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UnknownThree-dose vaccination-induced immune responses protect against SARS-CoV-2 Omicron BA.2: a population-based study in Hong Kong.
Not available
S-EPMC9786166 | biostudies-literature
UnknownSatellite-based estimates of long-term exposure to fine particulate matter are associated with C-reactive protein in 30 034 Taiwanese adults.
Not available
S-EPMC5837544 | biostudies-literature
UnknownLycium barbarum Extract Enhanced Neuroplasticity and Functional Recovery in 5xFAD Mice via Modulating Microglial Status of the Central Nervous System.
Not available
S-EPMC11576918 | biostudies-literature
UnknownHuman Intestinal Organoids Recapitulate Enteric Infections of Enterovirus and Coronavirus.
Not available
S-EPMC7940440 | biostudies-literature
UnknownGlobal prevalence of SARS-CoV-2 3CL protease mutations associated with nirmatrelvir or ensitrelvir resistance.
Not available
S-EPMC10101811 | biostudies-literature
UnknownEffective identification of Alzheimer's disease in mouse models via deep learning and motion analysis.
Not available
S-EPMC11647830 | biostudies-literature
UnknownBeneficial effect of combinational methylprednisolone and remdesivir in hamster model of SARS-CoV-2 infection.
Not available
S-EPMC7919885 | biostudies-literature
MetabolomicsDifferential role of sphingomyelin in influenza virus, rhinovirus and SARS-CoV-2 infection of Calu-3 cells
Host cell lipids play a pivotal role in the pathogenesis of respiratory virus infection. However, a direct comparison of the lipidomic profile of influenza virus and rhinovirus infections is lacking. In this study, we first compared the lipid profile of influenza virus and rhinovirus infection in a ...
2022-11-15 | MTBLS2352 | MetaboLights
UnknownDispersed Sensing Networks in Nano-Engineered Polymer Composites: From Static Strain Measurement to Ultrasonic Wave Acquisition.
Not available
S-EPMC5982692 | biostudies-literature
ProteomicsMulti-Omic analyses reveal aberrant differentiation trajectory with WNT1 Loss-of-Function in type XV osteogenesis imperfecta
Osteogenesis imperfecta (OI) is a serious genetic bone disorder characterized by congenital low bone mass, deformity and frequent fractures. Type XV OI is a moderate to severe form of skeletal dysplasia caused by WNT1 mutations. In this cohort study from southern China, we summarized the clinical ph...
ORGANISM(S): Homo sapiens (Human) 
2024-10-17 | PXD050841 | Pride
Human Bone Osteogenesis imperfecta 
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