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Life Sciences in Space Research|January 22, 2023
The COSPAR Planetary Protection Policy for robotic missions to Mars: A review of current scientific knowledge and future perspectivesKaren Olsson-Francis, Peter T Doran, Vyacheslav Ilyin, et al.
The Plant Journal : for Cell and Molecular Biology|August 20, 2013
The sacred lotus genome provides insights into the evolution of flowering plantsYun Wang, Guangyi Fan, Yiman Liu, et al.
Yi Chuan = Hereditas|March 11, 2025
Expert consensus on clinical genome sequencing interpretation and reportingYulan Lu, Guozhuang Li, Yaqiong Wang, et al.
Clinical and Translational Medicine|June 2, 2023
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanismNa He, Bao-Zhu Guan, Jie Wang, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 25, 2013
Monovalent antibody design and mechanism of action of onartuzumab, a MET antagonist with anti-tumor activity as a therapeutic agentMark Merchant, Xiaolei Ma, Henry R Maun, et al.
Brain : a Journal of Neurology|March 4, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopmentFang Liu, Chen Liang, Zhengchang Li, et al.
Neurology|October 16, 2025
Resective Surgery for Drug-Resistant Epilepsy in Patients With Tuberous Sclerosis Complex: A Prospective Nationwide Multicenter Cohort StudyZhirong Wei, Tinghong Liu, Dezhi Cao, et al.
Cell Reports. Medicine|January 4, 2023
CD8<sup>+</sup> T cell-intrinsic IL-6 signaling promotes resistance to anti-PD-L1 immunotherapyMahrukh A Huseni, Lifen Wang, Joanna E Klementowicz, et al.
Molecular Autism|December 20, 2018
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial modelHui Guo, Tianyun Wang, Huidan Wu, et al.
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