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1. M ⁴ esh: mmWave-Based 3D Human Mesh Construction for Multiple Subjects

   https://doi.org/10.1145/3560905.3568545  

   Xue, Hongfei; Cao, Qiming; Ju, Yan; Hu, Haochen; Wang, Haoyu; Zhang, Aidong; Su, Lu (November 2022, The 20th ACM Conference on Embedded Networked Sensor Systems (SenSys 2022))
2. Ag ⁺ Ion Binding to Human Metallothionein-2A Is Cooperative and Domain Specific

   https://doi.org/10.1021/acs.analchem.0c00829  

   Dong, Shiyu; Shirzadeh, Mehdi; Fan, Liqi; Laganowsky, Arthur; Russell, David H. (July 2020, Analytical Chemistry)

   null (Ed.)
3. Survival of aging CD264 ⁺ and CD264 ⁻ populations of human bone marrow mesenchymal stem cells is independent of colony‐forming efficiency

   https://doi.org/10.1002/bit.27195  

   Madsen, Sean_D; Jones, Sean_H; Tucker, H_Alan; Giler, Margaret_K; Muller, Dyllan_C; Discher, Carson_T; Russell, Katie_C; Dobek, Georgina_L; Sammarco, Mimi_C; Bunnell, Bruce_A; et al (November 2019, Biotechnology and Bioengineering)

   Abstract In vivo mesenchymal stem cell (MSC) survival is relevant to therapeutic applications requiring engraftment and potentially to nonengraftment applications as well. MSCs are a mixture of progenitors at different stages of cellular aging, but the contribution of this heterogeneity to the survival of MSC implants is unknown. Here, we employ a biomarker of cellular aging, the decoy TRAIL receptor CD264, to compare the survival kinetics of two cell populations in human bone marrow MSC (hBM‐MSC) cultures. Sorted CD264⁺hBM‐MSCs from two age‐matched donors have elevated β‐galactosidase activity, decreased differentiation potential and form in vitro colonies inefficiently relative to CD264⁻hBM‐MSCs. Counterintuitive to their aging phenotype, CD264⁺hBM‐MSCs exhibited comparable survival to matched CD264⁻hBM‐MSCs from the same culture during in vitro colony formation and in vivo when implanted ectopically in immunodeficient NIH III mice. In vitro and in vivo survival of these two cell populations were independent of colony‐forming efficiency. These findings have ramifications for the preparation of hBM‐MSC therapies given the prevalence of aging CD264⁺cells in hBM‐MSC cultures and the popularity of colony‐forming efficiency as a quality control metric in preclinical and clinical studies with MSCs. 

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4. Abstracts from the 19 ^th International Society for Research in Human Milk and Lactation Conference

   https://doi.org/10.1089/bfm.2018.29100.abstracts  

   Alatalo, D.; Hassanipour, F. (September 2018, Breastfeeding Medicine)
5. Advancing Human-Centric LED Lighting Using Na₂MgPO₄F:Eu²⁺

   https://doi.org/10.1021/acsami.1c00909  

   Hariyani, Shruti; Brgoch, Jakoah (March 2021, ACS Applied Materials & Interfaces)

   null (Ed.)

   The proliferation of energy-efficient light-emitting diode (LED) lighting has resulted in continued exposure to blue light, which has been linked to cataract formation, circadian disruption, and mood disorders. Blue light can be readily minimized in pursuit of “human-centric” lighting using a violet LED chip (λem ≈ 405 nm) downconverted by red, green, and blue-emitting phosphors. However, few phosphors efficiently convert violet light to blue light. This work reports a new phosphor that meets this demand. Na2MgPO4F:Eu2+ can be excited by a violet LED yielding an efficient, bright blue emission. The material also shows zero thermal quenching and has outstanding chromatic stability. The chemical robustness of the phosphor was also confirmed through prolonged exposure to water and high temperatures. A prototype device using a 405 nm LED, Na2MgPO4F:Eu2+, and a green and red-emitting phosphor produces a warm white light with a higher color rendering index than a commercially purchased LED light bulb while significantly reducing the blue component. These results demonstrate the capability of Na2MgPO4F:Eu2+ as a next-generation phosphor capable of advancing human-centric lighting. 

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