Lista de obras - Anna Fassio - Dominio Público Uruguay

APache Is an AP2-Interacting Protein Involved in Synaptic Vesicle Trafficking and Neuronal Development

artículo científico publicado en 2017

CGP 52432: a novel potent and selective GABAB autoreceptor antagonist in rat cerebral cortex.

artículo científico publicado en 1993

Characterization of the GABA autoreceptor in human neocortex as a pharmacological subtype of the GABAB receptor

artículo científico publicado en 1994

Clinical intrafamilial variability in lethal familial neonatal seizure disorder caused by TBC1D24 mutations

artículo científico publicado en 2016

Constitutive Inactivation of the PRRT2 Gene Alters Short-Term Synaptic Plasticity and Promotes Network Hyperexcitability in Hippocampal Neurons

artículo científico publicado en 2019

De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy.

artículo científico publicado en 2018

Entrapping of impermeant probes of different size into nonpermeabilized synaptosomes as a method to study presynaptic mechanisms

artículo científico publicado en 2000

Evidence for calcium-dependent vesicular transmitter release insensitive to tetanus toxin and botulinum toxin type F.

artículo científico publicado en 1999

Fibroblasts from FAD-linked presenilin 1 mutations display a normal unfolded protein response but overproduce Abeta42 in response to tunicamycin

artículo científico publicado en 2004

Formation, isomerisation and reduction of disulphide bonds during protein quality control in the endoplasmic reticulum

artículo científico publicado en 2002

Functional role of ATP binding to synapsin I in synaptic vesicle trafficking and release dynamics.

artículo científico publicado en 2014

GABA induces norepinephrine exocytosis from hippocampal noradrenergic axon terminals by a dual mechanism involving different voltage-sensitive calcium channels

artículo científico publicado en 1999

GABAB receptors as potential targets for drugs able to prevent excessive excitatory amino acid transmission in the spinal cord

article

Glutathione limits Ero1-dependent oxidation in the endoplasmic reticulum.

artículo científico publicado en 2004

Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy.

artículo científico publicado en 2014

Increased presynaptic protein kinase C activity and glutamate release in rats with a prenatally induced hippocampal lesion.

artículo científico publicado en 1997

Involvement of synaptic genes in the pathogenesis of autism spectrum disorders: the case of synapsins

artículo científico publicado en 2014

Lack of synapsin I reduces the readily releasable pool of synaptic vesicles at central inhibitory synapses

scientific article published on 01 December 2007

Molecular Machines Determining the Fate of Endocytosed Synaptic Vesicles in Nerve Terminals

artículo científico publicado en 2016

Neuronal hyperactivity causes Na+/H+ exchanger-induced extracellular acidification at active synapses.

artículo científico publicado en 2017

Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancy.

artículo científico publicado en 2013

PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery.

artículo científico publicado en 2016

PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity.

artículo científico publicado en 2018

Phosphorylation of synapsin I by cyclin-dependent kinase-5 sets the ratio between the resting and recycling pools of synaptic vesicles at hippocampal synapses.

artículo científico publicado en 2014

REST/NRSF-mediated intrinsic homeostasis protects neuronal networks from hyperexcitability.

artículo científico publicado en 2013

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

artículo científico publicado en 2011

SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth

scientific article published on 15 August 2013

Synapsin I senses membrane curvature by an amphipathic lipid packing sensor motif.

artículo científico publicado en 2011

Synapsins: from synapse to network hyperexcitability and epilepsy

artículo científico

TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features.

artículo científico publicado en 2016

TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons

artículo científico publicado en 2019

TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway

scientific journal article

TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy

artículo científico publicado en 2010

The CXXCXXC motif determines the folding, structure and stability of human Ero1-Lalpha

artículo científico publicado en 2000

The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons

artículo científico publicado en 2019

The highly conserved synapsin domain E mediates synapsin dimerization and phospholipid vesicle clustering

artículo científico publicado en 2010

The sensitivity of catecholamine release to botulinum toxin C1 and E suggests selective targeting of vesicles set into the readily releasable pool

artículo científico publicado en 2003

The synapsin domain E accelerates the exoendocytotic cycle of synaptic vesicles in cerebellar Purkinje cells

artículo científico publicado en 2006

Tyrosine phosphorylation of synapsin I by Src regulates synaptic-vesicle trafficking

artículo científico publicado en 2010

Lista de obras de Anna Fassio

APache Is an AP2-Interacting Protein Involved in Synaptic Vesicle Trafficking and Neuronal Development

CGP 52432: a novel potent and selective GABAB autoreceptor antagonist in rat cerebral cortex.

Characterization of the GABA autoreceptor in human neocortex as a pharmacological subtype of the GABAB receptor

Clinical intrafamilial variability in lethal familial neonatal seizure disorder caused by TBC1D24 mutations

Constitutive Inactivation of the PRRT2 Gene Alters Short-Term Synaptic Plasticity and Promotes Network Hyperexcitability in Hippocampal Neurons

De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy.

Entrapping of impermeant probes of different size into nonpermeabilized synaptosomes as a method to study presynaptic mechanisms

Evidence for calcium-dependent vesicular transmitter release insensitive to tetanus toxin and botulinum toxin type F.

Fibroblasts from FAD-linked presenilin 1 mutations display a normal unfolded protein response but overproduce Abeta42 in response to tunicamycin

Formation, isomerisation and reduction of disulphide bonds during protein quality control in the endoplasmic reticulum

Functional role of ATP binding to synapsin I in synaptic vesicle trafficking and release dynamics.

GABA induces norepinephrine exocytosis from hippocampal noradrenergic axon terminals by a dual mechanism involving different voltage-sensitive calcium channels

GABAB receptors as potential targets for drugs able to prevent excessive excitatory amino acid transmission in the spinal cord

Glutathione limits Ero1-dependent oxidation in the endoplasmic reticulum.

Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy.

Increased presynaptic protein kinase C activity and glutamate release in rats with a prenatally induced hippocampal lesion.

Involvement of synaptic genes in the pathogenesis of autism spectrum disorders: the case of synapsins

Lack of synapsin I reduces the readily releasable pool of synaptic vesicles at central inhibitory synapses

Molecular Machines Determining the Fate of Endocytosed Synaptic Vesicles in Nerve Terminals

Neuronal hyperactivity causes Na+/H+ exchanger-induced extracellular acidification at active synapses.

Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancy.

PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery.

PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity.

Phosphorylation of synapsin I by cyclin-dependent kinase-5 sets the ratio between the resting and recycling pools of synaptic vesicles at hippocampal synapses.

REST/NRSF-mediated intrinsic homeostasis protects neuronal networks from hyperexcitability.

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth

Synapsin I senses membrane curvature by an amphipathic lipid packing sensor motif.

Synapsins: from synapse to network hyperexcitability and epilepsy

TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features.

TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons

TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway

TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy

The CXXCXXC motif determines the folding, structure and stability of human Ero1-Lalpha

The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons

The highly conserved synapsin domain E mediates synapsin dimerization and phospholipid vesicle clustering

The sensitivity of catecholamine release to botulinum toxin C1 and E suggests selective targeting of vesicles set into the readily releasable pool

The synapsin domain E accelerates the exoendocytotic cycle of synaptic vesicles in cerebellar Purkinje cells

Tyrosine phosphorylation of synapsin I by Src regulates synaptic-vesicle trafficking