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Journal of Molecular and Cellular Cardiology|February 5, 2013
Polycystin-2 mutations lead to impaired calcium cycling in the heart and predispose to dilated cardiomyopathyJere Paavola, Simon Schliffke, Sandro Rossetti, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 8, 2026
Targeting 15-PGDH/15-oxoETE to mitigate inflammation and senescence in asthmaHongxia Bao, Jihong Ren, Kexin Zhao, et al.Plant Methods|November 4, 2024
Integrating dynamic high-throughput phenotyping and genetic analysis to monitor growth variation in foxtail milletZhenyu Wang, Jiongyu Hao, Xiaofan Shi, et al.Journal of Agricultural and Food Chemistry|May 16, 2022
Heterologous Expression of SiFBP, a Folate-Binding Protein from Foxtail Millet, Confers Increased Folate Content and Altered Amino Acid Profiles with Nutritional Potential to ArabidopsisSiyu Hou, Yijuan Zhang, Bing Zhao, et al.Proceedings of the National Academy of Sciences of the United States of America|October 13, 2010
The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretchNathan E Hellman, Yan Liu, Erin Merkel, et al.Journal of the Science of Food and Agriculture|June 10, 2021
Folate metabolic profiling and expression of folate metabolism-related genes during panicle development in foxtail millet (Setaria italica (L.) P. Beauv)Siyu Hou, Xiaxia Man, Boying Lian, et al.Small (Weinheim an Der Bergstrasse, Germany)|April 25, 2024
A High Efficiency, Low Resistance Antibacterial Filter Formed by Dopamine-Mediated In Situ Deposition of Silver onto Glass FibersZhaoxia Sun, Ying Kong, Liang Lan, et al.Neuropharmacology|September 8, 2023
Dexmedetomidine relieves inflammatory pain by enhancing GABAergic synaptic activity in pyramidal neurons of the anterior cingulate cortexLing Liu, Zhihao Luo, Yuanying Mai, et al.Free Radical Biology & Medicine|November 11, 2024
Restoration of mitochondrial function alleviates trigeminal neuropathic pain in miceJiajun Yang, Song Xie, Jiahao Guo, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2016
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1Zachry T Soens, Yuanyuan Li, Li Zhao, et al.Pageof 9