Results 191 to 200 of about 33,989 (317)
The FGF13 level is significantly downregulated in premature aging murine hearts subject to D‐galactose and Doxorubicin. FGF13 overexpression and deficiency exacerbated and alleviated Doxorubicin/D‐galactose‐induced myocardial aging characteristics and functional impairment, respectively.
Enzhao Shen+15 more
wiley +1 more source
MAGEA6 Engages a YY1‐Dependent Transcription to Dictate Perineural Invasion in Colorectal Cancer
This study investigates the role of MAGEA6 in perineural invasion (PNI) in colorectal cancer (CRC). MAGEA6 promotes CRC invasiveness by inhibiting YY1 ubiquitination, enhancing CXCL1 secretion, and recruiting Schwann cells. These findings highlight the potential of targeting the MAGEA6/YY1/CXCL1 axis for therapeutic strategies against PNI and tumor ...
Hao Wang+9 more
wiley +1 more source
Editorial: The role of post-translational modifications in cancer biology. [PDF]
Srivastava S, Tripathi A, Trivedi AK.
europepmc +1 more source
A ubiquitin conjugating enzyme encoded by African swine fever virus. [PDF]
Pascal Hingamp+3 more
openalex +1 more source
ESCRT-0 in Arabidopsis thaliana? Biochemische und zellbiologische Analyse von FYVE2 [PDF]
Herberth, Stefanie
core
Oral squamous cell carcinoma cells exhibit upregulated expression of GSDMD upon exposure to low‐dose cisplatin chemotherapy, which subsequently interacts with MMP14 through its N‐terminal domain, activating the epithelial‒mesenchymal transition (EMT) process and promoting the lymph node metastasis of oral squamous cell carcinoma.
Zixian Huang+9 more
wiley +1 more source
Author Correction: Visualization of the Cdc48 AAA+ ATPase protein unfolding pathway. [PDF]
Cooney I+7 more
europepmc +1 more source
Over-expression of ubiquitin carboxy terminal hydrolase-L1 induces apoptosis in breast cancer cells
Liu
openalex +2 more sources
To solve the challenge of PROTACs in clinical potential due to poor water solubility and membrane permeability, a nanodelivery system based on lipid nanodisks loaded with MZ1 prodrug (LND‐MZ1) to remodel the physicochemical and pharmacokinetic properties of PROTAC MZ1 is elaborately proposed.
Meichen Pan+6 more
wiley +1 more source