Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Carine Tellier-Lebegue"'
Autor:
Carine Tellier-Lebegue, Eléa Dizet, Emilie Ma, Xavier Veaute, Eric Coïc, Jean-Baptiste Charbonnier, Laurent Maloisel
Publikováno v:
PLoS Genetics, Vol 14, Iss 2, p e1007236 (2018)
[This corrects the article DOI: 10.1371/journal.pgen.1007119.].
Externí odkaz:
https://doaj.org/article/ba4343d950c641c28f528ae2004ba97d
Autor:
Carine Tellier-Lebegue, Eléa Dizet, Emilie Ma, Xavier Veaute, Eric Coïc, Jean-Baptiste Charbonnier, Laurent Maloisel
Publikováno v:
PLoS Genetics, Vol 13, Iss 12, p e1007119 (2017)
Replicative DNA polymerases cannot insert efficiently nucleotides at sites of base lesions. This function is taken over by specialized translesion DNA synthesis (TLS) polymerases to allow DNA replication completion in the presence of DNA damage. In e
Externí odkaz:
https://doaj.org/article/ffa8c3b1930d4be392ff350a6aaa94ce
Autor:
Lepakshi Ranjha, Pierre Chervy, Valérie Borde, Marie-Hélène Le Du, Laurent Maloisel, Jean-Baptiste Charbonnier, Giordano Reginato, Aurélien Thureau, Virginie Ropars, Emmanuelle Martini, Pierre Legrand, Jessica Andreani, Aurore Sanchez, Céline Adam, Petr Cejka, Jingqi Dai, Raphael Guerois, Carine Tellier-Lebegue
Publikováno v:
Proc Natl Acad Sci U S A
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2021, 118 (23), pp.e2022704118. ⟨10.1073/pnas.2022704118⟩
Proceedings of the National Academy of Sciences of the United States of America, 2021, 118 (23), pp.e2022704118. ⟨10.1073/pnas.2022704118⟩
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2021, 118 (23), pp.e2022704118. ⟨10.1073/pnas.2022704118⟩
Proceedings of the National Academy of Sciences of the United States of America, 2021, 118 (23), pp.e2022704118. ⟨10.1073/pnas.2022704118⟩
International audience; In budding yeast, the MutL homolog heterodimer Mlh1-Mlh3 (MutLγ) plays a central role in the formation of meiotic crossovers. It is also involved in the repair of a subset of mismatches besides the main mismatch repair (MMR)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05b3a333390522239b86cd01d2b897bf
https://europepmc.org/articles/PMC8201911/
https://europepmc.org/articles/PMC8201911/
Autor:
Serge Pin, Jean Armengaud, Stéphane Chédin, Gilles Lagniel, Laurent Marichal, Yves Boulard, Jean-Christophe Aude, Géraldine Klein, Carine Tellier-Lebegue, Jean Philippe Renault, Jean Labarre
Publikováno v:
Langmuir
Langmuir, 2018, 34 (18), pp.5312-5322. ⟨10.1021/acs.langmuir.8b00752⟩
Langmuir, American Chemical Society, 2018, 34 (18), pp.5312-5322. ⟨10.1021/acs.langmuir.8b00752⟩
Langmuir, 2018, 34 (18), pp.5312-5322. ⟨10.1021/acs.langmuir.8b00752⟩
Langmuir, American Chemical Society, 2018, 34 (18), pp.5312-5322. ⟨10.1021/acs.langmuir.8b00752⟩
International audience; Understanding the mechanisms involved in the interaction of proteins with inorganic surfaces is of major interest for both basic research and practical applications involving nanotechnology. From the list of cellular proteins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56df3d8fbd6153d929fc342ed2fb67f7
https://cea.hal.science/cea-01858455
https://cea.hal.science/cea-01858455
Autor:
Carine Tellier-Lebegue, Eléa Dizet, Emilie Ma, Xavier Veaute, Eric Coïc, Jean-Baptiste Charbonnier, Laurent Maloisel
Publikováno v:
PLoS Genetics
PLoS Genetics, Public Library of Science, 2018, 14 (2), pp.e1007236. ⟨10.1371/journal.pgen.1007236⟩
PLoS Genetics, 2018, 14 (2), pp.e1007236. ⟨10.1371/journal.pgen.1007236⟩
PLoS Genetics, Vol 14, Iss 2, p e1007236 (2018)
PLoS Genetics, Public Library of Science, 2018, 14 (2), pp.e1007236. ⟨10.1371/journal.pgen.1007236⟩
PLoS Genetics, 2018, 14 (2), pp.e1007236. ⟨10.1371/journal.pgen.1007236⟩
PLoS Genetics, Vol 14, Iss 2, p e1007236 (2018)
Replicative DNA polymerases cannot insert efficiently nucleotides at sites of base lesions. This function is taken over by specialized translesion DNA synthesis (TLS) polymerases to allow DNA replication completion in the presence of DNA damage. In e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::693b2d365fe39430e36216febeab8ddb
https://hal.archives-ouvertes.fr/hal-02184421
https://hal.archives-ouvertes.fr/hal-02184421
Autor:
Carine Tellier-Lebegue, Nicolas Siaud, Jean-Baptiste Charbonnier, Caroline Pouvelle, Sophie Salomé-Desnoulez, Patricia Kannouche, Agathe Bacquin, Bernard S. Lopez, Mylène Perderiset
Publikováno v:
Nucleic Acids Research
During replication, DNA damage can challenge replication fork progression and cell viability. Homologous Recombination (HR) and Translesion Synthesis (TLS) pathways appear as major players involved in the resumption and completion of DNA replication.
Autor:
Carine Tellier-Lebegue, Katheryn Meek, Mauro Modesti, Clément Nemoz, Satish K. Tadi, Jean-Baptiste Charbonnier, Stéphane Audebert, Sunetra Roy, Pascal Drevet
Publikováno v:
Cell Reports
Cell Reports, Elsevier Inc, 2016, 17 (2), pp.541-555. ⟨10.1016/j.celrep.2016.09.026⟩
Cell Reports, Vol 17, Iss 2, Pp 541-555 (2016)
Cell Reports, 2016, 17 (2), pp.541-555. ⟨10.1016/j.celrep.2016.09.026⟩
Cell Reports, Elsevier Inc, 2016, 17 (2), pp.541-555. ⟨10.1016/j.celrep.2016.09.026⟩
Cell Reports, Vol 17, Iss 2, Pp 541-555 (2016)
Cell Reports, 2016, 17 (2), pp.541-555. ⟨10.1016/j.celrep.2016.09.026⟩
International audience; In mammalian cells, classical non-homologous end joining (c-NHEJ) is critical for DNA double-strand break repair induced by ionizing radiation and during V(D)J recombination in developing B and T lymphocytes. Recently, PAXX wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dac7cb99d53d9d5a0dc79c58b7fa1f5b
https://www.hal.inserm.fr/inserm-01401845/document
https://www.hal.inserm.fr/inserm-01401845/document
Autor:
Bernard Gilquin, Floriana Londino, Josan A Márquez, Pierre Bonnesoeur, Claudine Dherin, Serge Boiteux, Marie-Hélène Le Du, Carine Tellier-Lebegue, Muriel Gondry, Jean-Baptiste Charbonnier, Pierre Legrand, Mireille Moutiez, Cathy Quemener, Emeric Gueneau
Publikováno v:
Nature Structural and Molecular Biology
Nature Structural and Molecular Biology, 2013, 20 (4), pp.461-468. ⟨10.1038/nsmb.2511⟩
Nature Structural and Molecular Biology, Nature Publishing Group, 2013, 20 (4), pp.461-468. ⟨10.1038/nsmb.2511⟩
Nature Structural and Molecular Biology, 2013, 20 (4), pp.461-468. ⟨10.1038/nsmb.2511⟩
Nature Structural and Molecular Biology, Nature Publishing Group, 2013, 20 (4), pp.461-468. ⟨10.1038/nsmb.2511⟩
International audience; Mismatch-repair factors have a prominent role in surveying eukaryotic DNA-replication fidelity and in ensuring correct meiotic recombination. These functions depend on MutL-homolog heterodimers with Mlh1. In humans, MLH1 mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4628b79c850f598d54d8c3dd780030a3
https://hal.science/hal-00817454
https://hal.science/hal-00817454
Autor:
Wikayatou Attanda, Jean-Baptiste Charbonnier, Bernard Gilquin, Sophie Zinn-Justin, Sylvaine Gasparini, Wei Wu, Howard J. Worman, Benjamin Bourgeois, Carine Tellier-Lebegue, Javier Pérez, Emilie Kondé, Sandrine Caputo
Publikováno v:
Biochemistry
Biochemistry, American Chemical Society, 2010, pp.8020-8032. ⟨10.1021/bi101153w⟩
Biochemistry, 2010, 49, pp.8020-8032. ⟨10.1021/bi101153w⟩
Biochemistry, American Chemical Society, 2010, pp.8020-8032. ⟨10.1021/bi101153w⟩
Biochemistry, 2010, 49, pp.8020-8032. ⟨10.1021/bi101153w⟩
MAN1, an integral protein of the inner nuclear membrane, influences transforming growth factor-β (TGF-β) signaling by directly interacting with R-Smads. Heterozygous loss of function mutations in the gene encoding MAN1 cause sclerosing bone dysplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac574b8082695a2f7058af2c438619f
https://hal.archives-ouvertes.fr/hal-00583792
https://hal.archives-ouvertes.fr/hal-00583792
Autor:
Satish K. Tadi, Carine Tellier-Lebègue, Clément Nemoz, Pascal Drevet, Stéphane Audebert, Sunetra Roy, Katheryn Meek, Jean-Baptiste Charbonnier, Mauro Modesti
Publikováno v:
Cell Reports, Vol 17, Iss 2, Pp 541-555 (2016)
In mammalian cells, classical non-homologous end joining (c-NHEJ) is critical for DNA double-strand break repair induced by ionizing radiation and during V(D)J recombination in developing B and T lymphocytes. Recently, PAXX was identified as a c-NHEJ
Externí odkaz:
https://doaj.org/article/c861e7cc7c714c09a07a270f4bfd07e7