Neurogenetics-IGTP

Welcome to the Functional and Translational NEUROGENETICS UNIT

[Neurogenetics-IGTP @NG_IGTP]

Desenvolupem una teràpia gènica innovadora per l’Atàxia de Friedreich i investiguem per trobar un tractament per la Chloe https://t.co/ZNAWTtXY3i vía @wordpressdotcom

[Neurogenetics-IGTP @NG_IGTP]

Published our study extending clinical-genetic features in POLR3A-related spastic ataxia: new mutations and a look into the phenotype.
J Neurol. 2019.@GTRecerca @ACAH_ataxiaCat @STOP_FA @FEDAES @hgermanstrias

[Neurogenetics-IGTP @NG_IGTP]

At the European meeting on Cell and Gene Therapy presenting the pre-clinical in vivo results obtained from the AAV-gene therapy to treat Friedreich’s Ataxia. @GTRecerca @hgermanstrias @FEDAES @STOP_FA @FEDER_ONG @ACAH_ataxiaCat

[Neurogenetics-IGTP @NG_IGTP]

Día internacional de la ataxia: aprovechamos la luz del Sincrotrón ALBA para descifrar la ataxia de Friedreich. @GTRecerca @hgermanstrias @ACAH_ataxiaCat

https://t.co/vGPMQ5dKgD

[Neurogenetics-IGTP @NG_IGTP]

Diada internacional de l'atàxia: el nostre grup a l'IGTP aprofita el llum del sincrotró ALBA per desxifrar l'atàxia de Friedreich. @GTRecerca @hgermanstrias @ACAH_ataxiaCat

https://t.co/geyftFWgkZ

[Neurogenetics-IGTP @NG_IGTP]

Award to our communication: an unstable ATTTC repeat mutation within Disabled 1 gene causes cerebellar Purkinje cell alterations, DAB1 RNA switch, and Reelin signalling dysregulation in SCA37. 6th international congress on spastic paraplegias and ataxias, Nice, France. @GTRecerca

[Neurogenetics-IGTP @NG_IGTP]

PhD Positions available on Gene Therapy https://t.co/mASxGXTKW1

[EFEciencia @EFEciencia]

Los padres de la edición genética creen hará falta debatir sus límites éticos https://t.co/23bPcgUaV2

[IGTP @GTRecerca]

Amics de Can Ruti "El millor talent al teu servei!" #GTRecerca https://t.co/uv4mihCC9G

[Rare Disease Report @RareDR]

Pope Francis Says Rare Disease Patients Deserve Our Commitment https://t.co/3o6qd3AQ1x @Pontifex @CatholicNewsSvc @vatican_en @GlobalGenes

[Neurogenetics-IGTP @NG_IGTP]

Recent Advances in the Treatment of Lysosomal Storage Diseases: Lysosomal exocytosis and lipid storage disorders http://t.co/P8sFqe8hM0

[Neurogenetics-IGTP @NG_IGTP]

Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Ty... - PubMed - NCBI http://t.co/N7SaUj1txH

[Neurogenetics-IGTP @NG_IGTP]

Study nearly triples the locations in the human genome that harbor micro... http://t.co/342qzUTxNg via @JeffersonUniv @EurekAlertAAAS

[genetic insidER @geneticinsidER]

Don’t miss new highlights in #NGS Technologies with @AntoniMatilla Save the date!! 16-17 April #geneticinsidER

[Neurogenetics-IGTP @NG_IGTP]

Functional characterization of Friedreich ataxia iPS-derived neuron... - PubMed - NCBI http://t.co/qIlxkQwZOA

[Neurogenetics-IGTP @NG_IGTP]

Neuroinflammation, mitochondrial defects and neurodegeneration in m... - PubMed - NCBI http://t.co/CZ6DCCr92O

[STOP FA @STOP_FA]

"Seguimos con buen rumbo" Nuestra newsletter está disponible en: http://t.co/RMEMpCAo31

[Espacios SaludInvestiga @eSaludInvestiga]

Comisión Europea y el Instituto Salud Carlos III firman acuerdo para estudio políticas de #salud para el #autismo http://t.co/95KfvWMWTc

[Rare Disease UK @rarediseaseuk]

The official @rarediseaseday video is now out! Watch it here: https://t.co/0YZHOr6WFh #rarediseaseday #livingwith a #raredisease

[Antoni Matilla @AntoniMatilla]

Científicos descubren un gen que rompe la ley de la herencia de Mendel http://t.co/ubMIhseZEb vía @la_informacion