Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Mei Juan Yu"'
Publikováno v:
Biochemical and Biophysical Research Communications. 419:1-6
Duchenne muscular dystrophy is the most prevalent inheritable muscle disease. Transplantation of autologous stem cells with gene direction is an ideal therapeutic approach for the disease. The current study aimed to investigate the restoration of myo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413fb9611bc1819f8288a8cbec66b439
https://doi.org/10.1016/j.bbrc.2012.01.029
https://doi.org/10.1016/j.bbrc.2012.01.029
Autor:
H. Meng, Mei-Juan Yu, Mei-Mei Gao, Na He, B. Qin, Wei-Ping Liao, Bing-Mei Li, Yi-Wu Shi, Yong-Hong Yi, Yue-Sheng Long, Xiao Rong Liu, Wei-Yi Deng
Publikováno v:
Genes, Brain and Behavior. 11:170-176
SCN1A is the most relevant epilepsy gene. Mutations of SCN1A generate phenotypes ranging from the extremely severe form of Dravet syndrome (DS) to a mild form of generalized epilepsy with febrile seizures plus (GEFS+). Mosaic SCN1A mutations have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7610eb4710b5be28e0c55e171a3ff604
https://doi.org/10.1111/j.1601-183x.2011.00756.x
https://doi.org/10.1111/j.1601-183x.2011.00756.x
HLA-B Alleles and Lamotrigine-Induced Cutaneous Adverse Drug Reactions in the Han Chinese Population
Publikováno v:
Basic & Clinical Pharmacology & Toxicology. 109:42-46
Lamotrigine (LTG) is a commonly used antiepileptic drug. However, the use of LTG is limited because of its cutaneous adverse drug reactions (cADRs) ranging from mild maculopapular eruption (MPE) to severe Stevens–Johnson syndrome (SJS) and toxic ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0895dbaf3fea9513937a816aed122410
https://doi.org/10.1111/j.1742-7843.2011.00681.x
https://doi.org/10.1111/j.1742-7843.2011.00681.x
Autor:
Xiao Rong Liu, Wei Yi Deng, Tian Li, Zhi Gang Lei, Shumin Duan, Shu Jun Xu, Yi Wu Shi, Yue Sheng Long, Yong Hong Yi, Tao Su, Weiwen Sun, Yang Zeng, Mei Juan Yu, Ping Deng, Zao C. Xu, Wei-Ping Liao
Publikováno v:
Epilepsia. 51:1669-1678
P>Purpose: Generalized epilepsy with febrile seizures plus (GEFS+) and severe myoclonic epilepsy in infancy (SMEI) are associated with sodium channel alpha-subunit type-1 gene (SCN1A) mutations. Febrile seizures and partial seizures occur in both GEF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d70e9dde46714ddc02f7e83224774977
https://doi.org/10.1111/j.1528-1167.2010.02645.x
https://doi.org/10.1111/j.1528-1167.2010.02645.x
Autor:
J.-L. Li, Chao Zhang, Mei-juan Yu, Zhengshan Liu, Tai-yun Liu, Xiao Lu, Yinxiang Zeng, Yi-Nuan Zhang, Shi-Ting Feng
Publikováno v:
Cytotherapy. 10:254-264
Mesenchymal stromal cells (MSC) are attractive candidates for the treatment of Duchenne muscular dystrophy (DMD) but how the donor MSC distribute in multiple organs and whether the increased dystrophin leads to a change in the pathology of mdx mice i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7aacaf2ea18ff28b8f96c9bbb2ceaab
https://doi.org/10.1080/14653240802020381
https://doi.org/10.1080/14653240802020381
Publikováno v:
Cytotherapy. 9:44-52
BackgroundThe value of transplantation of BM stem cells in aged (12-month-old) mdx was evaluated because it is thought to be a more ideal model for studying the praxiology of Duchenne muscular dystrophy (DMD). The possible mechanisms of stem cell dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aeab9b9d5a0ac173cb9de037d823f72
https://doi.org/10.1080/14653240601114815
https://doi.org/10.1080/14653240601114815
Autor:
Yi-Wu Shi, Wei-Ping Liao, Yue-Sheng Long, Li Chen, Wei-yi Deng, Mei-Juan Yu, Mei-Mei Gao, Yong-Hong Yi, Xiao-Rong Liu
Publikováno v:
Seizure. 19:443-445
Till now truncation mutations of voltage-gated sodium channel alpha subunit type I (SCN1A) gene were mostly found in severe myoclonic epilepsy of infancy (SMEI) patients. In this research we first identified two novel de novo truncation mutations (S6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d3c12297f5ac861b1dc6ba0db10578
https://doi.org/10.1016/j.seizure.2010.06.010
https://doi.org/10.1016/j.seizure.2010.06.010
Hla-B alleles and lamotrigine-induced cutaneous adverse drug reactions in the Han Chinese population
Autor:
Yi-Wu, Shi, Fu-Li, Min, Xiao-Rong, Liu, Li-Xuan, Zan, Mei-Mei, Gao, Mei-Juan, Yu, Wei-Ping, Liao
Publikováno v:
Basicclinical pharmacologytoxicology. 109(1)
Lamotrigine (LTG) is a commonly used antiepileptic drug. However, the use of LTG is limited because of its cutaneous adverse drug reactions (cADRs) ranging from mild maculopapular eruption (MPE) to severe Stevens-Johnson syndrome (SJS) and toxic epid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6a4624ce2d168b4b85c341882162c18
https://pubmed.ncbi.nlm.nih.gov/21306565
https://pubmed.ncbi.nlm.nih.gov/21306565
Autor:
Qi-Hua Zhao, Tao Su, Xun-Sha Sun, Yi-Wu Shi, Yue-Sheng Long, Yong-Hong Yi, Wei-Ping Liao, Zu-Ying Kuang, Xiao-Rong Liu, Guang-Fei Deng, Jia-Ming Qin, Mei-Juan Yu
Publikováno v:
Journal of molecular neuroscience : MN. 44(2)
Voltage-gated sodium channel α-subunit type III (Na(v)1.3) is mainly expressed in the central nervous system and is associated with neurological disorders. The expression of mouse Scn3a product (Na(v)1.3) mainly occurs in embryonic and early postnat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6d0490f2fc0c92db459fa81af01e19c
https://pubmed.ncbi.nlm.nih.gov/21271300
https://pubmed.ncbi.nlm.nih.gov/21271300
Autor:
Wei-Ping, Liao, Yi-Wu, Shi, Yue-Sheng, Long, Yang, Zeng, Tian, Li, Mei-Juan, Yu, Tao, Su, Ping, Deng, Zhi-Gang, Lei, Shu-Jun, Xu, Wei-Yi, Deng, Xiao-Rong, Liu, Wei-Wen, Sun, Yong-Hong, Yi, Zao C, Xu, Shumin, Duan
Publikováno v:
Epilepsia. 51(9)
Generalized epilepsy with febrile seizures plus (GEFS+) and severe myoclonic epilepsy in infancy (SMEI) are associated with sodium channel α-subunit type-1 gene (SCN1A) mutations. Febrile seizures and partial seizures occur in both GEFS+ and SMEI; s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6c25c7ee6bb8e0ae88a404809b213832
https://pubmed.ncbi.nlm.nih.gov/20550552
https://pubmed.ncbi.nlm.nih.gov/20550552