Lista de obras - Maria Teresa Carrì - Dominio Público Uruguay

A free cysteine residue at the dimer interface decreases conformational stability of Xenopus laevis copper,zinc superoxide dismutase

artículo científico publicado en 2000

A relationship between replicon size and supercoiled loop domains in the eukaryotic genome.

artículo científico publicado en 1982

ALS: focus on purinergic signalling.

artículo científico publicado en 2011

Abnormal sensitivity of cannabinoid CB1 receptors in the striatum of mice with experimental amyotrophic lateral sclerosis.

artículo científico publicado en 2010

Activation and induction by copper of Cu/Zn superoxide dismutase in Saccharomyces cerevisiae. Presence of an inactive proenzyme in anaerobic yeast

artículo científico publicado en 1991

Altered gene expression, mitochondrial damage and oxidative stress: converging routes in motor neuron degeneration.

artículo científico publicado en 2012

Amyotrophic Lateral Sclerosis: Mechanisms and Countermeasures

artículo científico publicado en 2009

Amyotrophic lateral sclerosis: new insights into underlying molecular mechanisms and opportunities for therapeutic intervention.

artículo científico

An electron microscope study of chromosomal DNA replication in different eukaryotic systems.

artículo científico publicado en 1982

Apoptosome inactivation rescues proneural and neural cells from neurodegeneration.

artículo científico publicado en 2004

Astroglial inhibition of NF-κB does not ameliorate disease onset and progression in a mouse model for amyotrophic lateral sclerosis (ALS)

artículo científico publicado en 2011

Bcl2-A1 interacts with pro-caspase-3: implications for amyotrophic lateral sclerosis.

artículo científico publicado en 2011

Bcl2a1 serves as a switch in death of motor neurons in amyotrophic lateral sclerosis

artículo científico publicado en 2006

Beta-amyloid causes downregulation of calcineurin in neurons through induction of oxidative stress.

artículo científico publicado en 2007

Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase

artículo científico publicado en 2000

Cell death in amyotrophic lateral sclerosis: interplay between neuronal and glial cells.

artículo científico publicado en 2004

Chaperonins dependent increase of Cu,Zn superoxide dismutase production in Escherichia coli

artículo científico publicado en 1993

Chromosome length and DNA loop size during early embryonic development of Xenopus laevis.

artículo científico publicado en 1993

Continuous monitoring of ascorbate transport through neuroblastoma cells with a ruthenium oxide hexacyanoferrate modified microelectrode.

artículo científico publicado en 2008

Copper-dependent oxidative stress, alteration of signal transduction and neurodegeneration in amyotrophic lateral sclerosis.

artículo científico publicado en 2001

Crystal structure of the cyanide-inhibitedXenopus laevisCu,Zn superoxide dismutase at 98 K

artículo científico publicado en 1994

Crystallisation and preliminary crystallographic analysis of recombinant Xenopus laevis Cu,Zn superoxide dismutase b.

artículo científico publicado en 1993

Cu,Zn-superoxide dismutase-dependent apoptosis induced by nitric oxide in neuronal cells

artículo científico publicado en 2000

Cystatin B and SOD1: protein–protein interaction and possible relation to neurodegeneration.

artículo científico publicado en 2014

Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis

artículo científico publicado en 2007

Cysteine Modifications in the Pathogenesis of ALS.

artículo científico publicado en 2017

Differential toxicity of TAR DNA-binding protein 43 isoforms depends on their submitochondrial localization in neuronal cells

artículo científico publicado en 2018

Diverse roles of FUS in Amyotrophic Lateral Sclerosis

artículo científico publicado en 2015

Dynamic NAD(P)H post-synaptic autofluorescence signals for the assessment of mitochondrial function in a neurodegenerative disease: monitoring the primary motor cortex of G93A mice, an amyotrophic lateral sclerosis model.

artículo científico publicado en 2009

Effect of Lys→Arg mutation on the thermal stability of Cu,Zn superoxide dismutase: influence on the monomer–dimer equilibrium

artículo científico publicado en 1996

Evaluation of the exposure to biomechanical overload of the upper limbs and clinical investigation in a female population employed in the manual loading of production lines in 2 ceramics factories

scientific article published on 01 November 1996

Evidence for co-regulation of Cu,Zn superoxide dismutase and metallothionein gene expression in yeast through transcriptional control by copper via the ACE 1 factor

artículo científico publicado en 1991

Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials.

artículo científico publicado en 2006

Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS mice.

artículo científico publicado en 2017

Glutaredoxin 1 is a major player in copper metabolism in neuroblastoma cells.

artículo científico publicado en 2013

Glutaredoxin 2 prevents aggregation of mutant SOD1 in mitochondria and abolishes its toxicity.

artículo científico publicado en 2010

Ice-bucket challenge should jolt funding

journal article; published in Nature on 2014-11-19

Impaired copper binding by the H46R mutant of human Cu,Zn superoxide dismutase, involved in amyotrophic lateral sclerosis

scientific article published on 01 December 1994

Impairment of glutamate transport and increased vulnerability to oxidative stress in neuroblastoma SH-SY5Y cells expressing a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis.

artículo científico publicado en 2004

Inactivation of cytochrome c oxidase by mutant SOD1s in mouse motoneuronal NSC-34 cells is independent from copper availability but is because of nitric oxide.

artículo científico publicado en 2009

Increase of Cu,Zn-superoxide dismutase activity during differentiation of human K562 cells involves activation by copper of a constantly expressed copper-deficient protein ⬇️

artículo científico publicado el 25 de diciembre de 1991

Inflammatory cytokines increase mitochondrial damage in motoneuronal cells expressing mutant SOD1.

artículo científico publicado en 2008

LRRK2 affects vesicle trafficking, neurotransmitter extracellular level and membrane receptor localization

artículo científico publicado en 2013

Lessons from models of SOD1-linked familial ALS.

artículo científico publicado en 2004

Metal uptake of recombinant cambialistic superoxide dismutase from Propionibacterium shermanii is affected by growth conditions of host Escherichia coli cells.

artículo científico publicado en 1995

Minocycline for patients with ALS

artículo científico publicado en 2008

Mitochondria and ALS: implications from novel genes and pathways.

artículo científico publicado en 2012

Mitochondria in the nervous system: From health to disease, Part I.

artículo científico publicado en 2017

Mitochondrial dynamism and the pathogenesis of Amyotrophic Lateral Sclerosis.

artículo científico publicado en 2015

Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine.

artículo científico publicado en 2003

Mitochondrial dysfunction in ALS ⬇️

artículo científico publicado el 2 de agosto de 2011

Mitochondrial redox signalling by p66Shc mediates ALS-like disease through Rac1 inactivation

artículo científico publicado en 2011

Mutant SOD1 and mitochondrial damage alter expression and splicing of genes controlling neuritogenesis in models of neurodegeneration.

artículo científico publicado en 2011

Mutation of Lys-120 and Lys-134 drastically reduces the catalytic rate of Cu,Zn superoxide dismutase

artículo científico publicado en 1994

Neurochemistry of SOD1 and familial amyotrophic lateral sclerosis

artículo científico publicado en 2001

Neuronal RNA-binding proteins in health and disease

artículo científico publicado en 2014

Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS.

artículo científico publicado en 2015

Old versus New Mechanisms in the Pathogenesis of ALS.

artículo científico publicado en 2016

Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis.

artículo científico publicado en 2001

Oxidative stress and mitochondrial damage in the pathogenesis of ALS: New perspectives.

artículo científico publicado en 2016

Oxidative stress and mitochondrial damage: importance in non-SOD1 ALS

artículo científico publicado en 2015

Pathways to mitochondrial dysfunction in ALS pathogenesis.

artículo científico publicado en 2016

Primary structure from amino acid and cDNA sequences of two Cu,Zn superoxide dismutase variants from Xenopus laevis

artículo científico publicado en 1989

Pur-alpha functionally interacts with FUS carrying ALS-associated mutations.

artículo científico publicado en 2015

Purification and characterization of Ag,Zn-superoxide dismutase from Saccharomyces cerevisiae exposed to silver

artículo científico publicado en 1994

Resistance to striatal dopamine depletion induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice expressing human mutant Cu,Zn superoxide dismutase.

artículo científico publicado en 2002

Role of LRRK2 in the regulation of dopamine receptor trafficking

artículo científico publicado en 2017

Role of zinc-coordination and of the glutathione redox couple in the redox susceptibility of human transcription factor Sp1.

artículo científico

S-Nitrosoglutathione Reductase Plays Opposite Roles in SH-SY5Y Models of Parkinson's Disease and Amyotrophic Lateral Sclerosis

artículo científico publicado en 2015

SIRT3 and mitochondrial metabolism in neurodegenerative diseases

artículo científico publicado en 2017

SOD1 and mitochondria in ALS: a dangerous liaison.

artículo científico

Structural insights into the multi-determinant aggregation of TDP-43 in motor neuron-like cells.

artículo científico publicado en 2016

Superoxide dismutase 1 modulates expression of transferrin receptor.

artículo científico publicado en 2006

Targets in ALS: designing multidrug therapies.

artículo científico publicado en 2006

Temperature-dependent protein folding in vivo--lower growth temperature increases yield of two genetic variants of Xenopus laevis Cu,Zn superoxide dismutase in Escherichia coli

artículo científico publicado el 14 de agosto de 1992

The Cu,Zn superoxide dismutase isoenzymes of Xenopus laevis: purification, identification of a heterodimer and differential heat sensitivity.

artículo científico publicado en 1990

The NADPH oxidase pathway is dysregulated by the P2X7 receptor in the SOD1-G93A microglia model of amyotrophic lateral sclerosis.

artículo científico publicado en 2013

The intriguing case of motor neuron disease: ALS and SMA come closer.

artículo científico

The proinflammatory action of microglial P2 receptors is enhanced in SOD1 models for amyotrophic lateral sclerosis.

artículo científico publicado en 2009

The relationship between chromosomal origins of replication and the nuclear matrix during the cell cycle

scientific article published on 01 June 1986

The sinister side of Italian soccer.

artículo científico publicado en 2003

The unfolded protein response in models of human mutant G93A amyotrophic lateral sclerosis.

artículo científico publicado en 2012

Three-dimensional structure of Xenopus laevis Cu,Zn superoxide dismutase b determined by X-ray crystallography at 1.5 A resolution.

artículo científico publicado en 1996

Tissue-specific deregulation of selected HDACs characterizes ALS progression in mouse models: pharmacological characterization of SIRT1 and SIRT2 pathways.

artículo científico publicado en 2014

Which TDP-43 aggregates are toxic in ALS?

artículo científico publicado en 2016

Xenopus laevis Cu,Zn superoxide dismutase B cDNA sequence.

artículo científico publicado en 1990

Lista de obras de Maria Teresa Carrì

A free cysteine residue at the dimer interface decreases conformational stability of Xenopus laevis copper,zinc superoxide dismutase

A relationship between replicon size and supercoiled loop domains in the eukaryotic genome.

ALS: focus on purinergic signalling.

Abnormal sensitivity of cannabinoid CB1 receptors in the striatum of mice with experimental amyotrophic lateral sclerosis.

Activation and induction by copper of Cu/Zn superoxide dismutase in Saccharomyces cerevisiae. Presence of an inactive proenzyme in anaerobic yeast

Altered gene expression, mitochondrial damage and oxidative stress: converging routes in motor neuron degeneration.

Amyotrophic Lateral Sclerosis: Mechanisms and Countermeasures

Amyotrophic lateral sclerosis: new insights into underlying molecular mechanisms and opportunities for therapeutic intervention.

An electron microscope study of chromosomal DNA replication in different eukaryotic systems.

Apoptosome inactivation rescues proneural and neural cells from neurodegeneration.

Astroglial inhibition of NF-κB does not ameliorate disease onset and progression in a mouse model for amyotrophic lateral sclerosis (ALS)

Bcl2-A1 interacts with pro-caspase-3: implications for amyotrophic lateral sclerosis.

Bcl2a1 serves as a switch in death of motor neurons in amyotrophic lateral sclerosis

Beta-amyloid causes downregulation of calcineurin in neurons through induction of oxidative stress.

Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase

Cell death in amyotrophic lateral sclerosis: interplay between neuronal and glial cells.

Chaperonins dependent increase of Cu,Zn superoxide dismutase production in Escherichia coli

Chromosome length and DNA loop size during early embryonic development of Xenopus laevis.

Continuous monitoring of ascorbate transport through neuroblastoma cells with a ruthenium oxide hexacyanoferrate modified microelectrode.

Copper-dependent oxidative stress, alteration of signal transduction and neurodegeneration in amyotrophic lateral sclerosis.

Crystal structure of the cyanide-inhibitedXenopus laevisCu,Zn superoxide dismutase at 98 K

Crystallisation and preliminary crystallographic analysis of recombinant Xenopus laevis Cu,Zn superoxide dismutase b.

Cu,Zn-superoxide dismutase-dependent apoptosis induced by nitric oxide in neuronal cells

Cystatin B and SOD1: protein–protein interaction and possible relation to neurodegeneration.

Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis

Cysteine Modifications in the Pathogenesis of ALS.

Differential toxicity of TAR DNA-binding protein 43 isoforms depends on their submitochondrial localization in neuronal cells

Diverse roles of FUS in Amyotrophic Lateral Sclerosis

Dynamic NAD(P)H post-synaptic autofluorescence signals for the assessment of mitochondrial function in a neurodegenerative disease: monitoring the primary motor cortex of G93A mice, an amyotrophic lateral sclerosis model.

Effect of Lys→Arg mutation on the thermal stability of Cu,Zn superoxide dismutase: influence on the monomer–dimer equilibrium

Evaluation of the exposure to biomechanical overload of the upper limbs and clinical investigation in a female population employed in the manual loading of production lines in 2 ceramics factories

Evidence for co-regulation of Cu,Zn superoxide dismutase and metallothionein gene expression in yeast through transcriptional control by copper via the ACE 1 factor

Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials.

Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS mice.

Glutaredoxin 1 is a major player in copper metabolism in neuroblastoma cells.

Glutaredoxin 2 prevents aggregation of mutant SOD1 in mitochondria and abolishes its toxicity.

Ice-bucket challenge should jolt funding

Impaired copper binding by the H46R mutant of human Cu,Zn superoxide dismutase, involved in amyotrophic lateral sclerosis

Impairment of glutamate transport and increased vulnerability to oxidative stress in neuroblastoma SH-SY5Y cells expressing a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis.

Inactivation of cytochrome c oxidase by mutant SOD1s in mouse motoneuronal NSC-34 cells is independent from copper availability but is because of nitric oxide.

Increase of Cu,Zn-superoxide dismutase activity during differentiation of human K562 cells involves activation by copper of a constantly expressed copper-deficient protein ⬇️

Inflammatory cytokines increase mitochondrial damage in motoneuronal cells expressing mutant SOD1.

LRRK2 affects vesicle trafficking, neurotransmitter extracellular level and membrane receptor localization

Lessons from models of SOD1-linked familial ALS.

Metal uptake of recombinant cambialistic superoxide dismutase from Propionibacterium shermanii is affected by growth conditions of host Escherichia coli cells.

Minocycline for patients with ALS

Mitochondria and ALS: implications from novel genes and pathways.

Mitochondria in the nervous system: From health to disease, Part I.

Mitochondrial dynamism and the pathogenesis of Amyotrophic Lateral Sclerosis.

Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine.

Mitochondrial dysfunction in ALS ⬇️

Mitochondrial redox signalling by p66Shc mediates ALS-like disease through Rac1 inactivation

Mutant SOD1 and mitochondrial damage alter expression and splicing of genes controlling neuritogenesis in models of neurodegeneration.

Mutation of Lys-120 and Lys-134 drastically reduces the catalytic rate of Cu,Zn superoxide dismutase

Neurochemistry of SOD1 and familial amyotrophic lateral sclerosis

Neuronal RNA-binding proteins in health and disease

Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS.

Old versus New Mechanisms in the Pathogenesis of ALS.

Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis.

Oxidative stress and mitochondrial damage in the pathogenesis of ALS: New perspectives.

Oxidative stress and mitochondrial damage: importance in non-SOD1 ALS

Pathways to mitochondrial dysfunction in ALS pathogenesis.

Primary structure from amino acid and cDNA sequences of two Cu,Zn superoxide dismutase variants from Xenopus laevis

Pur-alpha functionally interacts with FUS carrying ALS-associated mutations.

Purification and characterization of Ag,Zn-superoxide dismutase from Saccharomyces cerevisiae exposed to silver

Resistance to striatal dopamine depletion induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice expressing human mutant Cu,Zn superoxide dismutase.

Role of LRRK2 in the regulation of dopamine receptor trafficking

Role of zinc-coordination and of the glutathione redox couple in the redox susceptibility of human transcription factor Sp1.

S-Nitrosoglutathione Reductase Plays Opposite Roles in SH-SY5Y Models of Parkinson's Disease and Amyotrophic Lateral Sclerosis

SIRT3 and mitochondrial metabolism in neurodegenerative diseases

SOD1 and mitochondria in ALS: a dangerous liaison.

Structural insights into the multi-determinant aggregation of TDP-43 in motor neuron-like cells.

Superoxide dismutase 1 modulates expression of transferrin receptor.

Targets in ALS: designing multidrug therapies.

Temperature-dependent protein folding in vivo--lower growth temperature increases yield of two genetic variants of Xenopus laevis Cu,Zn superoxide dismutase in Escherichia coli

The Cu,Zn superoxide dismutase isoenzymes of Xenopus laevis: purification, identification of a heterodimer and differential heat sensitivity.

The NADPH oxidase pathway is dysregulated by the P2X7 receptor in the SOD1-G93A microglia model of amyotrophic lateral sclerosis.

The intriguing case of motor neuron disease: ALS and SMA come closer.

The proinflammatory action of microglial P2 receptors is enhanced in SOD1 models for amyotrophic lateral sclerosis.