Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Xiao-Zhou Liu"'
Publikováno v:
Cell Death and Disease, Vol 13, Iss 6, Pp 1-11 (2022)
Abstract Mutations in the GJB2 gene (encoding Connexin26(Cx26)) are the most common cause of hereditary deafness, accounting for about a quarter of all cases. Sensory epithelial damage is considered to be one of the main causes of deafness caused by
Externí odkaz:
https://doaj.org/article/a403c77eb04d40b5a174233b5f8f500a
Publikováno v:
Sensors, Vol 23, Iss 16, p 7106 (2023)
The surface defects on a shield subway tunnel can significantly affect the serviceability of the tunnel structure and may compromise operation safety. To effectively detect multiple surface defects, this study uses a tunnel inspection trolley (TIT) b
Externí odkaz:
https://doaj.org/article/5614298e236a41da818a58d4df41f9b8
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 10349 (2023)
The connexin gene family is the most prevalent gene that contributes to hearing loss. Connexins 26 and 30, encoded by GJB2 and GJB6, respectively, are the most abundantly expressed connexins in the inner ear. Connexin 43, which is encoded by GJA1, ap
Externí odkaz:
https://doaj.org/article/f88aad0405fe4387acdb9be4613e8c82
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Hearing loss is among the most common congenital sensory impairments. Genetic causes account for more than 50% of the cases of congenital hearing loss. The PTPRQ gene, encoding protein tyrosine phosphatase receptor Q, plays an important role in maint
Externí odkaz:
https://doaj.org/article/f1e9f571a3de4d57b80283b1a6825942
Publikováno v:
Applied Sciences, Vol 13, Iss 11, p 6681 (2023)
Surface cracks are typical defects in high-speed rail (HSR) slab tracks, which can cause structural deterioration and reduce the service reliability of the track system. However, the question of how to effectively detect and quantify the surface crac
Externí odkaz:
https://doaj.org/article/c769026cb4004d84909dea18319aff3f
Autor:
Xiao-zhou Liu, Yuan Jin, Sen Chen, Kai Xu, Le Xie, Yue Qiu, Xiao-hui Wang, Yu Sun, Wei-jia Kong
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2022)
Mutations in the GJB2 gene encoding connexin26 (Cx26) protein are one of the most common causes of hereditary deafness. Previous studies have found that different Cx26-null mouse models have severe hearing loss and deformity of the organ of Corti (OC
Externí odkaz:
https://doaj.org/article/1bfdc77929ba48c4a0515fc8205f9408
Publikováno v:
IEEE Access, Vol 8, Pp 156043-156052 (2020)
Track slab deformation has become a challenging issue in high-speed rail (HSR) operation in recent years. This article proposed a novel approach for track slab deformation monitoring based on computer vision techniques. The basic principle of visual
Externí odkaz:
https://doaj.org/article/76aacf8283af429e89167e6124b2b2f9
Publikováno v:
Fractal and Fractional, Vol 6, Iss 12, p 727 (2022)
The effect of track geometry on vehicle vibration is a major concern in high-speed rail (HSR) operation from the perspectives of ride comfort and safety. However, how to quantitatively characterize the relation between them remains a problem to be so
Externí odkaz:
https://doaj.org/article/991e0be97cee4262b0e8f4ee1c701fa8
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Sudden sensorineural hearing loss (SSNHL) is a common emergency in the world. Increasing evidence of imbalance of oxidant–antioxidant were found in SSNHL patients. Steroids combined with antioxidants may be a potential strategy for the treatment of
Externí odkaz:
https://doaj.org/article/6a5009966a804ac3b9641e6830ba0491
Autor:
Kai Xu, Sen Chen, Le Xie, Yue Qiu, Xue Bai, Xiao-Zhou Liu, Hui-Min Zhang, Xiao-Hui Wang, Yuan Jin, Yu Sun, Wei-Jia Kong
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2021)
The macrophage-related immune response is an important component of the cochlear response to different exogenous stresses, including noise, ototoxic antibiotics, toxins, or viral infection. However, the role of the immune response in hereditary deafn
Externí odkaz:
https://doaj.org/article/4358ede20cae4ad8a117b2b0c0860fc2