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Mapping the Fine-Scale Organization and Plasticity of the Brain Vasculature

Christoph Kirst , Sophie Skriabine , Alba Vieites-Prado , Thomas Topilko , Paul Bertin , et al.
Cell, 2020, 180 (4), pp.780-795.e25. ⟨10.1016/j.cell.2020.01.028⟩
Journal articles pasteur-02874557v1
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Spontaneous Mouse Behavior in Presence of Dissonance and Acoustic Roughness

Olivier Postal , Typhaine Dupont , Warren Bakay , Noémi Dominique , Christine Petit , et al.
Frontiers in Behavioral Neuroscience, 2020, 14, pp.588834. ⟨10.3389/fnbeh.2020.588834⟩
Journal articles hal-02989780v1

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.

Sandrine Passemard , Luigi Titomanlio , Monique Elmaleh , Alexandra Afenjar , Jean-Luc Alessandri , et al.
Neurology, 2009, 73 (12), pp.962-9. ⟨10.1212/WNL.0b013e3181b8799a⟩
Journal articles inserm-00420406v1

Hair Cell Afferent Synapses: Function and Dysfunction

Stuart Johnson , Saaid Safieddine , Mirna Mustapha , Walter Marcotti
Cold Spring Harbor Perspectives in Medicine, 2019, 9 (12), pp.a033175. ⟨10.1101/cshperspect.a033175⟩
Journal articles hal-02365401v1
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Shroom2, a myosin-VIIa- and actin-binding protein, directly interacts with ZO-1 at tight junctions.

Raphael Etournay , Ingrid Zwaenepoel , Isabelle Perfettini , Pierre Legrain , Christine Petit , et al.
Journal of Cell Science, 2007, 120 (16), pp.2838-50. ⟨10.1242/jcs.002568⟩
Journal articles pasteur-01545829v1
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Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy

Ana Fakin , Maja Šuštar , Jelka Brecelj , Crystel Bonnet , Christine Petit , et al.
Genes, 2019, 10 (12), pp.956. ⟨10.3390/genes10120956⟩
Journal articles hal-02408154v1
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Usher syndrome type 1–associated cadherins shape the photoreceptor outer segment

Cataldo Schietroma , Karine Parain , Amrit Estivalet , Asadollah Aghaie , Jacques Boutet de Monvel , et al.
Journal of Cell Biology, 2017, 216 (6), pp.1849 - 1864. ⟨10.1083/jcb.201612030⟩
Journal articles pasteur-01534475v1
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Functional characterisation of the mechano-electrical transduction complex of the auditory hair cells

Ménélik Labbe
Neurons and Cognition [q-bio.NC]. Université Pierre et Marie Curie - Paris VI, 2016. English. ⟨NNT : 2016PA066543⟩
Theses tel-01531928v1
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CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival

Vincent Michel , Kevin T Booth , Pranav Patni , Matteo Cortese , Hela Azaiez , et al.
EMBO Molecular Medicine, 2017, 9 (12), pp.1711 - 1731. ⟨10.15252/emmm.201708087⟩
Journal articles hal-01661175v1

The Auditory Hair Cell Ribbon Synapse: From Assembly to Function

Saaid Safieddine , Aziz El-Amraoui , Christine Petit
Annual Review of Neuroscience, 2012, 35, pp.509 - 528. ⟨10.1146/annurev-neuro-061010-113705⟩
Journal articles pasteur-03926768v1
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Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells

Aziz El-Amraoui , Christine Petit
Journal of Cell Science, 2005, 118 (20), pp.4593-4603. ⟨10.1242/jcs.02636⟩
Journal articles pasteur-03926862v1

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Philomena Mburu , Mirna Mustapha , Anabel Varela , Dominique Weil , Aziz El-Amraoui , et al.
Nature Genetics, 2003, 34, pp.421-428. ⟨10.1038/ng1208⟩
Journal articles pasteur-03926895v1
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Oscillations in the auditory system and their possible role

Boris Gourévitch , Claire Martin , Olivier Postal , Jos Eggermont
Neuroscience and Biobehavioral Reviews, 2020, 113, pp.507-528. ⟨10.1016/j.neubiorev.2020.03.030⟩
Journal articles hal-03066784v1

Connexins Responsible for Hereditary Deafness — The Tale Unfolds

Martine Cohen-Salmon , Francisco del Castillo , Christine Petit
Gap Junctions in Development and Disease, Springer Berlin Heidelberg, pp.111-134, 2005, ⟨10.1007/3-540-28621-7_6⟩
Book sections hal-04028261v1
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Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort

Vasily M Smirnov , Marco Nassisi , Saddek Mohand-Saïd , Crystel Bonnet , Anne Aubois , et al.
Investigative Ophthalmology & Visual Science, 2022, 63 (4), pp.25. ⟨10.1167/iovs.63.4.25⟩
Journal articles hal-03954493v1

Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutations

Oualid Sbai , Carine Monnier , Catherine Dode , Jean-Philippe Pin , Jean-Pierre Hardelin , et al.
FASEB Journal, 2014, 28 (8), pp.3734--44. ⟨10.1096/fj.13-243402⟩
Journal articles hal-01942940v1

Exocytotic Machineries of Vestibular Type I and Cochlear Ribbon Synapses Display Similar Intrinsic Otoferlin-Dependent Ca2+ Sensitivity But a Different Coupling to Ca2+ Channels

P. Vincent , Y. Bouleau , S. Safieddine , C. Petit , D. Dulon
Journal of Neuroscience, 2014, 34 (33), pp.10853-10869. ⟨10.1523/JNEUROSCI.0947-14.2014⟩
Journal articles hal-04178496v1

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family

Sara Salime , Zied Riahi , Soukaina Elrharchi , Lamiae Elkhattabi , Hicham Charoute , et al.
Gene, 2018, 659, pp.89-92. ⟨10.1016/j.gene.2018.03.042⟩
Journal articles pasteur-03219641v1
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Selective enhancement of low-gamma activity by tACS improves phonemic processing and reading accuracy in dyslexia

Silvia Marchesotti , Johanna Nicolle , Isabelle Merlet , Luc H Arnal , John P Donoghue , et al.
PLoS Biology, 2020, 18 (9), pp.e3000833. ⟨10.1371/journal.pbio.3000833⟩
Journal articles hal-02958984v1

A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family

Ghita Amalou , Crystel Bonnet , Zied Riahi , Aymane Bouzidi , Soukaina Elrharchi , et al.
International Journal of Pediatric Otorhinolaryngology, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
Journal articles pasteur-03215242v1
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Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells

Nicolas Michalski , Vincent Michel , Elisa Caberlotto , Gaëlle Lefèvre , Alexander van Aken , et al.
Pflügers Archiv European Journal of Physiology, 2009, 459 (1), pp.115-130. ⟨10.1007/s00424-009-0711-x⟩
Journal articles pasteur-02616476v1
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An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Crystel Bonnet , Zied Riahi , Sandra Chantot-Bastaraud , Luce Smagghe , Mélanie Letexier , et al.
European Journal of Human Genetics, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩
Journal articles pasteur-03215026v1
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Stem Cells and Gene Therapy in Progressive Hearing Loss: the State of the Art

Aida Nourbakhsh , Brett M. Colbert , Eric Nisenbaum , Aziz El-Amraoui , Derek M. Dykxhoorn , et al.
Journal of the Association for Research in Otolaryngology, 2021, 22 (2), pp.95-105. ⟨10.1007/s10162-020-00781-0⟩
Journal articles hal-03125733v1
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Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion

Joanna Schwenkgrub , Evan Harrell , Brice Bathellier , Julien Bouvier
Science Advances , 2020, 6 (49), pp.eabc6309. ⟨10.1126/sciadv.abc6309⟩
Journal articles hal-03043145v1

SpiCee: A Genetic Tool for Subcellular and Cell-Specific Calcium Manipulation

Oriol Ros , Yvrick Zagar , Sandrine Couvet , Alain Aghaie , Fiona Roche , et al.
Preprints, Working Papers, ... hal-02361424v1

Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage

Jean Defourny , Alain Aghaie , Isabelle Perfettini , Paul Avan , Sedigheh Delmaghani , et al.
Proceedings of the National Academy of Sciences of the United States of America, 2019, 116 (16), pp.8010-8017. ⟨10.1073/pnas.1821844116⟩
Journal articles hal-02318679v1
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Calcium- and Otoferlin-Dependent Exocytosis by Immature Outer Hair Cells

Maryline Beurg , Saaid Safieddine , Isabelle Roux , Yohan Bouleau , Christine Petit , et al.
Journal of Neuroscience, 2008, 28 (8), pp.1798-1803. ⟨10.1523/JNEUROSCI.4653-07.2008⟩
Journal articles hal-04159607v1
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Octopus Cells in the Posteroventral Cochlear Nucleus Provide the Main Excitatory Input to the Superior Paraolivary Nucleus

Richard A. Felix Il , Boris Gourévitch , Marcelo Gomez-Alvarez , Sara C. M. Leijon , Enrique Saldana , et al.
Frontiers in Neural Circuits, 2017, 11, pp.37. ⟨10.3389/fncir.2017.00037⟩
Journal articles hal-01556581v1
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Progrès de la thérapie génique : espoirs pour le syndrome d'Usher

Charlotte Calvet , Ghizlene Lahlou , Saaid Safieddine
Médecine/Sciences, 2018, 34 (10), pp.842 - 848. ⟨10.1051/medsci/2018210⟩
Journal articles hal-02365420v1
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Thérapie génique translationnelle des surdités et troubles vestibulaires d'origine génétique

Ghizlène Lahlou
Génétique. Sorbonne Université, 2020. Français. ⟨NNT : 2020SORUS090⟩
Theses tel-03907319v1