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UnknownLiquid Chromatography-Tandem Mass Spectrometry Assay of Leukocyte Acid α-Glucosidase for Post-Newborn Screening Evaluation of Pompe Disease.
Not available
S-EPMC5413112 | biostudies-literature
ProteomicsNaringenin targets PI3K p85alpha to suppress PI3K/AKT signaling pathway and ameliorate disordered MMP-9 secretion in cigarette smoke extract-induced alveolar macrophages in vitro
Naringenin has demonstrated potential therapeutic effects against cigarette smoke-induced lung injury; however, its underlying mechanisms of regulating matrix metalloproteinase-9 (MMP-9) in alveolar macrophages remain unclear. Methods: The regulatory mechanisms of naringenin in cigarette smoke extra...
ORGANISM(S): Mus Musculus 
2025-04-21 | PXD063137 |
UnknownN-acyl-O-phosphocholineserines: structures of a novel class of lipids that are biomarkers for Niemann-Pick C1 disease.
Not available
S-EPMC6672039 | biostudies-literature
UnknownEvaluation of Two Methods for Quantification of Glycosaminoglycan Biomarkers in Newborn Dried Blood Spots from Patients with Severe and Attenuated Mucopolysaccharidosis Type II.
Not available
S-EPMC8884011 | biostudies-literature
TranscriptomicsTranscriptomic analysis of breast cancer
Transcriptomic analysis of fresh breast cancer tissue versus normal tissues. The Study comprising 45 Saudi-Arabian subjects was designed to take advantage of transcriptomics to prospectively explore the roles of lifestyle and genetic susceptibility in the occurrence of breast cancer. Total RNA isola...
ORGANISM(S): Homo sapiens 
2014-04-15 | E-GEOD-36295 | biostudies-arrayexpress
UnknownExpression and Function of Group IIE Phospholipase A2 in Mouse Skin.
Not available
S-EPMC4957045 | biostudies-literature
ProteomicsQuantification profiles of enzyme activity, secretion and psychosine levels of Krabbe disease galactosylceramidase missense variants
Krabbe disease (KD) is an autosomal recessive lysosomal storage disorder caused by loss-offunction mutations in the GALC gene, which encodes for the enzyme galactosylceramidase (GALC). GALC is crucial for myelin metabolism. Functional deficiency of GALC leads to toxic accumulation of psychosine, dys...
ORGANISM(S): Homo sapiens (Human) 
2025-05-19 | PXD057472 | Pride
Secretion Missense mutation variant Galactosylceramidase Lysosomal storage disorder Lysosome Galc Psychosine Crispr-cas9 knockout cell Protein trafficking Krabbe disease Expression study Genotype-phenotype correlation Galactosylsphingosine Globoid cell leukodystrophy 
UnknownGalactosylceramidase deficiency and pathological abnormalities in cerebral white matter of Krabbe disease.
Not available
S-EPMC10474820 | biostudies-literature
UnknownThe role of group IIF-secreted phospholipase A2 in epidermal homeostasis and hyperplasia.
Not available
S-EPMC4612087 | biostudies-literature
UnknownA novel anti-inflammatory role for secretory phospholipase A2 in immune complex-mediated arthritis.
Not available
S-EPMC3058614 | biostudies-literature
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