Cargando…

Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome

Rett syndrome (RTT) is defined as a rare disease caused by mutations of the methyl-CpG binding protein 2 (MECP2). It is one of the most common causes of genetic mental retardation in girls, characterized by normal early psychomotor development, followed by severe neurologic regression. Hitherto, RTT...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zandl-Lang, Martina, Züllig, Thomas, Trötzmüller, Martin, Naegelin, Yvonne, Abela, Lucia, Wilken, Bernd, Scholl-Buergi, Sabine, Karall, Daniela, Kappos, Ludwig, Köfeler, Harald, Plecko, Barbara
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026385/ https://www.ncbi.nlm.nih.gov/pubmed/35448478 http://dx.doi.org/10.3390/metabo12040291

Ejemplares similares

A Metabolomics Workflow for Analyzing Complex Biological Samples Using a Combined Method of Untargeted and Target-List Based Approaches
por: Züllig, Thomas, et al.
Publicado: (2020)

Lipidomics—Paving the Road towards Better Insight and Precision Medicine in Rare Metabolic Diseases
por: Zandl-Lang, Martina, et al.
Publicado: (2023)

Lipidomics from sample preparation to data analysis: a primer
por: Züllig, Thomas, et al.
Publicado: (2019)

HIGH RESOLUTION MASS SPECTROMETRY IN LIPIDOMICS
por: Züllig, Thomas, et al.
Publicado: (2020)

Mass Spectrometry Based Lipidomics: An Overview of Technological Platforms
por: Köfeler, Harald C., et al.
Publicado: (2012)

Fingolimod in children with Rett syndrome: the FINGORETT study
por: Naegelin, Yvonne, et al.
Publicado: (2021)

Assessment of lipidomic species in hepatocyte lipid droplets from stressed mouse models
por: Hartler, Jürgen, et al.
Publicado: (2014)

Very long-/ and long Chain-3-Hydroxy Acyl CoA Dehydrogenase Deficiency correlates with deregulation of the mitochondrial fusion/fission machinery
por: Hagenbuchner, Judith, et al.
Publicado: (2018)

Metabolomics analysis of antiquitin deficiency in cultured human cells and plasma: Relevance to pyridoxine‐dependent epilepsy
por: Crowther, Lisa M., et al.
Publicado: (2022)

Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS
por: Blasco, H., et al.
Publicado: (2017)

Measuring and Validating the Levels of Brain-Derived Neurotrophic Factor in Human Serum
por: Naegelin, Yvonne, et al.
Publicado: (2018)

Quantitative analysis of N‐acylphosphatidylethanolamine molecular species in rat brain using solid‐phase extraction combined with reversed‐phase chromatography and tandem mass spectrometry
por: Triebl, Alexander, et al.
Publicado: (2016)

Abnormal Expression of Cerebrospinal Fluid Cation Chloride Cotransporters in Patients with Rett Syndrome
por: Duarte, Sofia Temudo, et al.
Publicado: (2013)

Comprehensive identification of age-related lipidome changes in rat amygdala during normal aging
por: Šmidák, Roman, et al.
Publicado: (2017)

Convergent cerebrospinal fluid proteomes and metabolic ontologies in humans and animal models of Rett syndrome
por: Zlatic, Stephanie A., et al.
Publicado: (2022)

Practice Effects of Mobile Tests of Cognition, Dexterity, and Mobility on Patients With Multiple Sclerosis: Data Analysis of a Smartphone-Based Observational Study
por: Woelfle, Tim, et al.
Publicado: (2021)

Human Milk Oligosaccharides Are Present in Amniotic Fluid and Show Specific Patterns Dependent on Gestational Age
por: Jantscher-Krenn, Evelyn, et al.
Publicado: (2022)

Wearable Sensor Technologies to Assess Motor Functions in People With Multiple Sclerosis: Systematic Scoping Review and Perspective
por: Woelfle, Tim, et al.
Publicado: (2023)

Recommendations for good practice in MS-based lipidomics
por: Köfeler, Harald C., et al.
Publicado: (2021)

Cerebrospinal fluid lipidomic fingerprint of obstructive sleep apnoea in Alzheimer’s disease
por: Dakterzada, Farida, et al.
Publicado: (2023)

Bilanz ziehen – Zahlen, Daten, Fakten
por: Karall, Daniela, et al.
Publicado: (2020)

Automated Annotation of Sphingolipids Including Accurate Identification of Hydroxylation Sites Using MS(n) Data
por: Hartler, Jürgen, et al.
Publicado: (2020)

Identification of Disease Markers in Human Cerebrospinal Fluid Using Lipidomic and Proteomic Methods
por: Fonteh, Alfred N., et al.
Publicado: (2006)

Lipid particles/droplets of the yeast Saccharomyces cerevisiae revisited: Lipidome meets Proteome
por: Grillitsch, Karlheinz, et al.
Publicado: (2011)

Nonalcoholic fatty liver disease stratification by liver lipidomics
por: Vvedenskaya, Olga, et al.
Publicado: (2021)

Asymmetric opening of the homopentameric 5-HT(3A) serotonin receptor in lipid bilayers
por: Zhang, Yingyi, et al.
Publicado: (2021)

Death Anxiety and Attitudes towards Death in Patients with Multiple Sclerosis: An Exploratory Study
por: Francalancia, Jara, et al.
Publicado: (2021)

Assessment of cognitive performance in multiple sclerosis using smartphone-based training games: a feasibility study
por: Pless, Silvan, et al.
Publicado: (2023)

Cerebrospinal fluid lipidomic biomarker signatures of demyelination for multiple sclerosis and Guillain–Barré syndrome
por: Péter, Mária, et al.
Publicado: (2020)

Lipidomic traits of plasma and cerebrospinal fluid in amyotrophic lateral sclerosis correlate with disease progression
por: Sol, Joaquim, et al.
Publicado: (2021)

Alteration in the Cerebrospinal Fluid Lipidome in Parkinson’s Disease: A Post-Mortem Pilot Study
por: Fernández-Irigoyen, Joaquín, et al.
Publicado: (2021)

Phospholipid oxidation generates potent anti-inflammatory lipid mediators that mimic structurally related pro-resolving eicosanoids by activating Nrf2
por: Bretscher, Peter, et al.
Publicado: (2015)

Cerebrospinal fluid from Alzheimer’s disease patients promotes tau aggregation in transgenic mice
por: Skachokova, Zhiva, et al.
Publicado: (2019)

Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD)
por: Karall, Daniela, et al.
Publicado: (2015)

Predictive Modeling of Alzheimer’s and Parkinson’s Disease Using Metabolomic and Lipidomic Profiles from Cerebrospinal Fluid
por: Hwangbo, Nathan, et al.
Publicado: (2022)

Untargeted plasma metabolomics identifies broad metabolic perturbations in glycogen storage disease type I
por: Mathis, Tamara, et al.
Publicado: (2021)

Natalizumab in cerebrospinal fluid and breastmilk of patients with multiple sclerosis
por: Callegari, Ilaria, et al.
Publicado: (2023)

A retrospective study on disease management in children and adolescents with phenylketonuria during the Covid-19 pandemic lockdown in Austria
por: Herle, Marion, et al.
Publicado: (2021)

Determination of Oxidized Phosphatidylcholines by Hydrophilic Interaction Liquid Chromatography Coupled to Fourier Transform Mass Spectrometry
por: Sala, Pia, et al.
Publicado: (2015)

Improved Characterization of Visual Evoked Potentials in Multiple Sclerosis by Topographic Analysis
por: Hardmeier, Martin, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_kso5537ongfavjompt5udcgmdr