Cesare Indiveri mainly focuses on Biochemistry, Liposome, Chromatography, Carnitine and Mitochondrion. In most of his Biochemistry studies, his work intersects topics such as Molecular biology. His research in Liposome focuses on subjects like Substrate, which are connected to Elution, Inner membrane and Catalysis.
His Chromatography research is multidisciplinary, incorporating elements of Synthetic membrane, Molecular mass, Cardiolipin, Polyacrylamide gel electrophoresis and Citrulline. His studies deal with areas such as Membrane and Carnitine transport as well as Carnitine. His Mitochondrion study integrates concerns from other disciplines, such as Glutamine transport, Glutaminase and Anaerobic glycolysis.
Biochemistry, Transporter, Carnitine, Amino acid and Antiporter are his primary areas of study. His work on Biochemistry deals in particular with Mitochondrion, Cysteine, Liposome, Glutamine and Amino acid transporter. His work on Organic cation transport proteins as part of his general Transporter study is frequently connected to Acetylcholine transport, thereby bridging the divide between different branches of science.
The study incorporates disciplines such as Membrane transport, Mutant, Site-directed mutagenesis and Carnitine transport in addition to Carnitine. His work in the fields of CD98 overlaps with other areas such as Molecular dynamics. His work in Antiporter addresses issues such as Citrulline, which are connected to fields such as Nigericin.
His main research concerns Biochemistry, Transporter, Amino acid, Amino acid transporter and Carnitine. Biochemistry is represented through his Membrane transport, Cysteine, Recombinant DNA, Glutamine and Mutant research. The concepts of his Transporter study are interwoven with issues in Sialic acid, Cholesterol and Function.
The various areas that Cesare Indiveri examines in his Amino acid study include Large Neutral Amino Acid-Transporter 1, Riboflavin, Antiporter and Metabolism. His Amino acid transporter research incorporates elements of SLC22A5, Binding site, Arginine, Stereochemistry and Energy metabolism. His Carnitine research includes themes of Transport protein, Inner mitochondrial membrane, Peroxisome, Kidney and Western blot.
His primary scientific interests are in Biochemistry, Transporter, Amino acid, Amino acid transporter and Glutamine. His Biochemistry study frequently intersects with other fields, such as Drug. His Transporter research integrates issues from Carnitine and Escherichia coli.
As part of one scientific family, Cesare Indiveri deals mainly with the area of Carnitine, narrowing it down to issues related to the SLC22A5, and often Transport protein. His Amino acid study combines topics from a wide range of disciplines, such as Pharmacophore, Stereochemistry, Docking and Antiporter. His studies in Amino acid transporter integrate themes in fields like Alanine, Virtual screening, Cysteine and Binding site.
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SLC38A9 is a component of the lysosomal amino acid sensing machinery that controls mTORC1
Manuele Rebsamen;Lorena Pochini;Taras Stasyk;Mariana E. G. de Araújo.
Nature (2015)
PNPLA3 has retinyl-palmitate lipase activity in human hepatic stellate cells
Carlo Pirazzi;Luca Valenti;Benedetta Maria Motta;Piero Pingitore.
Human Molecular Genetics (2014)
Mitochondrial metabolite carrier proteins: purification, reconstitution, and transport studies.
Ferdinando Palmieri;Cesare Indiveri;Faustino Bisaccia;Vito Iacobazzi.
Methods in Enzymology (1995)
Membrane transporters for the special amino acid glutamine: structure/function relationships and relevance to human health
Lorena Pochini;Mariafrancesca Scalise;Michele Galluccio;Cesare Indiveri.
Frontiers in Chemistry (2014)
Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder
Dora C. Tărlungeanu;Elena Deliu;Christoph P. Dotter;Majdi Kara.
Cell (2016)
The mitochondrial carnitine/acylcarnitine carrier: Function, structure and physiopathology
Cesare Indiveri;Vito Iacobazzi;Annamaria Tonazzi;Nicola Giangregorio.
Molecular Aspects of Medicine (2011)
Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function.
Piero Pingitore;Carlo Pirazzi;Rosellina Margherita Mancina;Benedetta Maria Motta.
Biochimica et Biophysica Acta (2014)
Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient
Marjan Huizing;Vito Iacobazzi;Lodewijk IJlst;Paul Savelkoul.
American Journal of Human Genetics (1997)
The mitochondrial carnitine carrier protein: cDNA cloning, primary structure and comparison with other mitochondrial transport proteins.
Cesare Indiveri;Vito Iacobazzi;Nicola Giangregorio;Ferdinando Palmieri.
Biochemical Journal (1997)
Mitochondrial metabolite transporters
F. Palmieri;F. Bisaccia;L. Capobianco;V. Dolce.
Biochimica et Biophysica Acta (1996)
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