D. W. Cleveland et al., “TRIP13 and APC15 drive mitotic exit by turnover of interphase- and unattached kinetochore-produced MCC,” Nat. Commun., vol. 9, no. 1, p. 4354, 2018.
 F. Gasset-Rosa et al., “Cytoplasmic TDP-43 De-mixing Independent of Stress Granules Drives Inhibition of Nuclear Import, Loss of Nuclear TDP-43, and Cell Death,” Neuron, Mar. 2019.
 T. Hoshiba et al., “Maintenance of Cartilaginous Gene Expression of Serially Subcultured Chondrocytes on Poly(2-Methoxyethyl Acrylate) Analogous Polymers,” Macromol. Biosci., vol. 17, no. 12, p. 1700297, Jun. 2017.
 J. Hwang et al., “Synthesis and Characterization of Functional Nanofilm-Coated Live Immune Cells,” ACS Appl. Mater. Interfaces, vol. 10, no. 21, pp. 17685–17692, 2018.
 V. G. Kartzev et al., “Discovery and optimization of cardenolides inhibiting HSF1 activation in human colon HCT-116 cancer cells,” Oncotarget, vol. 9, no. 43, 2018.
 D. H. Kim et al., “The AAA+ ATPase TRIP13 remodels HORMA domains through N‐terminal engagement and unfolding,” EMBO J., vol. 36, no. 16, pp. 2419–2434, 2017.
 S. W. Kim et al., “Mutual Destruction of Deep Lung Tumor Tissues by Nanodrug-Conjugated Stealth Mesenchymal Stem Cells,” Adv. Sci., vol. 5, no. 5, p. 1700860, Jun. 2018.
 T. Kimura et al., “Lipophagy maintains energy homeostasis in the kidney proximal tubule during prolonged starvation,” Autophagy , vol. 13, no. 10, pp. 1629–1647, 2017.
 H. Komura et al., “Alzheimer Aβ Assemblies Accumulate in Excitatory Neurons upon Proteasome Inhibition and Kill Nearby NAKα3 Neurons by Secretion,” iScience, 2019.
 Y. S. Lee and H. S. Jun, “Glucagon-like peptide-1 receptor agonist and glucagon increase glucose-stimulated insulin secretion in beta cells via distinct adenylyl cyclases,” Int. J. Med. Sci., vol. 15, no. 6, pp. 603–609, 2018.
 F. Louis, S. Kitano, J. F. Mano, and M. Matsusaki, “3D collagen microfibers stimulate the functionality of preadipocytes and maintain the phenotype of mature adipocytes for long term cultures,” Acta Biomater., vol. 84, pp. 194–207, Jan. 2019.
 F. Meitinger et al., “53BP1 and USP28 mediate p53 activation and G1 arrest after centrosome loss or extended mitotic duration,” J. Cell Biol., vol. 214, no. 2, pp. 155–166, 2016.
 M. H. Mosa et al., “Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in Munc18-2–Deficient Intestinal Organoids,” Cmgh, vol. 6, no. 4, pp. 477-493.e1, Aug. 2018.
 K. Nanki et al., “Divergent Routes toward Wnt and R-spondin Niche Independency during Human Gastric Carcinogenesis,” Cell, vol. 174, no. 4, pp. 856-869.e17, Aug. 2018.
 S. Santaguida et al., “Chromosome Mis-segregation Generates Cell-Cycle-Arrested Cells with Complex Karyotypes that Are Eliminated by the Immune System,” Dev. Cell, vol. 41, no. 6, pp. 638-651.e5, 2017.
 H. Seo et al., “A β1-tubulin–based megakaryocyte maturation reporter system identifies novel drugs that promote platelet production,” Blood Adv., vol. 2, no. 17, pp. 2262–2272, Sep. 2018.
 Y. Shimada et al., “FF-10502, an Antimetabolite with Novel Activity on Dormant Cells, Is Superior to Gemcitabine for Targeting Pancreatic Cancer Cells,” J. Pharmacol. Exp. Ther., vol. 366, no. 1, pp. 125–135, 2018.
 N. Sunamura, S. Iwashita, K. Enomoto, T. Kadoshima, and F. Isono, “Loss of the fragile X mental retardation protein causes aberrant differentiation in human neural progenitor cells,” Sci. Rep., vol. 8, no. 1, p. 11585, Dec. 2018.
 M. Tanaka et al., “Adhesion-based simple capture and recovery of circulating tumor cells using a blood-compatible and thermo-responsive polymer-coated substrate,” RSC Adv., vol. 6, no. 92, pp. 89103–89112, 2016.
 C. Zhang et al., “Mimicking Pathogenic Invasion with the Complexes of Au22(SG)18-Engineered Assemblies and Folic Acid,” ACS Nano, vol. 12, no. 5, pp. 4408–4418, 2018.
Link to article search site
Our Social Medias
We post our information to the following SNSs. Please follow us.
|Follow us||Share our application|
|@Yokogawa_LS||Share on Twitter|
|Yokogawa Life Science||Share on Facebook|
|Yokogawa Life Science||Share on LinkedIn|
Yokogawa's Official Social Media Account List
Les produits et solutions liés
Benchtop CQ1 Confocal System
The CellVoyager CQ1 provides the highest quality confocal images and extended live-cell imaging in a space-saving benchtop design.
Cycle et science de vie
Les systèmes d'analyse de contenus complexes de Yokogawa et les technologies confocales à double disque rotatif fournissent une imagerie cellulaire en direct à haute vitesse et en haute résolution, ce qui permet une recherche de pointe dans le monde entier.
High Content Analysis CellVoyager
Our high-content analysis (HCA) systems utilize powerful software to address a wide range of research applications from basic science to complex compound screening.