2004
DOI: 10.1016/j.ab.2004.04.004
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Toward fingerprinting cellular lipidomes directly from biological samples by two-dimensional electrospray ionization mass spectrometry

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Cited by 212 publications
(138 citation statements)
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“…Precursor ion scanning (PIS) and neutral loss scanning (NLS) for head group survey (HGS) and fatty acid survey (FAS), respectively, are typically performed in the positive or negative ion modes. PIS and NLS of the polar head groups of PLs are valuable techniques for detecting most molecular species within the same class of PLs [29][30][31][32][33][34][35]. PIS of carbonic anions was also very useful for identifying molecular species of PLs with specified fatty acyl chains as reported by Ekroos et al [29].…”
Section: Analytical Systems By Mass Spectrometry In Lipidomics J235mentioning
confidence: 82%
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“…Precursor ion scanning (PIS) and neutral loss scanning (NLS) for head group survey (HGS) and fatty acid survey (FAS), respectively, are typically performed in the positive or negative ion modes. PIS and NLS of the polar head groups of PLs are valuable techniques for detecting most molecular species within the same class of PLs [29][30][31][32][33][34][35]. PIS of carbonic anions was also very useful for identifying molecular species of PLs with specified fatty acyl chains as reported by Ekroos et al [29].…”
Section: Analytical Systems By Mass Spectrometry In Lipidomics J235mentioning
confidence: 82%
“…[29][30][31][32][33][34][35] There are two types of structure-related focused analysis by ESIMS/MS. Precursor ion scanning (PIS) and neutral loss scanning (NLS) for head group survey (HGS) and fatty acid survey (FAS), respectively, are typically performed in the positive or negative ion modes.…”
Section: Analytical Systems By Mass Spectrometry In Lipidomics J235mentioning
confidence: 99%
“…Identification of A-type ceramides in the stratum corneum of human skin Direct infusion of lipid extracts into a tandem mass spectrometer has been used for ceramide profiling in various samples such as mouse liver [27], rat brain tissues and cerebral endothelial cells [25], human plasma [28], and human skin fibroblasts cell [29]. In our previous study, this method was applied to N-type ceramide analysis in the skin stratum corneum [24].…”
Section: General Ms/ms Fragmentation Pattern Of A-type Ceramidesmentioning
confidence: 99%
“…Electrospray ionization mass spectrometry enables the identification and quantification of the cellular or tissue lipidomes directly from crude extracts of cell, tissue or organ samples [21][22][23] . The mass spectrometers that resolve fragments of entrant precursor ions of biomolecules in space domains enable identification and quantification in a class specific manner, referred to as automated shotgun lipid profiling [24] .…”
Section: Class Specific Analyses Of Lipids On Mass Analyzer Where Framentioning
confidence: 99%