Lista de obras - Giuseppe Fiermonte - Dominio Público Uruguay

A new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): a clinical, molecular, and functional study

scientific article published on 25 August 2011

A novel member of solute carrier family 25 (SLC25A42) is a transporter of coenzyme A and adenosine 3',5'-diphosphate in human mitochondria

artículo científico publicado en 2009

Abundant bacterial expression and reconstitution of an intrinsic membrane-transport protein from bovine mitochondria

artículo científico publicado en 1993

An adult with type 2 citrullinemia presenting in Europe

artículo científico publicado en 2008

Assignment of the human dicarboxylate carrier gene (DIC) to chromosome 17 band 17q25.3

artículo científico publicado en 1998

Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster.

artículo científico publicado en 2016

Citrin deficiency, a perplexing global disorder.

artículo científico publicado en 2008

Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells.

artículo científico publicado en 2017

Expression in Escherichia coli, functional characterization, and tissue distribution of isoforms A and B of the phosphate carrier from bovine mitochondria

scientific article published on 01 August 1998

Functional characterization of the partially purified Sac1p independent adenine nucleotide transport system (ANTS) from yeast endoplasmic reticulum

artículo científico publicado en 2018

Genomic organization and mapping of the gene (SLC25A19) encoding the human mitochondrial deoxynucleotide carrier (DNC).

artículo científico publicado en 2001

Glutamine-Derived Aspartate Biosynthesis in Cancer Cells: Role of Mitochondrial Transporters and New Therapeutic Perspectives

artículo científico publicado en 2022

ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins

artículo científico publicado en 2018

ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins

artículo científico publicado en 2018

Identification and functions of new transporters in yeast mitochondria.

artículo científico publicado en 2000

Identification of the human mitochondrial S-adenosylmethionine transporter: bacterial expression, reconstitution, functional characterization and tissue distribution

artículo científico publicado en 2004

Identification of the mitochondrial ATP-Mg/Pi transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution.

artículo científico publicado en 2004

Identification of the mitochondrial glutamate transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms

artículo científico publicado en 2002

Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy

artículo científico publicado en 2004

KRAS-regulated glutamine metabolism requires UCP2-mediated aspartate transport to support pancreatic cancer growth

artículo científico publicado en 2020

MTCH2/MIMP is a major facilitator of tBID recruitment to mitochondria

scientific journal article

Mitochondrial carriers of Ustilago maydis and Aspergillus terreus involved in itaconate production: same physiological role but different biochemical features

artículo científico publicado en 2019

Mitochondrial metabolite transporters.

artículo científico publicado en 1996

Mutant deoxynucleotide carrier is associated with congenital microcephaly

artículo científico publicado en 2002

Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts

artículo científico publicado en 2009

New insights about the structural rearrangements required for substrate translocation in the bovine mitochondrial oxoglutarate carrier

artículo científico publicado en 2016

Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2.

artículo científico publicado en 2016

Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes

artículo científico publicado en 2016

Nucleotide sequence of a human heart cDNA encoding the mitochondrial phosphate carrier

artículo científico publicado en 1991

Organization and sequence of the gene for the human mitochondrial dicarboxylate carrier: evolution of the carrier family

artículo científico publicado en 1999

Recombinant M protein-based ELISA test for detection of antibodies to canine coronavirus.

artículo científico publicado en 2003

Recombinant expression of the Ca(2+)-sensitive aspartate/glutamate carrier increases mitochondrial ATP production in agonist-stimulated Chinese hamster ovary cells

artículo científico publicado en 2003

Riboflavin responsive mitochondrial myopathy is a new phenotype of dihydrolipoamide dehydrogenase deficiency. The chaperon-like effect of vitamin B2

scholarly article by Rosalba Carrozzo published in September 2014

Sequence and pattern of expression of a bovine homologue of a human mitochondrial transport protein associated with Grave's disease.

artículo científico publicado en 1992

The complementary and divergent roles of uncoupling proteins 1 and 3 in thermoregulation.

artículo científico publicado en 2016

The human gene SLC25A29, of solute carrier family 25, encodes a mitochondrial transporter of basic amino acids

artículo científico publicado en 2014

The human mitochondrial deoxynucleotide carrier and its role in the toxicity of nucleoside antivirals

artículo científico publicado en 2001

The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

artículo científico publicado en 2015

The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms

scientific journal article

The mitochondrial oxoglutarate carrier: from identification to mechanism ⬇️

artículo científico publicado el 1 de febrero de 2013

The sequence, bacterial expression, and functional reconstitution of the rat mitochondrial dicarboxylate transporter cloned via distant homologs in yeast and Caenorhabditis elegans

artículo científico publicado en 1998

Tissue-specific expression of the two isoforms of the mitochondrial phosphate carrier in bovine tissues.

artículo científico publicado en 1996

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

scientific article published on 06 January 2014

Yeast mitochondrial carriers: bacterial expression, biochemical identification and metabolic significance.

artículo científico publicado en 2000

Lista de obras de Giuseppe Fiermonte

A new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): a clinical, molecular, and functional study

A novel member of solute carrier family 25 (SLC25A42) is a transporter of coenzyme A and adenosine 3',5'-diphosphate in human mitochondria

Abundant bacterial expression and reconstitution of an intrinsic membrane-transport protein from bovine mitochondria

An adult with type 2 citrullinemia presenting in Europe

Assignment of the human dicarboxylate carrier gene (DIC) to chromosome 17 band 17q25.3

Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster.

Citrin deficiency, a perplexing global disorder.

Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells.

Expression in Escherichia coli, functional characterization, and tissue distribution of isoforms A and B of the phosphate carrier from bovine mitochondria

Functional characterization of the partially purified Sac1p independent adenine nucleotide transport system (ANTS) from yeast endoplasmic reticulum

Genomic organization and mapping of the gene (SLC25A19) encoding the human mitochondrial deoxynucleotide carrier (DNC).

Glutamine-Derived Aspartate Biosynthesis in Cancer Cells: Role of Mitochondrial Transporters and New Therapeutic Perspectives

ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins

ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins

Identification and functions of new transporters in yeast mitochondria.

Identification of the human mitochondrial S-adenosylmethionine transporter: bacterial expression, reconstitution, functional characterization and tissue distribution

Identification of the mitochondrial ATP-Mg/Pi transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution.

Identification of the mitochondrial glutamate transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms

Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy

KRAS-regulated glutamine metabolism requires UCP2-mediated aspartate transport to support pancreatic cancer growth

MTCH2/MIMP is a major facilitator of tBID recruitment to mitochondria

Mitochondrial carriers of Ustilago maydis and Aspergillus terreus involved in itaconate production: same physiological role but different biochemical features

Mitochondrial metabolite transporters.

Mutant deoxynucleotide carrier is associated with congenital microcephaly

Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts

New insights about the structural rearrangements required for substrate translocation in the bovine mitochondrial oxoglutarate carrier

Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2.

Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes

Nucleotide sequence of a human heart cDNA encoding the mitochondrial phosphate carrier

Organization and sequence of the gene for the human mitochondrial dicarboxylate carrier: evolution of the carrier family

Recombinant M protein-based ELISA test for detection of antibodies to canine coronavirus.

Recombinant expression of the Ca(2+)-sensitive aspartate/glutamate carrier increases mitochondrial ATP production in agonist-stimulated Chinese hamster ovary cells

Riboflavin responsive mitochondrial myopathy is a new phenotype of dihydrolipoamide dehydrogenase deficiency. The chaperon-like effect of vitamin B2

Sequence and pattern of expression of a bovine homologue of a human mitochondrial transport protein associated with Grave's disease.

The complementary and divergent roles of uncoupling proteins 1 and 3 in thermoregulation.

The human gene SLC25A29, of solute carrier family 25, encodes a mitochondrial transporter of basic amino acids

The human mitochondrial deoxynucleotide carrier and its role in the toxicity of nucleoside antivirals

The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms

The mitochondrial oxoglutarate carrier: from identification to mechanism ⬇️

The sequence, bacterial expression, and functional reconstitution of the rat mitochondrial dicarboxylate transporter cloned via distant homologs in yeast and Caenorhabditis elegans

Tissue-specific expression of the two isoforms of the mitochondrial phosphate carrier in bovine tissues.

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

Yeast mitochondrial carriers: bacterial expression, biochemical identification and metabolic significance.