Results 121 to 130 of about 844,423 (151)

γ-Glutamylcyclotransferase Depletion Induces p15<sup>INK4b</sup> and p21<sup>Cip1</sup>-mediated Senescence <i>via</i> TGF-β2/SMAD3 Pathway Activation in Breast Cancer Cells. [PDF]

open access: yesCancer Genomics Proteomics
Kubota S   +11 more
europepmc   +1 more source

Junction-mediating and regulatory protein (JMY) is a promoting protein for radial migration of cortical neurons. [PDF]

open access: yesCell Death Discov
Chen XR   +12 more
europepmc   +1 more source

Live-cell single-vRNP imaging identifies viral gene expression signatures that shape influenza infection heterogeneity.

open access: yesCell Syst
Rabouw HH   +9 more
europepmc   +1 more source

Bombyx mori cell division cycle protein 37 promotes the proliferation of BmNPV

Pesticide Biochemistry and Physiology, 2021
Cell division cycle protein 37 (Cdc37) is a molecular chaperone that actively participates in many intracellular physiological and biochemical processes as well as pathogen infection. However, the function of Cdc37 in silkworm cells under Bombyx mori nucleopolyhedrovirus (BmNPV) infection is unknown.
Qian, Zhang   +6 more
openaire   +2 more sources

Discovery and Optimization of Small Molecules Targeting the Protein–Protein Interaction of Heat Shock Protein 90 (Hsp90) and Cell Division Cycle 37 as Orally Active Inhibitors for the Treatment of Colorectal Cancer

Journal of Medicinal Chemistry, 2020
Cell division cycle 37 (Cdc37) is known to work as a kinase-specific cochaperone, which selectively regulates the maturation of kinases through protein-protein interaction (PPI) with Hsp90. Directly disrupting the Hsp90-Cdc37 PPI is emerging as an alternative strategy to develop anticancer agents through a specific inhibition manner of kinase clients ...
Lei Wang   +7 more
openaire   +2 more sources

Targeting Cell division cycle 37: A Promising Novel Therapeutic Strategy

ChemMedChem
Cell division cycle 37 (CDC37) is a kinase‐specific HSP90 cochaperone that stabilizes oncogenic kinases and is frequently overexpressed in malignancies, making it a compelling therapeutic target. Herein, we systematically delineate therapeutic strategies aimed at inhibiting CDC37, including modulating its Ser13 phosphorylation switch through CK2 ...
Lixiao Zhang   +3 more
openaire   +1 more source

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