Area of research
Molecular Biology · Oncology
Research interest
Research interests include RNA modifications and cancer, RNA and protein synthesis mechanisms, Peptidase Inhibition and Analysis, and Cancer-related molecular mechanisms research.
The <scp>m6A</scp> demethylase <scp>FTO</scp> promotes C/ <scp>EBPβ</scp> ‐ <scp>LIP</scp> translation to perform oncogenic functions in breast cancer cells
Upstream open reading frame translation enhances immunogenic peptide presentation in mitotically arrested cancer cells
mTORC1 cooperates with tRNA wobble modification to sustain the protein synthesis machinery
Dual Ribosome Profiling reveals metabolic limitations of cancer and stromal cells in the tumor microenvironment
Upstream open reading frame translation enhances immunogenic peptide presentation in mitotically arrested cancer cells
P53-dependent hypusination of eIF5A affects mitochondrial translation and senescence immune surveillance
Identifying colorectal cancer-specific vulnerabilities in the Wnt-driven long non-coding transcriptome
Gene and protein sequence features augment HLA class I ligand predictions
DNMT and HDAC inhibition induces immunogenic neoantigens from human endogenous retroviral element-derived transcripts
The MTORC1-AHR pathway sustains translation and autophagy in tumours under tryptophan stress
Breast Cancer Metastatic Progression Requires mRNA Posttranscriptional Suppression
Cancer-associated fibroblasts require proline synthesis by PYCR1 for the deposition of pro-tumorigenic extracellular matrix
Roles of eIF5A in the immunosurveillance of cellular senescence
Author Correction: Cancer-associated fibroblasts require proline synthesis by PYCR1 for the deposition of pro-tumorigenic extracellular matrix
PYCR1-dependent proline synthesis in cancer-associated fibroblasts is required for the deposition of pro-tumorigenic extracellular matrix
Translatome analysis reveals altered serine and glycine metabolism in T-cell acute lymphoblastic leukemia cells
A fragment-like approach to PYCR1 inhibition
Myc coordinates transcription and translation to enhance transformation and suppress invasiveness