Results 201 to 210 of about 655,916 (248)
This paper reveals how human lactoferrin–albumin fusion (hLF‐HSA) potently suppresses lung adenocarcinoma cell migration. hLF‐HSA upregulates NHE7, leading to Golgi alkalization, disruption of the Golgi secretome, downregulation of MMP1, and reversal of EMT. These findings suggest a novel Golgi‐targeting strategy to suppress cancer cell migration.
Hana Nopia +3 more
wiley +1 more source
The evolution of ChatGPT-generated text in scientific medical publications. [PDF]
Saner FH +9 more
europepmc +1 more source
A novel signature integrating genome‐wide analysis with clinical factors predicts recurrence in stage II colorectal cancer and enables a new risk stratification to guide postoperative adjuvant chemotherapy. Clinical risk stratification for postoperative recurrence in patients with pathological stage II (pStage II) colorectal cancer (CRC) is essential ...
Mayuko Otomo +7 more
wiley +1 more source
Appropriate Use and Reporting of AI tools in Manuscript Preparation. [PDF]
Al-Quorain AA, Shaikh AK, Abdul Salam A.
europepmc +1 more source
Li Jianmin, Sisheng zhi yu (The Territory between Life and Death), Taibei, Academia Sinica, 2000, revised in 2001, 435 pages incl. illustrations (fine binding edition, ISBN 957-671-703-5; ordinary edition 957-671-704-3) [PDF]
Lo, V
core
Inhibition of Classical and Alternative Complement Pathway by Ravulizumab and Eculizumab
ABSTRACT Objective To explore the feasibility of classical (CH50) and alternative (AH50) complement pathway activity as potential biomarkers for treatment guidance and monitoring during therapy with ravulizumab in patients with generalized myasthenia gravis (gMG) and compare these to therapeutic drug monitoring under eculizumab.
Lea Gerischer +14 more
wiley +1 more source
Peer review: a collective commitment to knowledge and excellence. [PDF]
Belin D, Spires-Jones TL.
europepmc +1 more source
Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte +13 more
wiley +1 more source
Screening, sorting, and the feedback cycles that imperil peer review. [PDF]
Bergstrom CT, Gross K.
europepmc +1 more source

