Publications by authors named "G Mitra"

Sudden Stratospheric Warming (SSW) is a winter phenomenon initiated primarily by the enhanced stationary planetary waves (SPWs), characterized by an increase in polar stratospheric temperature by a few tens of kelvin for a few days. Wave-wave non-linear interaction can produce secondary waves, with sum and difference frequencies of the primary wave frequencies. The sun-synchronous semidiurnal tide is a major component at mid and high latitude middle atmosphere, which non-linearly interacts with the dominant SPW in the stratosphere to produce the zonally symmetric semidiurnal tide component (S0), as observed during two boreal SSWs.

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In the realm of biomedical advancement, extracellular vesicles (EVs) are revolutionizing our capacity to diagnose, monitor, and predict disease progression. However, the comprehensive exploration and clinical application of EVs face significant limitations due to the current isolation techniques. The size exclusion chromatography, commercial precipitation reagents, and ultracentrifugation are frequently employed, necessitating skilled operators and entailing challenges related to consistency, reproducibility, quality, and yields.

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Background: Through medicare, residents in Canada are entitled to medically necessary physician services without paying out of pocket, but still many people struggle to access primary care. We conducted a survey to explore people's experience with and priorities for primary care.

Methods: We conducted an online, bilingual survey of adults in Canada in fall 2022.

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Article Synopsis
  • Researchers analyzed genetic data from nearly 1 million individuals to create a comprehensive catalogue of human protein-coding variations, shedding light on gene function and the frequency of rare coding variants.
  • The study identified over 10 million missense and 1.1 million loss-of-function variants, discovering 1,751 novel genes with rare biallelic loss-of-function variants and 3,988 genes intolerant to these variants.
  • They estimate that 3% of people carry a clinically significant genetic variant and provide public access to their data to enhance genetic interpretation and support precision medicine.
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