Institut NeuroPSI - UMR9197
CNRS Université Paris-Saclay
Gif-Sur-Yvette
France

Dr. Cyrille VAILLEND

Directeur de Recherche
Cognition, Plasticité & Neuropathologies, Cognition, Plasticity & Neuropathologies

cyrille . vaillend(At)universite-paris-saclay . fr
+33(0) 1 69 15 49 85
ORCID : 0000-0002-8783-8185

Article dans une revue

2021

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Mirella Telles Salgueiro Barboni, André Maurício Passos Liber, Anneka Joachimsthaler, Amel Saoudi, Aurelie Goyenvalle, et al.. Altered visual processing in the mdx52 mouse model of Duchenne muscular dystrophy. Neurobiology of Disease, Elsevier, 2021, 152, pp.105288. ⟨10.1016/j.nbd.2021.105288⟩. ⟨hal-03196031⟩
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Mehdi Belmaati Cherkaoui, Ophélie Vacca, Charlotte Izabelle, Anne‐cécile Boulay, Claire Boulogne, et al.. Dp71 contribution to the molecular scaffold anchoring aquaporine‐4 channels in brain macroglial cells. Glia, Wiley, 2021, 69 (4), pp.954-970. ⟨10.1002/glia.23941⟩. ⟨hal-03035498⟩
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2020

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Philippine Aupy, Faouzi Zarrouki, Quentin Sandro, Cécile Gastaldi, Pierre-Olivier Buclez, et al.. Long-Term Efficacy of AAV9-U7snRNA-Mediated Exon 51 Skipping in mdx52 Mice. Molecular Therapy - Methods and Clinical Development, Nature Publishing Group, 2020, 17, pp.1037-1047. ⟨10.1016/j.omtm.2020.04.025⟩. ⟨hal-02912922⟩
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https://hal.archives-ouvertes.fr/hal-02912922/file/Aupy2020-mdx52-AAVU7.pdf BibTex
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Mirella Telles Salgueiro Barboni, Cyrille Vaillend, Anneka Joachimsthaler, André Maurício Passos Liber, Hanen Khabou, et al.. Rescue of Defective Electroretinographic Responses in Dp71-Null Mice With AAV-Mediated Reexpression of Dp71. Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2020, 61 (2), pp.11. ⟨10.1167/iovs.61.2.11⟩. ⟨hal-02520616⟩
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https://hal.archives-ouvertes.fr/hal-02520616/file/Barboni2020-ERG-Dp71.pdf BibTex
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Federica Briatore, Giulia Pregno, Silvia Di Angelantonio, Elena Frola, Maria Egle de Stefano, et al.. Dystroglycan Mediates Clustering of Essential GABAergic Components in Cerebellar Purkinje Cells. Frontiers in Molecular Neuroscience, Frontiers Media, 2020, 13 (9), pp.164. ⟨10.3389/fnmol.2020.00164⟩. ⟨hal-03009707⟩
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https://hal-cnrs.archives-ouvertes.fr/hal-03009707/file/Briatore2020-Front%20Mol%20neuro.pdf BibTex
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Tuy Nga Brignol, Dominique Mornet, Cecilia Montañez, Dora Fix Ventura, Cyrille Vaillend, et al.. What is the ocular phenotype associated with a single exon 78 deletion in Duchenne muscular dystrophy?. Journal of Human Genetics, Nature Publishing Group, 2020, 65 (8), pp.715-716. ⟨10.1038/s10038-020-0755-5⟩. ⟨hal-02640159⟩
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https://hal.archives-ouvertes.fr/hal-02640159/file/2020%20Brignol%20et%20al.%2C%20What%20is%20the.pdf BibTex
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Charlotte Castillon, Laurine Gonzalez, Florence Domenichini, Sandrine Guyon, Kévin da Silva, et al.. The intellectual disability PAK3 R67C mutation impacts cognitive functions and adult hippocampal neurogenesis. Human Molecular Genetics, Oxford University Press (OUP), 2020, 29 (12), pp.1950-1968. ⟨10.1093/hmg/ddz296⟩. ⟨hal-02459269⟩
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https://hal.archives-ouvertes.fr/hal-02459269/file/HMG-2019-D-00571.R1_Proof_hi%2029novembre19.pdf BibTex
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Jos G.M. Hendriksen, Mathula Thangarajh, Hermien Kan, Francesco Muntoni, Dr Aoki, et al.. 249th ENMC International Workshop: The role of brain dystrophin in muscular dystrophy: Implications for clinical care and translational research, Hoofddorp, The Netherlands, November 29th–December 1st 2019. Neuromuscular Disorders, Elsevier, 2020, 30 (9), pp.782-794. ⟨10.1016/j.nmd.2020.08.357⟩. ⟨hal-03009729⟩
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https://hal-cnrs.archives-ouvertes.fr/hal-03009729/file/NMD2020-249thENMC.pdf BibTex

2019

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Lora Martucci, Muriel Amar, Rémi Chaussenot, Gabriel Benet, Oscar Bauer, et al.. A multiscale analysis in CD38 −/− mice unveils major prefrontal cortex dysfunctions. FASEB Journal, Federation of American Society of Experimental Biology, 2019, 54, pp.fj.201800489R. ⟨10.1096/fj.201800489R⟩. ⟨hal-02111927⟩
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https://hal.archives-ouvertes.fr/hal-02111927/file/Martucci%20et%20al%202019.pdf BibTex
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Lora Martucci, Muriel Amar, Rémi Chaussenot, Gabriel Benet, Oscar Bauer, et al.. A multiscale analysis in CD38 −/− mice unveils major prefrontal cortex dysfunctions. FASEB Journal, Federation of American Society of Experimental Biology, 2019, 33 (5), pp.5823-5835. ⟨10.1096/fj.201800489R⟩. ⟨hal-02269129⟩
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https://hal.archives-ouvertes.fr/hal-02269129/file/Martucci%20et%20al%202019.pdf BibTex
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Sabrina Souttou, Roza Benabdesselam, Lourdes Siqueiros-Marquez, Madina Sifi, Maha Deliba, et al.. Expression and localization of dystrophins and β-dystroglycan in the hypothalamic supraoptic nuclei of rat from birth to adulthood. Acta Histochemica, Elsevier, 2019, 121 (2), pp.218-226. ⟨10.1016/j.acthis.2018.12.001⟩. ⟨hal-01968724⟩
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2018

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Rémi Chaussenot, Muriel Amar, Philippe Fossier, Cyrille Vaillend. Dp71-Dystrophin Deficiency Alters Prefrontal Cortex Excitation-Inhibition Balance and Executive Functions. Molecular Neurobiology, Humana Press, 2018, ⟨10.1007/s12035-018-1259-6⟩. ⟨hal-01854469⟩
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Romain Helleringer, Delphine Le Verger, Xia Li, Charlotte Izabelle, Rémi Chaussenot, et al.. Cerebellar synapse properties and cerebellum-dependent motor and non-motor performance in Dp71-null mice. Disease Models & Mechanisms, Cambridge Company of Biologists, 2018, ⟨10.1242/dmm.033258⟩. ⟨hal-01828161⟩
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2017

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Jorge Aragón, Mayram González-Reyes, José Romo-Yáñez, Ophélie Vacca, Guadalupe Aguilar-González, et al.. Dystrophin Dp71 Isoforms Are Differentially Expressed in the Mouse Brain and Retina: Report of New Alternative Splicing and a Novel Nomenclature for Dp71 Isoforms.. Molecular Neurobiology, Humana Press, 2017, 55 (2), pp.1376-1386. ⟨10.1007/s12035-017-0405-x⟩. ⟨hal-01485065⟩
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Karima Relizani, Graziella Griffith, Lucía Echevarría, Faouzi Zarrouki, Patricia Facchinetti, et al.. Efficacy and Safety Profile of Tricyclo-DNA Antisense Oligonucleotides in Duchenne Muscular Dystrophy Mouse Model. Molecular Therapy - Nucleic Acids, Nature Publishing Group, 2017, 8, pp.144-157. ⟨10.1016/j.omtn.2017.06.013⟩. ⟨hal-02407950⟩
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Cyrille Vaillend, Rémi Chaussenot. Relationships linking emotional, motor, cognitive and GABAergic dysfunctions in dystrophin-deficient mdx mice.. Human Molecular Genetics, Oxford University Press (OUP), 2017, 26 (6), pp.1041-1055. ⟨10.1093/hmg/ddx013⟩. ⟨hal-01443475⟩
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2016

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Rubén Miranda, Serge Laroche, Cyrille Vaillend. Reduced neuronal density in the CA1 anterodorsal hippocampus of the mdx mouse.. Neuromuscular Disorders, Elsevier, 2016, 26 (11), pp.775-781. ⟨10.1016/j.nmd.2016.08.006⟩. ⟨hal-01366180⟩
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2015

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Rémi Chaussenot, Jean-Marc Edeline, Benoit Le Bec, Nicole El Massioui, Serge Laroche, et al.. Cognitive dysfunction in the dystrophin-deficient mouse model of Duchenne muscular dystrophy: A reappraisal from sensory to executive processes.. Neurobiology of Learning and Memory, Elsevier, 2015, pp.S1074-7427. ⟨10.1016/j.nlm.2015.07.006⟩. ⟨hal-01179087⟩
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Aurélie Goyenvalle, Graziella Griffith, Arran Babbs, Samir El Andaloussi, Kariem Ezzat, et al.. Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers. Nature Medicine, Nature Publishing Group, 2015, 21 (3), pp.270-275. ⟨10.1038/nm.3765⟩. ⟨hal-02407968⟩
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Rubén Miranda, Flora Nagapin, Bruno Bozon, Serge Laroche, Thierry Aubin, et al.. Altered social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne muscular dystrophy.. Molecular Autism, BioMed Central, 2015, 6, pp.60. ⟨10.1186/s13229-015-0053-9⟩. ⟨hal-01240336⟩
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2013

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Elise Morice, Séverine Farley, Roseline Poirier, Glenn Dallérac, Carine Chagneau, et al.. Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin-Lowry syndrome.. Neurobiology of Disease, Elsevier, 2013, pp.156-168. ⟨10.1016/j.nbd.2013.05.016⟩. ⟨hal-00912776⟩
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Sara Vianello, Hua Yu, Vincent Voisin, Hafedh Haddad, Xun He, et al.. Arginine butyrate: a therapeutic candidate for Duchenne muscular dystrophy.. FASEB Journal, Federation of American Society of Experimental Biology, 2013, 27 (6), pp.2256-69. ⟨10.1096/fj.12-215723⟩. ⟨hal-00850330⟩
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2012

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Caroline Perronnet, Carine Chagneau, Pascale Le Blanc, Nathalie Samson-Desvignes, Dominique Mornet, et al.. Upregulation of brain utrophin does not rescue behavioral alterations in dystrophin-deficient mice.. Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (10), pp.2263-76. ⟨10.1093/hmg/dds047⟩. ⟨hal-00733451⟩
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2011

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Glenn Dallérac, Caroline Perronnet, Carine Chagneau, Pascale Leblanc-Veyrac, Nathalie Samson-Desvignes, et al.. Rescue of a dystrophin-like protein by exon skipping normalizes synaptic plasticity in the hippocampus of the mdx mouse. Neurobiology of Disease, Elsevier, 2011, 43 (3), pp.635-641. ⟨10.1016/j.nbd.2011.05.012⟩. ⟨hal-02325193⟩
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Ruben Miranda, Uri Nudel, Serge Laroche, Cyrille Vaillend. Altered presynaptic ultrastructure in excitatory hippocampal synapses of mice lacking dystrophins Dp427 or Dp71.. Neurobiology of Disease, Elsevier, 2011, pp.134-141. ⟨10.1016/j.nbd.2011.02.017⟩. ⟨hal-00719010⟩
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2010

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Cyrille Vaillend, Caroline Perronnet, Carine Ros, Carole Gruszczynski, Aurélie Goyenvalle, et al.. Rescue of a dystrophin-like protein by exon skipping in vivo restores GABAA-receptor clustering in the hippocampus of the mdx mouse.. Molecular Therapy, Nature Publishing Group, 2010, 18 (9), pp.1683-8. ⟨10.1038/mt.2010.134⟩. ⟨hal-01183355⟩
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2009

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Fatma Daoud, Aurora Candelario-Martínez, Jean-Marie Billard, Avi Avital, Malik Khelfaoui, et al.. Role of Mental Retardation-Associated Dystrophin-Gene Product Dp71 in Excitatory Synapse Organization, Synaptic Plasticity and Behavioral Functions. PLoS ONE, Public Library of Science, 2009, 4 (8), pp.e6574. ⟨10.1371/journal.pone.0006574⟩. ⟨hal-02325225⟩
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R. Miranda, C. SÉbriÉ, J. Degrouard, Brigitte Gillet, Danielle Jaillard, et al.. Reorganization of inhibitory synapses and increased PSD length of perforated excitatory synapses in hippocampal area CA1 of dystrophin-deficient mdx mice.. Cerebral Cortex, Oxford University Press (OUP), 2009, 19 (4), pp.876-88. ⟨10.1093/cercor/bhn135⟩. ⟨hal-00371156⟩
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Caroline Perronnet, Cyrille Vaillend. Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies.. Journal of Biomedicine and Biotechnology, Hindawi Publishing Corporation, 2009, 2010, pp.849426. ⟨10.1155/2010/849426⟩. ⟨hal-01183368⟩
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2008

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Fatma Daoud, Aurora Candelario-Martinez, Jean-Marie Billard, Avi Avital, Malik Khelfaoui, et al.. Role of mental retardation associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity, and behavioral functions.. PLoS ONE, Public Library of Science, 2008, 4 (8), pp.e6574. ⟨10.1371/journal.pone.0006574⟩. ⟨hal-00408818⟩
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Cyrille Vaillend, Roseline Poirier, Serge Laroche. Genes, Plasticity and Mental Retardation.. Behavioural Brain Research, Elsevier, 2008, 192 (1), pp.88-105. ⟨10.1016/j.bbr.2008.01.009⟩. ⟨hal-00320613⟩
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2007

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Roseline Poirier, S. Jacquot, Cyrille Vaillend, A. A. Soutthiphong, M. Libbey, et al.. Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior.. Behavior Genetics, Springer Verlag, 2007, 37 (1), pp.31-50. ⟨10.1007/s10519-006-9116-1⟩. ⟨hal-00190992⟩
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2004

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Cyrille Vaillend, Jean-Marie Billard, Serge Laroche. Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin-deficient Dmdmdx mouse. Neurobiology of Disease, Elsevier, 2004, 17 (1), pp.10-20. ⟨10.1016/j.nbd.2004.05.004⟩. ⟨hal-02325350⟩
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2002

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P. Dutar, Cyrille Vaillend, Cécile Viollet, Jean-Marie Billard, B. Potier, et al.. Spatial learning and synaptic hippocampal plasticity in type 2 somatostatin receptor knock-out mice. Neuroscience, Elsevier - International Brain Research Organization, 2002, 112 (2), pp.455-466. ⟨10.1016/s0306-4522(02)00074-x⟩. ⟨hal-02325393⟩
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Cyrille Vaillend, Susanne Mason, Matthew Cuttle, Bradley Alger. Mechanisms of Neuronal Hyperexcitability Caused by Partial Inhibition of Na + -K + -ATPases in the Rat CA1 Hippocampal Region. Journal of Neurophysiology, American Physiological Society, 2002, 88 (6), pp.2963-2978. ⟨10.1152/jn.00244.2002⟩. ⟨hal-02526498⟩
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Cyrille Vaillend, Claire Rampon, Sabrina Davis, Serge Laroche. Gene Control of Synaptic Plasticity and Memory Formation: Implications for Diseases and Therapeutic Strategies. Current Molecular Medicine, Bentham Science Publishers, 2002, 2 (7), pp.613-628. ⟨10.2174/1566524023361952⟩. ⟨hal-02526515⟩
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Cyrille Vaillend, Jean-Marie Billard. Facilitated CA1 hippocampal synaptic plasticity in dystrophin-deficient mice: Role for GABAA receptors?. Hippocampus, Wiley, 2002, 12 (6), pp.713-717. ⟨10.1002/hipo.10068⟩. ⟨hal-02325375⟩
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2000

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C. Viollet, Cyrille Vaillend, C. Videau, M.T. Bluet-Pajot, A. Ungerer, et al.. Involvement of sst2 somatostatin receptor in locomotor, exploratory activity and emotional reactivity in mice.. European Journal of Neuroscience, Wiley, 2000, 12 (10), pp.3761-70. ⟨10.1046/j.1460-9568.2000.00249.x⟩. ⟨hal-00168771⟩
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1999

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Cyrille Vaillend, Arielle Ungerer. Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins. Neuromuscular Disorders, Elsevier, 1999, 9 (5), pp.296-304. ⟨10.1016/s0960-8966(99)00029-2⟩. ⟨hal-02526547⟩
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Cyrille Vaillend, Arielle Ungerer, Jean-Marie Billard. Facilitated NMDA receptor-mediated synaptic plasticity in the hippocampal CA1 area of dystrophin-deficient mice. Synapse, Wiley-Blackwell, 1999, 33 (1), pp.59-70. ⟨hal-02325669⟩
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1998

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Cyrille Vaillend, Jean-Marie Billard, Thomas Claudepierre, Alvaro Rendon, P Dutar, et al.. Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin gene products. Neuroscience, Elsevier - International Brain Research Organization, 1998, 86 (1), pp.53-66. ⟨10.1016/s0306-4522(98)00023-2⟩. ⟨hal-02325684⟩
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1995

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Cyrille Vaillend, Alvaro Rendon, René Misslin, Arielle Ungerer. Influence of dystrophin-gene mutation onmdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks. Behavior Genetics, Springer Verlag, 1995, 25 (6), pp.569-579. ⟨10.1007/bf02327580⟩. ⟨hal-02526592⟩
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Chapitre d'ouvrage

2019

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Cyrille Vaillend, Faouzi Zarrouki, Ophélie Vacca. Gene Therapy for Central Nervous System in Duchenne Muscular Dystrophy. Muscle Gene Therapy, Springer International Publishing, pp.417-438, 2019, 978-3-030-03094-0. ⟨10.1007/978-3-030-03095-7_24⟩. ⟨hal-02192778⟩
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