Publications by authors named "U R Nair"

Article Synopsis
  • This study examined how selectively doping nickel oxide (NiO) films with lithium (Li) affects their structural, optical, and electrochemical properties.
  • The research found a significant relationship between the level of Li doping, conductivity, and bandgap modification, particularly highlighting the benefits of 0.5% Li doping.
  • The results indicated that 0.5% Li-doped NiO films had improved electrochemical behavior and efficiency compared to those with higher doping levels, as shown by their performance in impedance spectroscopy and current-voltage analysis.
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During the first two decades of the twenty-first century, we analyze the expansion of urban land cover, urban heat island (UHI), and urban pollution island (UPI) in the Houston Metropolitan Area (HMA) using land cover classifications derived from Landsat and land/aerosol products from NASA's Moderate Resolution Imaging Spectroradiometer. Our approach involves both direct utilization and fusion with in situ observations for a comprehensive characterization. We also examined how social vulnerability within the HMA changed during the study period and whether the synergy of UHI, UPI, and social vulnerability enhances environmental inequalities.

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Current prophylactic human immunodeficiency virus 1 (HIV-1) vaccine research aims to elicit broadly neutralizing antibodies (bnAbs). Membrane-proximal external region (MPER)-targeting bnAbs, such as 10E8, provide exceptionally broad neutralization, but some are autoreactive. Here, we generated humanized B cell antigen receptor knock-in mouse models to test whether a series of germline-targeting immunogens could drive MPER-specific precursors toward bnAbs.

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A key barrier to the development of vaccines that induce broadly neutralizing antibodies (bnAbs) against human immunodeficiency virus (HIV) and other viruses of high antigenic diversity is the design of priming immunogens that induce rare bnAb-precursor B cells. The high neutralization breadth of the HIV bnAb 10E8 makes elicitation of 10E8-class bnAbs desirable; however, the recessed epitope within gp41 makes envelope trimers poor priming immunogens and requires that 10E8-class bnAbs possess a long heavy chain complementarity determining region 3 (HCDR3) with a specific binding motif. We developed germline-targeting epitope scaffolds with affinity for 10E8-class precursors and engineered nanoparticles for multivalent display.

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