the c
Autor:
Robert L. Eoff, Sarah Eddy, Maroof K. Zafar, Leena Maddukuri, Erin E. Henninger, Zachary F. Pursell, Amit Ketkar
Publikováno v:
Biochemistry. 54(20)
We have investigated the action of the human DNA polymerase epsilon (hpol ε) and eta (hpol η) catalytic cores on G-quadruplex (G4) DNA substrates derived from the promoter of the c-MYC proto-oncogene. The translesion enzyme hpol η exhibits a 6.2-f
Autor:
A. Yasemin Göksenin, Hsu Chao, Eve Shinbrot, Erin E. Henninger, Zachary F. Pursell, David A. Wheeler, Kyle R. Covington, Chris Sander, Harshavardhan Doddapaneni, Donna M. Muzny, Nikolaus Schultz, Nils Weinhold, Richard A. Gibbs
Tumors with somatic mutations in the proofreading exonuclease domain of DNA polymerase epsilon (POLE-exo*) exhibit a novel mutator phenotype, with markedly elevated TCT→TAT and TCG→TTG mutations and overall mutation frequencies often exceeding 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f43cbabb266f532c9e375dc980060b0
https://europepmc.org/articles/PMC4216916/
https://europepmc.org/articles/PMC4216916/
Publikováno v:
The FASEB Journal. 28
While it is now appreciated that tumor cells contain thousands of mutations, identifying their source(s) has remained problematic. Whole genome sequencing from colorectal and endometrial cancers recently identified mutations in DNA polymerase (Pol) e