List of works - Ignasi Sahún

A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

scientific article published on 26 September 2009

AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway

scientific article published in February 2013

An animal model of compulsive food-taking behaviour

scientific article

Candidate genes for panic disorder: insight from human and mouse genetic studies.

scientific article published on June 2007

Carnitine palmitoyltransferase 1C deficiency causes motor impairment and hypoactivity.

scientific article published on 21 August 2013

Ceramide levels regulated by carnitine palmitoyltransferase 1C control dendritic spine maturation and cognition

scientific article

Cognition and hippocampal plasticity in the mouse is altered by monosomy of a genomic region implicated in Down syndrome

scientific article

DREAM controls the on/off switch of specific activity-dependent transcription pathways

scientific article

Developmental molecular and functional cerebellar alterations induced by PCP4/PEP19 overexpression: implications for Down syndrome.

scientific article published on 28 November 2013

Differential responses to anxiogenic drugs in a mouse model of panic disorder as revealed by Fos immunocytochemistry in specific areas of the fear circuitry.

scientific article published on 20 November 2006

Dissociation between CA3-CA1 synaptic plasticity and associative learning in TgNTRK3 transgenic mice.

scientific article

Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage

scientific article published on 4 May 2014

Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder

scientific article published on 15 July 2014

Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.

scientific article

Overexpression of Reelin prevents the manifestation of behavioral phenotypes related to schizophrenia and bipolar disorder.

scientific article

Reduced Mid1 Expression and Delayed Neuromotor Development in daDREAM Transgenic Mice

scientific article published on 3 May 2012

Targeting Dyrk1A with AAVshRNA attenuates motor alterations in TgDyrk1A, a mouse model of Down syndrome.

scientific article

Transgenic mice overexpressing the full-length neurotrophin receptor TrkC exhibit increased catecholaminergic neuron density in specific brain areas and increased anxiety-like behavior and panic reaction

scientific article published on 11 September 2006

List of works by Ignasi Sahún

A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway

An animal model of compulsive food-taking behaviour

Candidate genes for panic disorder: insight from human and mouse genetic studies.

Carnitine palmitoyltransferase 1C deficiency causes motor impairment and hypoactivity.

Ceramide levels regulated by carnitine palmitoyltransferase 1C control dendritic spine maturation and cognition

Cognition and hippocampal plasticity in the mouse is altered by monosomy of a genomic region implicated in Down syndrome

DREAM controls the on/off switch of specific activity-dependent transcription pathways

Developmental molecular and functional cerebellar alterations induced by PCP4/PEP19 overexpression: implications for Down syndrome.

Differential responses to anxiogenic drugs in a mouse model of panic disorder as revealed by Fos immunocytochemistry in specific areas of the fear circuitry.

Dissociation between CA3-CA1 synaptic plasticity and associative learning in TgNTRK3 transgenic mice.

Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage

Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder

Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.

Overexpression of Reelin prevents the manifestation of behavioral phenotypes related to schizophrenia and bipolar disorder.

Reduced Mid1 Expression and Delayed Neuromotor Development in daDREAM Transgenic Mice

Targeting Dyrk1A with AAVshRNA attenuates motor alterations in TgDyrk1A, a mouse model of Down syndrome.

Transgenic mice overexpressing the full-length neurotrophin receptor TrkC exhibit increased catecholaminergic neuron density in specific brain areas and increased anxiety-like behavior and panic reaction