SILEC: a protocol for generating and using isotopically labeled coenzyme A mass spectrometry standards - Wikidata - awgldk - TriplyDB

SILEC: a protocol for generating and using isotopically labeled coenzyme A mass spectrometry standards

SILEC: a protocol for generating and using isotopically labeled coenzyme A mass spectrometry standards

http://www.wikidata.org/entity/Q37242476

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Akt-dependent metabolic reprogramming regulates tumor cell histone acetylation Inhibition of neuronal cell mitochondrial complex I with rotenone increases lipid β-oxidation, supporting acetyl-coenzyme A levels.Metabolism of propionic acid to a novel acyl-coenzyme A thioester by mammalian cell lines and platelets.Stable isotope dilution liquid chromatography/mass spectrometry analysis of cellular and tissue medium- and long-chain acyl-coenzyme A thioesters Production of stable isotope-labeled acyl-coenzyme A thioesters by yeast stable isotope labeling by essential nutrients in cell culture Stable isotopes and LC-MS for monitoring metabolic disturbances in Friedreich's ataxia platelets.Regulation of lipid synthesis by the RNA helicase Mov10 controls Wnt5a production.Akt-mTORC1 signaling regulates Acly to integrate metabolic input to control of macrophage activation.Evidence for Intramyocardial Disruption of Lipid Metabolism and Increased Myocardial Ketone Utilization in Advanced Human Heart Failure.LC-quadrupole/Orbitrap high-resolution mass spectrometry enables stable isotope-resolved simultaneous quantification and ¹³C-isotopic labeling of acyl-coenzyme A thioesters.LC-MS Analysis of Human Platelets as a Platform for Studying Mitochondrial Metabolism.AMPK Activation and Metabolic Reprogramming by Tamoxifen through Estrogen Receptor-Independent Mechanisms Suggests New Uses for This Therapeutic Modality in Cancer Treatment Human platelets as a platform to monitor metabolic biomarkers using stable isotopes and LC-MS.Metabolomics: A Primer.Company profile: BluePen Biomarkers LLC – integrated biomarker solutions.Stable isotope labeling by essential nutrients in cell culture (SILEC) for accurate measurement of nicotinamide adenine dinucleotide metabolism.Characterization of histone acylations links chromatin modifications with metabolism Coenzyme A thioester formation of 11- and 15-oxo-eicosatetraenoic acid.Metabolic tracing analysis reveals substrate-specific metabolic deficits in platelet storage lesion.The role of fatty acid β-oxidation in lymphangiogenesis.Extraction and Analysis of Pan-metabolome Polar Metabolites by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS).

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SILEC: a protocol for generating and using isotopically labeled coenzyme A mass spectrometry standards

http://www.wikidata.org/entity/Q37242476

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 08 December 2011

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

SILEC: a protocol for generati ...... A mass spectrometry standards

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SILEC: a protocol for generati ...... A mass spectrometry standards.

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SILEC: a protocol for generati ...... A mass spectrometry standards

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SILEC: a protocol for generati ...... A mass spectrometry standards

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SILEC: a protocol for generati ...... A mass spectrometry standards.

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Nature Protocols

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SILEC: a protocol for generati ...... A mass spectrometry standards

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Ian A Blair

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Sankha S Basu

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Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

Stable isotope labeling by amino acids in cell culture, SILAC, as a simple and accurate approach to expression proteomics

Coenzyme A metabolism

A practical recipe for stable isotope labeling by amino acids in cell culture (SILAC)

Feasibility of pathways for transfer of acyl groups from mitochondria to the cytosol to form short chain acyl-CoAs in the pancreatic beta cell

A systematic approach to modeling, capturing, and disseminating proteomics experimental data.

High-throughput quantitative bioanalysis by LC/MS/MS.

Analysis of protein expression during oxidative stress in breast epithelial cells using a stable isotope labeled proteome internal standard.

Analytical strategies for identifying drug metabolites.

Systematic investigation of ion suppression and enhancement effects of fourteen stable-isotope-labeled internal standards by their native analogues using atmospheric-pressure chemical ionization and electrospray ionization and the relevance for mult

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1-12

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scholarly article

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10.1038/NPROT.2011.421

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1

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7

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2011-12-08T00:00:00Z

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22157971

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3802537

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