Mitochondrial transporters for ornithine and related amino acids: a review

Asymmetric Dimethylarginine (ADMA) in cardiovascular and renal disease

(2015) Patrícia Nessralla Alpoim et al.   CLINICA CHIMICA ACTA

Pathogenic potential of SLC25A15 mutations assessed by transport assays and complementation of Saccharomyces cerevisiae ORT1 null mutant

(2015) Carlo M.T. Marobbio et al.   MOLECULAR GENETICS AND METABOLISM

The hyperornithinemia–hyperammonemia-homocitrullinuria syndrome

(2015) Diego Martinelli et al.   Orphanet Journal of Rare Diseases

Nitric oxide and mitochondria in metabolic syndrome

(2015) Larisa Litvinova et al.   Frontiers in Physiology

The HumanSLC25A33andSLC25A36Genes of Solute Carrier Family 25 Encode Two Mitochondrial Pyrimidine Nucleotide Transporters

(2014) Maria Antonietta Di Noia et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The Human GeneSLC25A29, of Solute Carrier Family 25, Encodes a Mitochondrial Transporter of Basic Amino Acids

(2014) Vito Porcelli et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mitochondrial transporters of the SLC25 family and associated diseases: a review

(2014) Ferdinando Palmieri   JOURNAL OF INHERITED METABOLIC DISEASE

A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: Functional analysis of the mutant protein

(2014) Nagehan Ersoy Tunalı et al.   MOLECULAR GENETICS AND METABOLISM

Homoarginine, kidney function and cardiovascular mortality risk

(2014) A. Tomaschitz et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

UCP2 transports C4 metabolites out of mitochondria, regulating glucose and glutamine oxidation

(2014) A. Vozza et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Structures of yeast mitochondrial ADP/ATP carriers support a domain-based alternating-access transport mechanism

(2014) J. J. Ruprecht et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

BASIC AMINO ACID CARRIER 2 gene expression modulates arginine and urea content and stress recovery in Arabidopsis leaves

(2014) Séverine Planchais et al.   Frontiers in Plant Science

The Saccharomyces cerevisiae gene YPR011c encodes a mitochondrial transporter of adenosine 5′-phosphosulfate and 3′-phospho-adenosine 5′-phosphosulfate

(2013) Simona Todisco et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Genome-Wide Association Study Identifies 3 Genomic Loci Significantly Associated With Serum Levels of Homoarginine

(2013) Marcus E. Kleber et al.   Circulation-Cardiovascular Genetics

Neuronal Nitric Oxide Synthase and Sympathetic Nerve Activity in Neurovascular and Metabolic Systems

(2013) Yutang Wang et al.   CURRENT NEUROVASCULAR RESEARCH

The mitochondrial oxoglutarate carrier: from identification to mechanism

(2012) Magnus Monné et al.   JOURNAL OF BIOENERGETICS AND BIOMEMBRANES

The peroxisomal NAD+ carrier of Arabidopsis thaliana transports coenzyme A and its derivatives

(2012) Gennaro Agrimi et al.   JOURNAL OF BIOENERGETICS AND BIOMEMBRANES

Substrate Specificity of the Two Mitochondrial Ornithine Carriers Can Be Swapped by Single Mutation in Substrate Binding Site

(2012) Magnus Monné et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The mitochondrial transporter family SLC25: Identification, properties and physiopathology

(2012) Ferdinando Palmieri   MOLECULAR ASPECTS OF MEDICINE

The substrate specificity of mitochondrial carriers: Mutagenesis revisited

(2012) Magnus Monné et al.   MOLECULAR MEMBRANE BIOLOGY

Evolution, structure and function of mitochondrial carriers: a review with new insights

(2011) Ferdinando Palmieri et al.   PLANT JOURNAL

Homoarginine, Cardiovascular Risk, and Mortality

(2010) Winfried März et al.   CIRCULATION

Mitochondrial metabolite transport

(2010) Ferdinando Palmieri et al.   Essays in Biochemistry

Mutations in the Hyperosmotic Stress-Responsive Mitochondrial BASIC AMINO ACID CARRIER2 Enhance Proline Accumulation in Arabidopsis

(2010) I. Toka et al.   PLANT PHYSIOLOGY

Amino acids: metabolism, functions, and nutrition

(2009) Guoyao Wu   AMINO ACIDS

Structure and function of mitochondrial carriers - Role of the transmembrane helix P and G residues in the gating and transport mechanism

(2009) Ferdinando Palmieri et al.   FEBS LETTERS

Identification of novel mutations in theSLC25A15gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study

(2009) Alessandra Tessa et al.   HUMAN MUTATION

Molecular Identification and Functional Characterization ofArabidopsis thalianaMitochondrial and Chloroplastic NAD+Carrier Proteins

(2009) Ferdinando Palmieri et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The Human and Mouse SLC25A29 Mitochondrial Transporters Rescue the Deficient Ornithine Metabolism in Fibroblasts of Patients With the Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome

(2009) Josée A Camacho et al.   PEDIATRIC RESEARCH

Diseases caused by defects of mitochondrial carriers: A review

(2008) Ferdinando Palmieri   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Endothelial Arginase II

(2008) Sungwoo Ryoo et al.   CIRCULATION RESEARCH

Peroxisomal ATP Import Is Essential for Seedling Development in Arabidopsis thaliana

(2008) N. Linka et al.   PLANT CELL

Proteomic Identification and Characterization of a Novel Peroxisomal Adenine Nucleotide Transporter Supplying ATP for Fatty Acid  -Oxidation in Soybean and Arabidopsis

(2008) Y. Arai et al.   PLANT CELL

Identification of a Novel Adenine Nucleotide Transporter in the Endoplasmic Reticulum of Arabidopsis

(2008) M. Leroch et al.   PLANT CELL

Characterization of the Arabidopsis Brittle1 transport protein and impact of reduced activity on plant metabolism

(2008) Simon Kirchberger et al.   PLANT JOURNAL

Novel Proteins, Putative Membrane Transporters, and an Integrated Metabolic Network Are Revealed by Quantitative Proteomic Analysis of Arabidopsis Cell Culture Peroxisomes

(2008) H. Eubel et al.   PLANT PHYSIOLOGY

Hyperornithinemia–hyperammonemia–homocitrullinuria syndrome with stroke-like imaging presentation: Clinical, biochemical and molecular analysis

(2007) Zuhair N. Al-Hassnan et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES