Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Yufen GUO"'
Autor:
Suyang Wang, Chen Yang Xu, Yiming Zhu, Wenjuan Ding, Jieyu Hu, Baicheng Xu, Yufen Guo, Xiaowen Liu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Usher syndrome type 3 (USH3) is an autosomal recessive inherited disorder caused by pathogenic variants in the CLRN1 gene. Object To evaluate the genotype-phenotype correlation of Usher syndrome type 3 (USH3) in a deaf-blind Chine
Externí odkaz:
https://doaj.org/article/ed6db7d936d6494dacbd30cccaa7664a
Autor:
Suyang Wang, Yi‐Ming Zhu, ChenYang Xu, Wenjuan Ding, Hui Jia, Panpan Bian, Baicheng Xu, Yufen Guo, Xiaowen Liu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 2, Pp n/a-n/a (2024)
Abstract Objective We aimed to evaluate the genotype–phenotype relationship in two Chinese family members with enlarged vestibular aqueduct (EVA). Methods We collected blood samples and clinical data from each pedigree family member. Genomic DNA wa
Externí odkaz:
https://doaj.org/article/1cd562f148bc43639d023abb66e6a0ac
Publikováno v:
Journal of International Advanced Otology, Vol 18, Iss 2, Pp 92-95 (2022)
Externí odkaz:
https://doaj.org/article/40da2e8d26434322a8701e72041a42ad
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 10 (2022)
The unicellular flagellate algae Poterioochromonas malhamensis is a potential fucoxanthin-rich resource for sustainable and cost-effective fucoxanthin production. Light and nutrients are critical regulators for the accumulation of fucoxanthin in P. m
Externí odkaz:
https://doaj.org/article/edeb21d62db24a089292626b19df8360
Autor:
Panpan Bian Master, Baicheng Xu Doctor, Xiaoyun Zhao Master, YiMing Zhu Doctor, Chi Chen Master, XingJian Chen Master, Xiaowen Liu Doctor, Yanli Wang Master, Yufen Guo Doctor
Publikováno v:
Inquiry: The Journal of Health Care Organization, Provision, and Financing, Vol 59 (2022)
Background : The GJB2 gene is the most common deafness gene, and epidemic characteristics have obvious racial specificity. Our study aimed to investigate the prevalence and ethnic specificity of the GJB2 gene in deafness in major ethnic groups in Nor
Externí odkaz:
https://doaj.org/article/413dafbbece74bf68abb63f5692a8acc
Publikováno v:
Stem Cell Research, Vol 61, Iss , Pp 102761- (2022)
More than 120 genes have been reported to be associated with deafness, and deletion of the TBL1X gene may cause deafness in humans. In this study, we generated an induced pluripotent stem cell (iPSC) line from dermal fibroblasts of a 34-year-old deaf
Externí odkaz:
https://doaj.org/article/763f9f4bbda84a64a0e60837b45c9cfb
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
ObjectiveTo investigate the effects of NK4 gene on the properties and tumorigenicity in laryngeal squamous cell carcinoma cell.MethodsHere, we used the attenuated Salmonella carrying the NK4 gene to transfect the AMC-HN-8 cells and detected the expre
Externí odkaz:
https://doaj.org/article/576b932660674485b52b2818229d1043
Publikováno v:
Journal of International Medical Research, Vol 49 (2021)
Objective Mutations in GJB2 , SLC26A4 , and mitochondrial (mt)DNA 12S rRNA genes are the main cause of nonsyndromic hearing impairment. The present study analyzed these mutations in ethnic minority and Han Chinese patients with nonsyndromic hearing i
Externí odkaz:
https://doaj.org/article/f2716bf8cd7f4b1ab03022b827f002e4
Autor:
Junxiong Hu, Jianbao Xu, Chao Zhu, Qi Li, Zaka Ullah, Fengkui Liu, Weiwei Li, Yufen Guo, Xinluo Zhao, Liwei Liu
Publikováno v:
AIP Advances, Vol 7, Iss 5, Pp 055315-055315-7 (2017)
We demonstrate a facile approach to significantly enhance the heat dissipation potential of conventional aluminum (Al) heat sinks by mechanically coating graphene nanosheets. For Al and graphene-coated Al heat sinks, the change in temperature with ch
Externí odkaz:
https://doaj.org/article/2044b7d9de3a42f29f74eaf3ebcc5f35
Publikováno v:
Acta Oto-Laryngologica. 143:134-140