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

Human organoids for rapid validation of gene variants linked to cochlear malformations.

利用人类类器官快速验证与耳蜗畸形相关的基因变异

Zafeer Mohammad Faraz, Ramzan Memoona, Duman Duygu, Mutlu Ahmet, Seyhan Serhat, Kalcioglu M Tayyar, Fitoz Suat, DeRosa Brooke A, Guo Shengru, Dykxhoorn Derek M, Tekin Mustafa

Postural correlates of visual incentives: application to food and alcohol stimuli

视觉激励的姿势相关性:应用于食物和酒精刺激

Duman, Duygu; Kızılışık, Sumeyye; Zitouni, Amel; Campanella, Salvatore; Lelard, Thierry; Akounach, Mbarka; Mouras, Harold

Siblings with a Homozygous Variant in the NHP2 Gene: A Case Report and Review of Literature

NHP2基因纯合变异的兄弟姐妹:病例报告及文献综述

Sürücü Kara, İlknur; Duman, Duygu; Bademci, Güney; Kuloglu, Zarife; Kaynak Sahap, Seda; Tekin, Mustafa; Eminoğlu, Fatma Tuba

Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2.

遗传性听力损失的遗传异质性:纤毛运动蛋白 TOGARAM2 的潜在作用

Ramzan Memoona, Zafeer Mohammad Faraz, Abad Clemer, Guo Shengru, Owrang Daniel, Alper Ozgul, Mutlu Ahmet, Atik Tahir, Duman Duygu, Bademci Guney, Vona Barbara, Kalcioglu Mahmut Tayyar, Walz Katherina, Tekin Mustafa

Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss

在常染色体显性遗传性感觉神经性听力损失家族中鉴定出新的MYH14变异

Duman, Duygu; Ramzan, Memoona; Subasioglu, Asli; Mutlu, Ahmet; Peart, LéShon; Seyhan, Serhat; Guo, Shengru; Ila, Kadri; Balta, Burhan; Kalcioglu, Mahmut Tayyar; Bademci, Guney; Tekin, Mustafa

Dispersed DNA variants underlie hearing loss in South Florida's minority population

南佛罗里达州少数族裔人群听力损失的根本原因在于分散的DNA变异。

Peart, LéShon; Gonzalez, Joanna; Morel Swols, Dayna; Duman, Duygu; Saridogan, Turcin; Ramzan, Memoona; Zafeer, Mohammad Faraz; Liu, Xue Zhong; Eshraghi, Adrien A; Hoffer, Michael E; Angeli, Simon I; Bademci, Guney; Blanton, Susan; Smith, Carson; Telischi, Fred F; Tekin, Mustafa

Novel GPR156 variants confirm its role in moderate sensorineural hearing loss

新型 GPR156 变异体证实了其在中度感音神经性听力损失中的作用

Ramzan, Memoona; Bozan, Nazim; Seyhan, Serhat; Zafeer, Mohammad Faraz; Ayral, Aburrahman; Duman, Duygu; Bademci, Guney; Tekin, Mustafa

Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice

MINAR2基因(编码膜整合型NOTCH2相关受体2)的突变会导致人类和小鼠耳聋。

Bademci, Guney; Lachgar-Ruiz, María; Deokar, Mangesh; Zafeer, Mohammad Faraz; Abad, Clemer; Yildirim Baylan, Muzeyyen; Ingham, Neil J; Chen, Jing; Sineni, Claire J; Vadgama, Nirmal; Karakikes, Ioannis; Guo, Shengru; Duman, Duygu; Singh, Nitu; Harlalka, Gaurav; Jain, Shirish P; Chioza, Barry A; Walz, Katherina; Steel, Karen P; Nasir, Jamal; Tekin, Mustafa

Whole Mitochondrial Genome Analysis in Turkish Patients with Mitochondrial Diseases

土耳其线粒体疾病患者的全线粒体基因组分析

Gencer Öncül, Emine Begüm; Duman, Duygu; Eminoğlu, Fatma Tuba; Aktuna, Süleyman; Duman, Mustafa Türker

Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development

控制 GDF6 表达的长程顺式调控元件对耳朵发育至关重要。

Bademci, Guney; Abad, Clemer; Cengiz, Filiz B; Seyhan, Serhat; Incesulu, Armagan; Guo, Shengru; Fitoz, Suat; Atli, Emine Ikbal; Gosstola, Nicholas C; Demir, Selma; Colbert, Brett M; Seyhan, Gozde Cosar; Sineni, Claire J; Duman, Duygu; Gurkan, Hakan; Morton, Cynthia C; Dykxhoorn, Derek M; Walz, Katherina; Tekin, Mustafa