(Q28279470)

Metabolic and functional aspects of sulfogalactolipids

published in

Molecular Neurobiology

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volume

37

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issue

2-3

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page(s)

93-103

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cites work

1 reference

https://api.crossref.org/works/10.1007%2FS12035-008-8022-3

Functional compartments of sulphatide metabolism in cultured living cells: evidence for the involvement of a novel sulphatide-degrading pathway

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-008-8022-3

The role of apolipoprotein E in lipid metabolism in the central nervous system

21 January 2018

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Correction of metachromatic leukodystrophy in the mouse model by transplantation of genetically modified hematopoietic stem cells

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-008-8022-3

Accumulation of sulfatide in neuronal and glial cells of arylsulfatase A deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-008-8022-3

Delay of myelin formation in arylsulphatase A-deficient mice

21 January 2018

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12 December 2020

Principles of lysosomal membrane digestion: stimulation of sphingolipid degradation by sphingolipid activator proteins and anionic lysosomal lipids

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12 December 2020

Potential mechanisms contributing to sulfatide depletion at the earliest clinically recognizable stage of Alzheimer's disease: a tale of shotgun lipidomics

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12 December 2020

Oligodendroglial progenitor cell therapy limits central neurological deficits in mice with metachromatic leukodystrophy.

1 reference

12 December 2020

Two mammalian longevity assurance gene (LAG1) family members, trh1 and trh4, regulate dihydroceramide synthesis using different fatty acyl-CoA donors

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12 December 2020

Exocytosis of storage material in a lysosomal disorder

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12 December 2020

Assembly of myelin by association of proteolipid protein with cholesterol- and galactosylceramide-rich membrane domains

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12 December 2020

Enzyme, cell and gene-based therapies for metachromatic leukodystrophy

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12 December 2020

Cerebroside sulfotransferase forms homodimers in living cells

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12 December 2020

Hyperactivity, neuromotor defects, and impaired learning and memory in a mouse model for metachromatic leukodystrophy.

1 reference

12 December 2020

Lipid dynamics in neurons

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12 December 2020

Reversible inhibition of oligodendrocyte progenitor differentiation by a monoclonal antibody against surface galactolipids

1 reference

12 December 2020

Oligodendrocyte-specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT-deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level

1 reference

12 December 2020

Regulation of integrin growth factor interactions in oligodendrocytes by lipid raft microdomains

1 reference

12 December 2020

Roles of KATP channels as metabolic sensors in acute metabolic changes

1 reference

12 December 2020

In vivo gene therapy of metachromatic leukodystrophy by lentiviral vectors: correction of neuropathology and protection against learning impairments in affected mice

1 reference

12 December 2020

Association of beta 1 integrin with focal adhesion kinase and paxillin in differentiating Schwann cells.

1 reference

12 December 2020

Specificity and potential mechanism of sulfatide deficiency in Alzheimer's disease: an electrospray ionization mass spectrometric study

1 reference

12 December 2020

A mammalian fatty acid hydroxylase responsible for the formation of alpha-hydroxylated galactosylceramide in myelin

1 reference

12 December 2020

Intracellular sulfatide expression in a subpopulation of astrocytes in primary cultures

1 reference

12 December 2020

A myelin galactolipid, sulfatide, is essential for maintenance of ion channels on myelinated axon but not essential for initial cluster formation.

1 reference

12 December 2020

Biochemical studies of the late infantile form of metachromatic leukodystrophy.

1 reference

12 December 2020

The UDP‐Galactose:Ceramide Galactosyltransferase: Expression Pattern in Oligodendrocytes and Schwann Cells During Myelination and Substrate Preference for Hydroxyceramide

1 reference

12 December 2020

The human FA2H gene encodes a fatty acid 2-hydroxylase

1 reference

12 December 2020

Partial cure of established disease in an animal model of metachromatic leukodystrophy after intracerebral adeno-associated virus-mediated gene transfer

1 reference

12 December 2020

cDNA cloning, genomic cloning, and tissue-specific regulation of mouse cerebroside sulfotransferase

1 reference

12 December 2020

Increasing sulfatide synthesis in myelin-forming cells of arylsulfatase A-deficient mice causes demyelination and neurological symptoms reminiscent of human metachromatic leukodystrophy

1 reference

12 December 2020

Chemistry and functional distribution of sulfoglycolipids

1 reference

12 December 2020

Stimulation of oligodendrocyte differentiation in culture by growth in the presence of a monoclonal antibody to sulfated glycolipid

1 reference

12 December 2020

Molecular cloning and expression of cDNA encoding human 3'-phosphoadenylylsulfate:galactosylceramide 3'-sulfotransferase

1 reference

12 December 2020

Sulfatide with short fatty acid dominates in astrocytes and neurons

1 reference

12 December 2020

Long-term expression and transfer of arylsulfatase A into brain of arylsulfatase A-deficient mice transplanted with bone marrow expressing the arylsulfatase A cDNA from a retroviral vector

1 reference

12 December 2020

Synthesis of cerebroside by brain from uridine diphosphate galactose and ceramide containing hydroxy fatty acid

1 reference

12 December 2020

Mice deficient for the HNK-1 sulfotransferase show alterations in synaptic efficacy and spatial learning and memory

1 reference

12 December 2020

Tenascin-R is an intrinsic autocrine factor for oligodendrocyte differentiation and promotes cell adhesion by a sulfatide-mediated mechanism.

1 reference

12 December 2020

Synthesis of non-hydroxy-galactosylceramides and galactosyldiglycerides by hydroxy-ceramide galactosyltransferase

1 reference

12 December 2020

Sulfatide and GM1 ganglioside modulate the high-affinity dopamine uptake in rat striatal synaptosomes: evidence for the involvement of their ionic charges

1 reference

12 December 2020

Neuromotor alterations and cerebellar deficits in aged arylsulfatase A-deficient transgenic mice

1 reference

12 December 2020

Gene therapy: prospects for glycolipid storage diseases

1 reference

12 December 2020

Rafts in adult peripheral nerve myelin contain major structural myelin proteins and myelin and lymphocyte protein (MAL) and CD59 as specific markers

1 reference

12 December 2020

Novel role for apolipoprotein E in the central nervous system. Modulation of sulfatide content

1 reference

12 December 2020

Does paranode formation and maintenance require partitioning of neurofascin 155 into lipid rafts?

1 reference

12 December 2020

Expression of the myelin and oligodendrocyte progenitor marker sulfatide in neurons and astrocytes of adult rat brain

1 reference

12 December 2020

Nodal protrusions, increased Schmidt-Lanterman incisures, and paranodal disorganization are characteristic features of sulfatide-deficient peripheral nerves.

1 reference

12 December 2020

Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism

1 reference

12 December 2020

C16:0 sulfatide inhibits insulin secretion in rat beta-cells by reducing the sensitivity of KATP channels to ATP inhibition.

1 reference

12 December 2020

Gene therapy of metachromatic leukodystrophy

1 reference

12 December 2020

FA2H-dependent fatty acid 2-hydroxylation in postnatal mouse brain

1 reference

12 December 2020

Apolipoprotein E and Alzheimer's disease

1 reference

12 December 2020

rMAL is a glycosphingolipid-associated protein of myelin and apical membranes of epithelial cells in kidney and stomach

1 reference

12 December 2020

Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy

1 reference

12 December 2020

Sulfatide is a negative regulator of oligodendrocyte differentiation: development in sulfatide-null mice

1 reference

12 December 2020

Characterization of a rat gene, rMAL, encoding a protein with four hydrophobic domains in central and peripheral myelin

1 reference

12 December 2020

The cell biology of glycosphingolipids.

1 reference

12 December 2020

Sulfatide storage in neurons causes hyperexcitability and axonal degeneration in a mouse model of metachromatic leukodystrophy.

1 reference

12 December 2020

Myelination in the absence of galactocerebroside and sulfatide: normal structure with abnormal function and regional instability.

1 reference

12 December 2020

Novel candidate disease for gene therapy: metachromatic leukodystrophy

1 reference

12 December 2020

A role for apolipoprotein E, apolipoprotein A-I, and low density lipoprotein receptors in cholesterol transport during regeneration and remyelination of the rat sciatic nerve

1 reference

12 December 2020

Localization of annexin II in the paranodal regions and Schmidt-Lanterman incisures in the peripheral nervous system.

1 reference

12 December 2020

Glial regulation of the axonal membrane at nodes of Ranvier

1 reference

12 December 2020

Mass spectrometric analysis reveals changes in phospholipid, neutral sphingolipid and sulfatide molecular species in progressive epilepsy with mental retardation, EPMR, brain: a case study

1 reference

12 December 2020

Embryonic stem cell-based reduction of central nervous system sulfatide storage in an animal model of metachromatic leukodystrophy.

1 reference

12 December 2020

Enzyme replacement improves nervous system pathology and function in a mouse model for metachromatic leukodystrophy

1 reference

12 December 2020

Intracerebral adeno-associated virus-mediated gene transfer in rapidly progressive forms of metachromatic leukodystrophy.

1 reference

12 December 2020

The way we view cellular (glyco)sphingolipids.

1 reference

12 December 2020

Regulatory effect of sulphatides on BKCa channels

1 reference

12 December 2020

Gene therapy of metachromatic leukodystrophy reverses neurological damage and deficits in mice

1 reference

12 December 2020

Enzymatic activation of voltage-gated potassium channels.

1 reference

12 December 2020

Cerebrospinal fluid sulfatide is decreased in subjects with incipient dementia

1 reference

12 December 2020

Substantial sulfatide deficiency and ceramide elevation in very early Alzheimer's disease: potential role in disease pathogenesis

1 reference

12 December 2020

Negative regulation of oligodendrocyte differentiation by galactosphingolipids

1 reference

12 December 2020

The oligodendrocyte and its many cellular processes

1 reference

12 December 2020

Laminin-sulfatide binding initiates basement membrane assembly and enables receptor signaling in Schwann cells and fibroblasts

1 reference

12 December 2020

Mannose 6-phosphate receptors: new twists in the tale

1 reference

12 December 2020

The raft-associated protein MAL is required for maintenance of proper axon--glia interactions in the central nervous system

1 reference

12 December 2020

Endosomes and lysosomes play distinct roles in sulfatide-induced neuroblastoma apoptosis: potential mechanisms contributing to abnormal sulfatide metabolism in related neuronal diseases

1 reference

12 December 2020

Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis

1 reference

12 December 2020

Oligodendrocytes assist in the maintenance of sodium channel clusters independent of the myelin sheath.

1 reference

12 December 2020

Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophies.

1 reference

12 December 2020

Lysosomal sulfatide storage in the brain of arylsulfatase A-deficient mice: cellular alterations and topographic distribution

1 reference

12 December 2020

Specific downregulation and mistargeting of the lipid raft-associated protein MAL in a glycolipid storage disorder

1 reference

12 December 2020

Sulfatide and Na+-K+-ATPase: a salinity-sensitive relationship in the gill basolateral membrane of rainbow trout

1 reference

12 December 2020

Sulfatide is essential for the maintenance of CNS myelin and axon structure

1 reference

12 December 2020

Reduced brain cholesterol content in arylsulfatase A-deficient mice.

1 reference

12 December 2020

A neutral galactocerebroside sulfate sulfatidase from mouse brain

1 reference

12 December 2020

A spontaneously immortalized Schwann cell line to study the molecular aspects of metachromatic leukodystrophy

1 reference

12 December 2020

Paranodal axoglial junction is required for the maintenance of the Nav1.6-type sodium channel in the node of Ranvier in the optic nerves but not in peripheral nerve fibers in the sulfatide-deficient mice

1 reference

12 December 2020

Composition and biophysical properties of myelin lipid define the neurological defects in galactocerebroside- and sulfatide-deficient mice

1 reference

12 December 2020

Astrocytes synthesize apolipoprotein E and metabolize apolipoprotein E-containing lipoproteins

1 reference

12 December 2020

Regulation of fish gill Na(+)-K(+)-ATPase by selective sulfatide-enriched raft partitioning during seawater adaptation

1 reference

12 December 2020

Early signs of neurolipidosis-related behavioural alterations in a murine model of metachromatic leukodystrophy.

1 reference

12 December 2020

Metachromatic leukodystrophy: molecular genetics and an animal model

1 reference

12 December 2020

Differential expression of (dihydro)ceramide synthases in mouse brain: oligodendrocyte-specific expression of CerS2/Lass2.

1 reference

12 December 2020

Enzymatic Synthesis of Galactocerebroside by a Galactosyltransferase from Embryonic Chicken Brain

1 reference

12 December 2020

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

1 reference

12 December 2020

Paranodal junction formation and spermatogenesis require sulfoglycolipids

1 reference

12 December 2020

Mammalian Lass6 and its related family members regulate synthesis of specific ceramides

1 reference

12 December 2020

Jamming the endosomal system: lipid rafts and lysosomal storage diseases.

1 reference

12 December 2020

Secondary accumulation of gangliosides in lysosomal storage disorders

1 reference

12 December 2020

Association of the Golgi UDP-galactose transporter with UDP-galactose:ceramide galactosyltransferase allows UDP-galactose import in the endoplasmic reticulum

1 reference

12 December 2020

Bone marrow stem cell-based gene transfer in a mouse model for metachromatic leukodystrophy: effects on visceral and nervous system disease manifestations

1 reference

12 December 2020

Reversal of non-hydroxy:alpha-hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP-galactose:ceramide galactosyltransferase

1 reference

12 December 2020

Increased hippocampal and cortical beta oscillations in mice deficient for the HNK-1 sulfotransferase.

1 reference

12 December 2020

High cholesterol level is essential for myelin membrane growth

1 reference

12 December 2020

The metabolism and function of sphingolipids and glycosphingolipids.

1 reference

12 December 2020

Role of K(ATP) channels in protection against neuronal excitatory insults

1 reference

12 December 2020

Laminin binds specifically to sulfated glycolipids

1 reference

12 December 2020

TRAM, LAG1 and CLN8: members of a novel family of lipid-sensing domains?

1 reference

12 December 2020