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Shiwei Qiu

tsinghua university

H指数:9

被引数:324

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Functional characterization of MFSD3 in auditory system and zebrafish embryogenesis

MFSD3在听觉系统及斑马鱼胚胎发育中的功能鉴定

Frontiers in Genetics

IF2.8

2025-10-010

OAAI

MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss (vol 41, pg 3448, 2018)

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

IF5.8

2025-05-010

OAAI

Single Administration of AAV-mAtp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2-Induced Lysosomal Dysfunction in Hair Cells

单次AAV-mAtp6v1b2基因治疗可挽救由毛细胞中Atp6v1b2诱导的溶酶体功能障碍引起的听力和前庭功能障碍。

ADVANCED SCIENCE

IF14.1

2025-03-111

OAAI

Are Guilt-Prone Power-Holders Less Corrupt? Evidence From Two Online Experiments

SOCIAL PSYCHOLOGICAL AND PERSONALITY SCIENCE

IF3.3

2023-05-221

PRE

Pyrite-enhanced Sludge Digestion via Stimulation of Direct Interspecies Electron Transfer between Syntrophic Propionate- and Sulfur-oxidizing Bacteria and Methanogens: Genome-centric Metagenomics Evidence

CHEMICAL ENGINEERING JOURNAL

IF13.2

2023-01-0130

PRE

ROS-Responsive Nanoparticle as a Berberine Carrier for OHC-Targeted Therapy of Noise-Induced Hearing Loss

ROS响应纳米粒作为小檗碱载体用于噪声性听力损失的OHC靶向治疗

ACS APPLIED MATERIALS & INTERFACES

IF8.2

2021-02-0240

PREAI

Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms

JOURNAL OF MEDICAL GENETICS

IF3.7

2020-07-3113

PREAI

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability

IF10.8

2019-07-0131

OAAI

MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

IF5.8

2018-03-0642

OAAI

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

JOURNAL OF MEDICAL GENETICS

IF3.7

2018-02-1616

OAAI