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

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

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

毛里塔尼亚一个患有非综合征性听力障碍的家族中,PJVK基因存在剪接改变变异。

Salame, Malak; Bonnet, Crystel; Singh-Estivalet, Amrit; Brahim, Selma Mohamed; Roux, Solene; Boussaty, Ely Cheikh; Hadrami, Mouna; Hamed, Cheikh Tijani; Sidi, Abdellahi M'hamed; Veten, Fatimetou; Petit, Christine; Houmeida, Ahmed

Murine nuclear tyrosyl-tRNA synthetase deficiency leads to fat storage deficiency and hearing loss

小鼠核酪氨酰-tRNA合成酶缺乏导致脂肪储存缺陷和听力丧失

Julia A Jones, Jiadong Zhou, Jianjie Dong, Salvador Huitron-Resendiz, Ely Boussaty, Eduardo Chavez, Na Wei, Calin Dan Dumitru, Yosuke Morodomi, Taisuke Kanaji, Allen F Ryan, Rick Friedman, Tong Zhou, Sachiko Kanaji, Matthew Wortham, Simon Schenk, Amanda J Roberts, Xiang-Lei Yang

The genomic landscape of Ménière's disease: a path to endolymphatic hydrops

梅尼埃病的基因组图谱:通往内淋巴积水的途径

Fisch, Kathleen M; Rosenthal, Sara Brin; Mark, Adam; Sasik, Roman; Nasamran, Chanond A; Clifford, Royce; Derebery, M Jennifer; Boussaty, Ely; Jepsen, Kristen; Harris, Jeffrey; Friedman, Rick A

Altered Fhod3 expression involved in progressive high-frequency hearing loss via dysregulation of actin polymerization stoichiometry in the cuticular plate

Fhod3 表达改变与进行性高频听力损失有关,这是由于角质层中的肌动蛋白聚合化学计量失调所致

Ely Cheikh Boussaty, Yuzuru Ninoyu, Leonardo R Andrade, Qingzhong Li, Ryu Takeya, Hideki Sumimoto, Takahiro Ohyama, Karl J Wahlin, Uri Manor, Rick A Friedman

Cochlear transcriptome analysis of an outbred mouse population (CFW)

杂交小鼠种群(CFW)的耳蜗转录组分析

Ely Cheikh Boussaty #, Neil Tedeschi #, Mark Novotny, Yuzuru Ninoyu, Eric Du, Clara Draf, Yun Zhang, Uri Manor, Richard H Scheuermann #, Rick Friedman #

Attenuation of Age-Related Hearing Impairment in Senescence-Accelerated Mouse Prone 8 (SAMP8) Mice Treated with Fatty Acid Synthase Inhibitor CMS121

用脂肪酸合成酶抑制剂CMS121治疗可减轻衰老加速易感小鼠8(SAMP8)的年龄相关性听力障碍

Pham, Tammy B; Boussaty, Ely Cheikh; Currais, Antonio; Maher, Pamela; Schubert, David R; Manor, Uri; Friedman, Rick A

Cochlear transcriptome analysis of an outbred mouse population (CFW)

杂交小鼠种群(CFW)的耳蜗转录组分析

Ely Cheikh Boussaty, Neil Tedeschi, Mark Novotny, Yuzuru Ninoyu, Eric Du, Clara Draf, Yun Zhang, Uri Manor, Richard H Scheuermann, Rick Friedman

The Genetics of Variation of the Wave 1 Amplitude of the Mouse Auditory Brainstem Response

小鼠听觉脑干反应第一波振幅变异的遗传学

Ely Cheikh Boussaty,Danielle Gillard,Joel Lavinsky,Pezhman Salehi,Juemei Wang,Aline Mendonça,Hooman Allayee,Uri Manor,Rick Adam Friedman

The Genetics of Variation of the Wave 1 Amplitude of the Mouse Auditory Brainstem Response

小鼠听觉脑干反应波 1 振幅变异的遗传学

Ely Cheikh Boussaty, Danielle Gillard, Joel Lavinsky, Pezhman Salehi, Juemei Wang, Aline Mendonça, Hooman Allayee, Uri Manor, Rick Adam Friedman