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Aging and Disease|August 24, 2019
Two Novel Mutations and a de novo Mutation in PSEN1 in Early-onset Alzheimer's DiseaseYu-Sheng Li, Zhi-Hua Yang, Yao Zhang, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|September 8, 2021
Pseudolaric Acid B Attenuates High Salt Intake-Induced Hypertensive Left Ventricular Remodeling by Modulating Monocyte/Macrophage PhenotypesFang-Fang Yu, Guo-Hong Yang, Shao-Bo Chen, et al.
The Neuroradiology Journal|May 23, 2022
Autoimmune disease of head and neck, imaging, and clinical reviewAlireza Paydar, Zachary B Jenner, Tyrell J Simkins, et al.
BMC Plant Biology|June 1, 2012
Novel variants of HMW glutenin subunits from Aegilops section Sitopsis species in relation to evolution and wheat breedingQian-Tao Jiang, Jian Ma, Yu-Ming Wei, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 21, 2017
NLRP3 Gene Deletion Attenuates Angiotensin II-Induced Phenotypic Transformation of Vascular Smooth Muscle Cells and Vascular RemodelingXing-Sheng Ren, Ying Tong, Li Ling, et al.
ACS Nano|February 2, 2017
Operando Grazing Incidence Small-Angle X-ray Scattering/X-ray Diffraction of Model Ordered Mesoporous Lithium-Ion Battery AnodesSarang M Bhaway, Zhe Qiang, Yanfeng Xia, et al.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi = Zhonghua Shiyan He Linchuang Bingduxue Zazhi = Chinese Journal of Experimental and Clinical Virology|January 29, 2010
[Analysis for clinical and genetic characteristics of a sporadic FFI case]Sheng-li Xia, Yu-ming Xu, Qiang Xu, et al.
BMC Plant Biology|June 19, 2015
Genome-wide analysis of the gene families of resistance gene analogues in cotton and their response to Verticillium wiltJie-Yin Chen, Jin-Qun Huang, Nan-Yang Li, et al.
Biomedicines|August 27, 2021
miR-31-5p Promotes Oxidative Stress and Vascular Smooth Muscle Cell Migration in Spontaneously Hypertensive Rats via Inhibiting FNDC5 ExpressionBing Zhou, Lu-Lu Wu, Fen Zheng, et al.
Neuromuscular Disorders : NMD|July 1, 2019
Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregatesHai-Yang Luo, Lu Zhao, Cheng-Yuan Mao, et al.
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