Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yuebei, Luo"'
Autor:
Wei Zhang, Bing Wen, Jun Lu, Yawen Zhao, Daojun Hong, Zhe Zhao, Cheng Zhang, Yuebei Luo, Xueliang Qi, Yingshuang Zhang, Xueqin Song, Yuying Zhao, Chongbo Zhao, Jing Hu, Huan Yang, Zhaoxia Wang, Chuanzhu Yan, Yun Yuan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Abstract Background Neutral lipid storage disease with myopathy (NLSDM) is a rare clinical heterogeneous disorder caused by mutations in the patatin-like phospholipase domain-containing 2 (PNPLA2) gene. NLSDM usually presents skeletal myopathy, cardi
Externí odkaz:
https://doaj.org/article/33eba440eda848c2a7e7857afba47c25
Publikováno v:
Mediators of Inflammation, Vol 2020 (2020)
This study is aimed at exploring the expression pattern and methylation level of G0S2 in the peripheral blood mononuclear cells (PBMCs) of myasthenia gravis (MG) patients with positive acetylcholine receptor (AChR) autoantibodies and revealing the re
Externí odkaz:
https://doaj.org/article/5bcb111f32b04662bd01f09731139d04
Autor:
Xiaoqing Lv, Feng Lin, Wenjing Wu, Hui Wang, Yuebei Luo, Zhiqiang Wang, Chuanzhu Yan, He Lv, Sushan Luo, Pengfei Lin
Publikováno v:
Human Molecular Genetics.
Limb-girdle muscular dystrophy R7 (LGMDR7) is an autosomal recessive hereditary muscular dystrophy caused by mutations in titin-cap (TCAP). Here, we summarized the clinical characteristics and TCAP mutations in a Chinese cohort of 30 patients with LG
Autor:
Qiuming, Zeng, Xiaohua, Dong, Chunyun, Ruan, Bo, Hu, Yuebei, Luo, Zhaohui, Luo, Liqun, Xu, Hao, Zhou, Runqi, Wang, Huan, Yang
Publikováno v:
Journal of neuroimmunology. 300
The pathophysiologic significance of the CD16
Publikováno v:
BMC Medical Genomics; 2015, Vol. 8 Issue 1, p1-16, 16p