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Microbiota and Neurological Disorders: A Gut Feeling.Iron-sulfur cluster biogenesis in mammalian cells: New insights into the molecular mechanisms of cluster deliveryMitochondrial Bol1 and Bol3 function as assembly factors for specific iron-sulfur proteins.MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis DisorderClinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency.Spectrum of combined respiratory chain defects.Mis-targeting of the mitochondrial protein LIPT2 leads to apoptotic cell deathAssembly of Lipoic Acid on Its Cognate Enzymes: an Extraordinary and Essential Biosynthetic Pathway.Lipoyltransferase 1 Gene Defect Resulting in Fatal Lactic Acidosis in Two Siblings.Roles of Fe-S proteins: from cofactor synthesis to iron homeostasis to protein synthesis.Lipid metabolism in mitochondrial membranes.Lipoic acid and lipoic acid analogs in cancer metabolism and chemotherapy.The spectrum of pyruvate oxidation defects in the diagnosis of mitochondrial disorders.Epigenetic Treatment of Neurodegenerative Disorders: Alzheimer and Parkinson Diseases.Immunomodulatory activities of alpha lipoic acid with a special focus on its efficacy in preventing miscarriage.Differential diagnosis of lipoic acid synthesis defects.Novel compound heterozygous LIAS mutations cause glycine encephalopathy.IBA57 mutations abrogate iron-sulfur cluster assembly leading to cavitating leukoencephalopathy.Bioprotective carnitinoids: lipoic acid, butyrate, and mitochondria-targeting to treat radiation injury: mitochondrial drugs come of age.Lipoic acid metabolism and mitochondrial redox regulation.Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy.Epigenetic Treatment of Neurodegenerative Ophthalmic Disorders: An Eye Toward the Future.The Antioxidant Cofactor Alpha-Lipoic Acid May Control Endogenous Formaldehyde Metabolism in Mammals.In Vivo Roles of Fatty Acid Biosynthesis Enzymes in Biosynthesis of Biotin and α-Lipoic Acid in Corynebacterium glutamicum.A novel synthetic chemical entity (UPEI-800) is neuroprotective in vitro and in an in vivo rat model of oxidative stress.Iron Sulfur and Molybdenum Cofactor Enzymes Regulate the Drosophila Life Cycle by Controlling Cell Metabolism.Suppression of a cancer stem-like phenotype mediated by alpha-lipoic acid in human lung cancer cells through down-regulation of β-catenin and Oct-4.Acute loss of iron-sulfur clusters results in metabolic reprogramming and generation of lipid droplets in mammalian cells.Protein moonlighting elucidates the essential human pathway catalyzing lipoic acid assembly on its cognate enzymes
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Lipoic acid biosynthesis defects.
@en
type
label
Lipoic acid biosynthesis defects.
@en
prefLabel
Lipoic acid biosynthesis defects.
@en
P2093
P2860
P1476
Lipoic acid biosynthesis defects
@en
P2093
Antonia Ribes
René G Feichtinger
Wolfgang Sperl
P2860
P2888
P304
P356
10.1007/S10545-014-9705-8
P577
2014-04-29T00:00:00Z
P5875
P6179
1009257492