Results 301 to 310 of about 14,901,455 (379)
Suicide in Elementary School-Aged Children and Early Adolescents
A. Sheftall+6 more
semanticscholar +1 more source
TTT and R2TP chaperone complexes are required for the assembly and activation of mTORC1. WAC directly interacts with components of TTT, R2TP, and mTORC1, and these interactions are affected by the availability of glucose and glutamine, correlating with changes in mTORC1 activity.
Sofía Cabezudo+11 more
wiley +1 more source
In this research, a rat model of asthma was created using OVA, and polydatin served as an intervention. By inhibiting ferroautophagy mediated by NCOA4 and averting ferroptosis, polydatin has been demonstrated to reduce asthma. This work presents new ideas for investigating the mechanism of polydatin's ability to alleviate asthma, in addition to ...
Wei Li+5 more
wiley +1 more source
Regenerating aged bone marrow via a nitric oxide nanopump. [PDF]
Li K+10 more
europepmc +1 more source
Art. XIV.—Brief Notes on the Age and Authenticity of the Works of Âryabhaṭa, Varâhamihira, Brahmagupta, Bhaṭṭotpala, and Bhâskarâchârya [PDF]
Bhâu Dâjî
openalex +1 more source
Beyond p‐values: Assessing clinical significance in acupuncture research
Abstract In acupuncture randomized controlled trials (RCTs), the proper interpretation of results requires a thorough understanding of key statistical concepts such as p‐value, effect size, and the minimal clinically important difference (MCID). This paper explores the relationships among these metrics and their implications for assessing the clinical ...
Changzhen Gong
wiley +1 more source
Global Burden of Alzheimer's disease and other dementias in adults aged 65 years and older, 1991-2021: population-based study. [PDF]
Xiaopeng Z+6 more
europepmc +1 more source
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao+34 more
wiley +1 more source