Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Xian‐Guo Fu"'
Autor:
Wen-jing Yang, Ai-zhen Yan, Yong-jun Xu, Xiao-yan Guo, Xian-guo Fu, Dan Li, Juan Liao, Duo Zhang, Feng-hua Lan
Publikováno v:
BMC Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
Abstract Background The disease gene of fragile X syndrome, FMR1 gene, encodes fragile X mental retardation protein (FMRP). The alternative splicing (AS) of FMR1 can affect the structure and function of FMRP. However, the biological functions of alte
Externí odkaz:
https://doaj.org/article/cdb14d04becc443eb8323dac6660e2ec
Autor:
Xian‐Guo Fu, Zhao Huang, Su‐Juan Zhou, Jing Yang, Yun‐Juan Peng, Luo‐Yuan Cao, Hua Guo, Guang‐Hui Wu, Ying‐Hua Lin, Bao‐Ying Huang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background Trichilemmal cysts (TCs) are common intradermal or subcutaneous cysts, which are commonly sporadic and rarely autosomal dominantly inherited. However, little is known about the disease‐determining genes in families with TCs exhi
Externí odkaz:
https://doaj.org/article/19aed055de6e42cf8976d7cb3889256c
Publikováno v:
Fa yi xue za zhi. 38(3)
To establish the ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method to detect ethanol metabolites phosphatidylethanol (PEth) in whole blood.An appropriate amount of aqueous solution including 1% formic acid was added
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5fb71849d3a9866d5d773ac7da791758
https://pubmed.ncbi.nlm.nih.gov/36221832
https://pubmed.ncbi.nlm.nih.gov/36221832
Publikováno v:
Phytotaxa. 491:85-91
Tetrataenium mianguaqi, a traditionally used medicinal herb in Cangyuan County, SW Yunnan, China, is described as a species new to science and illustrated. Molecular phylogenetic analysis based on nuclear ITS well supports its belonging to Tetrataeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::982dded80d7226015fd81198bfe47e77
https://doi.org/10.11646/phytotaxa.491.1.10
https://doi.org/10.11646/phytotaxa.491.1.10
Autor:
Fenghua Lan, Wen-jing Yang, Juan Liao, Yong-jun Xu, Xiao-yan Guo, Xian-guo Fu, Dan Li, Ai-zhen Yan, Duo Zhang, Feng-hua Lan
The disease gene of fragile X syndrome, FMR1 gene, encodes fragile X mental retardation protein (FMRP). The alternative splicing of FMR1 can affect the structure and function of FMRP. However, the biological functions of alternatively spliced isoform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3317b4c393ef7aa02ce9b1e8ac89b985
https://doi.org/10.21203/rs.2.20949/v1
https://doi.org/10.21203/rs.2.20949/v1
Autor:
Gen Bin Huang, Zi Chun Chen, Luo Yuan Cao, Jing Yang, Yong Tong Xin, Xian Guo Fu, Qi Fang Lin, Long Teng Yao
Publikováno v:
Journal of Clinical Neurology (Seoul, Korea)
BACKGROUND AND PURPOSE Five single-nucleotide polymorphisms (SNPs) (rs4379368, rs10504861, rs10915437, rs12134493 and rs13208321) were recently identified in a Western population with migraine. These migraine-associated SNPs have not been evaluated i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48f9996b57a86a43f932fcb0de31815f
http://europepmc.org/articles/PMC5242144
http://europepmc.org/articles/PMC5242144
Autor:
Ai-zhen Yan, Wen-jing Yang, Duo Zhang, Juan Liao, Feng-hua Lan, Yong-jun Xu, Xian-guo Fu, De-zhu Zheng, Xiao-yan Guo
Publikováno v:
Gene. 731:144359
FMRP is an RNA-binding protein, loss of which causes fragile X syndrome (FXS). FMRP has several isoforms resulted from alternative splicing (AS) of fragile X mental retardation 1 (FMR1) gene, but their biological functions are still poorly understood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd6e457d1463f192152a56cc7ce03e7
https://doi.org/10.1016/j.gene.2020.144359
https://doi.org/10.1016/j.gene.2020.144359
Autor:
De-zhu Zheng, Yuxiang Lin, Ai-zhen Yan, Duo Zhang, Feng-hua Lan, Qingqin Li, Juan Liao, Xian-guo Fu
Publikováno v:
Molecular Medicine Reports. 12:1957-1962
Fragile X mental retardation 1 gene (FMR1) expression is associated with fragile X syndrome (FXS) and exhibits several splicing products. However, the proportion of spliced isoforms that are expressed in different tissues remains unclear. In the pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccdff0a634943440904b73850eaaf17c
https://doi.org/10.3892/mmr.2015.3574
https://doi.org/10.3892/mmr.2015.3574
Publikováno v:
Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 36(12)
To explore the role of miR-205 in regulating epithelial-messenchymal transition (EMT) in proximal tubular cell line HK-2 cells and the underlying mechanism.HK-2 cells transfected with miR-205 mimics or a scrambled control sequence were examined for m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cda1ebab210e0c59888222b48c0ce97f
https://pubmed.ncbi.nlm.nih.gov/27998868
https://pubmed.ncbi.nlm.nih.gov/27998868
Autor:
Bo Li, Ai-Zhen Yan, Shui-di Yan, Xian-Guo Fu, Duo Zhang, Jian Zeng, Long-Feng Ke, Feng-Hua Lan
Publikováno v:
PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS. 37:445-450
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd67c85a85e37284f8e6f4cafa587fcb
https://doi.org/10.3724/sp.j.1206.2009.00526
https://doi.org/10.3724/sp.j.1206.2009.00526