Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Clara Benoit‐Pilven"'
Publikováno v:
Genome Biology, Vol 25, Iss 1, Pp 1-27 (2024)
Abstract Background Variation in X chromosome inactivation (XCI) in human-induced pluripotent stem cells (hiPSCs) can impact their ability to model biological sex biases. The gene-wise landscape of X chromosome gene dosage remains unresolved in femal
Externí odkaz:
https://doaj.org/article/948460aec0694b3eb9427830f6390bc9
Autor:
Anne‐Sophie Hatat, Clara Benoit‐Pilven, Amélie Pucciarelli, Florence deFraipont, Lucie Lamothe, Pascal Perron, Amandine Rey, Matteo Giaj Levra, Anne‐Claire Toffart, Didier Auboeuf, Beatrice Eymin, Sylvie Gazzeri
Publikováno v:
Molecular Oncology, Vol 16, Iss 19, Pp 3490-3508 (2022)
Despite the initial efficacy of using tyrosine kinase inhibitors of epidermal growth factor receptors (EGFR‐TKIs) for treating patients with non‐small cell lung cancer (NSCLC), resistance inevitably develops. Recent studies highlight a link betwe
Externí odkaz:
https://doaj.org/article/b72c5db1e289451ca303938baa5d229b
Autor:
Clara Benoit-Pilven, Alicia Besson, Audrey Putoux, Claire Benetollo, Clément Saccaro, Justine Guguin, Gabriel Sala, Audric Cologne, Marion Delous, Gaetan Lesca, Richard A Padgett, Anne-Louise Leutenegger, Vincent Lacroix, Patrick Edery, Sylvie Mazoyer
Publikováno v:
PLoS ONE, Vol 15, Iss 7, p e0235655 (2020)
Biallelic variants in RNU4ATAC, a non-coding gene transcribed into the minor spliceosome component U4atac snRNA, are responsible for three rare recessive developmental diseases, namely Taybi-Linder/MOPD1, Roifman and Lowry-Wood syndromes. Next-genera
Externí odkaz:
https://doaj.org/article/c65c22bed0df489ab421b2e558d11852
Autor:
Deepak Khatri, Audrey Putoux, Audric Cologne, Sophie Kaltenbach, Alicia Besson, Eloïse Bertiaux, Justine Guguin, Adèle Fendler, Marie A. Dupont, Clara Benoit-Pilven, Leila Qebibo, Samira Ahmed-Elie, Séverine Audebert-Bellanger, Pierre Blanc, Thomas Rambaud, Martin Castelle, Gaëlle Cornen, Sarah Grotto, Agnès Guët, Laurent Guibaud, Caroline Michot, Sylvie Odent, Lyse Ruaud, Elise Sacaze, Virginie Hamel, Rémy Bordonné, Anne-Louise Leutenegger, Patrick Edery, Lydie Burglen, Tania Attié-Bitach, Sylvie Mazoyer, Marion Delous
Publikováno v:
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, 2023, 120 (9), pp.e2102569120. ⟨10.1073/pnas.2102569120⟩
Proceedings of the National Academy of Sciences of the United States of America, 2023, 120 (9), pp.e2102569120. ⟨10.1073/pnas.2102569120⟩
In the human genome, about 750 genes contain one intron excised by the minor spliceosome. This spliceosome comprises its own set of snRNAs, among which U4atac. Its noncoding gene, RNU4ATAC , has been found mutated in Taybi-Linder (TALS/microcephalic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff8ec8d20ada31707836e9ec93fa4cca
https://univ-rennes.hal.science/hal-04021151
https://univ-rennes.hal.science/hal-04021151
Autor:
null Anne‐Sophie Hatat, null Clara Benoit‐Pilven, null Amélie Pucciarelli, null Florence de Fraipont, null Lucie Lamothe, null Pascal Perron, null Amandine Rey, null Matteo Giaj Levra, null Anne‐Claire Toffart, null Didier Auboeuf, null Beatrice Eymin, null Sylvie Gazzeri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4320f37af9e374056fb6ad0a26775d77
https://doi.org/10.1002/1878-0261.13229/v2/response1
https://doi.org/10.1002/1878-0261.13229/v2/response1
Autor:
Deepak Khatri, Audrey Putoux, Audric Cologne, Sophie Kaltenbach, Alicia Besson, Eloïse Bertiaux, Justine Guguin, Adèle Fendler, Marie A. Dupont, Clara Benoit-Pilven, Sarah Grotto, Lyse Ruaud, Caroline Michot, Martin Castelle, Agnès Guët, Laurent Guibaud, Virginie Hamel, Rémy Bordonné, Anne-Louise Leutenegger, Tania Attié-Bitach, Patrick Edery, Sylvie Mazoyer, Marion Delous
In the human genome, about 750 genes contain one intron excised by the minor spliceosome. This spliceosome comprises its own set of snRNAs, among which U4atac. Its non-coding gene,RNU4ATAC, has been found mutated in Taybi-Linder (MOPD1/TALS), Roifman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d73912952aca0e6d7322911d9b0fce9c
https://doi.org/10.1101/2021.12.12.21266616
https://doi.org/10.1101/2021.12.12.21266616
Autor:
U. Ashraf, Sandie Munier, Vincent Navratil, Vincent Lacroix, Guillaume Fournier, Nadia Naffakh, Clara Benoit-Pilven, Odile Sismeiro, Cécile Ligneau, Jean-Yves Coppée
Publikováno v:
NAR Genomics and Bioinformatics
NAR Genomics and Bioinformatics, Oxford University Press, 2020, 2 (4), ⟨10.1093/nargab/lqaa095⟩
NAR Genomics and Bioinformatics, 2020, 2 (4), ⟨10.1093/nargab/lqaa095⟩
NAR Genomics and Bioinformatics, Oxford University Press, 2020, 2 (4), ⟨10.1093/nargab/lqaa095⟩
NAR Genomics and Bioinformatics, 2020, 2 (4), ⟨10.1093/nargab/lqaa095⟩
Influenza A viruses (IAVs) use diverse mechanisms to interfere with cellular gene expression. Although many RNA-seq studies have documented IAV-induced changes in host mRNA abundance, few were designed to allow an accurate quantification of changes i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcff2ff4f1eef7229d25a981c4f621da
https://hal.archives-ouvertes.fr/hal-03021806
https://hal.archives-ouvertes.fr/hal-03021806
Autor:
Claire Benetollo, Gabriel Sala, Sylvie Mazoyer, Anne-Louise Leutenegger, Alicia Besson, Justine Guguin, Clément Saccaro, Marion Delous, Gaetan Lesca, Vincent Lacroix, Clara Benoit-Pilven, Audrey Putoux, Patrick Edery, Richard A. Padgett, Audric Cologne
Publikováno v:
PLoS ONE
PLoS ONE, 2020, 15 (7), pp.e0235655. ⟨10.1371/journal.pone.0235655⟩
PLoS ONE, Public Library of Science, 2020, 15 (7), pp.e0235655. ⟨10.1371/journal.pone.0235655⟩
PLoS ONE, Vol 15, Iss 7, p e0235655 (2020)
PLoS ONE, 2020, 15 (7), pp.e0235655. ⟨10.1371/journal.pone.0235655⟩
PLoS ONE, Public Library of Science, 2020, 15 (7), pp.e0235655. ⟨10.1371/journal.pone.0235655⟩
PLoS ONE, Vol 15, Iss 7, p e0235655 (2020)
International audience; Biallelic variants in RNU4ATAC, a non-coding gene transcribed into the minor spliceosome component U4atac snRNA, are responsible for three rare recessive developmental diseases, namely Taybi-Linder/MOPD1, Roifman and Lowry-Woo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdfd207a43e278f43fc3f603b4e4fff6
https://pubmed.ncbi.nlm.nih.gov/32628740
https://pubmed.ncbi.nlm.nih.gov/32628740
Autor:
Martin Dutertre, Didier Auboeuf, Iris Tanaka, Olivier Saulnier, Clara Benoit-Pilven, Ivan Bièche, Alina Chakraborty, Frederic Pouzoulet, Stéphan Vagner, Dalila Labiod, Olivier Delattre, Sophie Vacher, Eric Lam
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, 2020, Ahead of print. ⟨10.1093/nar/gkz1213⟩
Nucleic Acids Research, 2020, Ahead of print. ⟨10.1093/nar/gkz1213⟩
Besides analyses of specific alternative splicing (AS) variants, little is known about AS regulatory pathways and programs involved in anticancer drug resistance. Doxorubicin is widely used in breast cancer chemotherapy. Here, we identified 1723 AS e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00852853d7911c09194fc3f6d72ffac2
http://hdl.handle.net/10044/1/75656
http://hdl.handle.net/10044/1/75656
Autor:
Amandine Campan-Fournier, Sylvie Mazoyer, Aimee D C Paulussen, Alicia Besson, Audric Cologne, Vincent Lacroix, Annick Toutain, Anne-Louise Leutenegger, Audrey Putoux, Patrick Edery, Clara Benoit-Pilven, Chaim M. Roifman, Christine E. M. de Die-Smulders, Lucile Pinson, Michael B. Bober
Publikováno v:
RNA
RNA, Cold Spring Harbor Laboratory Press, 2019, pp.1-21. ⟨10.1261/rna.071423.119⟩
RNA, 2019, pp.1-21. ⟨10.1261/rna.071423.119⟩
Rna-A Publication of the Rna Society, 25(9), 1130-1149. Cold Spring Harbor Laboratory Press
RNA, Cold Spring Harbor Laboratory Press, 2019, pp.1-21. ⟨10.1261/rna.071423.119⟩
RNA, 2019, pp.1-21. ⟨10.1261/rna.071423.119⟩
Rna-A Publication of the Rna Society, 25(9), 1130-1149. Cold Spring Harbor Laboratory Press
Minor intron splicing plays a central role in human embryonic development and survival. Indeed, biallelic mutations in RNU4ATAC, transcribed into the minor spliceosomal U4atac snRNA, are responsible for three rare autosomal recessive multimalformatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::295cf4813d8c203cc5cd9305e6501c60
https://hal.inria.fr/hal-02305628
https://hal.inria.fr/hal-02305628