Zobrazeno 1 - 10
of 2 560
pro vyhledávání: '"S., Herman"'
Publikováno v:
npj Digital Medicine, Vol 7, Iss 1, Pp 1-6 (2024)
Current regulatory frameworks for artificial intelligence-based clinical decision support (AICDS) are insufficient to ensure safety, effectiveness, and equity at the bedside. The oversight of clinical laboratory testing, which requires federal- and h
Externí odkaz:
https://doaj.org/article/636d6503e42c4473a3fe506f0b0db4ad
Autor:
Kyle S. Herman
Publikováno v:
Sustainable Environment, Vol 10, Iss 1 (2024)
The growing need to address climate change through sustainability governance has amplified the importance of Sustainable Transitions Research (STR). Despite its interdisciplinary scope and methodological variety, STR continues to face divisions betwe
Externí odkaz:
https://doaj.org/article/87facb1dc18945deaa349a3b7056e400
Autor:
Kyle S. Herman
Publikováno v:
Sustainable Futures, Vol 7, Iss , Pp 100209- (2024)
The White House claims that Biden's Climate Agenda is “the most ambitious ever.” While the Inflation Reduction Act (IRA) and the Infrastructure Jobs Act (IJA) indeed do earmark billions of dollars for clean energy technologies, they also direct s
Externí odkaz:
https://doaj.org/article/28915a70f7684e878b759ca5f3f0f10a
Autor:
William G. La Cava, Paul C. Lee, Imran Ajmal, Xiruo Ding, Priyanka Solanki, Jordana B. Cohen, Jason H. Moore, Daniel S. Herman
Publikováno v:
npj Digital Medicine, Vol 6, Iss 1, Pp 1-14 (2023)
Abstract Machine learning (ML) models trained for triggering clinical decision support (CDS) are typically either accurate or interpretable but not both. Scaling CDS to the panoply of clinical use cases while mitigating risks to patients will require
Externí odkaz:
https://doaj.org/article/aae04f346cfd45fbaa7d279a18b6938b
Publikováno v:
Gastro Hep Advances, Vol 2, Iss 1, Pp 8-15 (2023)
Background and Aims: Thrombocytopenia is present in up to 76% of patients with chronic liver disease, and lower platelet counts (PCs) are associated with greater severity of portal hypertension. In this study, we assess the relationship of PC in pati
Externí odkaz:
https://doaj.org/article/49b01fb3de24417a8f6433567d27325c
Publikováno v:
Environmental Research Communications, Vol 6, Iss 12, p 125006 (2024)
Recent research underscores the importance of ensuring that net-zero pathways are perceived as legitimate and socially acceptable, as public attitudes can trigger significant backlash. This article investigates the narratives surrounding industrial d
Externí odkaz:
https://doaj.org/article/a77c446d542c41e5851be8b2043db665
Autor:
Andrzej A. Romaniuk, Lore G. Troalen, Robin Bendrey, Jeremy S. Herman, Olwyn Owen, Catherine Smith
Publikováno v:
Royal Society Open Science, Vol 10, Iss 4 (2023)
Micromammals, like rodents and shrews, adapt rapidly to take advantage of new food sources, habitats and ecological niches, frequently thriving in anthropogenic environments. Their remains, often retrieved during archaeological investigations, can be
Externí odkaz:
https://doaj.org/article/51d65fc4448a4dcbb6c3dd1de5d0cb4d
Autor:
Richard P. Oleksak, Rafik Addou, Bharat Gwalani, John P. Baltrus, Tao Liu, J. Trey Diulus, Arun Devaraj, Gregory S. Herman, Ömer N. Doğan
Publikováno v:
npj Materials Degradation, Vol 5, Iss 1, Pp 1-17 (2021)
Abstract Current and future power systems require chromia-forming alloys compatible with high-temperature CO2. Important questions concerning the mechanisms of oxidation and carburization remain unanswered. Herein we shed light onto these processes b
Externí odkaz:
https://doaj.org/article/aa0f478cc73d4c50aa8fe14ee21dd54f
Publikováno v:
Molecular Autism, Vol 11, Iss 1, Pp 1-13 (2020)
Abstract Background Partial or an entire deletion of SHANK3 are considered as major drivers in the Phelan–McDermid syndrome, in which 75% of patients are diagnosed with autism spectrum disorder (ASD). During the recent years, there was an increasin
Externí odkaz:
https://doaj.org/article/09578129a97d4d7f9ce85dee36328243
Autor:
Hequn Liu, Jesse Barnes, Erika Pedrosa, Nathaniel S. Herman, Franklin Salas, Ping Wang, Deyou Zheng, Herbert M. Lachman
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-16 (2020)
Abstract Background Lowe syndrome (LS) is caused by loss-of-function mutations in the X-linked gene OCRL, which codes for an inositol polyphosphate 5-phosphatase that plays a key role in endosome recycling, clathrin-coated pit formation, and actin po
Externí odkaz:
https://doaj.org/article/dd11e8258a334c02b7c31968977e764c