Lista de obras - Liliya Euro - Dominio Público Uruguay

ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia

artículo científico publicado en 2017

Atomistic Molecular Dynamics Simulations of Mitochondrial DNA Polymerase γ: Novel Mechanisms of Function and Pathogenesis

artículo científico publicado en 2017

Carrier Frequency of a Common Mutation of Carnitine Palmitoyltransferase 1A Deficiency and Long-Term Follow-Up in Finland ⬇️

artículo científico publicado el 29 de septiembre de 2011

Conserved lysine residues of the membrane subunit NuoM are involved in energy conversion by the proton-pumping NADH:ubiquinone oxidoreductase (Complex I).

artículo científico publicado en 2008

Editing activity for eliminating mischarged tRNAs is essential in mammalian mitochondria

artículo científico publicado en 2017

Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3

artículo científico publicado en 2014

Electrostatic interactions between FeS clusters in NADH:ubiquinone oxidoreductase (Complex I) from Escherichia coli

scientific article published on 13 February 2008

Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy

artículo científico publicado en 2011

High affinity cation-binding sites in Complex I from Escherichia coli.

artículo científico publicado en 2009

Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy

artículo científico publicado en 2018

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism

artículo científico publicado en 2016

Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy

artículo científico publicado en 2012

Muscle NAD+ depletion and Serpina3n as molecular determinants of murine cancer cachexia - the effects of blocking myostatin and activins

artículo científico publicado en 2020

Real-time electron transfer in respiratory complex I

artículo científico publicado en 2008

Redox regulation of GRPEL2 nucleotide exchange factor for mitochondrial HSP70 chaperone

Role of the conserved arginine 274 and histidine 224 and 228 residues in the NuoCD subunit of complex I from Escherichia coli.

artículo científico publicado en 2007

SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease

artículo científico publicado en 2020

Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation

artículo científico publicado en 2015

The role of the invariant glutamate 95 in the catalytic site of Complex I from Escherichia coli.

artículo científico publicado en 2008

Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy

artículo científico publicado en 2013

Lista de obras de Liliya Euro

ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia

Atomistic Molecular Dynamics Simulations of Mitochondrial DNA Polymerase γ: Novel Mechanisms of Function and Pathogenesis

Carrier Frequency of a Common Mutation of Carnitine Palmitoyltransferase 1A Deficiency and Long-Term Follow-Up in Finland ⬇️

Conserved lysine residues of the membrane subunit NuoM are involved in energy conversion by the proton-pumping NADH:ubiquinone oxidoreductase (Complex I).

Editing activity for eliminating mischarged tRNAs is essential in mammalian mitochondria

Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3

Electrostatic interactions between FeS clusters in NADH:ubiquinone oxidoreductase (Complex I) from Escherichia coli

Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy

High affinity cation-binding sites in Complex I from Escherichia coli.

Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism

Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy

Muscle NAD+ depletion and Serpina3n as molecular determinants of murine cancer cachexia - the effects of blocking myostatin and activins

Real-time electron transfer in respiratory complex I

Redox regulation of GRPEL2 nucleotide exchange factor for mitochondrial HSP70 chaperone

Role of the conserved arginine 274 and histidine 224 and 228 residues in the NuoCD subunit of complex I from Escherichia coli.

SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease

Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation

The role of the invariant glutamate 95 in the catalytic site of Complex I from Escherichia coli.

Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy