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

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

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

Abstracts from the 15th International Myopia Conference: Wenzhou, P.R. China. 23-27 September 2015

第十五届国际近视大会摘要:中国温州,2015年9月23-27日

Bonnet, Crystel; Riahi, Zied; Chantot-Bastaraud, Sandra; Smagghe, Luce; Letexier, Mélanie; Marcaillou, Charles; Lefèvre, Gaëlle M; Hardelin, Jean-Pierre; El-Amraoui, Aziz; Singh-Estivalet, Amrit; Mohand-Saïd, Saddek; Kohl, Susanne; Kurtenbach, Anne; Sliesoraityte, Ieva; Zobor, Ditta; Gherbi, Souad; Testa, Francesco; Simonelli, Francesca; Banfi, Sandro; Fakin, Ana; Glavač, Damjan; Jarc-Vidmar, Martina; Zupan, Andrej; Battelino, Saba; Martorell Sampol, Loreto; Claveria, Maria Antonia; Catala Mora, Jaume; Dad, Shzeena; Møller, Lisbeth B; Rodriguez Jorge, Jesus; Hawlina, Marko; Auricchio, Alberto; Sahel, José-Alain; Marlin, Sandrine; Zrenner, Eberhart; Audo, Isabelle; Petit, Christine; Benavente-Perez, Alexandra; Nour, Ann; Ansel, Tobin; Abarr, Kathleen; Yan, Luying; Roden, Keisha; Troilo, David; Lu, Chanyi; Pan, Miaozhen; Zheng, Min; Qu, Jia; Zhou, Xiangtian; Wildsoet, Christine F; Lu, Fan; Zhou, Xiangtian; Chen, Jie; Bao, Jinhua; Hu, Liang; Wang, Qinmei; Jin, Zibing; Qu, Jia; Rucker, Frances; Britton, Stephanie; Hanowsky, Stephan; Spatcher, Molly; Kuo, Hui-Ying; Ke, Ching-Hsiu; Kuo, I-Hsin; Peng, Chien-Chun; Sun, Han-Yin; Morgan, Ian G; Guggenheim, Jeremy A; Shah, Rupal L; Williams, Cathy; Yang, Jinglei; Reinach, Peter S; Zhang, Sen; Pan, Miaozhen; Sun, Wenfeng; Liu, Bo; Li, Fen; Li, Xiaoqing; Zhao, Aihua; Chen, Tianlu; Jia, Wei; Qu, Jia; Zhou, Xiangtian; Jiang, Jun; Wu, Haoran; Lu, Fan; Tsubota, Kazuo; Ozawa, Hiroko; Torii, Hidemasa; Takamizawa, Shigemasa; Kurihara, Toshihide; Negishi, Kazuno; Graef, Klaus; Rathbun, Daniel; Schaeffel, Frank; Ghodsi, Ladan; Stell, William K; Pardue, Machelle T; Chakraborty, Ranjay; Park, Han na; Sidhu, Curran S; Iuvone, P Michael; Collins, Michael J; Srinvasalu, Nethrajeith; McFadden, Sally A; Baird, Paul N; Iuvone, P Michael; Artal, Pablo; Cho, Pauline; Cheung, SW; Wu, Pei-Chang; Hoang, Quan V; McFadden, Sally A; Chakraborty, Ranjay; Lee, Duk C; Landis, Erica G; Bergen, Michael A; Sidhu, Curran; Hattar, Samer; Iuvone, P Michael; Stone, Richard A; Pardue, Machelle T; Metlapally, Ravi; Li, Ruiqin; Xu, Qinglin; Zhong, Hong; Pan, Chenglin; Lan, Weizhong; Li, Xiaoning; Chen, Ling; Yang, Zhikuan; Read, Scott A; Saw, Seang-Mei; Weng, Shi-Jun; Wu, Xiao-Hua; Qian, Kang-Wei; Li, Yun-Yun; Xu, Guo-Zhong; Huang, Furong; Zhou, Xiangtian; Qu, Jia; Yang, Xiong-Li; Zhong, Yong-Mei; Smith, Earl L III; Arumugam, Baskar; Hung, Li-Fang; Ostrin, Lisa A; Trier, Klaus; Jong, Monica; Holden, Brien A; Lam, Thomas Chuen; Shan, Samantha; Zuo, Bing; McFadden, Sally A; Tse, Dennis Yan-yin; Bian, Jingfang; Li, King-Kit; Liu, Quan; To, Chi-ho; Gawne, Timothy J; Siegwart, John T Jr; Ward, Alexander H; Norton, Thomas T; Zhou, Xiangtian; Zhang, Yan; Liu, Yue; Ho, Carol; Phan, Eileen; Hang, Abraham; Eng, Emily; Wildsoet, Christine

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

阿尔及利亚 Usher 综合征患者相关基因的多样性

Abdi, Samia; Bahloul, Amel; Behlouli, Asma; Hardelin, Jean-Pierre; Makrelouf, Mohamed; Boudjelida, Kamel; Louha, Malek; Cheknene, Ahmed; Belouni, Rachid; Rous, Yahia; Merad, Zahida; Selmane, Djamel; Hasbelaoui, Mokhtar; Bonnet, Crystel; Zenati, Akila; Petit, Christine

Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients

全外显子组测序在重度耳聋的突尼斯患者中发现了 Usher 综合征基因突变

Riahi, Zied; Bonnet, Crystel; Zainine, Rim; Lahbib, Saida; Bouyacoub, Yosra; Bechraoui, Rym; Marrakchi, Jihène; Hardelin, Jean-Pierre; Louha, Malek; Largueche, Leila; Ben Yahia, Salim; Kheirallah, Moncef; Elmatri, Leila; Besbes, Ghazi; Abdelhak, Sonia; Petit, Christine

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness

EPS8 编码耳蜗毛细胞立体纤毛的肌动蛋白结合蛋白,是导致常染色体隐性重度耳聋的新致病基因。

Behlouli, Asma; Bonnet, Crystel; Abdi, Samia; Bouaita, Aïcha; Lelli, Andrea; Hardelin, Jean-Pierre; Schietroma, Cataldo; Rous, Yahia; Louha, Malek; Cheknane, Ahmed; Lebdi, Hayet; Boudjelida, Kamel; Makrelouf, Mohamed; Zenati, Akila; Petit, Christine