Publications by authors named "Max M Wang"

Elicitation of effective antitumor immunity following cancer vaccination requires the selective activation of distinct effector cell populations and pathways. Here we report a therapeutic approach for generating potent T cell responses using a modular vaccination platform technology capable of inducing directed immune activation, termed the Protein-like Polymer (PLP). PLPs demonstrate increased proteolytic resistance, high uptake by antigen-presenting cells (APCs), and enhanced payload-specific T cell responses.

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Background: Female underrepresentation in oncology clinical trials can result in outcome disparities. We evaluated female participant representation in US oncology trials by intervention type, cancer site, and funding.

Materials And Methods: Data were extracted from the publicly available Aggregate Analysis of ClinicalTrials.

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In this Minireview, we describe synthetic polymers densely functionalized with sequence-defined biomolecular sidechains. We focus on synthetic brush polymers of oligonucleotides, oligosaccharides, and oligopeptides, prepared via graft-through polymerization from biomolecule functionalized monomers. The resulting structures are brush polymers wherein a biomolecular graft is positioned at each monomer backbone unit.

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Background: Molecular diagnostics can allow some patients with indeterminate thyroid nodule cytopathology to avoid diagnostic hemithyroidectomy; however, the testing is costly. We hypothesized that molecular testing with the intention of preventing unnecessary diagnostic hemithyroidectomy would be cost-effective if this test was applied selectively based on sonographic risk of malignancy.

Methods: A Markov model was constructed depicting a 40-year-old patient with a cytologically indeterminate thyroid nodule.

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Astrocytes express a variety of G protein-coupled receptors and might influence cognitive functions, such as learning and memory. However, the roles of astrocytic Gs-coupled receptors in cognitive function are not known. We found that humans with Alzheimer's disease (AD) had increased levels of the Gs-coupled adenosine receptor A2A in astrocytes.

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Article Synopsis
  • Imbalances in excitatory and inhibitory activity in the brain, especially due to apoE4 and amyloid-β (Aβ), disrupt memory function in Alzheimer’s disease (AD).
  • Researchers transplanted embryonic interneuron progenitors into aged mouse models to see if this could restore normal brain activity and cognitive function.
  • The transplanted interneurons successfully matured and integrated into the brain circuitry, leading to improved learning and memory, showing potential for cell replacement therapy in treating AD-related cognitive deficits.
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Apolipoprotein (apo) E4 is the major genetic risk factor for Alzheimer's disease (AD). ApoE4 has sex-dependent effects, whereby the risk of developing AD is higher in apoE4-expressing females than males. However, the mechanism underlying the sex difference, in relation to apoE4, is unknown.

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