Search Results - "Coppee, Frederique"

Olfactory and gustatory dysfunctions as a clinical presentation of mild-to-moderate forms of the coronavirus disease (COVID-19): a multicenter European study by Lechien, Jerome R., Chiesa-Estomba, Carlos M., De Siati, Daniele R., Horoi, Mihaela, Le Bon, Serge D., Rodriguez, Alexandra, Dequanter, Didier, Blecic, Serge, El Afia, Fahd, Distinguin, Lea, Chekkoury-Idrissi, Younes, Hans, Stéphane, Delgado, Irene Lopez, Calvo-Henriquez, Christian, Lavigne, Philippe, Falanga, Chiara, Barillari, Maria Rosaria, Cammaroto, Giovanni, Khalife, Mohamad, Leich, Pierre, Souchay, Christel, Rossi, Camelia, Journe, Fabrice, Hsieh, Julien, Edjlali, Myriam, Carlier, Robert, Ris, Laurence, Lovato, Andrea, De Filippis, Cosimo, Coppee, Frederique, Fakhry, Nicolas, Ayad, Tareck, Saussez, Sven

“…Objective To investigate the occurrence of olfactory and gustatory dysfunctions in patients with laboratory-confirmed COVID-19 infection. Methods Patients with…”
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The FSHD atrophic myotube phenotype is caused by DUX4 expression by Vanderplanck, Céline, Ansseau, Eugénie, Charron, Sébastien, Stricwant, Nadia, Tassin, Alexandra, Laoudj-Chenivesse, Dalila, Wilton, Steve D, Coppée, Frédérique, Belayew, Alexandra

“…Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat array in which we identified the double homeobox 4 (DUX4)…”
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An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies by Bosnakovski, Darko, Xu, Zhaohui, Ji Gang, Eun, Galindo, Cristi L, Liu, Mingju, Simsek, Tugba, Garner, Harold R, Agha-Mohammadi, Siamak, Tassin, Alexandra, Coppée, Frédérique, Belayew, Alexandra, Perlingeiro, Rita R, Kyba, Michael

“…Facioscapulohumeral muscular dystrophy (FSHD) is caused by an unusual deletion with neomorphic activity. This deletion derepresses genes in cis ; however which…”
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DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1 by Dixit, Manjusha, Ansseau, Eugénie, Tassin, Alexandra, Winokur, Sara, Shi, Rongye, Qian, Hong, Sauvage, Sébastien, Mattéotti, Christel, van Acker, Anne M, Leo, Oberdan, Figlewicz, Denise, Barro, Marietta, Laoudj-Chenivesse, Dalila, Belayew, Alexandra, Coppée, Frédérique, Chen, Yi-Wen

“…Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder linked to contractions of the D4Z4 repeat array in the subtelomeric region of…”
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Molecular and cellular biology of PCSK9: impact on glucose homeostasis by Tchéoubi, Sègbédé E. R., Akpovi, Casimir D., Coppée, Frédérique, Declèves, Anne-Emilie, Laurent, Sophie, Agbangla, Clément, Burtea, Carmen

“…Proprotein convertase substilisin/kexin 9 (PCSK9) inhibitors (PCSK9i) revolutionised the lipid-lowering therapy. However, a risk of type 2 diabetes mellitus…”
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DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo by Wallace, Lindsay M., Garwick, Sara E., Mei, Wenyan, Belayew, Alexandra, Coppee, Frederique, Ladner, Katherine J., Guttridge, Denis, Yang, Jing, Harper, Scott Q.

“…Objective: Facioscapulohumeral muscular dystrophy (FSHD) is associated with D4Z4 repeat contraction on human chromosome 4q35. This genetic lesion does not…”
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Antisense Oligonucleotides Used to Target the DUX4 mRNA as Therapeutic Approaches in FaciosScapuloHumeral Muscular Dystrophy (FSHD) by Ansseau, Eugénie, Vanderplanck, Céline, Wauters, Armelle, Harper, Scott Q, Coppée, Frédérique, Belayew, Alexandra

“…FacioScapuloHumeral muscular Dystrophy (FSHD) is one of the most prevalent hereditary myopathies and is generally characterized by progressive muscle atrophy…”
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DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy? by Tassin, Alexandra, Laoudj‐Chenivesse, Dalila, Vanderplanck, Céline, Barro, Marietta, Charron, Sébastien, Ansseau, Eugénie, Chen, Yi‐Wen, Mercier, Jacques, Coppée, Frédérique, Belayew, Alexandra

“…Facioscapulohumeral muscular dystrophy (FSHD) is one of the most frequent hereditary muscle disorders. It is linked to contractions of the D4Z4 repeat array in…”
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FSHD myotubes with different phenotypes exhibit distinct proteomes by Tassin, Alexandra, Leroy, Baptiste, Laoudj-Chenivesse, Dalila, Wauters, Armelle, Vanderplanck, Céline, Le Bihan, Marie-Catherine, Coppée, Frédérique, Wattiez, Ruddy, Belayew, Alexandra

“…Facioscapulohumeral muscular dystrophy (FSHD) is a progressive muscle disorder linked to a contraction of the D4Z4 repeat array in the 4q35 subtelomeric…”
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Dux4 controls migration of mesenchymal stem cells through the Cxcr4-Sdf1 axis by Dmitriev, Petr, Kiseleva, Ekaterina, Kharchenko, Olga, Ivashkin, Evgeny, Pichugin, Andrei, Dessen, Philippe, Robert, Thomas, Coppée, Frédérique, Belayew, Alexandra, Carnac, Gilles, Laoudj-Chenivesse, Dalila, Lipinski, Marc, Vasiliev, Andrei, Vassetzky, Yegor S

“…We performed transcriptome profiling of human immortalized myoblasts (MB) transiently expressing double homeobox transcription factor 4 (DUX4) and double…”
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Overexpression of the double homeodomain protein DUX4c interferes with myofibrillogenesis and induces clustering of myonuclei by Vanderplanck, Céline, Tassin, Alexandra, Ansseau, Eugénie, Charron, Sébastien, Wauters, Armelle, Lancelot, Céline, Vancutsem, Kelly, Laoudj-Chenivesse, Dalila, Belayew, Alexandra, Coppée, Frédérique

“…Facioscapulohumeral muscular dystrophy (FSHD) is associated with DNA hypomethylation at the 4q35 D4Z4 repeat array. Both the causal gene DUX4 and its homolog…”
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DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferation by Ansseau, Eugénie, Laoudj-Chenivesse, Dalila, Marcowycz, Aline, Tassin, Alexandra, Vanderplanck, Céline, Sauvage, Sébastien, Barro, Marietta, Mahieu, Isabelle, Leroy, Axelle, Leclercq, India, Mainfroid, Véronique, Figlewicz, Denise, Mouly, Vincent, Butler-Browne, Gillian, Belayew, Alexandra, Coppée, Frédérique

“…Facioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to contractions of the D4Z4 repeat array in 4q35. We have previously identified a…”
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The Krüppel-like Factor 15 as a Molecular Link between Myogenic Factors and a Chromosome 4q Transcriptional Enhancer Implicated in Facioscapulohumeral Dystrophy by Dmitriev, Petr, Petrov, Andrei, Ansseau, Eugenie, Stankevicins, Luiza, Charron, Sébastien, Kim, Elena, Bos, Tomas Jan, Robert, Thomas, Turki, Ahmed, Coppée, Frédérique, Belayew, Alexandra, Lazar, Vladimir, Carnac, Gilles, Laoudj, Dalila, Lipinski, Marc, Vassetzky, Yegor S.

“…Facioscapulohumeral muscular dystrophy (FSHD), a dominant hereditary disease with a prevalence of 7 per 100,000 individuals, is associated with a partial…”
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The Role of D4Z4-Encoded Proteins in the Osteogenic Differentiation of Mesenchymal Stromal Cells Isolated from Bone Marrow by de la Kethulle de Ryhove, Laurence, Ansseau, Eugénie, Nachtegael, Charlotte, Pieters, Karlien, Vanderplanck, Céline, Geens, Mieke, Sermon, Karen, Wilton, Steve D, Coppée, Frédérique, Lagneaux, Laurence, Belayew, Alexandra

“…Facioscapulohumeral muscular dystrophy (FSHD) is associated with an activation of the double homeobox 4 (DUX4) gene, which we previously identified within the…”
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Clinical and epidemiological characteristics of 1420 European patients with mild‐to‐moderate coronavirus disease 2019 by Lechien, Jerome R., Chiesa‐Estomba, Carlos M., Place, Sammy, Van Laethem, Yves, Cabaraux, Pierre, Mat, Quentin, Huet, Kathy, Plzak, Jan, Horoi, Mihaela, Hans, Stéphane, Rosaria Barillari, Maria, Cammaroto, Giovanni, Fakhry, Nicolas, Martiny, Delphine, Ayad, Tareck, Jouffe, Lionel, Hopkins, Claire, Saussez, Sven, Blecic, Serge, De Siati, Daniele R., Leich, Pierre, Souchay, Christel, Rossi, Camelia, Journe, Fabrice, Hsieh, Julien, Ris, Laurence, El Afia, Fahd, Harmegnies, Bernard, Distinguin, Lea, Chekkoury‐Idrissi, Younes, Circiu, Marta, Lavigne, Philippe, Lopez Delgado, Irene, Calvo‐Henriquez, Christian, Falanga, Chiara, Coppee, Frederique, Bon, Serge D, Rodriguez, Alexandra, Dequanter, Didier, Cornelis, Jean‐Philippe, Vergez, Sebastien, Koenen, Lukas, Giuditta, Mannelli, Molteni, Gabriele, Tucciarone, Manuel, Radulesco, Thomas, Khalife, Mohamad, Fourneau, Anne‐Francoise, Cherifi, Soraya, Manto, Mario, Michel, Justin, Radulesco, Thomas, Molteni, Gabriele, Tucciarone, Manuel, Mannelli, Giuditta, Cantarella, Giovanna

“…Background The clinical presentation of European patients with mild‐to‐moderate COVID‐19 infection is still unknown. Objective To study the clinical…”
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Helicase-like transcription factor exhibits increased expression and altered intracellular distribution during tumor progression in hypopharyngeal and laryngeal squamous cell carcinomas by Capouillez, Aurélie, Decaestecker, Christine, Filleul, Olivier, Chevalier, Dominique, Coppée, Frederique, Leroy, Xavier, Belayew, Alexandra, Saussez, Sven

“…The helicase-like transcription factor (HLTF) belongs to the SWI/SNF family of proteins that use the energy from adenosine triphosphate hydrolysis to remodel…”
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Induction of a local muscular dystrophy using electroporation in vivo: an easy tool for screening therapeutics by Derenne, Aline, Tassin, Alexandra, Nguyen, Thuy Hang, De Roeck, Estelle, Jenart, Vincianne, Ansseau, Eugénie, Belayew, Alexandra, Coppée, Frédérique, Declèves, Anne-Emilie, Legrand, Alexandre

“…Intramuscular injection and electroporation of naked plasmid DNA (IMEP) has emerged as a potential alternative to viral vector injection for transgene…”
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Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? by Richards, Mark, Coppée, Frédérique, Thomas, Nick, Belayew, Alexandra, Upadhyaya, Meena

“…Facioscapulohumeral muscular dystrophy (FSHD) is the third most common muscular dystrophy after the dystrophinopathies and myotonic dystrophy and is associated…”
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Homologous Transcription Factors DUX4 and DUX4c Associate with Cytoplasmic Proteins during Muscle Differentiation by Ansseau, Eugénie, Eidahl, Jocelyn O, Lancelot, Céline, Tassin, Alexandra, Matteotti, Christel, Yip, Cassandre, Liu, Jian, Leroy, Baptiste, Hubeau, Céline, Gerbaux, Cécile, Cloet, Samuel, Wauters, Armelle, Zorbo, Sabrina, Meyer, Pierre, Pirson, Isabelle, Laoudj-Chenivesse, Dalila, Wattiez, Ruddy, Harper, Scott Q, Belayew, Alexandra, Coppée, Frédérique

“…Hundreds of double homeobox (DUX) genes map within 3.3-kb repeated elements dispersed in the human genome and encode DNA-binding proteins. Among these, we…”
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The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins by Claus, Clothilde, Slavin, Moriya, Ansseau, Eugénie, Lancelot, Céline, Bah, Karimatou, Lassche, Saskia, Fiévet, Manon, Greco, Anna, Tomaiuolo, Sara, Tassin, Alexandra, Dudome, Virginie, Kusters, Benno, Declèves, Anne-Emilie, Laoudj-Chenivesse, Dalila, van Engelen, Baziel G M, Nonclercq, Denis, Belayew, Alexandra, Kalisman, Nir, Coppée, Frédérique

“…We have previously demonstrated that double homeobox 4 centromeric (DUX4C) encoded for a functional DUX4c protein upregulated in dystrophic skeletal muscles…”
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