Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ru-Yi Han"'
Autor:
Pei Wang, Sen Li, Yang Zou, Ru-Yi Han, Ping Wang, De-Ping Song, Cheng-Bin Wang, Xiao-Qing Chen
Publikováno v:
Animals, Vol 12, Iss 14, p 1764 (2022)
Entamoeba spp. is a common zoonotic intestinal protozoan that can parasitize most vertebrates, including humans and pigs, causing severe intestinal diseases and posing a serious threat to public health. However, the available data on Entamoeba spp. i
Externí odkaz:
https://doaj.org/article/d8beec7f47994db997cdea1b73e42469
Autor:
You-Yuan Zhuang, Lue Xiang, Xin-Ran Wen, Ren-Juan Shen, Ning Zhao, Si-Si Zheng, Ru-Yi Han, Jia Qu, Fan Lu, Zi-Bing Jin
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Previous study has identified SLC7A14 as a new causative gene of retinitis pigmentosa (RP). However, the role of SLC7A14 has not been fully characterized. The goal of this study was to investigate the biological features of slc7a14 in zebrafish. To d
Externí odkaz:
https://doaj.org/article/c632fdfc940e49ee9c57a91ea6a45dfa
Autor:
Xiu-Feng Huang, Lue Xiang, Wan Cheng, Fei-Fei Cheng, Kai-Wen He, Bo-Wen Zhang, Si-Si Zheng, Ru-Yi Han, Yi-Han Zheng, Xiao-Tao Xu, Huan-Yun Yu, Wenjuan Zhuang, Yuk Fai Leung, Zi-Bing Jin
Publikováno v:
Experimental and Molecular Medicine, Vol 50, Iss 4, Pp 1-11 (2018)
Hereditary eye disease: Looking for blindness in the family tree In-depth genomic analysis of the family of a young man with severe visual impairment reveals a new gene involved in eye development. Ocular coloboma encompasses various hereditary disor
Externí odkaz:
https://doaj.org/article/34777f933ab945848b41bdcdce3d2b5d
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 6 (2018)
Over recent decades, zebrafish has been established as a sophisticated vertebrate model for studying human ocular diseases due to its high fecundity, short generation time and genetic tractability. With the invention of morpholino (MO) technology, it
Externí odkaz:
https://doaj.org/article/5b05a59c20ce4e6d90b6ed492118cea7
Publikováno v:
Transboundary and emerging diseasesReferences.
Enterocytozoon bieneusi is an important pathogen that is responsible for over 90% of documented cases of human microsporidiosis worldwide, causing a threat to public health and husbandry development. In immunocompromised patients, it can cause persis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0cd2d52fa2da4517de130879634418c
https://pubmed.ncbi.nlm.nih.gov/36193011
https://pubmed.ncbi.nlm.nih.gov/36193011
Autor:
Pei, Wang, Sen, Li, Yang, Zou, Ru-Yi, Han, Ping, Wang, De-Ping, Song, Cheng-Bin, Wang, Xiao-Qing, Chen
Publikováno v:
Animals : an open access journal from MDPI. 12(14)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0436ef300e682dce8309d9ae5a55cc7
https://pubmed.ncbi.nlm.nih.gov/35883310
https://pubmed.ncbi.nlm.nih.gov/35883310
Autor:
Yi-Han Zheng, Ru-Yi Han, Huan-Yun Yu, Xiu-Feng Huang, Lue Xiang, Si-Si Zheng, Bo-Wen Zhang, Fei-Fei Cheng, Wan Cheng, Wenjuan Zhuang, Kai-Wen He, Yuk Fai Leung, Zi-Bing Jin, Xiao-Tao Xu
Publikováno v:
Experimental and Molecular Medicine, Vol 50, Iss 4, Pp 1-11 (2018)
Experimental & Molecular Medicine
Experimental & Molecular Medicine
Ocular coloboma is a developmental structural defect of the eye that often occurs as complex ocular anomalies. However, its genetic etiology remains largely unexplored. Here we report the identification of mutation (c.331C>T, p.R111C) in the IPO13 ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::721e2c4d61efc43867b601b9f78cfdd4
https://doaj.org/article/34777f933ab945848b41bdcdce3d2b5d
https://doaj.org/article/34777f933ab945848b41bdcdce3d2b5d
Autor:
Wei-Qin Liu, Xiu-Feng Huang, Wan Cheng, Ren-Juan Shen, Si-Si Zheng, Xiao-Long Fang, Ru-Yi Han, You-Yuan Zhuang, Xiaoling Liu, Zi-Bing Jin, Lue Xiang, Zhen-Ji Chen, Xue-Jiao Chen
Publikováno v:
Human Mutation.
Retinitis pigmentosa (RP) is the most common manifestation of inherited retinal diseases with high degree of genetic, allelic, and phenotypic heterogeneity. CEP250 encodes the C-Nap1 protein and has been associated with various retinal phenotypes. He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aafcd0f0367b840ae45abacfd8463b0c
https://doi.org/10.1002/humu.23759
https://doi.org/10.1002/humu.23759
Autor:
You-Yuan Zhuang, Si-Si Zheng, Lue Xiang, Ru-Yi Han, Zhen-Ji Chen, Xiu-Feng Huang, Xiao-Long Fang, Wan Cheng, Ren-Juan Shen, Xiaoling Liu, Zi-Bing Jin
Publikováno v:
SSRN Electronic Journal.
Background: Retinitis pigmentosa (RP) is the most common manifestation of inherited retinal diseases that primarily affects photoreceptor function, and is generally exhibited with high degree of genetic, allelic and phenotypic heterogeneity. CEP250 e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7e6dec0d2ae8f9f0a913b643b6b97c9
https://doi.org/10.2139/ssrn.3228881
https://doi.org/10.2139/ssrn.3228881
Autor:
Si-Si Zheng, Xianglian Ge, Feng Gu, Ru-Yi Han, Qingjie Min, Ye-Wen Lin, Fayu Yang, Yi-Han Zheng, Xinping Yu, Lulu Cheng, Jia Qu, Jin-Ling Xu, Jie Tian
To identify the genetic defects of a Chinese patient with sporadic retinitis pigmentosa (RP).Ophthalmologic examinations were performed on the sporadic RP patient, 144 genes associated with retinal diseases were scanned with capture next generation s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::758766bd8feee0e5726793b95e022928
https://europepmc.org/articles/PMC4990571/
https://europepmc.org/articles/PMC4990571/
