日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The interpeduncular nucleus blunts the rewarding effect of nicotine.

脚间核减弱了尼古丁的奖赏效应

Jehl Joachim, Ciscato Maria, Vicq Eléonore, Guyon Nicolas, Dejean de la Batie Gabrielle, Mondoloni Sarah, Frangieh Jacinthe, Mohayyaei Monir, Nguyen Claire, Pons Stéphanie, Maskos Uwe, Hardelin Jean-Pierre, Marti Fabio, Corringer Pierre-Jean, Faure Philippe, Mourot Alexandre

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity

马格里布和约旦语前孤立性耳聋和厄舍尔综合征的遗传学:利用纯合子的潜力

Riahi, Zied; Boucher, Sophie; Abdi, Samia; Wong Jun Tai, Fabienne; Singh-Estivalet, Amrit; Aghaie, Asadollah; Niasme-Grare, Magali; Hardelin, Jean-Pierre; Behlouli, Asma; Dahmani, Malika; Talbi, Sonia; Bouyacoub, Yosra; Mkaouar, Rahma; Charfeddine, Cherine; Amalou, Ghita; Bakhchane, Amina; Bousfiha, Amale; Salime, Sara; Elrharchi, Soukaina; Salame, Malak; Hadrami, Mouna; Boussaty, Ely; Charoute, Hicham; Detsouli, Mustapha; Snoussi, Khalid; Rouba, Hassan; Hachmi, Hala El; Veten, Fatimetou; Meiloud, Ghlana; Marrakchi, Jihene; Zainine, Rim; Chahed, Houda; Besbes, Ghazi; Trabelsi, Mediha; Mrad, Ridha; Kraoua, Ichraf; Ouhab, Sofiane; Djennaoui, Djamel; Boudjenah, Farid; Chouery, Eliane; Mustapha, Mirna; Houmeida, Ahmed; Barakat, Abdelhamid; Khodja, Fatima Ammar; Makrelouf, Mohamed; Zenati, Akila; Beltaief, Najeh; Abdelhak, Sonia; Petit, Christine; Bonnet, Crystel

Digital Implementation of Oscillatory Neural Network for Image Recognition Applications

用于图像识别应用的振荡神经网络的数字实现

Abernot, Madeleine; Gil, Thierry; Jiménez, Manuel; Núñez, Juan; Avellido, María J; Linares-Barranco, Bernabé; Gonos, Théophile; Hardelin, Tanguy; Todri-Sanial, Aida

Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells

原钙粘蛋白-15 与支架蛋白 whirlin 的相互作用支持其在耳蜗毛细胞中锚定毛束侧链

Vincent Michel #, Elise Pepermans #, Jacques Boutet de Monvel, Patrick England, Sylvie Nouaille, Alain Aghaie, Florent Delhommel, Nicolas Wolff, Isabelle Perfettini, Jean-Pierre Hardelin, Christine Petit, Amel Bahloul0

Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model

双重AAV介导的基因疗法可恢复DFNB9小鼠模型的听力

Akil, Omar; Dyka, Frank; Calvet, Charlotte; Emptoz, Alice; Lahlou, Ghizlene; Nouaille, Sylvie; Boutet de Monvel, Jacques; Hardelin, Jean-Pierre; Hauswirth, William W; Avan, Paul; Petit, Christine; Safieddine, Saaid; Lustig, Lawrence R

Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G

局部基因疗法可持久恢复 Usher 综合征 1G 型小鼠模型的前庭功能

Emptoz, Alice; Michel, Vincent; Lelli, Andrea; Akil, Omar; Boutet de Monvel, Jacques; Lahlou, Ghizlene; Meyer, Anaïs; Dupont, Typhaine; Nouaille, Sylvie; Ey, Elody; Franca de Barros, Filipa; Beraneck, Mathieu; Dulon, Didier; Hardelin, Jean-Pierre; Lustig, Lawrence; Avan, Paul; Petit, Christine; Safieddine, Saaid

Spectrin βV adaptive mutations and changes in subcellular location correlate with emergence of hair cell electromotility in mammalians

哺乳动物毛细胞电动力的出现与Spectrin βV的适应性突变和亚细胞定位变化相关

Cortese, Matteo; Papal, Samantha; Pisciottano, Francisco; Elgoyhen, Ana Belén; Hardelin, Jean-Pierre; Petit, Christine; Franchini, Lucia Florencia; El-Amraoui, Aziz

Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses

Otoferlin 可作为听觉毛细胞带状突触中囊泡融合和囊泡池补充的 Ca2+ 传感器

Nicolas Michalski, Juan D Goutman, Sarah Marie Auclair, Jacques Boutet de Monvel, Margot Tertrais, Alice Emptoz, Alexandre Parrin, Sylvie Nouaille, Marc Guillon, Martin Sachse, Danica Ciric, Amel Bahloul, Jean-Pierre Hardelin, Roger Bryan Sutton, Paul Avan, Shyam S Krishnakumar, James E Rothman, Did

Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery

毛细胞机电转导机制亚膜支架蛋白 harmonin 的构象转换

Amel Bahloul, Elise Pepermans, Bertrand Raynal, Nicolas Wolff, Florence Cordier, Patrick England, Sylvie Nouaille, Bruno Baron, Aziz El-Amraoui, Jean-Pierre Hardelin, Dominique Durand, Christine Petit

Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.

CDC14A 基因突变编码一种参与毛细胞纤毛发生的蛋白磷酸酶,导致常染色体隐性遗传的重度至极重度耳聋

Delmaghani Sedigheh, Aghaie Asadollah, Bouyacoub Yosra, El Hachmi Hala, Bonnet Crystel, Riahi Zied, Chardenoux Sebastien, Perfettini Isabelle, Hardelin Jean-Pierre, Houmeida Ahmed, Herbomel Philippe, Petit Christine