Reactome | Fiermonte, G

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Fiermonte, G Show undefined attributes

created	[InstanceEdit:372446] D'Eustachio, P, 2008-06-26 18:02:55
dbId	372488
displayName	Fiermonte, G
firstname	Giuseppe
initial	G
modified	[InstanceEdit:8855056] D'Eustachio, Peter, 2016-01-30
publications	[LiteratureReference:9837338] A novel member of solute carrier family 25 (SLC25A42) is a transporter of coenzyme A and adenosine 3',5'-diphosphate in human mitochondria [LiteratureReference:372484] Identification of the human mitochondrial oxodicarboxylate carrier. Bacterial expression, reconstitution, functional characterization, tissue distribution, and chromosomal location [LiteratureReference:374019] The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms [LiteratureReference:8875620] Identification of the mitochondrial glutamate transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms [LiteratureReference:372842] Organization and sequence of the gene for the human mitochondrial dicarboxylate carrier: evolution of the carrier family [LiteratureReference:9959723] Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study [LiteratureReference:8959787] The human gene SLC25A29, of solute carrier family 25, encodes a mitochondrial transporter of basic amino acids [LiteratureReference:8855055] Identification of the human mitochondrial S-adenosylmethionine transporter: bacterial expression, reconstitution, functional characterization and tissue distribution [LiteratureReference:8875837] Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy [LiteratureReference:9959738] The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
schemaClass	Person
surname	Fiermonte

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