Lista de obras - Diana Zala - Dominio Público Uruguay

Allele-specific silencing of mutant huntingtin in rodent brain and human stem cells

artículo científico publicado en 2014

B13 axonal transport, energy supply and huntingtin

CA150 expression delays striatal cell death in overexpression and knock-in conditions for mutant huntingtin neurotoxicity.

artículo científico publicado en 2006

Dysregulation of gene expression in primary neuron models of Huntington's disease shows that polyglutamine-related effects on the striatal transcriptome may not be dependent on brain circuitry.

artículo científico publicado en 2008

Genetic and pharmacological inhibition of calcineurin corrects the BDNF transport defect in Huntington's disease

artículo científico publicado en 2009

Huntingtin is required for mitotic spindle orientation and mammalian neurogenesis

artículo científico publicado en 2010

Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons

artículo científico publicado en 2008

Huntingtin's function in axonal transport is conserved in Drosophila melanogaster

artículo científico publicado en 2013

Huntington's disease: from huntingtin function and dysfunction to therapeutic strategies.

artículo científico publicado en 2006

Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin

artículo científico publicado en 2006

Lentiviral-mediated gene transfer to model triplet repeat disorders

artículo científico publicado en 2004

Long-term lentiviral-mediated expression of ciliary neurotrophic factor in the striatum of Huntington's disease transgenic mice

artículo científico publicado en 2004

Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway

scientific journal article

Modulation of AMPA receptor surface diffusion restores hippocampal plasticity and memory in Huntington's disease models

artículo científico publicado en 2018

Mutant Huntingtin alters retrograde transport of TrkB receptors in striatal dendrites.

artículo científico publicado en 2013

NanoPaint: A Tool for Rapid and Dynamic Imaging of Membrane Structural Plasticity at the Nanoscale

scientific article published on 03 October 2019

Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease.

artículo científico publicado en 2001

Phosphorylation of mutant huntingtin at S421 restores anterograde and retrograde transport in neurons.

artículo científico publicado en 2008

Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment

artículo científico publicado en 2005

Releasing the brake: restoring fast axonal transport in neurodegenerative disorders.

artículo científico

S.04.03 BDNF/TrkB signaling, axonal and dendritic transport and neurodegeneration in Huntington's disease

Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport.

artículo científico publicado en 2016

Sulfobetaine-Vinylimidazole Block Copolymers: A Robust Quantum Dot Surface Chemistry Expanding Bioimaging's Horizons

artículo científico publicado en 2015

The advantage of channeling nucleotides for very processive functions

artículo científico publicado en 2017

Unexpected link between Huntington disease and Rett syndrome

artículo científico publicado en 2012

Vapor Pressure and Liquid Heat Capacity of Perhydroacenaphthylene and Perhydrophenanthrene

Vesicular glycolysis provides on-board energy for fast axonal transport

artículo científico publicado en 2013

Lista de obras de Diana Zala

Allele-specific silencing of mutant huntingtin in rodent brain and human stem cells

B13 axonal transport, energy supply and huntingtin

CA150 expression delays striatal cell death in overexpression and knock-in conditions for mutant huntingtin neurotoxicity.

Dysregulation of gene expression in primary neuron models of Huntington's disease shows that polyglutamine-related effects on the striatal transcriptome may not be dependent on brain circuitry.

Genetic and pharmacological inhibition of calcineurin corrects the BDNF transport defect in Huntington's disease

Huntingtin is required for mitotic spindle orientation and mammalian neurogenesis

Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons

Huntingtin's function in axonal transport is conserved in Drosophila melanogaster

Huntington's disease: from huntingtin function and dysfunction to therapeutic strategies.

Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin

Lentiviral-mediated gene transfer to model triplet repeat disorders

Long-term lentiviral-mediated expression of ciliary neurotrophic factor in the striatum of Huntington's disease transgenic mice

Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway

Modulation of AMPA receptor surface diffusion restores hippocampal plasticity and memory in Huntington's disease models

Mutant Huntingtin alters retrograde transport of TrkB receptors in striatal dendrites.

NanoPaint: A Tool for Rapid and Dynamic Imaging of Membrane Structural Plasticity at the Nanoscale

Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease.

Phosphorylation of mutant huntingtin at S421 restores anterograde and retrograde transport in neurons.

Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment

Releasing the brake: restoring fast axonal transport in neurodegenerative disorders.

S.04.03 BDNF/TrkB signaling, axonal and dendritic transport and neurodegeneration in Huntington's disease

Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport.

Sulfobetaine-Vinylimidazole Block Copolymers: A Robust Quantum Dot Surface Chemistry Expanding Bioimaging's Horizons

The advantage of channeling nucleotides for very processive functions

Unexpected link between Huntington disease and Rett syndrome

Vapor Pressure and Liquid Heat Capacity of Perhydroacenaphthylene and Perhydrophenanthrene

Vesicular glycolysis provides on-board energy for fast axonal transport