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UnknownPhenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis.
Not available
S-EPMC9469212 | biostudies-literature
TranscriptomicsGenome-wide analysis of serum starved prelamin A-accumulating hMSCs gene expression.
Analysis of serum starved prelamin A-accumulating hMSCs at gene expression level. The hypothesis tested in the present study was that prelamin A accumulation induces the dysregulation of genes that are essensial for cell survival under a stress condition such as serum starvation. The results provide...
ORGANISM(S): Homo sapiens 
2014-06-23 | E-GEOD-52563 | biostudies-arrayexpress
UnknownTMPRSS4: A Novel Tumor Prognostic Indicator for the Stratification of Stage IA Tumors and a Liquid Biopsy Biomarker for NSCLC Patients.
Not available
S-EPMC6947244 | biostudies-literature
UnknownTargeting the extra domain A of fibronectin for cancer therapy with CAR-T cells.
Not available
S-EPMC9351345 | biostudies-literature
UnknownIdentification of a novel synthetic lethal vulnerability in non-small cell lung cancer by co-targeting TMPRSS4 and DDR1.
Not available
S-EPMC6817908 | biostudies-literature
UnknownCirculating Levels of the Interferon-γ-Regulated Chemokines CXCL10/CXCL11, IL-6 and HGF Predict Outcome in Metastatic Renal Cell Carcinoma Patients Treated with Antiangiogenic Therapy.
Not available
S-EPMC8201218 | biostudies-literature
UnknownSRC family kinase (SFK) inhibitor dasatinib improves the antitumor activity of anti-PD-1 in NSCLC models by inhibiting Treg cell conversion and proliferation.
Not available
S-EPMC7931761 | biostudies-literature
UnknownId1 and PD-1 Combined Blockade Impairs Tumor Growth and Survival of KRAS-mutant Lung Cancer by Stimulating PD-L1 Expression and Tumor Infiltrating CD8+ T Cells.
Not available
S-EPMC7693788 | biostudies-literature
ProteomicsCOQ4 Affinity Enrichment Mass Spectrometry
Affinity enrichment mass spectrometry experiment to identify protein-protein interactions of hCOQ4-FLAG WT and hCOQ4-FLAG D164A.
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
2023-10-26 | MSV000093201 | MassIVE
UnknownConversion Ability of Immunotherapy in Hepatocellular Carcinoma: Insights from the International Converse Study.
Not available
S-EPMC12503878 | biostudies-literature
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