Results 171 to 180 of about 297,769 (330)
USP35 Acts as a Deubiquitinating Enzyme for ID3 to Promote Immune Escape in Colorectal Cancer
USP35 stabilizes ID3 expression by deubiquitinating the K2/K30 site, thereby upregulating PD‐L1 and promoting immune escape in colorectal cancer. IU1, an inhibitor of USP35 enzyme activity, has been shown to inhibit USP35, thereby accelerating ID3 degradation, enhancing CD8+ T cell killing, and reversing the immunosuppressive microenvironment ...
Wenxin Chen +9 more
wiley +1 more source
Basic : Upper Limit of normal alanine aminotransferase (ALT) and aspartate aminotransferase (AST) and its modulating factors in Korean (초) [PDF]
Dae Won Jun +4 more
openalex
Clinical Features of Hepatitis C Virus Carriers With Persistently normal Alanine Aminotransferase Levels [PDF]
Hirofumi Uto +4 more
openalex +1 more source
Clinical Non-invasive Model to Predict Liver Inflammation in Chronic Hepatitis B With Alanine Aminotransferase ≤ 2 Upper Limit of Normal [PDF]
Shanshan Chen, Haijun Huang
openalex +1 more source
FeCo dual‐atom catalyst (FeCo‐N‐DAC) with ultrahigh metal loading (Fe > 5.4%, Co > 4.8%) is developed for synergistic photothermal‐chemodynamic immunotherapy. FeCo‐N‐DAC penetrates deep‐seated tissues, eradicates MRSA biofilms, and reprograms immune‐inflammatory pathways via multi‐omics‐validated mechanisms.
Shihao Xu +11 more
wiley +1 more source
O‐017: An immunochromatographic test for measurement of alanine aminotransferase 1 (ALT1) at point‐of‐care [PDF]
openalex +1 more source
In non‐MASH‐HCC, L‐carnitine promotes tumor progression primarily through its classical role in enhancing fatty acid oxidation (FAO). However, in MASH‐HCC, where FAO is markedly suppressed, L‐carnitine shifts from this canonical function to serve instead as an intracellular acetyl group buffer.
Chuqi Xia +11 more
wiley +1 more source
Primary hyperoxaluria type 1 caused by peroxisome-to-mitochondrion mistargeting of alanine : glyoxylate aminotransferase [PDF]
Karl Lhotta +5 more
openalex +1 more source
Donor‐derived tdTomato+ mature hepatocytes were FACS‐isolated and transplanted into Fah−/− host mice. During regeneration, these cells convert into proliferative, unipotent Afp+ rHeps. Their plasticity is governed by a PPARγ/AFP‐dependent metabolic switch, segregating into pro‐proliferative Afplow and pro‐survival Afphigh subpopulations.
Ting Fang +12 more
wiley +1 more source

