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UnknownHomology-model-guided site-specific mutagenesis reveals the mechanisms of substrate binding and product-regulation of adenosine kinase from Leishmania donovani.
Not available
S-EPMC1386000 | biostudies-literature
MetabolomicsNon-targeted multimodal metabolomics and lipidomics data from ovine rumen fluid fractions

From an animal production and health perspective, our understanding of the metabolites in ruminant biofluids, particularly rumen fluid across different host species is poorly understood. Metabolomics is a powerful and sensitive approach for investigating low molecular weight metabolite profiles p...

2021-08-23 | MTBLS1717 | MetaboLights
UnknownSimple Bisthiocarbonohydrazone as a Sensitive, Selective, Colorimetric, and Ratiometric Fluorescent Chemosensor for Picric Acids.
Not available
S-EPMC6641181 | biostudies-literature
UnknownInhibition of Staphylococcus aureus and Pseudomonas aeruginosa Biofilm and Virulence by Active Fraction of Syzygium cumini (L.) Skeels Leaf Extract: In-Vitro and In Silico Studies.
Not available
S-EPMC6328409 | biostudies-literature
UnknownA cross talk between the immunization and edible vaccine: Current challenges and future prospects.
Not available
S-EPMC7449231 | biostudies-literature
UnknownGenomic Clues of a Multidrug-Resistant Bacterium from Cultured Domestic Silkworm (Bombyx mori L.).
Not available
S-EPMC9202366 | biostudies-literature
TranscriptomicsExpression profile of peripheral blood of healthy individuals phenotyped based on â??Prakritiâ?? concept of Ayurveda
Immense phenotypic variability exists among healthy individuals which is a consequence of both genetic and environmental effects. Genome wide expression variability is a powerful tool for capturing these expression variations and hence can give insights into genotype phenotype correlations. In the a...
ORGANISM(S): Homo sapiens 
2010-05-26 | E-GEOD-7883 | biostudies-arrayexpress
UnknownAnalysis of the topology of Vibrio cholerae NorM and identification of amino acid residues involved in norfloxacin resistance.
Not available
S-EPMC1635172 | biostudies-literature
MetabolomicsSMN deficiency perturbs monoamine neurotransmitter metabolism in spinal muscular atrophy

Beyond motor neuron degeneration, homozygous mutations in the survival motor neuron 1 (SMN1) gene cause multiorgan and metabolic defects in patients with spinal muscular atrophy (SMA). However, the precise biochemical features of these alterations and the age of onset in the brain and peripheral ...

2023-11-27 | MTBLS8784 | MetaboLights
UnknownMutational analysis of the active-site residues crucial for catalytic activity of adenosine kinase from Leishmania donovani.
Not available
S-EPMC1134988 | biostudies-literature
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