Lipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models

Neuropathy in Tangier disease: A clinicopathologic study and a review of the literature

(2010) V. Pietrini et al.   ACTA NEUROLOGICA SCANDINAVICA

Peroxisomes, lipid metabolism and lipotoxicity

(2010) R.J.A. Wanders et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS

Sjögren-Larsson syndrome in Sweden. A clinical, genetic and epidemiological study

(2010) Sten Jagell et al.   CLINICAL GENETICS

Smith-Lemli-Opitz Syndrome: Neuropathological and Ophthalmological Observations

(2010) Marcella Fierro et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

(2010) Katherine J. Dick et al.   HUMAN MUTATION

Metabolic acetate therapy improves phenotype in the tremor rat model of Canavan disease

(2010) Peethambaran Arun et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolism

(2010) Paul P. Van Veldhoven   JOURNAL OF LIPID RESEARCH

Pyruvate carboxylase deficiency: Mechanisms, mimics and anaplerosis

(2010) Isaac Marin-Valencia et al.   MOLECULAR GENETICS AND METABOLISM

Myelination and the trophic support of long axons

(2010) Klaus-Armin Nave   NATURE REVIEWS NEUROSCIENCE

Two new test methods to quantify motor deficits in a marmoset model for Parkinson's disease

(2009) Peternella S. Verhave et al.   BEHAVIOURAL BRAIN RESEARCH

Oligodendroglial impact on axonal function and survival – a hypothesis

(2009) Celia Michèle Kassmann et al.   CURRENT OPINION IN NEUROLOGY

On the biogenesis of myelin membranes: Sorting, trafficking and cell polarity

(2009) Wia Baron et al.   FEBS LETTERS

Absence of oligodendroglial glucosylceramide synthesis does not result in CNS myelin abnormalities or alter the dysmyelinating phenotype of CGT-deficient mice

(2009) Laleh Saadat et al.   GLIA

Defects in myelination, paranode organization and Purkinje cell innervation in the ether lipid-deficient mouse cerebellum

(2009) Andre Teigler et al.   HUMAN MOLECULAR GENETICS

Adult Ceramide Synthase 2 (CERS2)-deficient Mice Exhibit Myelin Sheath Defects, Cerebellar Degeneration, and Hepatocarcinomas

(2009) Silke Imgrund et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Cholesterol Regulates the Endoplasmic Reticulum Exit of the Major Membrane Protein P0 Required for Peripheral Myelin Compaction

(2009) G. Saher et al.   JOURNAL OF NEUROSCIENCE

Specific Loss of Brain ABCA1 Increases Brain Cholesterol Uptake and Influences Neuronal Structure and Function

(2009) J. M. Karasinska et al.   JOURNAL OF NEUROSCIENCE

Lack of aspartoacylase activity disrupts survival and differentiation of neural progenitors and oligodendrocytes in a mouse model of Canavan disease

(2009) Shalini Kumar et al.   JOURNAL OF NEUROSCIENCE RESEARCH

Are Astrocytes the Missing Link Between Lack of Brain Aspartoacylase Activity and the Spongiform Leukodystrophy in Canavan Disease?

(2009) Morris H. Baslow et al.   NEUROCHEMICAL RESEARCH

Peroxisomes, Myelination, and Axonal Integrity in the CNS

(2009) Myriam Baes et al.   NEUROSCIENTIST

Effect of cholesterol on structural and mechanical properties of membranes depends on lipid chain saturation

(2009) Jianjun Pan et al.   PHYSICAL REVIEW E

Ablation of cholesterol biosynthesis in neural stem cells increases their VEGF expression and angiogenesis but causes neuron apoptosis

(2009) K. Saito et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

SCAP is required for timely and proper myelin membrane synthesis

(2009) Mark H. G. Verheijen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia

(2008) Simon Edvardson et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Sphingomyelin Synthase 2 Deficiency Attenuates NFκB Activation

(2008) Tiruneh K. Hailemariam et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Plasmalogens participate in very-long-chain fatty acid-induced pathology

(2008) P. Brites et al.   BRAIN

Safety of statins

(2008) William Virgil Brown   CURRENT OPINION IN LIPIDOLOGY

Phosphatidic acid mediates demyelination in Lpin1 mutant mice

(2008) K. Nadra et al.   GENES & DEVELOPMENT

Lovastatin induces the formation of abnormal myelin-like membrane sheets in primary oligodendrocytes

(2008) Olaf Maier et al.   GLIA

Nur7 Is a Nonsense Mutation in the Mouse Aspartoacylase Gene That Causes Spongy Degeneration of the CNS

(2008) M. Traka et al.   JOURNAL OF NEUROSCIENCE

Absence of 2-Hydroxylated Sphingolipids Is Compatible with Normal Neural Development But Causes Late-Onset Axon and Myelin Sheath Degeneration

(2008) I. Zoller et al.   JOURNAL OF NEUROSCIENCE

The Role and Metabolism of Sulfatide in the Nervous System

(2008) Matthias Eckhardt   MOLECULAR NEUROBIOLOGY

Inhibition of Rho Family Functions by Lovastatin Promotes Myelin Repair in Ameliorating Experimental Autoimmune Encephalomyelitis

(2008) A. S. Paintlia et al.   MOLECULAR PHARMACOLOGY

Membrane lipids: where they are and how they behave

(2008) Gerrit van Meer et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Expression of Pyruvate Carboxylase in Cultured Oligodendroglial, Microglial and Ependymal Cells

(2008) Radovan Murin et al.   NEUROCHEMICAL RESEARCH

The Mystery and Magic of Glia: A Perspective on Their Roles in Health and Disease

(2008) Ben A. Barres   NEURON

A simple and universal method for the separation and identification of phospholipid molecular species

(2008) Kim Retra et al.   RAPID COMMUNICATIONS IN MASS SPECTROMETRY

Parameters related to lipid metabolism as markers of myelination in mouse brain

(2003) Evan D. Muse et al.   JOURNAL OF NEUROCHEMISTRY