Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lianhua Su"'
Autor:
Xixi Xiao, Ruijia Feng, Mingshan Wang, Hanqi Sun, Tianzhen Jing, Lianhua Su, You Fan, Zuojun Hu, Shenming Wang, Siwen Wang
Publikováno v:
BMC Surgery, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Background Thrombotic popliteal artery aneurysm (PAA) with acute lower limb ischemia (ALI) is a serious disease leading to amputation. The choice of emergency procedures is not clearly defined, and the difference in therapeutic efficiency be
Externí odkaz:
https://doaj.org/article/f3244a1f4974467d811942f4a7f88856
Autor:
Jianfeng Jiang, Yuqing Hao, Biao He, Lianhua Su, Xuezheng Li, Xiangxiang Liu, Chuanwei Chen, Lijuan Chen, Zihan Zhao, Shijiang Mi, Xuming Deng, Wenjie Gong, Changchun Tu
Publikováno v:
J Virol
Members of the genus Hepacivirus have a broad range of hosts, with at least 14 species identified. To date, a highly pathogenic hepacivirus causing severe disease in animals has not been found. Here, by using high-throughput sequencing, a new hepaciv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f9fbadf4cc2400423bcccb043dbe0a4
https://europepmc.org/articles/PMC9472637/
https://europepmc.org/articles/PMC9472637/
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveAuditory neuropathy spectrum disease (ANSD) is caused by both environmental and genetic causes and is defined by a failure in peripheral auditory neural transmission but normal outer hair cells function. To date, 13 genes identified as poten
Externí odkaz:
https://doaj.org/article/47379ab4e97d4bfca424674bf870cdee
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Hearing loss affecting about 2/1000 newborns is the most common congenital disease. Genetic defects caused approximately 70% of patients who have non-syndromic hearing loss. We recruited 13 Chinese Han deafness families who tested negative for GJB2,
Externí odkaz:
https://doaj.org/article/08629ef3fd3840ab86e9557b36f571fe
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
The Kölliker’s organ is a transient cellular cluster structure in the development of the mammalian cochlea. It gradually degenerates from embryonic columnar cells to cuboidal cells in the internal sulcus at postnatal day 12 (P12)–P14, with the c
Externí odkaz:
https://doaj.org/article/517d9ac471db42e687f8476530af40f5
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Hereditary deafness is one of the most common human birth defects. GJB2 gene mutation is the most genetic etiology. Gap junction protein 26 (connexin26, Cx26) encoded by the GJB2 gene, which is responsible for intercellular substance transfer and sig
Externí odkaz:
https://doaj.org/article/02063b04d1534b059568bc76c2038346
Autor:
Lianhua Sun, Dekun Gao, Junmin Chen, Shule Hou, Yue Li, Yuyu Huang, Fabio Mammano, Jianyong Chen, Jun Yang
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
Mutations in the GJB2 gene that encodes connexin 26 (Cx26) are the predominant cause of prelingual hereditary deafness, and the most frequently encountered variants cause complete loss of protein function. To investigate how Cx26 deficiency induces d
Externí odkaz:
https://doaj.org/article/5d32b36ce3f94bc6aadf20dc53d62ebd
Autor:
Jianyong Chen, Dekun Gao, Junmin Chen, Shule Hou, Baihui He, Yue Li, Shuna Li, Fan Zhang, Xiayu Sun, Yulian Jin, Lianhua Sun, Jun Yang
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
The hair cells of the cochlea play a decisive role in the process of hearing damage and recovery, yet knowledge of their regeneration process is still limited. Greater epithelial ridge (GER) cells, a type of cell present during cochlear development t
Externí odkaz:
https://doaj.org/article/7fb52564919d4d02a7d1b583dd32e9e9
Autor:
Jianyong Chen, Dekun Gao, Junmin Chen, Shule Hou, Baihui He, Yue Li, Shuna Li, Fan Zhang, Xiayu Sun, Fabio Mammano, Lianhua Sun, Jun Yang, Guiliang Zheng
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Greater epithelial ridge cells, a transient neonatal cell group in the cochlear duct, which plays a crucial role in the functional maturation of hair cell, structural development of tectorial membrane, and refinement of audio localization before hear
Externí odkaz:
https://doaj.org/article/5b4697d8e4374c9b949902a3a9fe5d0f
Autor:
Shule Hou, Penghui Chen, Jiarui Chen, Junmin Chen, Lianhua Sun, Jianyong Chen, Baihui He, Yue Li, Huan Qin, Yuren Hong, Shuna Li, Jingchun He, Dekun Gao, Fabio Mammano, Jun Yang
Publikováno v:
Neural Plasticity, Vol 2020 (2020)
Autophagy and apoptosis have a complex interplay in the early embryo development. The development of spiral ganglion neurons (SGNs) in addition to Corti’s organ in the mammalian cochlea remains crucial in the first two-week postnatal period. To inv
Externí odkaz:
https://doaj.org/article/018c9e951bd145498b7dfdc3a805a3a1