Claire Rougeulle - Publications

Affiliations: 
Centre Epigenetique et Destin Cellulaire Université Paris Diderot - Paris 7, Paris, Île-de-France, France 

59 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Rosspopoff O, Cazottes E, Huret C, Loda A, Collier AJ, Casanova M, Rugg-Gunn PJ, Heard E, Ouimette JF, Rougeulle C. Species-specific regulation of XIST by the JPX/FTX orthologs. Nucleic Acids Research. 51: 2177-2194. PMID 36727460 DOI: 10.1093/nar/gkad029  0.75
2022 Mahadik K, Rougeulle C. Study of X Chromosome Activity Status in Human Naive Pluripotent Stem Cells Using RNA-FISH. Methods in Molecular Biology (Clifton, N.J.). 2416: 239-255. PMID 34870840 DOI: 10.1007/978-1-0716-1908-7_15  0.503
2021 Heard E, Rougeulle C. Digging into X chromosome inactivation. Science (New York, N.Y.). 374: 942-943. PMID 34793229 DOI: 10.1126/science.abm1857  0.446
2021 Moscatelli M, Rougeulle C. [Latest insights on X-chromosome inactivation: When general principles should be revisited]. Medecine Sciences : M/S. 37: 152-158. PMID 33591258 DOI: 10.1051/medsci/2020278  0.514
2020 Ouimette JF, Rougeulle C. Many XCI-ting routes to reach the eXACT dose. Nature Cell Biology. PMID 33257807 DOI: 10.1038/s41556-020-00608-3  0.664
2020 Cazottes E, Rougeulle C. Straight to the X: Modeling Human X Chromosome Inactivation in hESCs by FGF Signal Blockade. Cell Stem Cell. 27: 352-353. PMID 32888422 DOI: 10.1016/J.Stem.2020.08.008  0.535
2020 Patrat C, Ouimette JF, Rougeulle C. X chromosome inactivation in human development. Development (Cambridge, England). 147. PMID 31900287 DOI: 10.1242/Dev.183095  0.78
2019 Casanova M, Moscatelli M, Chauvière LÉ, Huret C, Samson J, Liyakat Ali TM, Rosspopoff O, Rougeulle C. A primate-specific retroviral enhancer wires the XACT lncRNA into the core pluripotency network in humans. Nature Communications. 10: 5652. PMID 31827084 DOI: 10.1038/S41467-019-13551-1  0.531
2018 John RM, Rougeulle C. Developmental Epigenetics: Phenotype and the Flexible Epigenome. Frontiers in Cell and Developmental Biology. 6: 130. PMID 30364270 DOI: 10.3389/Fcell.2018.00130  0.306
2018 Furlan G, Gutierrez Hernandez N, Huret C, Galupa R, van Bemmel JG, Romito A, Heard E, Morey C, Rougeulle C. The Ftx Noncoding Locus Controls X Chromosome Inactivation Independently of Its RNA Products. Molecular Cell. 70: 462-472.e8. PMID 29706539 DOI: 10.1016/J.Molcel.2018.03.024  0.566
2018 Kilens S, Meistermann D, Moreno D, Chariau C, Gaignerie A, Reignier A, Lelièvre Y, Casanova M, Vallot C, Nedellec S, Flippe L, Firmin J, Song J, Charpentier E, Lammers J, ... ... Rougeulle C, et al. Parallel derivation of isogenic human primed and naive induced pluripotent stem cells. Nature Communications. 9: 360. PMID 29367672 DOI: 10.1038/S41467-017-02107-W  0.415
2017 Sahakyan A, Plath K, Rougeulle C. Regulation of X-chromosome dosage compensation in human: mechanisms and model systems. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 372. PMID 28947660 DOI: 10.1098/Rstb.2016.0363  0.586
2016 Vallot C, Rougeulle C. Single-cell Visualization of Chromosome Transcriptional Territories by RNA-paint. Bio-Protocol. 6. PMID 29082283 DOI: 10.21769/BioProtoc.1914  0.407
2016 Vallot C, Patrat C, Collier AJ, Huret C, Casanova M, Liyakat Ali TM, Tosolini M, Frydman N, Heard E, Rugg-Gunn PJ, Rougeulle C. XACT Noncoding RNA Competes with XIST in the Control of X Chromosome Activity during Human Early Development. Cell Stem Cell. PMID 27989768 DOI: 10.1016/J.Stem.2016.10.014  0.585
2016 Cantone I, Bagci H, Dormann D, Dharmalingam G, Nesterova T, Brockdorff N, Rougeulle C, Vallot C, Heard E, Chaligne R, Merkenschlager M, Fisher AG. Ordered chromatin changes and human X chromosome reactivation by cell fusion-mediated pluripotent reprogramming. Nature Communications. 7: 12354. PMID 27507283 DOI: 10.1038/Ncomms12354  0.557
2016 Vallot C, Ouimette JF, Rougeulle C. Establishment of X chromosome inactivation and epigenomic features of the inactive X depend on cellular contexts. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 38: 869-80. PMID 27389958 DOI: 10.1002/Bies.201600121  0.773
2016 Casanova M, Ali TM, Rougeulle C. Enlightening the contribution of the dark matter to the X chromosome inactivation process in mammals. Seminars in Cell & Developmental Biology. PMID 27174438 DOI: 10.1016/J.Semcdb.2016.05.003  0.561
2016 Furlan G, Rougeulle C. Function and evolution of the long noncoding RNA circuitry orchestrating X-chromosome inactivation in mammals. Wiley Interdisciplinary Reviews. Rna. 7: 702-22. PMID 27173581 DOI: 10.1002/Wrna.1359  0.611
2016 Ouimette JF, Rougeulle C. How Many Non-coding RNAs Does It Take to Compensate Male/Female Genetic Imbalance? Advances in Experimental Medicine and Biology. 886: 33-49. PMID 26659486 DOI: 10.1007/978-94-017-7417-8_3  0.762
2015 Chen H, Aksoy I, Gonnot F, Osteil P, Aubry M, Hamela C, Rognard C, Hochard A, Voisin S, Fontaine E, Mure M, Afanassieff M, Cleroux E, Guibert S, Chen J, ... ... Rougeulle C, et al. Reinforcement of STAT3 activity reprogrammes human embryonic stem cells to naive-like pluripotency. Nature Communications. 6: 7095. PMID 25968054 DOI: 10.1038/Ncomms8095  0.357
2015 Vallot C, Ouimette JF, Makhlouf M, Féraud O, Pontis J, Côme J, Martinat C, Bennaceur-Griscelli A, Lalande M, Rougeulle C. Erosion of X Chromosome Inactivation in Human Pluripotent Cells Initiates with XACT Coating and Depends on a Specific Heterochromatin Landscape. Cell Stem Cell. 16: 533-46. PMID 25921272 DOI: 10.1016/J.Stem.2015.03.016  0.786
2015 Lazorthes S, Vallot C, Briois S, Aguirrebengoa M, Thuret JY, St Laurent G, Rougeulle C, Kapranov P, Mann C, Trouche D, Nicolas E. A vlincRNA participates in senescence maintenance by relieving H2AZ-mediated repression at the INK4 locus. Nature Communications. 6: 5971. PMID 25601475 DOI: 10.1038/Ncomms6971  0.421
2014 Makhlouf M, Ouimette JF, Oldfield A, Navarro P, Neuillet D, Rougeulle C. A prominent and conserved role for YY1 in Xist transcriptional activation. Nature Communications. 5: 4878. PMID 25209548 DOI: 10.1038/Ncomms5878  0.772
2013 Vallot C, Rougeulle C. Long non-coding RNAs and human X-chromosome regulation: a coat for the active X chromosome. Rna Biology. 10: 1262-5. PMID 23948700 DOI: 10.4161/Rna.25802  0.617
2013 Vallot C, Rougeulle C. [X chromosome inactivation in human: XACT and XIST, a non coding RNA for each X]. Medecine Sciences : M/S. 29: 223-5. PMID 23452612 DOI: 10.1051/Medsci/2013292024  0.539
2013 Vallot C, Huret C, Lesecque Y, Resch A, Oudrhiri N, Bennaceur-Griscelli A, Duret L, Rougeulle C. XACT, a long noncoding transcript coating the active X chromosome in human pluripotent cells. Nature Genetics. 45: 239-41. PMID 23334669 DOI: 10.1038/Ng.2530  0.59
2011 Romito A, Rougeulle C. Origin and evolution of the long non-coding genes in the X-inactivation center. Biochimie. 93: 1935-42. PMID 21820484 DOI: 10.1016/J.Biochi.2011.07.009  0.534
2011 Makhlouf M, Rougeulle C. Linking X chromosome inactivation to pluripotency: Necessity or fate? Trends in Molecular Medicine. 17: 329-36. PMID 21411371 DOI: 10.1016/J.Molmed.2011.02.001  0.589
2011 Chureau C, Chantalat S, Romito A, Galvani A, Duret L, Avner P, Rougeulle C. Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region. Human Molecular Genetics. 20: 705-18. PMID 21118898 DOI: 10.1093/Hmg/Ddq516  0.558
2010 Navarro P, Oldfield A, Legoupi J, Festuccia N, Dubois A, Attia M, Schoorlemmer J, Rougeulle C, Chambers I, Avner P. Molecular coupling of Tsix regulation and pluripotency. Nature. 468: 457-60. PMID 21085182 DOI: 10.1038/Nature09496  0.491
2010 Mitjavila-Garcia MT, Bonnet ML, Yates F, Haddad R, Oudrhiri N, Féraud O, Magniez A, Makhlouf M, Vallot C, Rougeulle C, Bennaceur-Griscelli A, Turhan AG. Partial reversal of the methylation pattern of the X-linked gene HUMARA during hematopoietic differentiation of human embryonic stem cells. Journal of Molecular Cell Biology. 2: 291-8. PMID 20823083 DOI: 10.1093/Jmcb/Mjq026  0.417
2010 Fritsch L, Robin P, Mathieu JR, Souidi M, Hinaux H, Rougeulle C, Harel-Bellan A, Ameyar-Zazoua M, Ait-Si-Ali S. A subset of the histone H3 lysine 9 methyltransferases Suv39h1, G9a, GLP, and SETDB1 participate in a multimeric complex. Molecular Cell. 37: 46-56. PMID 20129054 DOI: 10.1016/J.Molcel.2009.12.017  0.304
2009 Navarro P, Chantalat S, Foglio M, Chureau C, Vigneau S, Clerc P, Avner P, Rougeulle C. A role for non-coding Tsix transcription in partitioning chromatin domains within the mouse X-inactivation centre. Epigenetics & Chromatin. 2: 8. PMID 19615107 DOI: 10.1186/1756-8935-2-8  0.469
2009 Rougeulle C. [X inactivation in embryonic stem cells is controlled by pluripotent genes]. Medecine Sciences : M/S. 25: 234-5. PMID 19361384 DOI: 10.1051/Medsci/2009253234  0.45
2008 Navarro P, Chambers I, Karwacki-Neisius V, Chureau C, Morey C, Rougeulle C, Avner P. Molecular coupling of Xist regulation and pluripotency. Science (New York, N.Y.). 321: 1693-5. PMID 18802003 DOI: 10.1126/Science.1160952  0.547
2008 Mitjavila-Garcia MT, Yates F, Bonnet M, Rougeulle C, Makhlouf M, Feraud O, Magniez A, Bennaceur-Griscelli A, Turhan AG. X-Linked Clonality Analysis of Human Embryonic Stem Cells ( hESC ) Before and after induction of Hematopoietic Differentiation Blood. 112: 4784-4784. DOI: 10.1182/Blood.V112.11.4784.4784  0.433
2006 Navarro P, Page DR, Avner P, Rougeulle C. Tsix-mediated epigenetic switch of a CTCF-flanked region of the Xist promoter determines the Xist transcription program. Genes & Development. 20: 2787-92. PMID 17043308 DOI: 10.1101/Gad.389006  0.453
2006 Ciaudo C, Bourdet A, Cohen-Tannoudji M, Dietz HC, Rougeulle C, Avner P. Nuclear mRNA degradation pathway(s) are implicated in Xist regulation and X chromosome inactivation. Plos Genetics. 2: e94. PMID 16789828 DOI: 10.1371/Journal.Pgen.0020094  0.543
2005 Navarro P, Pichard S, Ciaudo C, Avner P, Rougeulle C. Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation. Genes & Development. 19: 1474-84. PMID 15964997 DOI: 10.1101/Gad.341105  0.514
2004 Rougeulle C, Avner P. The role of antisense transcription in the regulation of X-inactivation. Current Topics in Developmental Biology. 63: 61-89. PMID 15536014 DOI: 10.1016/S0070-2153(04)63003-1  0.489
2004 Landers M, Bancescu DL, Le Meur E, Rougeulle C, Glatt-Deeley H, Brannan C, Muscatelli F, Lalande M. Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. Nucleic Acids Research. 32: 3480-92. PMID 15226413 DOI: 10.1093/Nar/Gkh670  0.39
2004 Rougeulle C, Chaumeil J, Sarma K, Allis CD, Reinberg D, Avner P, Heard E. Differential histone H3 lys-9 and lys-27 methylation profiles on the X chromosome Molecular and Cellular Biology. 24: 5475-5484. PMID 15169908 DOI: 10.1128/Mcb.24.12.5475-5484.2004  0.52
2004 Morey C, Navarro P, Debrand E, Avner P, Rougeulle C, Clerc P. The region 3' to Xist mediates X chromosome counting and H3 Lys-4 dimethylation within the Xist gene. The Embo Journal. 23: 594-604. PMID 14749728 DOI: 10.1038/Sj.Emboj.7600071  0.589
2003 Rougeulle C, Avner P. Controlling X-inactivation in mammals: what does the centre hold? Seminars in Cell & Developmental Biology. 14: 331-40. PMID 15015740 DOI: 10.1016/J.Semcdb.2003.09.014  0.511
2003 Rougeulle C, Navarro P, Avner P. Promoter-restricted H3 Lys 4 di-methylation is an epigenetic mark for monoallelic expression. Human Molecular Genetics. 12: 3343-8. PMID 14570711 DOI: 10.1093/Hmg/Ddg351  0.413
2002 Rougeulle C, Heard E. Antisense RNA in imprinting: spreading silence through Air. Trends in Genetics : Tig. 18: 434-7. PMID 12175797 DOI: 10.1016/S0168-9525(02)02749-X  0.387
2002 Bourdet A, Rougeulle C. Inactivation du chromosome X chez la souris : les tendancescisettranspour 2002 MéDecine/Sciences. 18: 532-534. DOI: 10.1051/Medsci/2002185532  0.473
2001 Heard E, Rougeulle C, Arnaud D, Avner P, Allis CD, Spector DL. Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation. Cell. 107: 727-38. PMID 11747809 DOI: 10.1016/S0092-8674(01)00598-0  0.516
1999 Dudley AM, Rougeulle C, Winston F. The Spt components of SAGA facilitate TBP binding to a promoter at a post-activator-binding step in vivo Genes and Development. 13: 2940-2945. PMID 10580001 DOI: 10.1101/Gad.13.22.2940  0.345
1998 Rougeulle C, Lalande M. Angelman syndrome: how many genes to remain silent? Neurogenetics. 1: 229-37. PMID 10732796 DOI: 10.1007/S100480050034  0.387
1998 Rougeulle C, Cardoso C, Fontés M, Colleaux L, Lalande M. An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript. Nature Genetics. 19: 15-6. PMID 9590281 DOI: 10.1038/Ng0598-15  0.326
1997 Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, Malzac P, Roëckel N, Taviaux S, Lefranc JL, Cau P, Berta P, Lalande M, Muscatelli F. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genetics. 17: 357-61. PMID 9354807 DOI: 10.1038/Ng1197-357  0.405
1997 Simmler MC, Heard E, Rougeulle C, Cruaud C, Weissenbach J, Avner P. Localization and expression analysis of a novel conserved brain expressed transcript, Brx/BRX, lying within the Xic/XIC candidate region. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 760-6. PMID 9321471 DOI: 10.1007/S003359900561  0.513
1996 Heard E, Kress C, Mongelard F, Courtier B, Rougeulle C, Ashworth A, Vourc'h C, Babinet C, Avner P. Transgenic mice carrying an Xist-containing YAC. Human Molecular Genetics. 5: 441-50. PMID 8845836 DOI: 10.1093/Hmg/5.4.441  0.537
1996 Rougeulle C, Avner P. Cloning and characterization of a murine brain specific gene Bpx and its human homologue lying within the Xic candidate region. Human Molecular Genetics. 5: 41-9. PMID 8789438 DOI: 10.1093/Hmg/5.1.41  0.48
1994 Simmler MC, Cattanach BM, Rasberry C, Rougeulle C, Avner P. Mapping the murine Xce locus with (CA)n repeats. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 523-30. PMID 8118102 DOI: 10.1007/Bf00364788  0.474
1994 Rougeulle C, Colleaux L, Dujon B, Avner P. Generation and characterization of an ordered lambda clone array for the 460-kb region surrounding the murine Xist sequence. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 416-23. PMID 7726900 DOI: 10.1007/Bf00357001  0.416
1993 Colleaux L, Rougeulle C, Avner P, Dujon B. Rapid physical mapping of YAC inserts by random integration of I-Sce I sites. Human Molecular Genetics. 2: 265-71. PMID 8499915 DOI: 10.1093/Hmg/2.3.265  0.33
1993 Heard E, Simmler MC, Larin Z, Rougeulle C, Courtier B, Lehrach H, Avner P. Physical mapping and YAC contig analysis of the region surrounding Xist on the mouse X chromosome. Genomics. 15: 559-69. PMID 8468050 DOI: 10.1006/Geno.1993.1108  0.527
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