Publications by authors named "M G Farber"

Objective: To investigate which preoperative factors most impact the 5-year survival of patients undergoing fenestrated/branched endovascular aortic repair (F/BEVAR) and to identify modifiable elements that, if time allows, should be actively managed and adequately controlled preoperatively.

Methods: Patients treated for aortic aneurysms with complex anatomy using either patient-specific company-manufactured or off-the-shelf F/BEVAR devices were included. The exposure of interest was aneurysm type (group I: type I-III thoracoabdominal aneurysms vs group II: type IV thoracoabdominal aneurysms vs group III: juxtarenal or suprarenal aneurysms), and the primary outcome was 5-year risk of all-cause mortality.

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  • Lipid accumulation in macrophages is linked to their role in promoting tumor growth, emphasizing their importance in cancer biology.
  • The text outlines a workflow for studying how macrophages interact with lipid-laden tumor cells, detailing methods for identifying and analyzing these macrophages in mouse tumors.
  • This research aims to reveal the origins of lipids that contribute to the formation of lipid-laden macrophages and their potential to enhance cancer malignancy across different types of cancer.
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Introduction: A secondary loss of response (LOR) to infliximab (IFX) therapy for inflammatory bowel disease (IBD) is typically associated with low IFX trough levels, often with high levels of neutralizing antibodies to IFX (ATI). A small subset of patients on long-term therapy experience a "nonimmune" LOR, without ATI and with desired IFX trough levels ≥5 μg/mL, regarded as a LOR to the mechanism of action of IFX. However, this currently accepted IFX goal level is largely derived from observations of patients within the first year of therapy and may not apply to those on treatment beyond 1 year.

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  • - Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer with increasing rates in the US and Europe, primarily linked to the Merkel cell polyomavirus (MCPyV), although its cell of origin is still uncertain.
  • - The study introduced MCPyV antigens into different cancer cell lines to analyze how they affect DNA methylation and gene expression, revealing that MCPyV-LT alters DNA methylation in both cell lines while MCPyV-sT only impacted one.
  • - Findings indicate significant changes in gene expression patterns, particularly in MCC13 cells, with downregulated genes in immune pathways suggesting potential targets for new immunotherapies for MCC, along with confirmation that MCPyV-LT regulates gene
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