Moran Lisa L - OmicsDI

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Unknown (7)
Metabolomics (1)
Proteomics (1)

Organisms

Mus musculus (1)

Repository

MetaboLights (1)
pride (1)

Tissue

Kidney (1)

Disease

Autosomal recessive polycystic kidney disease (1)

Technology Type

Mass spectrometry (1)
Bottom-up proteomics (1)
Data-dependent acquisition (1)
Mass Spectrometry (1)

Instrument Platform

Liquid Chromatography MS - negative - reverse phase (1)
Liquid Chromatography MS - positive - reverse phase (1)

Publication Date

2025 (1)
2026 (1)

CHEBI ID

CHEBI:1157 (1)
CHEBI:15356 (1)
CHEBI:15428 (1)
CHEBI:15573 (1)
CHEBI:15611 (1)
CHEBI:156381 (1)
CHEBI:15698 (1)
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CHEBI:16414 (1)
CHEBI:16610 (1)
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CHEBI:16750 (1)
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CHEBI:16946 (1)
CHEBI:16977 (1)
CHEBI:17148 (1)
CHEBI:17196 (1)
CHEBI:17285 (1)
CHEBI:17562 (1)
CHEBI:17822 (1)

Metabolite Name

2'-deoxycytidine (1)
4-amino-5-aminomethyl-2-methylpyrimidine (1)
4-aminobenzoic acid (1)
Adenosine 5'-monophosphate (1)
Arginine (1)
Cysteine (1)
Cytidine (1)
Cytosine (1)
Ectoine (1)
Folic acid (1)
Gamma-aminobutyric acid (1)
Glutamine (1)
Glutathione (1)
Glycine (1)
Guanosine (1)
Homoserine betaine (1)
L-asparagine (1)
L-ornithine (1)
L-tyrosine (1)
Sarcosine (1)
Spermidine (1)
Taurine (1)
Tryptamine (1)

Release Date

2023 (4)
2025 (1)
2021 (1)
2016 (1)

Lab affiliation

Center for Translational Research, Children’s National Research Institute, Children’s National Hospital, Washington,DC, United States & Children’s Hospital of Philadelphia, Philadelphia, PA, United States (1)

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Advancing Reef Monitoring Techniques through Exometabolomics: Quantification of Labile Dissolved Organic Metabolites on Coral Reefs

Extracellular chemical cues constitute much of the language of life among marine organisms from microbes to mammals. These chemical cues shape foraging and feeding strategies, symbiotic interactions, selection of mates and habitats, and the transfer of energy and nutrient...

2025-07-16 | MTBLS9008 | MetaboLights

Disruption of the human Cystin-1 myristoyl-electrostatic switch causes autosomal recessive polycystic kidney disease (ARPKD)

Autosomal recessive polycystic kidney disease (ARPKD; MIM#263200) is primarily caused by pathogenic variants in PKHD1, which encodes fibrocystin/polyductin (FPC). The Cys1cpk/cpk (cpk) mouse expresses a renal lesion that closely phenocopies ARPKD. Cys1-encoded cystin is a myristoylated protein that ...

ORGANISM(S): Mus musculus (Mouse)

2026-04-13 | PXD048013 | Pride