Zobrazeno 1 - 10
of 164
pro vyhledávání: '"EYA4"'
Autor:
Junfang Xue, Linyi Xie, Qiuchen Zheng, Fen Xiong, Xiedong Wu, Jialin Fan, Yang Zhang, Dayong Wang, Qiujing Zhang, Qiuju Wang
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background EYA4 variants are responsible for DFNA10 deafness. Due to its insidious onset and slow progression, hearing loss in autosomal dominant non-syndromic hearing loss (ADNSHL) is usually challenging to detect early in clinical settings
Externí odkaz:
https://doaj.org/article/1819332b461a4428bcb90f358303584e
Publikováno v:
Molecular Cancer, Vol 22, Iss 1, Pp 1-18 (2023)
Abstract The Eyes Absent (EYA) family of proteins is an atypical group of four dual-functioning protein phosphatases (PP), which have been linked to many vital cellular processes and organogenesis pathways. The four family members of this PP family p
Externí odkaz:
https://doaj.org/article/84a501a5d1624c18945c54c7315e35a6
Akademický článek
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Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2023)
BackgroundNoise-induced hearing loss (NIHL) has always been a global public health problem, which is related to noise exposure and genetic factors. Many researchers have tried to identify the polymorphisms that cause different individuals' susceptibi
Externí odkaz:
https://doaj.org/article/c739f97009c7439a970538b44eec801d
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-12 (2022)
Abstract Background Hereditary hearing loss is a heterogeneous class of disorders that exhibits various patterns of inheritance and involves many genes. Variants in the EYA4 gene in DFNA10 are known to lead to postlingual, progressive, autosomal domi
Externí odkaz:
https://doaj.org/article/ed5db3586bfb4cbdb792f077515afb09
Autor:
Chenxi Li, Zhaohui Liu, Guohua Xu, Shibin Wu, Yunhui Peng, Ruinuan Wu, Shukun Zhao, Xiaoqi Liao, Runhua Lin
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 28, Iss 6, Pp 456-465 (2022)
Background: Intestinal metaplasia (IM) of the gastric cardia is an important premalignant lesion. However, there is limited information concerning its epidemiological and molecular features. Herein, we aimed to provide an overview of the epidemiologi
Externí odkaz:
https://doaj.org/article/4be00f1ded504cbdad91376a6e4e3479
Akademický článek
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Autor:
Wei Dong, Junming Bi, Hongwei Liu, Dong Yan, Qingqing He, Qianghua Zhou, Qiong Wang, Ruihui Xie, Yinjie Su, Meihua Yang, Tianxin Lin, Jian Huang
Publikováno v:
Molecular Cancer, Vol 18, Iss 1, Pp 1-16 (2019)
Abstract Background Circular RNAs (circRNAs) have been considered to mediate occurrence and development of human cancers, generally acting as microRNA (miRNA) sponges to regulate downstream genes expression. However, the aberrant expression profile a
Externí odkaz:
https://doaj.org/article/ae11ba9ab5bd42aea3c7bc209aadf4c4
Publikováno v:
Biomedicines, Vol 10, Iss 9, p 2125 (2022)
Sensorineural hearing loss is one of the most common inherited sensory disorders. Functional classifications of deafness genes have shed light on genotype- and mechanism-based pharmacological approaches and on gene therapy strategies. In this study,
Externí odkaz:
https://doaj.org/article/87b81e6f97044dd1bc4973601b69e155
Autor:
Yanfang Mi, Danhua Liu, Beiping Zeng, Yongan Tian, Hui Zhang, Bei Chen, Juanli Zhang, Hong Xue, Wenxue Tang, Yulin Zhao, Hongen Xu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 1, Pp n/a-n/a (2021)
Abstract Background Autosomal dominant hearing loss (ADHL) accounts for about 20% of all hereditary non‐syndromic HL. Truncating mutations of the EYA4 gene can cause either non‐syndromic ADHL or syndromic ADHL with cardiac abnormalities. It has b
Externí odkaz:
https://doaj.org/article/19ec8a09492f4e1f90435ea9926f26be