Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Franck, Court"'
Autor:
Cecilia Rengifo Rojas, Jil Cercy, Sophie Perillous, Céline Gonthier-Guéret, Bertille Montibus, Stéphanie Maupetit-Méhouas, Astrid Espinadel, Marylou Dupré, Charles C. Hong, Kenichiro Hata, Kazuhiko Nakabayashi, Antonius Plagge, Tristan Bouschet, Philippe Arnaud, Isabelle Vaillant, Franck Court
Publikováno v:
HGG Advances, Vol 5, Iss 2, Pp 100271- (2024)
Summary: It is only partially understood how constitutive allelic methylation at imprinting control regions (ICRs) interacts with other regulation levels to drive timely parental allele-specific expression along large imprinted domains. The Peg13-Kcn
Externí odkaz:
https://doaj.org/article/d7cbd17169d146879f77c972bc9cd96b
Autor:
Elisa Le Boiteux, Franck Court, Pierre‐Olivier Guichet, Catherine Vaurs‐Barrière, Isabelle Vaillant, Emmanuel Chautard, Pierre Verrelle, Bruno M. Costa, Lucie Karayan‐Tapon, Anne Fogli, Philippe Arnaud
Publikováno v:
Molecular Oncology, Vol 15, Iss 8, Pp 1995-2010 (2021)
In human, the 39 coding HOX genes and 18 referenced noncoding antisense transcripts are arranged in four genomic clusters named HOXA, B, C, and D. This highly conserved family belongs to the homeobox class of genes that encode transcription factors r
Externí odkaz:
https://doaj.org/article/fed95548f2564556b60979aca372b0ee
Autor:
Elisa Le Boiteux, Pierre-Olivier Guichet, Konstantin Masliantsev, Bertille Montibus, Catherine Vaurs-Barriere, Céline Gonthier-Gueret, Emmanuel Chautard, Pierre Verrelle, Lucie Karayan-Tapon, Anne Fogli, Franck Court, Philippe Arnaud
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 9, p 4743 (2022)
Glioblastomas represent approximatively half of all gliomas and are the most deadly and aggressive form. Their therapeutic resistance and tumor relapse rely on a subpopulation of cells that are called Glioma Stem Cells (GSCs). Here, we investigated t
Externí odkaz:
https://doaj.org/article/eaa16bcefe1a4cf78d9d79e9ad983d0e
Autor:
Stéphanie Maupetit‐Mehouas, Franck Court, Céline Bourgne, Agnès Guerci‐Bresler, Pascale Cony‐Makhoul, Hyacinthe Johnson, Gabriel Etienne, Philippe Rousselot, Denis Guyotat, Alexandre Janel, Eric Hermet, Sandrine Saugues, Juliette Berger, Philippe Arnaud, Marc G. Berger
Publikováno v:
Molecular Oncology, Vol 12, Iss 6, Pp 814-829 (2018)
Despite the high efficiency of tyrosine kinase inhibitors (TKI), some patients with chronic myeloid leukemia (CML) will display residual disease that can become resistant to treatment, indicating intraclonal heterogeneity in chronic‐phase CML (CP
Externí odkaz:
https://doaj.org/article/b9748f2553f944a0a5f7f0ba157e2821
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains
Autor:
David Monk, Joannella Morales, Johan T. den Dunnen, Silvia Russo, Franck Court, Dirk Prawitt, Thomas Eggermann, Jasmin Beygo, Karin Buiting, Zeynep Tümer, the Nomenclature group of the European Network for Human Congenital Imprinting Disorders
Publikováno v:
Epigenetics, Vol 13, Iss 2, Pp 117-121 (2018)
The analysis of DNA methylation has become routine in the pipeline for diagnosis of imprinting disorders, with many publications reporting aberrant methylation associated with imprinted differentially methylated regions (DMRs). However, comparisons b
Externí odkaz:
https://doaj.org/article/8c2fc76343b646629c10575a2b21ff9b
Autor:
Marie-Elisa Pinson, Franck Court, Aymeric Masson, Yoan Renaud, Allison Fantini, Ophélie Bacoeur-Ouzillou, Marie Barriere, Bruno Pereira, Pierre-Olivier Guichet, Emmanuel Chautard, Lucie Karayan-Tapon, Pierre Verrelle, Philippe Arnaud, Catherine Vaurs-Barrière
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, In press
Human Molecular Genetics, 2022, 31 (15), pp.2606-2622. ⟨10.1093/hmg/ddac056⟩
Human Molecular Genetics, In press
Human Molecular Genetics, 2022, 31 (15), pp.2606-2622. ⟨10.1093/hmg/ddac056⟩
Besides the consequences of retrotransposition, long interspersed element 1 (L1) retrotransposons can affect the host genome through their antisense promoter. In addition to the sense promoter, the evolutionarily recent L1 retrotransposons, which are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c76312db2c614ceea8bf32459fa44595
https://doi.org/10.1093/hmg/ddac056
https://doi.org/10.1093/hmg/ddac056
Autor:
Marta Sanchez-Delgado, Franck Court, Enrique Vidal, Jose Medrano, Ana Monteagudo-Sánchez, Alex Martin-Trujillo, Chiharu Tayama, Isabel Iglesias-Platas, Ivanela Kondova, Ronald Bontrop, Maria Eugenia Poo-Llanillo, Tomas Marques-Bonet, Kazuhiko Nakabayashi, Carlos Simón, David Monk
Publikováno v:
PLoS Genetics, Vol 12, Iss 11, p e1006427 (2016)
Thousands of regions in gametes have opposing methylation profiles that are largely resolved during the post-fertilization epigenetic reprogramming. However some specific sequences associated with imprinted loci survive this demethylation process. He
Externí odkaz:
https://doaj.org/article/0e4b89b8a6004bec95c52f9a1c7cafd9
Autor:
Philippe Arnaud, Franck Court
Publikováno v:
Oncotarget
Oncotarget, Impact journals, 2017, 8, pp.4110-4124
Oncotarget, 2017, 8, pp.4110-4124
HAL
Oncotarget, Impact journals, 2017, 8, pp.4110-4124
Oncotarget, 2017, 8, pp.4110-4124
HAL
// Franck Court 1, 2, 3 , Philippe Arnaud 1, 2, 3 1 CNRS-UMR 6293, Clermont-Ferrand, 63001, France 2 INSERM-U1103, Clermont-Ferrand, 63001, France 3 Universite Clermont Auvergne, GReD Laboratory, Clermont-Ferrand, 63000, France Correspondence to: Phi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db9234c03913597b655fddb24758c481
http://europepmc.org/articles/PMC5354816
http://europepmc.org/articles/PMC5354816
Autor:
Mélanie Müller-Barthélémy, Elisa Le Boiteux, Franck Court, Julian Biau, Lucie Karayan-Tapon, Toufic Khalil, Pierre Verrelle, Philippe Arnaud, Jean-Louis Kemeny, Anne Fogli, Catherine Vaurs-Barrière, Bruno Pereira, Emmanuel Chautard
Publikováno v:
Genome Research
Genome Research, 2019, 29 (10), pp.1605-1621. ⟨10.1101/gr.249219.119⟩
Genome Research, Cold Spring Harbor Laboratory Press, 2019, 29 (10), pp.1605-1621. ⟨10.1101/gr.249219.119⟩
Genome Research, 2019, 29 (10), pp.1605-1621. ⟨10.1101/gr.249219.119⟩
Genome Research, Cold Spring Harbor Laboratory Press, 2019, 29 (10), pp.1605-1621. ⟨10.1101/gr.249219.119⟩
In cancer cells, aberrant DNA methylation is commonly associated with transcriptional alterations, including silencing of tumor suppressor genes. However, multiple epigenetic mechanisms, including polycomb repressive marks, contribute to gene deregul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a976cd21f9127bb91cbb3859bc871cd6
https://doi.org/10.1101/gr.249219.119
https://doi.org/10.1101/gr.249219.119
Autor:
Catherine Vaurs-Barrière, Elisa Le Boiteux, Isabelle Vaillant, Anne Fogli, Bruno M. Costa, Pierre Verrelle, Emmanuel Chautard, Lucie Karayan-Tapon, Pierre-Olivier Guichet, Franck Court, Philippe Arnaud
Publikováno v:
Molecular Oncology
Molecular Oncology, Elsevier, 2021, ⟨10.1002/1878-0261.12944⟩
Molecular Oncology, 2021, ⟨10.1002/1878-0261.12944⟩
Molecular Oncology, Vol 15, Iss 8, Pp 1995-2010 (2021)
Molecular Oncology, Elsevier, 2021, ⟨10.1002/1878-0261.12944⟩
Molecular Oncology, 2021, ⟨10.1002/1878-0261.12944⟩
Molecular Oncology, Vol 15, Iss 8, Pp 1995-2010 (2021)
In human, the 39 coding HOX genes and 18 referenced noncoding antisense transcripts are arranged in four genomic clusters named HOXA, B, C, and D. This highly conserved family belongs to the homeobox class of genes that encode transcription factors r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c663b7f53d6cfea16f45f720db7c7867
https://hal.archives-ouvertes.fr/hal-03172071/document
https://hal.archives-ouvertes.fr/hal-03172071/document
