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BMC Medical Genetics|December 4, 2016
Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactylyXingping Guo, Chunying Song, Yaping Shi, et al.
Bone Research|May 3, 2019
DMP1 prevents osteocyte alterations, FGF23 elevation and left ventricular hypertrophy in mice with chronic kidney diseaseCorey Dussold, Claire Gerber, Samantha White, et al.
International Immunopharmacology|October 22, 2024
Advances in mesenchymal stem cell-centered stem cell therapy in the treatment of hypoxic-ischemic injuryLixin Qi, Lei Hu, Rengcheng Qian, et al.
Scientific Reports|November 1, 2017
Klotho Inhibits Interleukin-8 Secretion from Cystic Fibrosis Airway EpitheliaStefanie Krick, Nathalie Baumlin, Sheyla Paredes Aller, et al.
Gene|April 28, 2025
Research progress of gene editing technology in neurological diseasesXiuying Gao, Chunting Zhou, Yani Feng, et al.
Psychopharmacology|August 8, 2025
Application of nanomaterials in central nervous system disordersYixuan Deng, Yani Feng, Bangming Ye, et al.
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