Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Huayuan Ou"'
Autor:
Renjie Cui, Dingli Chen, Na Li, Ming Cai, Teng Wan, Xueqiang Zhang, Meiqin Zhang, Sichen Du, Huayuan Ou, Jianjun Jiao, Nan Jiang, Shuangxia Zhao, Huaidong Song, Xuedong Song, Duan Ma, Jin Zhang, Shouxia Li
Publikováno v:
Journal of Cellular and Molecular Medicine. 26:4292-4304
Nonsyndromic cleft palate only (NSCP) is a common congenital malformation worldwide. In this study, we report a three-generation pedigree with NSCP following the autosomal-dominant pattern. Whole-exome sequencing and Sanger sequencing revealed that o
Autor:
Meiqin Zhang, Jin Zhang, Duan Ma, Nan Jiang, Sichen Du, Jing Ma, Huayuan Ou, Xiaorong Li, Renjie Cui
Publikováno v:
Human Gene Therapy. 30:155-167
Gaucher disease (GD) is an autosomal recessive lysosomal storage disorder caused by mutations in the GBA gene. Enzyme replacement treatment is the most effective therapy available for type 1 GD patients, but it is very expensive and does not improve
Autor:
Huayuan Ou, Tinglan Chen, Meiqin Zhang, Nan Jiang, Sichen Du, Renjie Cui, Runsheng Ge, Jin Zhang, Duan Ma
Publikováno v:
Journal of Cellular and Molecular Medicine
Recent studies have demonstrated that aberrant long non‐coding RNAs (lncRNAs) expression are suggested to be closely associated with multiple human diseases, lung cancer included. However, the roles of lncRNAs in lung cancer are not well understood
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1868:118858
Protein phosphatase 2A (PP2A) complex comprises an extended family of intracellular protein serine/threonine phosphatases, that participate in different signaling transduction pathways. Different functions of PP2As are determined by the variety of re