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Original

Functional characterization of residues within the carnitine/acylcarnitine translocase RX2PANAAXF distinct motif

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Pages 152-163 | Received 09 May 2007, Published online: 09 Jul 2009

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Magnus Monné, Ferdinando Palmieri & Edmund R. S. Kunji. (2013) The substrate specificity of mitochondrial carriers: Mutagenesis revisited. Molecular Membrane Biology 30:2, pages 149-159.
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Magnus Monné & Ferdinando Palmieri. 2014. Exchangers. Exchangers 289 320 .
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Cesare Indiveri, Vito Iacobazzi, Annamaria Tonazzi, Nicola Giangregorio, Vittoria Infantino, Paolo Convertini, Lara Console & Ferdinando Palmieri. (2011) The mitochondrial carnitine/acylcarnitine carrier: Function, structure and physiopathology. Molecular Aspects of Medicine 32:4-6, pages 223-233.
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Nicola Giangregorio, Annamaria Tonazzi, Lara Console, Cesare Indiveri & Ferdinando Palmieri. (2010) Site-directed mutagenesis of charged amino acids of the human mitochondrial carnitine/acylcarnitine carrier: Insight into the molecular mechanism of transport. Biochimica et Biophysica Acta (BBA) - Bioenergetics 1797:6-7, pages 839-845.
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Ferdinando Palmieri & Ciro Leonardo Pierri. (2010) Structure and function of mitochondrial carriers - Role of the transmembrane helix P and G residues in the gating and transport mechanism. FEBS Letters 584:9, pages 1931-1939.
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Annamaria Tonazzi, Nicola Giangregorio, Cesare Indiveri & Ferdinando Palmieri. (2009) Site-directed mutagenesis of the His residues of the rat mitochondrial carnitine/acylcarnitine carrier: Implications for the role of His-29 in the transport pathway. Biochimica et Biophysica Acta (BBA) - Bioenergetics 1787:8, pages 1009-1015.
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Alessandra Tessa, Giuseppe Fiermonte, Carlo Dionisi-Vici, Eleonora Paradies, Matthias R. Baumgartner, Yin-Hsiu Chien, Carmela Loguercio, Helene Ogier de Baulny, Marie-Cecile Nassogne, Manuel Schiff, Federica Deodato, Giancarlo Parenti, S. Lane Rutledge, M. Antonia Vilaseca, Mariarosa A.B. Melone, Gioacchino Scarano, Luiz Aldamiz-Echevarría, Guy Besley, John Walter, Eugenia Martinez-Hernandez, Jose M. Hernandez, Ciro L. Pierri, Ferdinando Palmieri & Filippo M. Santorelli. (2009) Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study . Human Mutation 30:5, pages 741-748.
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Ferdinando Palmieri. (2008) Diseases caused by defects of mitochondrial carriers: A review. Biochimica et Biophysica Acta (BBA) - Bioenergetics 1777:7-8, pages 564-578.
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