Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mylène Perderiset"'
Autor:
Michael Schertzer, Arturo Londoño-Vallejo, Aaron Mendez-Bermudez, Michelle Debatisse, Mylène Perderiset, Karine Jamet, Geneviève Almouzni, Jing Ye, Nicolas Nottet, Eric Gilson, Stephane Koundrioukoff, Marie Josèphe Giraud-Panis, Macarena Mowinckel, Liudmyla Lototska, Agurtzane Irizar, Olivier Croce, Serge Bauwens, Mare Paule Teulade-Fichou
Publikováno v:
Molecular Cell
Molecular Cell, Elsevier, 2018, 70 (3), pp.449-461.e5. ⟨10.1016/j.molcel.2018.03.036⟩
Molecular Cell, 2018, 70 (3), pp.449-461.e5. ⟨10.1016/j.molcel.2018.03.036⟩
Molecular Cell, Elsevier, 2018, 70 (3), pp.449-461.e5. ⟨10.1016/j.molcel.2018.03.036⟩
Molecular Cell, 2018, 70 (3), pp.449-461.e5. ⟨10.1016/j.molcel.2018.03.036⟩
Summary Hard-to-replicate regions of chromosomes (e.g., pericentromeres, centromeres, and telomeres) impede replication fork progression, eventually leading, in the event of replication stress, to chromosome fragility, aging, and cancer. Our knowledg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73ce31d58e8e99c896076015a236ff9f
https://hal.archives-ouvertes.fr/hal-02104993
https://hal.archives-ouvertes.fr/hal-02104993
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f08c7b181825d1e1e71818851d133e
https://doi.org/10.1093/nar/gkt397
https://doi.org/10.1093/nar/gkt397
Autor:
Sascha Emilie Liberti, Vilhelm A. Bohr, Lene Juel Rasmussen, Guido Keijzers, Jean-Baptiste Charbonnier, Mylène Perderiset, Finn Cilius Nielsen, Jing Wang, Sofie Dabros Andersen, Alfred May, Simona Miron
Publikováno v:
DNA Repair
DNA Repair, 2011, 10, pp.73-86. ⟨10.1016/j.dnarep.2010.09.023⟩
DNA Repair, Elsevier, 2011, 10, pp.73-86. ⟨10.1016/j.dnarep.2010.09.023⟩
DNA Repair, 2011, 10, pp.73-86. ⟨10.1016/j.dnarep.2010.09.023⟩
DNA Repair, Elsevier, 2011, 10, pp.73-86. ⟨10.1016/j.dnarep.2010.09.023⟩
Human exonuclease 1 (hEXO1) is implicated in DNA metabolism, including replication, recombination and repair, substantiated by its interactions with PCNA, DNA helicases BLM and WRN, and several DNA mismatch repair (MMR) proteins. We investigated the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3e16ab96c7acd73cdb1c8a85929a599
https://doi.org/10.1016/j.dnarep.2010.09.023
https://doi.org/10.1016/j.dnarep.2010.09.023
Publikováno v:
Crystal Growth & Design. 7:2140-2146
Most small GTPases, whether free or complexed to their effectors, diffract to 2.0 A resolution or better. Here, the complex between a small GTPase and its effector was screened in the classic way using the sparse matrix method, and large single cryst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cee07807de0cea536ff622c3d7b5faf
https://doi.org/10.1021/cg700698d
https://doi.org/10.1021/cg700698d
Autor:
Julie Ménétrey, Karine Regazzoni, Anne Splingard, Lucien Cabanié, Ahmed El Marjou, J. Cicolari, Amber L. Wells, Mylène Perderiset, Fatima Hamoudi, Anne Houdusse, Jean de Gunzburg
Publikováno v:
Journal of Biological Chemistry. 282:1905-1915
RGK proteins, encompassing Rad, Gem, Rem1, and Rem2, constitute an intriguing branch of the Ras superfamily; their expression is regulated at the transcription level, they exhibit atypical nucleotide binding motifs, and they carry both large N- and C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c021a34f3c2dcea2b813f2c7821ab1b6
https://doi.org/10.1074/jbc.m604363200
https://doi.org/10.1074/jbc.m604363200
Autor:
Arturo Londoño-Vallejo, Michael Schertzer, Florent Dingli, Patrick Revy, Tangui Le Guen, Mylène Perderiset, Barbara Bardoni, Damarys Loew, Jean-Pierre de Villartay, Karina Jouravleva
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2015, 43 (3), pp.1834-1847. ⟨10.1093/nar/gku1402⟩
Nucleic Acids Research, 2015, 43 (3), pp.1834-1847. ⟨10.1093/nar/gku1402⟩
Nucleic Acids Research, Oxford University Press, 2015, 43 (3), pp.1834-1847. 〈10.1093/nar/gku1402〉
Nucleic Acids Research, Oxford University Press, 2015, 43 (3), pp.1834-1847. ⟨10.1093/nar/gku1402⟩
Nucleic Acids Research, 2015, 43 (3), pp.1834-1847. ⟨10.1093/nar/gku1402⟩
Nucleic Acids Research, Oxford University Press, 2015, 43 (3), pp.1834-1847. 〈10.1093/nar/gku1402〉
Hoyeraal-Hreidarsson syndrome (HHS) is a severe form of Dyskeratosis congenita characterized by developmental defects, bone marrow failure and immunodeficiency and has been associated with telomere dysfunction. Recently, mutations in Regulator of Tel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b10c3063aa748cbc39ac5ff6297cce24
https://hal.sorbonne-universite.fr/hal-01278052
https://hal.sorbonne-universite.fr/hal-01278052
Autor:
Ronald A. Milligan, Anne Houdusse, Jamel Chelly, Mylène Perderiset, Fiona Francis, Carolyn A. Moores
Publikováno v:
Molecular Cell. 14(6):833-839
Neurons undertake an amazing journey from the center of the developing mammalian brain to the outer layers of the cerebral cortex. Doublecortin, a component of the microtubule cytoskeleton, is essential in postmitotic neurons and was identified becau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50e0ddff337687ea5b5ae5b8eb43a6b3
Publikováno v:
Methods in cell biology. 115
Doublecortin (DCX) is a microtubule (MT)-stabilizing protein essential for neuronal migration during human brain development. Missense mutations in DCX cause severe brain defects. This implies that the many other MT-stabilizing proteins in neurons ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::682fe21d7aecd65d2162f26468ad64a1
https://pubmed.ncbi.nlm.nih.gov/23973064
https://pubmed.ncbi.nlm.nih.gov/23973064
Autor:
Tangui Le Guen, Gérard Couillault, Laetitia Gaillard, Jean Soulier, Capucine Picard, Jean-Pierre de Villartay, Fabien Touzot, Patrick Nitschke, Isabelle Callebaut, Arturo Londoño-Vallejo, Michael Schertzer, Nada Jabado, Alain Fischer, Mylène Perderiset, Wassila Carpentier, Patrick Revy, Laurent Jullien
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2013, 22 (16), pp.3239-3249. ⟨10.1093/hmg/ddt178⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (16), pp.3239-3249. ⟨10.1093/hmg/ddt178⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (16), pp.3239-3249. 〈10.1093/hmg/ddt178〉
Human Molecular Genetics, 2013, 22 (16), pp.3239-3249. ⟨10.1093/hmg/ddt178⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (16), pp.3239-3249. ⟨10.1093/hmg/ddt178⟩
Human Molecular Genetics, Oxford University Press (OUP), 2013, 22 (16), pp.3239-3249. 〈10.1093/hmg/ddt178〉
International audience; Hoyeraal-Hreidarsson syndrome (HHS), a severe variant of dyskeratosis congenita (DC), is characterized by early onset bone marrowfailure, immunodeficiency and developmental defects. Several factors involved in telomere length
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da1b430ede84442e129d5950bb176817
https://pubmed.ncbi.nlm.nih.gov/23591994
https://pubmed.ncbi.nlm.nih.gov/23591994
Doublecortin (DCX) is a microtubule (MT)-stabilizing protein essential for neuronal migration during human brain development. Missense mutations in DCX cause severe brain defects. This implies that the many other MT-stabilizing proteins in neurons ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bada6f02e0ddf0beef7bd4dd080e8247
https://doi.org/10.1016/b978-0-12-407757-7.00003-7
https://doi.org/10.1016/b978-0-12-407757-7.00003-7