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

The Role of Antenatal Ultrasound in the Detection of Goldston Syndrome: A Case Report and Review of Literature

产前超声在戈尔德斯顿综合征检测中的作用:病例报告及文献综述

Gupta, Isha; Gangwal, Ashish; Sharma, Rahul; Mittal, Mukesh; Mannan, Naima

A middle-aged male with necrotic lung mass

一名中年男性,肺部有坏死性肿块。

Tyagi, Rahul; Mittal, Saurabh; Madan, Karan; Mohan, Anant; Hadda, Vijay; Bhalla, Ashu Seith

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

PDE1C 基因的显性变异与非综合征性听力损失有关

Li Wang, Yong Feng, Denise Yan, Litao Qin, M'hamed Grati, Rahul Mittal, Tao Li, Abhiraami Kannan Sundhari, Yalan Liu, Prem Chapagain, Susan H Blanton, Shixiu Liao, Xuezhong Liu

Combination Therapy with c-Met and Src Inhibitors Induces Caspase-Dependent Apoptosis of Merlin-Deficient Schwann Cells and Suppresses Growth of Schwannoma Cells

c-Met 和 Src 抑制剂联合治疗可诱导 Merlin 缺陷型雪旺细胞发生 Caspase 依赖性凋亡,并抑制雪旺细胞瘤细胞的生长

Marisa A Fuse, Stephani Klingeman Plati, Sarah S Burns, Christine T Dinh, Olena Bracho, Denise Yan, Rahul Mittal, Rulong Shen, Julia N Soulakova, Alicja J Copik, Xue Zhong Liu, Fred F Telischi, Long-Sheng Chang, Maria Clara Franco, Cristina Fernandez-Valle

Ponatinib promotes a G1 cell-cycle arrest of merlin/NF2-deficient human schwann cells

帕纳替尼促使缺乏 Merlin/NF2 的人类雪旺细胞进入 G1 细胞周期停滞

Alejandra M Petrilli, Jeanine Garcia, Marga Bott, Stephani Klingeman Plati, Christine T Dinh, Olena R Bracho, Denise Yan, Bing Zou, Rahul Mittal, Fred F Telischi, Xue-Zhong Liu, Long-Sheng Chang, D Bradley Welling, Alicja J Copik, Cristina Fernández-Valle

Serotonin Activates Bacterial Quorum Sensing and Enhances the Virulence of Pseudomonas aeruginosa in the Host

血清素激活细菌群体感应并增强宿主铜绿假单胞菌的毒力

Leslie D Knecht, Gregory O'Connor, Rahul Mittal, Xue Z Liu, Pirouz Daftarian, Sapna K Deo, Sylvia Daunert

A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60

编码耳蜗纹内皮中表达的有机阳离子转运蛋白的 SLC22A4 突变导致人类隐性非综合征性听力损失 DFNB60

Mariem Ben Said, M'hamed Grati, Takahiro Ishimoto, Bing Zou, Imen Chakchouk, Qi Ma, Qi Yao, Bouthaina Hammami, Denise Yan, Rahul Mittal, Noritaka Nakamichi, Abdelmonem Ghorbel, Lingling Neng, Mustafa Tekin, Xiao Rui Shi, Yukio Kato, Saber Masmoudi, Zhongmin Lu, Mounira Hmani, Xuezhong Liu1

MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform

MYO3A 导致人类显性耳聋并与原钙粘蛋白 15-CD2 异构体相互作用

M'hamed Grati, Denise Yan, Manmeet H Raval, Tom Walsh, Qi Ma, Imen Chakchouk, Abhiraami Kannan-Sundhari, Rahul Mittal, Saber Masmoudi, Susan H Blanton, Mustafa Tekin, Mary-Claire King, Christopher M Yengo, Xue Zhong Liu

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

DCDC2 的错义突变导致人类隐性耳聋 DFNB66,可能是通过干扰感觉毛细胞和支持细胞纤毛长度调节来实现的

M'hamed Grati, Imen Chakchouk, Qi Ma, Mariem Bensaid, Alexandra Desmidt, Nouha Turki, Denise Yan, Aissette Baanannou, Rahul Mittal, Nabil Driss, Susan Blanton, Amjad Farooq, Zhongmin Lu, Xue Zhong Liu, Saber Masmoudi

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing

FAM65B 是听觉所必需的毛细胞纤毛膜相关蛋白

Oscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, Alexandra DeSmidt, Joseph Foster 2nd, Lei Cao, Guney Bademci, Suna Tokgoz-Yilmaz, Duygu Duman, F Basak Cengiz, Clemer Abad, Rahul Mittal, Susan Blanton, Xue Z Liu, Amjad Farooq, Katherina Walz, Zhongmin Lu, Mustafa Tekin