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UnknownFrom genome to drug lead: identification of a small-molecule inhibitor of the SARS virus.
Not available
S-EPMC7119130 | biostudies-literature
MetabolomicsPreterm birth is associated with xenobiotics and predicted by the vaginal metabolome
Spontaneous preterm birth (sPTB) is a leading cause of maternal and neonatal morbidity and mortality, yet its prevention and early risk stratification are limited. Previous investigations have suggested that vaginal microbes and metabolites may be implicated in sPTB. Here we performed untargeted met...
2022-11-21 | MTBLS702 | MetaboLights
MetabolomicsHomeostasis of the biosynthetic E. coli metabolome
Metabolite concentrations vary across conditions and such metabolome changes are relevant for metabolic and gene regulation. Here, we used LC-MS/MS to explore metabolite concentration changes in Escherichia coli. We measured 101 primary metabolites in 19 experimental conditions that include v...
2022-11-02 | MTBLS4249 | MetaboLights
UnknownA Precise Method to Evaluate 360 Degree Measures of Optic Cup and Disc Morphology in an African American Cohort and Its Genetic Applications.
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S-EPMC8701339 | biostudies-literature
Unknown<i>KIF21A</i>-associated peripheral neuropathy defined by impaired binding with TUBB3.
Not available
S-EPMC11773626 | biostudies-literature
UnknownGenome sequencing reveals novel noncoding variants in PLA2G6 and LMNB1 causing progressive neurologic disease.
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S-EPMC9000935 | biostudies-literature
UnknownCytokine-like protein 1-induced survival of monocytes suggests a combined strategy targeting MCL1 and MAPK in CMML.
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S-EPMC8233685 | biostudies-literature
UnknownRelation of koniocellular layers of dorsal lateral geniculate to inferior pulvinar nuclei in common marmosets.
Not available
S-EPMC6928438 | biostudies-literature
UnknownGenome-wide association studies of TDP-43 proteinopathy and hippocampal sclerosis reveal shared genetic associations with APOE and TMEM106B.
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S-EPMC12598407 | biostudies-literature
UnknownTargeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases.
Not available
S-EPMC9613861 | biostudies-literature
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