Lista de obras -

A switch in metabolism precedes increased mitochondrial biogenesis in respiratory chain-deficient mouse hearts

artículo científico publicado en 2004

Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons

artículo científico publicado en 2011

Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome

artículo científico publicado en 2011

Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo

artículo científico publicado en 2019

Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo

artículo científico publicado en 2011

Increased mitochondrial mass in mitochondrial myopathy mice

artículo científico publicado en 2002

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs

artículo científico publicado en 2012

MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulation

scientific journal article

MTERF3 is a negative regulator of mammalian mtDNA transcription

artículo científico publicado en 2007

MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals

artículo científico publicado en 2013

MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome

artículo científico publicado en 2011

Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcription

artículo científico publicado en 2010

Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome

artículo científico publicado en 2009

MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome

artículo científico publicado en 2008

Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy.

artículo científico publicado en 2012

Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

artículo científico publicado en 2012

Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance

artículo científico publicado en 2006

SOD2 overexpression: enhanced mitochondrial tolerance but absence of effect on UCP activity

artículo científico publicado en 2005

Secondary metabolic effects in complex I deficiency

artículo científico publicado en 2005

Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene

artículo científico publicado en 2009

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production

artículo científico publicado en 2005

TEFM regulates both transcription elongation and RNA processing in mitochondria.

artículo científico publicado en 2019

The bicoid stability factor controls polyadenylation and expression of specific mitochondrial mRNAs in Drosophila melanogaster

artículo científico publicado en 2011

Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion

artículo científico publicado en 2010

Lista de obras de

A switch in metabolism precedes increased mitochondrial biogenesis in respiratory chain-deficient mouse hearts

Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons

Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome

Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo

Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo

Increased mitochondrial mass in mitochondrial myopathy mice

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs

MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulation

MTERF3 is a negative regulator of mammalian mtDNA transcription

MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals

MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome

Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcription

Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome

MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome

Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy.

Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance

SOD2 overexpression: enhanced mitochondrial tolerance but absence of effect on UCP activity

Secondary metabolic effects in complex I deficiency

Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production

TEFM regulates both transcription elongation and RNA processing in mitochondria.

The bicoid stability factor controls polyadenylation and expression of specific mitochondrial mRNAs in Drosophila melanogaster

Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion