Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Hai-zhu Chen"'
Autor:
Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-ze Zheng, Liang-liang Qiu, Zhi-xian Ye, Hai-zhu Chen, Min-ting Lin, Ning Wang, Zhi-qiang Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-18 (2023)
Abstract Background Limb-girdle muscular dystrophies (LGMDs) are a group of heterogeneous inherited diseases predominantly characterized by limb-girdle muscle weakness and dystrophic changes on histological analysis. The frequency of LGMD subtypes va
Externí odkaz:
https://doaj.org/article/80189a10ec2d46fb8dda201e21e194aa
Autor:
Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Yun-Lu Li, Chong Wang, Zhi-Yuan Zhao, Xue-Jing Huang, Kai-Jun Lin, Zi-Ling Ye, Bi-Wei Lin, Shunyan Hong, Jitan Zheng, Yao-Bin Liu, Xiang-Ping Yao, Dehao Yang, Ying-Qian Lu, Hai-Zhu Chen, Erwei Zuo, Guang Yang, Hong-Tao Wang, Chen-Wei Huang, Xiao-Hong Lin, Zhidong Cen, Lu-Lu Lai, Yan-Ke Zhang, Xi Li, Tianmin Lai, Jingjing Lin, Dan-Dan Zuo, Min-Ting Lin, Chia-Wei Liou, Qing-Xia Kong, Chuan-Zhu Yan, Zhi-Qi Xiong, Ning Wang, Wei Luo, Cui-Ping Zhao, Xuewen Cheng, Wan-Jin Chen
Publikováno v:
Cell Discovery, Vol 8, Iss 1, Pp 1-17 (2022)
Abstract Brain calcification is a critical aging-associated pathology and can cause multifaceted neurological symptoms. Cerebral phosphate homeostasis dysregulation, blood-brain barrier defects, and immune dysregulation have been implicated as major
Externí odkaz:
https://doaj.org/article/9415229f27c04eb299808dca7e144e8f
Autor:
Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 22, Pp 2753-2755 (2021)
Externí odkaz:
https://doaj.org/article/eecb6fd1948e4082a8be5b5932908fe6
Autor:
Hai-Zhu Chen, Ming Jin, Nai-Qing Cai, Xiao-Dan Lin, Xin-Yi Liu, Liu-Qing Xu, Min-Ting Lin, Feng Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu, Yi Cui
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 13, Pp 1615-1618 (2019)
Externí odkaz:
https://doaj.org/article/2fff0e1a423c42e1902353678b37ef51
Autor:
Xiao-Dan Lin, Jun-Jie He, Feng Lin, Hai-Zhu Chen, Liu-Qing Xu, Wei Hu, Nai-Qing Cai, Min-Ting Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 18, Pp 2164-2171 (2018)
Background: Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric muscular deficit of facial, shoulder-girdle muscles, and descending to lower limb muscles, but it exists in several extramuscular manifestations or overlapping s
Externí odkaz:
https://doaj.org/article/e16c5af090ef4ddcb0ee68da2b7a287f
Publikováno v:
Tongxin xuebao, Vol 35, Pp 1-8 (2014)
The data locality is divided into two levels.One is called the node data locality,which placing tasks on nodes that contain their input data.The other one is called the rack data locality,which placing tasks on nodes whose rack contains their input d
Externí odkaz:
https://doaj.org/article/bc020130517a4f21896d6f3d73532813
Autor:
Hai-Zhu Chen, Min-Ting Lin, Lin Lin, Liangliang Qiu, Guo-Rong Xu, Lili Wang, Feng Lin, Zhixian Ye, Nai-Qing Cai, Xiao-Dan Lin, Ming Jin, Zhi-Qiang Wang, Ning Wang, Jun-Jie He
Publikováno v:
Journal of Medical Genetics. 57:777-785
PurposeTo analyse the clinical spectrum, genetic features, specific D4Z4 hypomethylation status and genotype–phenotype correlations for somatic mosaicism in facioscapulohumeral dystrophy (FSHD).MethodsThis was a prospective, hospital-based, case–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6728f17907b0b3eaf306dbaf611384f6
https://doi.org/10.1136/jmedgenet-2019-106638
https://doi.org/10.1136/jmedgenet-2019-106638
Autor:
Min-Ting Lin, Hai-Zhu Chen, Nai-Qing Cai, Zhixian Ye, Ning Wang, Feng Lin, Guo-Rong Xu, Lili Wang, Liangliang Qiu, Ming Jin
Publikováno v:
Neuromuscular Disorders. 30:137-143
Limb girdle muscular dystrophy LGMD R7 telethonin-related is a rare autosomal recessive muscle disorder characterized by proximal muscle weakness of pelvic and shoulder girdles. Mutation in TCAP is responsible for LGMD R7, and the disease has a wide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aceaacdadce60b65ef3cba2b72c81891
https://doi.org/10.1016/j.nmd.2019.12.004
https://doi.org/10.1016/j.nmd.2019.12.004
Publikováno v:
Current medical science. 42(6)
Due to the rarity of angioimmunoblastic T-cell lymphoma (AITL), very limited data concerning its incidence patterns and prognostic factors are available. This study aimed to explore the incidence, characteristics, survival outcomes, and prognostic fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90a364a73f92f1923887bf38510c5c42
https://pubmed.ncbi.nlm.nih.gov/36547871
https://pubmed.ncbi.nlm.nih.gov/36547871
Autor:
Yidi Sun, Ying-Qian Lu, Lixiang Ma, Changyang Zhou, Wan-Jin Chen, Lu-Lu Lai, He Li, Min-Ting Lin, Xiaowen Shen, Qifang Wang, Hui Yang, Wenqin Ying, Linyu Shi, Xiang Lin, Shuang Wu, Jin-Jing Li, Ning Wang, Qi-Jie Zhang, Adrian R. Krainer, Erwei Zuo, Xin-Xin Guo, Hai-Zhu Chen, Cheng Tang, Xinde Hu
Publikováno v:
National Science Review
We here report a genome-editing strategy to correct spinal muscular atrophy (SMA). Rather than directly targeting the pathogenic exonic mutations, our strategy employed Cas9 and guide-sgRNA for the targeted disruption of intronic splicing-regulatory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12409ee1e044a102bdb596c00d044557
https://doi.org/10.1093/nsr/nwz131
https://doi.org/10.1093/nsr/nwz131