Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Zhixian Ye"'
Publikováno v:
Advances in Aerodynamics, Vol 4, Iss 1, Pp 1-28 (2022)
Abstract A comparative study about riblets-controlled turbulent boundary layers has been performed to investigate the turbulence characteristics associated with drag reduction in a compressive flat-plate flow (where the free-stream Mach number is 0.7
Externí odkaz:
https://doaj.org/article/d11f268fdcd949d48946bd5319ce2d2f
Autor:
Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Aim to identify potential biomarkers to assess therapeutic efficacy for hereditary spastic paraplegias type 5 (SPG5) by investigating the clinical, cerebrospinal fluid (CSF) and magnetic resonance imaging (MRI) features. Methods W
Externí odkaz:
https://doaj.org/article/0491c80a17724709923abc9594b987c2
Autor:
Fuze Zheng, Long Chen, Liangliang Qiu, Lin Lin, Xin Lin, Qifang He, Lili Wang, Zhixian Ye, Minting Lin, Zhiqiang Wang
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102678- (2022)
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common muscular dystrophy. FSHD type 1 (FSHD1) is caused by multicopy contraction of D4Z4 repeats on chromosome 4q35. Human induced pluripotent stem cell (hiPSC) lines serve as importan
Externí odkaz:
https://doaj.org/article/2a87b206256f48d2923ce82ef8b3b264
Autor:
Zhiqiang Wang, Liangliang Qiu, Minting Lin, Long Chen, Fuze Zheng, Lin Lin, Feng Lin, Zhixian Ye, Xiaodan Lin, Junjie He, Lili Wang, Xin Lin, Qifang He, Wanjin Chen, Yi Lin, Ying Fu, Ning Wang
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 18, Iss , Pp 100323- (2022)
Summary: Background: Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a rare disease, which is often underdiagnosed due to its heterogeneous presentations and complex molecular genetic basis, leading to a lack of population-based epidemiology
Externí odkaz:
https://doaj.org/article/1c941babb7814c839f8752c100d31eff
Correction to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5
Autor:
Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/5ef776ba5f034881883d8f94061a4a73
Publikováno v:
2022 IEEE/RSJ International Conference on Intelligent Robots and Systems (IROS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba52b7ffaea4cd9e4196be149dbfce1
https://doi.org/10.1109/iros47612.2022.9981220
https://doi.org/10.1109/iros47612.2022.9981220
Autor:
Liangliang Qiu, Long Chen, Fuze Zheng, Ying Zheng, Xin Lin, Qifang He, Lin Lin, Lili Wang, Zhixian Ye, Minting Lin, Yi Lin, Ying Fu, Zhi-qiang Wang, Ning Wang
Background: Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a rare, hereditary, and progressive muscular dystrophy characterized by weakness and wasting of the facial (facio-) and shoulder-upper arm (scapulo-humeral-) muscles. The clinical s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89329baf05b32291c0832364a28962fc
https://doi.org/10.21203/rs.3.rs-2006739/v1
https://doi.org/10.21203/rs.3.rs-2006739/v1
Publikováno v:
Traitement du Signal. Dec2019, Vol. 36 Issue 6, p501-506. 6p.
In this paper, we present a systematic approach for high-performance and efficient trajectory tracking control of autonomous wheel loaders. With the nonlinear dynamic model of a wheel loader, nonlinear model predictive control (MPC) is used in offlin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0dffdc226d7eb174a3e806a18ae0fd2
http://arxiv.org/abs/2203.08944
http://arxiv.org/abs/2203.08944
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