Lista de obras - Olga Corti - Dominio Público Uruguay

Adenovirus in the brain: recent advances of gene therapy for neurodegenerative diseases.

artículo científico publicado en 1998

Autophagy in neurodegeneration: New insights underpinning therapy for neurological diseases

artículo científico publicado en 2020

Behavioral phenotyping of Parkin-deficient mice: looking for early preclinical features of Parkinson's disease

artículo científico publicado en 2014

Conditional NF-L transgene expression in mice for in vivo analysis of turnover and transport rate of neurofilaments

artículo científico publicado en 2007

Divergent sequences in the 5' region of cDNA suggest alternative splicing as a mechanism for the generation of carnitine acetyltransferases with different subcellular localizations

artículo científico publicado en 1994

ER-stress-associated functional link between Parkin and DJ-1 via a transcriptional cascade involving the tumor suppressor p53 and the spliced X-box binding protein XBP-1.

artículo científico publicado en 2013

Functional interplay between Parkin and Drp1 in mitochondrial fission and clearance

artículo científico publicado en 2014

Integration of genetically modified adult astrocytes into the lesioned rat spinal cord

artículo científico publicado en 2006

Intracerebral tetracycline-dependent regulation of gene expression in grafts of neural precursors.

artículo científico publicado en 1996

Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson disease

artículo científico publicado en 2010

Long-term doxycycline-controlled expression of human tyrosine hydroxylase after direct adenovirus-mediated gene transfer to a rat model of Parkinson's disease.

artículo científico publicado en 1999

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

scientific journal article

Mechanisms of mitochondrial quality control in autosomal recessive Parkinson's disease

artículo científico publicado en 2015

Mitochondrial dysfunctions in Parkinson's disease

artículo científico

Mitochondrial quality control turns out to be the principal suspect in parkin and PINK1-related autosomal recessive Parkinson's disease ⬇️

artículo científico publicado el 30 de noviembre de 2012

Molecular cloning of cDNAs encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1.

artículo científico publicado en 1994

NF-κB pathway controls mitochondrial dynamics.

artículo científico publicado en 2015

Parkin acts as a transcription factor modulating presenilin-1 and presenilin-2 promoter transactivations

artículo científico publicado en 2013

Parkin and Parkinson's: more than homonymy?

artículo científico publicado en 2001

Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathy

artículo científico publicado en 2009

Parkin differently regulates presenilin-1 and presenilin-2 functions by direct control of their promoter transcription

artículo científico publicado en 2013

Parkin occurs in a stable, non-covalent, approximately 110-kDa complex in brain

scientific journal article

Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death.

artículo científico publicado en 2003

Parkin protects dopaminergic neurons from excessive Wnt/beta-catenin signaling

artículo científico publicado en 2009

Parkin, alpha-synuclein and other molecular aspects of Parkinson's disease

artículo científico publicado en 2002

Parkin-knockout mice did not display increased vulnerability to intranasal administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

artículo científico publicado en 2013

Parkinson's disease: what have we learned from the genes responsible for familial forms?

artículo científico publicado en 2003

Phosphoproteomic screening identifies Rab GTPases as novel downstream targets of PINK1.

artículo científico publicado en 2015

Probes of ubiquitin E3 ligases enable systematic dissection of parkin activation

artículo científico publicado en 2016

Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function

artículo científico publicado en 2005

The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations

artículo científico publicado en 2016

The endoplasmic reticulum/mitochondria interface: a subcellular platform for the orchestration of the functions of the PINK1-Parkin pathway?

artículo científico

The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration.

artículo científico publicado en 2003

Tissue- and cell-specific mitochondrial defect in Parkin-deficient mice

artículo científico publicado en 2014

Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease.

artículo científico publicado en 2009

What genetics tells us about the causes and mechanisms of Parkinson's disease

artículo científico

[A versatile ubiquitin ligase: guardian of mitochondrial quality and antibacterial immunity?]

artículo científico publicado en 2014

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

artículo científico publicado en 2016

Lista de obras de Olga Corti

Adenovirus in the brain: recent advances of gene therapy for neurodegenerative diseases.

Autophagy in neurodegeneration: New insights underpinning therapy for neurological diseases

Behavioral phenotyping of Parkin-deficient mice: looking for early preclinical features of Parkinson's disease

Conditional NF-L transgene expression in mice for in vivo analysis of turnover and transport rate of neurofilaments

Divergent sequences in the 5' region of cDNA suggest alternative splicing as a mechanism for the generation of carnitine acetyltransferases with different subcellular localizations

ER-stress-associated functional link between Parkin and DJ-1 via a transcriptional cascade involving the tumor suppressor p53 and the spliced X-box binding protein XBP-1.

Functional interplay between Parkin and Drp1 in mitochondrial fission and clearance

Integration of genetically modified adult astrocytes into the lesioned rat spinal cord

Intracerebral tetracycline-dependent regulation of gene expression in grafts of neural precursors.

Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson disease

Long-term doxycycline-controlled expression of human tyrosine hydroxylase after direct adenovirus-mediated gene transfer to a rat model of Parkinson's disease.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Mechanisms of mitochondrial quality control in autosomal recessive Parkinson's disease

Mitochondrial dysfunctions in Parkinson's disease

Mitochondrial quality control turns out to be the principal suspect in parkin and PINK1-related autosomal recessive Parkinson's disease ⬇️

Molecular cloning of cDNAs encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1.

NF-κB pathway controls mitochondrial dynamics.

Parkin acts as a transcription factor modulating presenilin-1 and presenilin-2 promoter transactivations

Parkin and Parkinson's: more than homonymy?

Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathy

Parkin differently regulates presenilin-1 and presenilin-2 functions by direct control of their promoter transcription

Parkin occurs in a stable, non-covalent, approximately 110-kDa complex in brain

Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death.

Parkin protects dopaminergic neurons from excessive Wnt/beta-catenin signaling

Parkin, alpha-synuclein and other molecular aspects of Parkinson's disease

Parkin-knockout mice did not display increased vulnerability to intranasal administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

Parkinson's disease: what have we learned from the genes responsible for familial forms?

Phosphoproteomic screening identifies Rab GTPases as novel downstream targets of PINK1.

Probes of ubiquitin E3 ligases enable systematic dissection of parkin activation

Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function

The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations

The endoplasmic reticulum/mitochondria interface: a subcellular platform for the orchestration of the functions of the PINK1-Parkin pathway?

The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration.

Tissue- and cell-specific mitochondrial defect in Parkin-deficient mice

Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease.

What genetics tells us about the causes and mechanisms of Parkinson's disease

[A versatile ubiquitin ligase: guardian of mitochondrial quality and antibacterial immunity?]

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)