Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Yingyin Liang"'
Autor:
Liang Wang, Min Xu, Dawei Liu, Yingyin Liang, Pinning Feng, Huan Li, Yuling Zhu, Ruojie He, Jinfu Lin, Huili Zhang, Ziyu Liao, Cheng Zhang
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Background Dystrophinopathy, a common neuromuscular disorder, includes Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). Many researches are currently ongoing to develop curative approaches, which results in an urgent ne
Externí odkaz:
https://doaj.org/article/c1a68b14084149a8adc06fc97ab13a56
Publikováno v:
Biomolecules & Biomedicine, Vol 15, Iss 2 (2015)
The aim of our study was to determine the role of dystrophin hydrophobic regions in the pathogenesis of Duchenne (DMD) and Becker (BMD) muscular dystrophies, by the Kyte-Doolittle scale mean hydrophobicity profile and 3D molecular models. A total of
Externí odkaz:
https://doaj.org/article/450a01cee5d64715b07eb675552471f3
Publikováno v:
Marine Biotechnology. 25:109-122
A marine aerobic denitrifying bacterium was isolated and identified as Pseudomonas stutzeri BBW831 from the seabed silt of Beibu Gulf in China. According to the genome analysis, P. stutzeri BBW831 possessed a total of 14 genes (narG, narH, narI, narJ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1916ee2b89a28756e4ca825e0c3020a
https://doi.org/10.1007/s10126-022-10185-1
https://doi.org/10.1007/s10126-022-10185-1
Autor:
Jiqing, Cao, Yaqin, Li, Yingyin, Liang, Fei, Chen, Huili, Zhang, Yuling, Zhu, Juan, Yang, Shanwei, Feng, Cheng, Zhang
Publikováno v:
In Cytotherapy September 2015 17(9):1213-1219
Publikováno v:
Neuromuscular Disorders. 31:456-461
Twins with Duchenne muscular dystrophy (DMD) have been widely studied. We report the first rare case of monozygotic triplets with DMD who shared consistent phenotypes, including delayed motor and language milestones, muscle wasting and weakness, join
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::945b096b87e0d60c795c4e56a6c31a1a
https://doi.org/10.1016/j.nmd.2021.02.005
https://doi.org/10.1016/j.nmd.2021.02.005
Autor:
Jinfu Lin, Ruojie He, Huili Zhang, Cheng Zhang, Pinning Feng, Yuling Zhu, Ziyu Liao, Huan Li, Liang Wang, Dawei Liu, Min Xu, Yingyin Liang
Publikováno v:
BMC Neurology
BMC Neurology, Vol 21, Iss 1, Pp 1-11 (2021)
BMC Neurology, Vol 21, Iss 1, Pp 1-11 (2021)
Background Dystrophinopathy, a common neuromuscular disorder, includes Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). Many researches are currently ongoing to develop curative approaches, which results in an urgent need for bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12eb2fd54ac2335109ecad9e7e7e8819
https://doi.org/10.1186/s12883-021-02382-7
https://doi.org/10.1186/s12883-021-02382-7
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2021 (2021)
BioMed Research International, Vol 2021 (2021)
Parkinson’s disease (PD) is an incurable progressive disorder resulting from neurodegeneration, and apoptosis is considered a dominant mechanism underlying the process of neurodegeneration. MicroRNAs (miRNAs), which are small and noncoding RNAs inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1831ab4eb3cb8217a703ddfde329879d
http://europepmc.org/articles/PMC7806375
http://europepmc.org/articles/PMC7806375
Autor:
Fu Xiong, Xiaofeng Wei, Huajie Huang, Dan Guo, Xuelian Zhang, Jian Wang, Hengbiao Sun, Yingyin Liang, Xiangmin Xu
Publikováno v:
Experimental and Therapeutic Medicine
Hypophosphatasia (HPP) is a rare hereditary systemic disease that is characterized by defective bone and/or dental mineralization, and is caused by mutations in the alkaline phosphatase gene (ALPL). The present study investigated the ALPL mutation in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a76ae96e916bd340e905beecf3027462
https://doi.org/10.3892/etm.2020.9281
https://doi.org/10.3892/etm.2020.9281
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 42(5)
Vestibular migraine (VM) has been recently receiving increasing attention as an independent disease concept. It is a common cause of dizziness or headache; however, it was not clearly defined until 2018. Its diagnosis mainly relies on clinical histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4607e4e44ddd5592d4e887792a5cc8b
https://pubmed.ncbi.nlm.nih.gov/33666767
https://pubmed.ncbi.nlm.nih.gov/33666767
Autor:
YINGYIN LIANG1 lyyin@mail.sysu.edu.cn, GUIDIAN LI2, SONGLIN CHEN1, RONGXING HE2, XIANGXUE ZHOU1, YINGMING CHEN2, XUE XU1, RONGLAN ZHU1, CHENG ZHANG1
Publikováno v:
Biomedical Reports. Aug2017, Vol. 7 Issue 2, p193-196. 4p.