Related references
Note: Only part of the references are listed.Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation
Sabrina Dusi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
MAM (mitochondria-associated membranes) in mammalian cells: Lipids and beyond
Jean E. Vance
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2014)
Polyunsaturated fatty acids inhibit stimulated coupling between the ER Ca2+ sensor STIM1 and the Ca2+ channel protein Orai1 in a process that correlates with inhibition of stimulated STIM1 oligomerization
David Holowka et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2014)
Pantethine treatment is effective in recovering the disease phenotype induced by ketogenic diet in a pantothenate kinase-associated neurodegeneration mouse model
Dario Brunetti et al.
BRAIN (2014)
Plasma and Erythrocyte Fatty Acids Reflect Intakes of Saturated and n-6 PUFA within a Similar Time Frame
Leanne Hodson et al.
JOURNAL OF NUTRITION (2014)
Plasma phospholipids identify antecedent memory impairment in older adults
Mark Mapstone et al.
NATURE MEDICINE (2014)
Membrane Lipids Tune Synaptic Transmission by Direct Modulation of Presynaptic Potassium Channels
Mario Carta et al.
NEURON (2014)
Efficacy and safety of deferiprone for the treatment of pantothenate kinase-associated neurodegeneration (PKAN) and neurodegeneration with brain iron accumulation (NBIA): Results from a four years follow-up
Giovanni Cossu et al.
PARKINSONISM & RELATED DISORDERS (2014)
Impairment of Drosophila Orthologs of the Human Orphan Protein C19orf12 Induces Bang Sensitivity and Neurodegeneration
Arcangela Iuso et al.
PLOS ONE (2014)
Mitochondrial lipid trafficking
Takashi Tatsuta et al.
TRENDS IN CELL BIOLOGY (2014)
Cell death and diseases related to oxidative stress: 4-hydroxynonenal (HNE) in the balance
S. Dalleau et al.
CELL DEATH AND DIFFERENTIATION (2013)
Disorders of phospholipids, sphingolipids and fatty acids biosynthesis: toward a new category of inherited metabolic diseases
F. Lamari et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2013)
Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism
Cigdem Koroglu et al.
JOURNAL OF MEDICAL GENETICS (2013)
Mitochondria-associated ER membranes in Alzheimer disease
Eric A. Schon et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2013)
Mitochondrial membrane protein associated neurodegenration: A novel variant of neurodegeneration with brain iron accumulation
Eva C. Schulte et al.
MOVEMENT DISORDERS (2013)
Iron metabolism in the CNS: implications for neurodegenerative diseases
Tracey A. Rouault
NATURE REVIEWS NEUROSCIENCE (2013)
Proteomic Mapping of Mitochondria in Living Cells via Spatially Restricted Enzymatic Tagging
Hyun-Woo Rhee et al.
SCIENCE (2013)
Interaction of aldehydes derived from lipid peroxidation and membrane proteins
Stefania Pizzimenti et al.
FRONTIERS IN PHYSIOLOGY (2013)
Disturbed brain phospholipid and docosahexaenoic acid metabolism in calcium-independent phospholipase A2-VIA (iPLA2β)-knockout mice
Yewon Cheon et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2012)
Neurodegeneration with brain iron accumulation Clinical syndromes and neuroimaging
Hyman M. Schipper
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2012)
Severe disturbance in the Ca2 signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6
Mikhail Strokin et al.
HUMAN MOLECULAR GENETICS (2012)
Pantothenate kinase-associated neurodegeneration: altered mitochondria membrane potential and defective respiration in Pank2 knock-out mouse model
Dario Brunetti et al.
HUMAN MOLECULAR GENETICS (2012)
Associations of polyunsaturated fatty acids with residual depression or anxiety in older people with major depression
Ayesha Jadoon et al.
JOURNAL OF AFFECTIVE DISORDERS (2012)
Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations
Valerio Leoni et al.
MOLECULAR GENETICS AND METABOLISM (2012)
A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathy
Rita Horvath et al.
MOVEMENT DISORDERS (2012)
Lipidomics identifies cardiolipin oxidation as a mitochondrial target for redox therapy of brain injury
Jing Ji et al.
NATURE NEUROSCIENCE (2012)
Fats and Factors: Lipid Profiles Associate with Personality Factors and Suicidal History in Bipolar Subjects
Simon J. Evans et al.
PLOS ONE (2012)
Germline Deletion of Pantothenate Kinases 1 and 2 Reveals the Key Roles for CoA in Postnatal Metabolism
Matthew Garcia et al.
PLOS ONE (2012)
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
Monika B. Hartig et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Genetics of Neurodegeneration with Brain Iron Accumulation
Allison Gregory et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2011)
Lipid peroxidation and neurodegenerative disease
Tanea T. Reed
FREE RADICAL BIOLOGY AND MEDICINE (2011)
Central Nervous System Dysfunction in a Mouse Model of FA2H Deficiency
Kathleen A. Potter et al.
GLIA (2011)
The relevance of iron in the pathogenesis of Parkinson's disease
Jeswinder Sian-Huelsmann et al.
JOURNAL OF NEUROCHEMISTRY (2011)
Neuroaxonal Dystrophy in Calcium-Independent Phospholipase A2β Deficiency Results from Insufficient Remodeling and Degeneration of Mitochondrial and Presynaptic Membranes
Goichi Beck et al.
JOURNAL OF NEUROSCIENCE (2011)
2-hydroxylated sphingomyelin profiles in cells from patients with mutated fatty acid 2-hydroxylase
Phyllis Dan et al.
LIPIDS IN HEALTH AND DISEASE (2011)
Sodium Leak Channels in Neuronal Excitability and Rhythmic Behaviors
Dejian Ren
NEURON (2011)
Genetic Ablation of PLA2G6 in Mice Leads to Cerebellar Atrophy Characterized by Purkinje Cell Loss and Glial Cell Activation
Zhengshan Zhao et al.
PLOS ONE (2011)
Three Faces of the Same Gene: FA2H Links Neurodegeneration with Brain Iron Accumulation, Leukodystrophies, and Hereditary Spastic Paraplegias
Susanne A. Schneider et al.
ANNALS OF NEUROLOGY (2010)
Defective FA2H Leads to a Novel Form of Neurodegeneration with Brain Iron Accumulation (NBIA)
Michael C. Kruer et al.
ANNALS OF NEUROLOGY (2010)
Fatty acid 2-Hydroxylation in mammalian sphingolipid biology
Hiroko Hama
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2010)
Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation
L. Timmermann et al.
BRAIN (2010)
Protection of Pancreatic β-Cells by Group VIA Phospholipase A2-Mediated Repair of Mitochondrial Membrane Peroxidation
Zhengshan Zhao et al.
ENDOCRINOLOGY (2010)
Mutation of FA2H Underlies a Complicated Form of Hereditary Spastic Paraplegia (SPG35)
Katherine J. Dick et al.
HUMAN MUTATION (2010)
Fatty Acid 2-Hydroxylase Mediates Diffusional Mobility of Raft-associated Lipids, GLUT4 Level, and Lipogenesis in 3T3-L1 Adipocytes
Lin Guo et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Imaging decreased brain docosahexaenoic acid metabolism and signaling in iPLA2β (VIA)-deficient mice
Mireille Basselin et al.
JOURNAL OF LIPID RESEARCH (2010)
Lipidomics reveals a remarkable diversity of lipids in human plasma
Oswald Quehenberger et al.
JOURNAL OF LIPID RESEARCH (2010)
Cystamine metabolism and brain transport properties: clinical implications for neurodegenerative diseases
Melanie Bousquet et al.
JOURNAL OF NEUROCHEMISTRY (2010)
Pantethine rescues a Drosophila model for pantothenate kinase-associated neurodegeneration
Anil Rana et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Establishment of an Improved Mouse Model for Infantile Neuroaxonal Dystrophy That Shows Early Disease Onset and Bears a Point Mutation in Pla296
Haruka Wada et al.
AMERICAN JOURNAL OF PATHOLOGY (2009)
Cytochrome c/cardiolipin relations in mitochondria: a kiss of death
Valerian E. Kagan et al.
FREE RADICAL BIOLOGY AND MEDICINE (2009)
Fatty acid 2-hydroxylase regulates cAMP-induced cell cycle exit in D6P2T Schwannoma cells
Nathan L. Alderson et al.
JOURNAL OF LIPID RESEARCH (2009)
Working towards an exegesis for lipids in biology
H. Alex Brown et al.
NATURE CHEMICAL BIOLOGY (2009)
Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia
Simon Edvardson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations
Ibrahim Malik et al.
AMERICAN JOURNAL OF PATHOLOGY (2008)
Glucose homeostasis, insulin secretion, and islet phospholipids in mice that overexpress iPLA2β in pancreatic β-cells and in iPLA2β-null mice
Shunzhong Bao et al.
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM (2008)
Oxidative stress and mitochondrial dysfunction in neurodegeneration; cardiolipin a critical target?
Simon Pope et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2008)
Intracellular phospholipase A2 group IVA and group VIA play important roles in Wallerian degeneration and axon regeneration after peripheral nerve injury
Ruben Lopez-Vales et al.
BRAIN (2008)
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease
Jose Bras et al.
FEBS JOURNAL (2008)
De novo CoA biosynthesis is required to maintain DNA integrity during development of the Drosophila nervous system
Floris Bosveld et al.
HUMAN MOLECULAR GENETICS (2008)
Neuroaxonal dystrophy caused by group VIA phospholipase A2 deficiency in mice:: A model of human neurodegenerative disease
Koei Shinzawa et al.
JOURNAL OF NEUROSCIENCE (2008)
Absence of 2-hydroxylated sphingolipids is compatible with normal neural development but causes late-onset axon and myelin sheath degeneration
Inge Zoeller et al.
JOURNAL OF NEUROSCIENCE (2008)
Imaging neuroinflammation in Alzheimer's disease with radiolabeled arachidonic acid and PET
Giuseppe Esposito et al.
JOURNAL OF NUCLEAR MEDICINE (2008)
Orai, STIM1 and iPLA2β:: a view from a different perspective
Victoria M. Bolotina
JOURNAL OF PHYSIOLOGY-LONDON (2008)
Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)
M. A. Kurian et al.
NEUROLOGY (2008)
Thematic review series: Glycerolipids - Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes
Michael Schlame
JOURNAL OF LIPID RESEARCH (2008)
FA2H is responsible for the formation of 2-hydroxy galactolipids in peripheral nervous system myelin
Eduardo N. Maldonado et al.
JOURNAL OF LIPID RESEARCH (2008)
Omega-3 fatty acids as treatments for mental illness: which disorder and which fatty acid?
Brian M. Ross et al.
LIPIDS IN HEALTH AND DISEASE (2007)
Arachidonic acid metabolism in brain physiology and pathology: lessons from genetically altered mouse models
Francesca Bosetti
JOURNAL OF NEUROCHEMISTRY (2007)
Selective early cardiolipin peroxidation after traumatic brain injury: An oxidative lipidomics analysis
Huelya Bayir et al.
ANNALS OF NEUROLOGY (2007)
Resolvin E1 and protectin D1 activate inflammation-resolution programmes
Jan M. Schwab et al.
NATURE (2007)
Deprivation of pantothenic acid elicits a movement disorder and azoospermia in a mouse model of pantothenate kinase-associated neurodegeneration
Y. M. Kuo et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2007)
Bipolar phospholipid sensing by TRPC5 calcium channel
D. J. Beech
BIOCHEMICAL SOCIETY TRANSACTIONS (2007)
Ca2+-independent phospholipase A2-dependent Gating of TRPM8 by lysophospholipids
Fabien Vanden Abeele et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
FA2H-dependent fatty acid 2-hydroxylation in postnatal mouse brain
Nathan L. Alderson et al.
JOURNAL OF LIPID RESEARCH (2006)
PPAR:: a new pharmacological target for neuroprotection in stroke and neurodegenerative diseases
R. Bordet et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2006)
Plasma phosphatidylcholine docosahexaenoic acid content and risk of dementia and Alzheimer disease - The Framingham heart study
Ernst J. Schaefer et al.
ARCHIVES OF NEUROLOGY (2006)
PLA2G6 mutation underlies infantile neuroaxonal dystrophy
Shareef Khateeb et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Calcium-independent phospholipase A2 localizes in and protects mitochondria during apoptotic induction by staurosporine
Konstantin Seleznev et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
Neil V. Morgan et al.
NATURE GENETICS (2006)
Identification of a novel CoA synthase isoform, which is primarily expressed in the brain
I Nemazanyy et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Altered neuronal mitochondrial coenzyme a synthesis in neurodegeneration with brain iron accumulation caused by abnormal processing, stability, and catalytic activity of mutant pantothenate kinase 2
PT Kotzbauer et al.
JOURNAL OF NEUROSCIENCE (2005)
Deficiency of pantothenate kinase 2 (Pank2) in mice leads to retinal degeneration and azoospermia
YM Kuo et al.
HUMAN MOLECULAR GENETICS (2005)
A novel mechanism for the store-operated calcium influx pathway
T Smani et al.
NATURE CELL BIOLOGY (2004)
The human FA2H gene encodes a fatty acid 2-hydroxylase
NL Alderson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Glycerophosphocholine is elevated in cerebrospinal fluid of Alzheimer patients
A Walter et al.
NEUROBIOLOGY OF AGING (2004)
Subcellular localization and regulation of coenzyme a synthase
A Zhyvoloup et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Decreased lysophosphatidylcholine/phosphatidylcholine ratio in cerebrospinal fluid in Alzheimer's disease
C Mulder et al.
JOURNAL OF NEURAL TRANSMISSION (2003)
Apoptotic cells induce migration of phagocytes via caspase-3-mediated release of a lipid attraction signal
K Lauber et al.
CELL (2003)
Novel docosatrienes and 17S-resolvins generated from docosahexaenoic acid in murine brain, human blood, and glial cells -: Autacoids in anti-inflammation
S Hong et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Molecular cloning of CoA synthase - The missing link in CoA biosynthesis
A Zhyvoloup et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome
B Zhou et al.
NATURE GENETICS (2001)
α-synuclein occurs in lipid-rich high molecular weight complexes, binds fatty acids, and shows homology to the fatty acid-binding proteins
R Sharon et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Fatty acid analysis of blood plasma of patients with Alzheimer's disease, other types of dementia, and cognitive impairment
JA Conquer et al.
LIPIDS (2000)
The role of dietary n-6 and n-3 fatty acids in the developing brain
SM Innis
DEVELOPMENTAL NEUROSCIENCE (2000)
Share Paper
