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Nicotine inhibits the VTA-to-amygdala dopamine pathway to promote anxiety.
Nguyen C, Mondoloni S, Le Borgne T, Centeno I, Come M, Jehl J, Solié C, Reynolds LM, Durand-de Cuttoli R, Tolu S, Valverde S, Didienne S, Hannesse B, Fiancette JF, Pons S, Maskos U, Deroche-Gamonet V, Dalkara D, Hardelin JP, Mourot A, Marti F, Faure P. Nguyen C, et al. Among authors: hardelin jp. Neuron. 2021 Aug 18;109(16):2604-2615.e9. doi: 10.1016/j.neuron.2021.06.013. Epub 2021 Jul 8. Neuron. 2021. PMID: 34242565 Free article.
[Congenital deafness forms: progressing toward gene therapy?].
Hardelin JP, Safieddine S. Hardelin JP, et al. Med Sci (Paris). 2019 Dec;35(12):1213-1215. doi: 10.1051/medsci/2019233. Epub 2020 Jan 6. Med Sci (Paris). 2019. PMID: 31903944 Free article. French. No abstract available.
Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes.
Delmaghani S, Defourny J, Aghaie A, Beurg M, Dulon D, Thelen N, Perfettini I, Zelles T, Aller M, Meyer A, Emptoz A, Giraudet F, Leibovici M, Dartevelle S, Soubigou G, Thiry M, Vizi ES, Safieddine S, Hardelin JP, Avan P, Petit C. Delmaghani S, et al. Among authors: hardelin jp. Cell. 2015 Nov 5;163(4):894-906. doi: 10.1016/j.cell.2015.10.023. Cell. 2015. PMID: 26544938 Free article.
[Kallmann De Morsier syndrome: FGF-signaling insufficiency?].
Dodé C, Hardelin JP. Dodé C, et al. Among authors: hardelin jp. Med Sci (Paris). 2004 Aug-Sep;20(8-9):793-8. doi: 10.1051/medsci/2004208-9793. Med Sci (Paris). 2004. PMID: 15361347 Free article. Review. French.
EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.
Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C. Behlouli A, et al. Among authors: hardelin jp. Orphanet J Rare Dis. 2014 Apr 17;9:55. doi: 10.1186/1750-1172-9-55. Orphanet J Rare Dis. 2014. PMID: 24741995 Free PMC article.
Stereocilin-deficient mice reveal the origin of cochlear waveform distortions.
Verpy E, Weil D, Leibovici M, Goodyear RJ, Hamard G, Houdon C, Lefèvre GM, Hardelin JP, Richardson GP, Avan P, Petit C. Verpy E, et al. Among authors: hardelin jp. Nature. 2008 Nov 13;456(7219):255-8. doi: 10.1038/nature07380. Epub 2008 Oct 8. Nature. 2008. PMID: 18849963 Free PMC article.
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.
Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, Pepermans E, Estivalet A, Carette D, Aghaie A, Ebermann I, Lelli A, Iribarne M, Hardelin JP, Weil D, Sahel JA, El-Amraoui A, Petit C. Sahly I, et al. Among authors: hardelin jp. J Cell Biol. 2012 Oct 15;199(2):381-99. doi: 10.1083/jcb.201202012. Epub 2012 Oct 8. J Cell Biol. 2012. PMID: 23045546 Free PMC article.
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.
Delmaghani S, Aghaie A, Bouyacoub Y, El Hachmi H, Bonnet C, Riahi Z, Chardenoux S, Perfettini I, Hardelin JP, Houmeida A, Herbomel P, Petit C. Delmaghani S, et al. Among authors: hardelin jp. Am J Hum Genet. 2016 Jun 2;98(6):1266-1270. doi: 10.1016/j.ajhg.2016.04.015. Am J Hum Genet. 2016. PMID: 27259055 Free PMC article.
92 results