Zobrazeno 1 - 10
of 26
pro vyhledávání: '"MESH: Hair Cells, Auditory"'
Autor:
Henry Houlden, Thomas Haaf, Pratishtha Varshney, Christian Beetz, Hamid Galehdari, Lucy A Dunbar, Alireza Sedaghat, Richard J.H. Smith, Michael R. Bowl, Aziz El-Amraoui, Kevin T. Booth, David Murphy, Neda Mazaheri, Sandrine Vitry, Kumar N. Alagramam, Ben Fowler, Shruthi VijayKumar, Aboulfazl Rad, Hela Azaiez, Cassidy Petree, Barbara Vona, Sheng-Jia Lin, Gholamreza Shariati, Reza Maroofian, Franz Rüschendorf, Gaurav K. Varshney
Publikováno v:
Human Genetics
Human Genetics, 2021, 140 (6), pp.915-931. ⟨10.1007/s00439-020-02254-z⟩
Human Genetics, Springer Verlag, 2021, 140 (6), pp.915-931. ⟨10.1007/s00439-020-02254-z⟩
Human Genetics, 2021, 140 (6), pp.915-931. ⟨10.1007/s00439-020-02254-z⟩
Human Genetics, Springer Verlag, 2021, 140 (6), pp.915-931. ⟨10.1007/s00439-020-02254-z⟩
Deafness, the most frequent sensory deficit in humans, is extremely heterogeneous with hundreds of genes involved. Clinical and genetic analyses of an extended consanguineous family with pre-lingual, moderate-to-profound autosomal recessive sensorine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ec2c6de213429b2f5213b9170fe9c29
https://doi.org/10.1007/s00439-020-02254-z
https://doi.org/10.1007/s00439-020-02254-z
Autor:
Aziz El-Amraoui, Stuart L. Johnson, Christine Petit, Michelle Simon, Prashanthini Jeyarajan, Lauren Chessum, Michael R. Bowl, Sherylanne Newton, Andrea Lelli, Helena Rr Wells, Frances M K Williams, Andrew Parker, Joanne Dorning, Didier Dulon, Susan Morse, Suhasini R. Gopal, Steve D.M. Brown, Sedigheh Delmaghani, Philomena Mburu, Christopher T. Esapa, Ronna Hertzano, Sara Wells, Debbie Williams, Carlos A. Aguilar, Kumar N. Alagramam, Pranav Patni, Thibault Peineau, Walter Marcotti, Laura F. Corns, Sally J. Dawson, Gemma F. Codner, Lucy A Dunbar
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Wiley Open Access, 2019, 11 (9), pp.e10288. ⟨10.15252/emmm.201910288⟩
EMBO Molecular Medicine, 2019, 11 (9), pp.e10288. ⟨10.15252/emmm.201910288⟩
EMBO Molecular Medicine, Vol 11, Iss 9, Pp n/a-n/a (2019)
EMBO Molecular Medicine, Wiley Open Access, 2019, 11 (9), pp.e10288. ⟨10.15252/emmm.201910288⟩
EMBO Molecular Medicine, 2019, 11 (9), pp.e10288. ⟨10.15252/emmm.201910288⟩
EMBO Molecular Medicine, Vol 11, Iss 9, Pp n/a-n/a (2019)
International audience; Hearing relies on mechanically gated ion channels present in the actin-rich stereocilia bundles at the apical surface of cochlear hair cells. Our knowledge of the mechanisms underlying the formation and maintenance of the soun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edaae1d8c8cc8054398a9affa8ff41c6
https://hal-pasteur.archives-ouvertes.fr/pasteur-03261798/document
https://hal-pasteur.archives-ouvertes.fr/pasteur-03261798/document
Genes Involved in the Development and Physiology of Both the Peripheral and Central Auditory Systems
Autor:
Nicolas Michalski, Christine Petit
Publikováno v:
Annual Review of Neuroscience
Annual Review of Neuroscience, Annual Reviews, 2019, 42, pp.67-86. ⟨10.1146/annurev-neuro-070918-050428⟩
Annual Review of Neuroscience, 2019, 42, pp.67-86. ⟨10.1146/annurev-neuro-070918-050428⟩
Annual Review of Neuroscience, Annual Reviews, 2019, 42, pp.67-86. ⟨10.1146/annurev-neuro-070918-050428⟩
Annual Review of Neuroscience, 2019, 42, pp.67-86. ⟨10.1146/annurev-neuro-070918-050428⟩
International audience; The genetic approach, based on the study of inherited forms of deafness, has proven to be particularly effective for deciphering the molecular mechanisms underlying the development of the peripheral auditory system, the cochle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e1d88a021d7a73171f52e66d9a7729
https://hal-pasteur.archives-ouvertes.fr/pasteur-02874563/file/MichalskiPetit_Maintext_31August2018.pdf
https://hal-pasteur.archives-ouvertes.fr/pasteur-02874563/file/MichalskiPetit_Maintext_31August2018.pdf
Autor:
Christine Petit, Florent Delhommel, Benjamin Bardiaux, Julia Chamot-Rooke, Michael Nilges, Sébastien Brier, Florence Cordier, Amel Bahloul, Bertrand Raynal, Sylvie Nouaille, Nicolas Wolff, Baptiste Colcombet-Cazenave, Guillaume Bouvier
Publikováno v:
Structure
Structure, Elsevier (Cell Press), 2017, 25 (11), pp.1645-1656.e5. ⟨10.1016/j.str.2017.08.013⟩
Structure, 2017, 25 (11), pp.1645-1656.e5. ⟨10.1016/j.str.2017.08.013⟩
Structure, Elsevier (Cell Press), 2017, 25 (11), pp.1645-1656.e5. ⟨10.1016/j.str.2017.08.013⟩
Structure, 2017, 25 (11), pp.1645-1656.e5. ⟨10.1016/j.str.2017.08.013⟩
International audience; Hearing relies on the transduction of sound-evoked vibrations into electric signals, occurring in the stereocilia bundle of hair cells. The bundle is organized in a staircase pattern formed by rows of packed stereocilia. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf6c0f0829c16de0cf89456ba92ad039
https://hal-pasteur.archives-ouvertes.fr/pasteur-02883914
https://hal-pasteur.archives-ouvertes.fr/pasteur-02883914
Publikováno v:
Hearing Research
Hearing Research, Elsevier, 2006, 221 (1-2), pp.119-27. ⟨10.1016/j.heares.2006.08.010⟩
Hearing Research, Elsevier, 2006, 221 (1-2), pp.119-27. ⟨10.1016/j.heares.2006.08.010⟩
International audience; The therapeutic efficacy of cochlear infusion of methylprednisolone (MP) after an impulse noise trauma (170dB SPL peak) was evaluated in guinea pigs. The compound action potential threshold shifts were measured over a 14 days
Autor:
Sylviane Hoos, Jean-Pierre Hardelin, Christine Petit, Vincent Michel, Patrick England, Anne Houdusse, Amel Bahloul, Sylvie Nouaille
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2010, 19 (18), pp.3557-3565. ⟨10.1093/hmg/ddq271⟩
Human Molecular Genetics, 2010, 19 (18), pp.3557-3565. ⟨10.1093/hmg/ddq271⟩
International audience; Cadherin-23 is a component of early transient lateral links of the auditory sensory cells' hair bundle, the mechanoreceptive structure to sound. This protein also makes up the upper part of the tip links that control gating of
Autor:
Christine Petit, Dominique Weil, Michel Leibovici, Vincent Michel, Isabelle Foucher, Nadège Cayet, Raphaël Etournay, Jean-Pierre Hardelin, Jacques Boutet de Monvel, Léa Lepelletier
Publikováno v:
Development (Cambridge, England)
Development (Cambridge, England), 2010, 137 (8), pp.1373-83. ⟨10.1242/dev.045138⟩
Development (Cambridge, England), Company of Biologists, 2010, 137 (8), pp.1373-83. ⟨10.1242/dev.045138⟩
Development (Cambridge, England), 2010, 137 (8), pp.1373-83. ⟨10.1242/dev.045138⟩
Development (Cambridge, England), Company of Biologists, 2010, 137 (8), pp.1373-83. ⟨10.1242/dev.045138⟩
International audience; Epithelial cells acquire diverse shapes relating to their different functions. This is particularly relevant for the cochlear outer hair cells (OHCs), whose apical and basolateral shapes accommodate the functioning of these ce
Autor:
Elisa Caberlotto, Jean-Yves Tinevez, Christine Petit, Christophe Houbron, Guy P. Richardson, Emilie Bizard, Pascal Martin, Vincent Michel, Nicolas Michalski, Alexander F. J. van Aken, Gaelle M. Lefèvre, Jean-Pierre Hardelin, Corné J. Kros, Dominique Weil
Publikováno v:
Pflügers Archiv European Journal of Physiology
Pflügers Archiv European Journal of Physiology, Springer Verlag, 2009, 459 (1), pp.115-130. ⟨10.1007/s00424-009-0711-x⟩
Pflügers Archiv European Journal of Physiology, 2009, 459 (1), pp.115-130. ⟨10.1007/s00424-009-0711-x⟩
Pflugers Archiv
Pflügers Archiv European Journal of Physiology, Springer Verlag, 2009, 459 (1), pp.115-130. ⟨10.1007/s00424-009-0711-x⟩
Pflügers Archiv European Journal of Physiology, 2009, 459 (1), pp.115-130. ⟨10.1007/s00424-009-0711-x⟩
Pflugers Archiv
We assessed the involvement of harmonin-b, a submembranous protein containing PDZ domains, in the mechanoelectrical transduction machinery of inner ear hair cells. Harmonin-b is located in the region of the upper insertion point of the tip link that
Autor:
Xavier Estivill, Frédéric Venail, Maria L. Arbonés, Ester Ballana, Jing Wang, Assumpció Bosch, Jean-Luc Puel
Publikováno v:
Neuroscience Letters
Neuroscience Letters, Elsevier, 2008, 442 (2), pp.134-9. ⟨10.1016/j.neulet.2008.06.060⟩
Neuroscience Letters, Elsevier, 2008, 442 (2), pp.134-9. ⟨10.1016/j.neulet.2008.06.060⟩
International audience; Congenital deafness, affecting 1 in 1000 neonates, can lead to major problems in speech, cognitive and psychosocial development. Congenital deafness is mainly caused by mutations in connexins, hemi-channel proteins forming gap
Autor:
Nicolas Michalski, Christine Petit
Publikováno v:
Pflügers Archiv European Journal of Physiology
Pflügers Archiv European Journal of Physiology, Springer Verlag, 2015, 467 (1), pp.49-72. ⟨10.1007/s00424-014-1552-9⟩
Pflügers Archiv European Journal of Physiology, 2015, 467 (1), pp.49-72. ⟨10.1007/s00424-014-1552-9⟩
Pflügers Archiv-European Journal of Physiology
Pflugers Archiv
Pflügers Archiv European Journal of Physiology, Springer Verlag, 2015, 467 (1), pp.49-72. ⟨10.1007/s00424-014-1552-9⟩
Pflügers Archiv European Journal of Physiology, 2015, 467 (1), pp.49-72. ⟨10.1007/s00424-014-1552-9⟩
Pflügers Archiv-European Journal of Physiology
Pflugers Archiv
International audience; The hair bundles of cochlear hair cells play a central role in the auditory mechano-electrical transduction (MET) process. The identification of MET components and of associated molecular complexes by biochemical approaches is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b16ebf3ff0bdf171704aeb6b1c60e62d
https://hal-pasteur.archives-ouvertes.fr/pasteur-01472836
https://hal-pasteur.archives-ouvertes.fr/pasteur-01472836