Diseases caused by defects of mitochondrial carriers: a review
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Suggested guidelines for the diagnosis and management of urea cycle disordersMutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaNutritional and Hormonal Regulation of Citrate and Carnitine/Acylcarnitine Transporters: Two Mitochondrial Carriers Involved in Fatty Acid MetabolismMitochondrial disorders in children: toward development of small-molecule treatment strategiesMitochondrial Glutathione in Diabetic NephropathyResources, challenges and way forward in rare mitochondrial diseases researchMitochondrial disease in childhood: nuclear encodedPower(2): the power of yeast genetics applied to the powerhouse of the cellStrategies of bacterial over expression of membrane transporters relevant in human health: the successful case of the three members of OCTN subfamilyStructures of yeast mitochondrial ADP/ATP carriers support a domain-based alternating-access transport mechanismIdentification and functional characterization of a novel mitochondrial carrier for citrate and oxoglutarate in Saccharomyces cerevisiae.The Mtm1p carrier and pyridoxal 5'-phosphate cofactor trafficking in yeast mitochondria.Heptahelical protein PQLC2 is a lysosomal cationic amino acid exporter underlying the action of cysteamine in cystinosis therapyBiochemical diagnosis of mitochondrial disordersMitochondrial metabolite transportPhysiological and pathological roles of mitochondrial SLC25 carriersThe mechanism of transport by mitochondrial carriers based on analysis of symmetryMTCH2/MIMP is a major facilitator of tBID recruitment to mitochondriaThe evolutionary trajectory of mitochondrial carrier family during metazoan evolutionCardiolipin, a critical determinant of mitochondrial carrier protein assembly and function.The human and mouse SLC25A29 mitochondrial transporters rescue the deficient ornithine metabolism in fibroblasts of patients with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.The human gene SLC25A29, of solute carrier family 25, encodes a mitochondrial transporter of basic amino acids.SLC25A1, or CIC, is a novel transcriptional target of mutant p53 and a negative tumor prognostic markerPotential Use of Chemoprotectants against the Toxic Effects of Cyanotoxins: A Review.WormNet v3: a network-assisted hypothesis-generating server for Caenorhabditis elegans.Development of head organizer of the mouse embryo depends on a high level of mitochondrial metabolism.The biochemical properties of the mitochondrial thiamine pyrophosphate carrier from Drosophila melanogaster.Potential therapeutic benefits of strategies directed to mitochondria.Role of carnitine in diseaseMitochondrial uptake of thiamin pyrophosphate: physiological and cell biological aspects.Changes in mitochondrial carriers exhibit stress-specific signatures in INS-1Eβ-cells exposed to glucose versus fatty acids.Carnitine-acylcarnitine translocase deficiency: experience with four cases in Spain and review of the literature.Thiamin uptake by pancreatic acinar cells: effect of chronic alcohol feeding/exposure.Comparative analysis between endometrial proteomes of pregnant and non-pregnant ewes during the peri-implantation period.TMFoldRec: a statistical potential-based transmembrane protein fold recognition tool.Synthesis and cytotoxicity studies of 1-propenyl-1,3-dihydro-benzimidazol-2-one.Molecular Basis of MgATP Selectivity of the Mitochondrial SCaMC Carrier.Subcellular Distribution of NAD+ between Cytosol and Mitochondria Determines the Metabolic Profile of Human Cells.OXPHOS mutations and neurodegenerationThe mitochondrial citrate transporter, CIC, is essential for mitochondrial homeostasis.
P2860
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P2860
Diseases caused by defects of mitochondrial carriers: a review
description
2008 nî lūn-bûn
@nan
2008 թուականին հրատարակուած գիտական յօդուած
@hyw
2008 թվականին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Diseases caused by defects of mitochondrial carriers: a review
@ast
Diseases caused by defects of mitochondrial carriers: a review
@en
Diseases caused by defects of mitochondrial carriers: a review
@nl
type
label
Diseases caused by defects of mitochondrial carriers: a review
@ast
Diseases caused by defects of mitochondrial carriers: a review
@en
Diseases caused by defects of mitochondrial carriers: a review
@nl
prefLabel
Diseases caused by defects of mitochondrial carriers: a review
@ast
Diseases caused by defects of mitochondrial carriers: a review
@en
Diseases caused by defects of mitochondrial carriers: a review
@nl
P3181
P1476
Diseases caused by defects of mitochondrial carriers: a review
@en
P2093
Ferdinando Palmieri
P304
P3181
P356
10.1016/J.BBABIO.2008.03.008
P407
P577
2008-01-01T00:00:00Z