A5085105850- Cephalopods and Marine Biology
- Hearing, Cochlea, Tinnitus, Genetics
- Pediatric health and respiratory diseases
- IL-33, ST2, and ILC Pathways
- Paleontology and Stratigraphy of Fossils
- Marine and environmental studies
- Ion channel regulation and function
- Vestibular and auditory disorders
- Eosinophilic Esophagitis
Central Hospital of Wuhan
2023-2025
General Hospital of Central Theater Command
2023-2025
Wuhan Third Hospital
2025
Tongren Hospital
2025
KCNQ4 is a common genetic cause of nonsyndromic autosomal dominant hearing loss. We have identified the family in China with (c.701A>G; p.His234Arg) missense variation. In this study, survey and analysis were performed to investigate audiological characteristics Chinese family. The medical history members was collected, underwent pure tone audiometry, acoustic immittance, physical examination. proband additionally examined by ABR (auditory brainstem response) DPOAE (distortion product...
Type 2 innate lymphoid cells (ILC2s) and NLRP3 inflammasome are related to allergic inflammatory responses. inhibitor MCC950 was demonstrated ameliorate rhinitis (AR) in animal models.