Publications by authors named "Susamita Kesh"

Article Synopsis
  • The NIH-funded Consortium of Eosinophilic Gastrointestinal Disease Researchers (CEGIR) formed a diversity committee to combat systemic racism and implicit bias in the care and research of eosinophilic gastrointestinal diseases (EGIDs).
  • The committee established mission statements, integrated diversity discussions into meetings, and launched educational initiatives, such as a speaker series and a publication library.
  • Their research agenda aims to address demographic understanding, reduce bias in literature, investigate health disparities, and create a framework for ongoing projects to enhance diversity, equity, inclusion, and accessibility (DEIA) in EGID research and care.
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Acquired angioedema (AAE) is a rare form of angioedema (AE) and is often associated with lymphoproliferative conditions and/or anti-C1 esterase inhibitor (C1-INH) antibodies without clear treatment consensus. Current treatments have been reported to have variable effectiveness with different safety concerns. A large Italian cohort of patients with AAE was previously found to respond well to tranexamic acid (TXA).

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Objective: To review the various types of angioedema including diagnosis and treatment.

Data Sources: PubMed search of articles in the English language of various types of angioedema.

Study Selections: Articles on the subject matter were selected and reviewed.

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Background: Pulmonary fat embolism (FE) in patients after major bone fracture and other trauma may lead to acute respiratory distress, but few clinical evidence of lung injury remains, and there is a dearth of histopathologic information after the initial recovery. We recently reported histologic changes in the lungs of a patient who died after cesarian delivery, which were similar to a rat model of FE. In this model, we found that despite an apparent full recovery, modest fibrotic damage persisted up to 6 weeks.

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The primary objective of this study is to functionally characterize and provide molecular evidence of large neutral amino acid transporter (LAT1) in human derived prostate cancer cells (PC-3). We carried out the uptake of [3H]-tyrosine to assess the functional activity of LAT1. Reverse transcription-polymerase chain reaction (RT-PCR) analysis is carried out to confirm the molecular expression of LAT1.

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