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Journal Abstract Search

320 related items for PubMed ID: 22020112

  • 1. The mitochondrial carnitine/acylcarnitine carrier: function, structure and physiopathology.
    Indiveri C, Iacobazzi V, Tonazzi A, Giangregorio N, Infantino V, Convertini P, Console L, Palmieri F.
    Mol Aspects Med; 2011 Aug; 32(4-6):223-33. PubMed ID: 22020112
    [Abstract] [Full Text] [Related]

  • 2. Carnitine-acylcarnitine translocase deficiency, clinical, biochemical and genetic aspects.
    Rubio-Gozalbo ME, Bakker JA, Waterham HR, Wanders RJ.
    Mol Aspects Med; 2004 Aug; 25(5-6):521-32. PubMed ID: 15363639
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  • 3. Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency.
    Iacobazzi V, Invernizzi F, Baratta S, Pons R, Chung W, Garavaglia B, Dionisi-Vici C, Ribes A, Parini R, Huertas MD, Roldan S, Lauria G, Palmieri F, Taroni F.
    Hum Mutat; 2004 Oct; 24(4):312-20. PubMed ID: 15365988
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  • 4. Functional characterization of residues within the carnitine/acylcarnitine translocase RX2PANAAXF distinct motif.
    De Lucas JR, Indiveri C, Tonazzi A, Perez P, Giangregorio N, Iacobazzi V, Palmieri F.
    Mol Membr Biol; 2008 Feb; 25(2):152-63. PubMed ID: 18307102
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  • 7. Identification by site-directed mutagenesis of a hydrophobic binding site of the mitochondrial carnitine/acylcarnitine carrier involved in the interaction with acyl groups.
    Tonazzi A, Console L, Giangregorio N, Indiveri C, Palmieri F.
    Biochim Biophys Acta; 2012 May; 1817(5):697-704. PubMed ID: 22365929
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  • 8. Post-translational modification by acetylation regulates the mitochondrial carnitine/acylcarnitine transport protein.
    Giangregorio N, Tonazzi A, Console L, Indiveri C.
    Mol Cell Biochem; 2017 Feb; 426(1-2):65-73. PubMed ID: 27864727
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  • 11. The human gene SLC25A29, of solute carrier family 25, encodes a mitochondrial transporter of basic amino acids.
    Porcelli V, Fiermonte G, Longo A, Palmieri F.
    J Biol Chem; 2014 May 09; 289(19):13374-84. PubMed ID: 24652292
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  • 12. Evidence for a short-chain carnitine-acylcarnitine translocase in mitochondria specifically related to the metabolism of branched-chain amino acids.
    Roe DS, Roe CR, Brivet M, Sweetman L.
    Mol Genet Metab; 2000 Jan 09; 69(1):69-75. PubMed ID: 10655160
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  • 13. Carnitine and carnitine palmitoyltransferase in fatty acid oxidation and ketosis.
    Hoppel CL.
    Fed Proc; 1982 Oct 09; 41(12):2853-7. PubMed ID: 7128831
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  • 14. Carnitine palmitoyltransferase 2 and carnitine/acylcarnitine translocase are involved in the mitochondrial synthesis and export of acylcarnitines.
    Violante S, Ijlst L, Te Brinke H, Tavares de Almeida I, Wanders RJ, Ventura FV, Houten SM.
    FASEB J; 2013 May 09; 27(5):2039-44. PubMed ID: 23322164
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  • 15. Identification of two novel mutations of the carnitine/acylcarnitine translocase (CACT) gene in a patient with CACT deficiency.
    Ogawa A, Yamamoto S, Kanazawa M, Takayanagi M, Hasegawa S, Kohno Y.
    J Hum Genet; 2000 May 09; 45(1):52-5. PubMed ID: 10697964
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  • 17. The mitochondrial carnitine/acylcarnitine carrier is regulated by hydrogen sulfide via interaction with C136 and C155.
    Giangregorio N, Tonazzi A, Console L, Lorusso I, De Palma A, Indiveri C.
    Biochim Biophys Acta; 2016 Jan 09; 1860(1 Pt A):20-7. PubMed ID: 26459002
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  • 18. Conformation-dependent accessibility of Cys-136 and Cys-155 of the mitochondrial rat carnitine/acylcarnitine carrier to membrane-impermeable SH reagents.
    Giangregorio N, Tonazzi A, Indiveri C, Palmieri F.
    Biochim Biophys Acta; 2007 Nov 09; 1767(11):1331-9. PubMed ID: 17961500
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  • 19. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
    Stanley CA.
    Adv Pediatr; 1987 Nov 09; 34():59-88. PubMed ID: 3318304
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  • 20. Glutathione controls the redox state of the mitochondrial carnitine/acylcarnitine carrier Cys residues by glutathionylation.
    Giangregorio N, Palmieri F, Indiveri C.
    Biochim Biophys Acta; 2013 Nov 09; 1830(11):5299-304. PubMed ID: 23948593
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