Ana Gorostidi

Ana Gorostidi

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Ana Gorostidi

Ana Gorostidi

Publications by authors named "Ana Gorostidi"

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Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons.

J Neuroinflammation 2016 11 18;13(1):295. Epub 2016 Nov 18.

Laboratory of Stem Cells and Neural Repair, Inbiomed, Paseo Mikeletegi, 81, E-20009, San Sebastian, Spain.

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http://dx.doi.org/10.1186/s12974-016-0761-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116223PMC
November 2016

SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor.

ASN Neuro 2015 Jul-Aug;7(4). Epub 2015 Aug 21.

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA Departments of Psychiatry and Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA Friedman Brain and Mindich Child Health and Development Institutes, Icahn School of Medicine at Mount Sinai, New York, NY, USA

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http://journals.sagepub.com/doi/10.1177/1759091415598290
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http://dx.doi.org/10.1177/1759091415598290DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550298PMC
March 2016

Assessing the role of TUBA4A gene in frontotemporal degeneration.

Neurobiol Aging 2016 Feb 5;38:215.e13-215.e14. Epub 2015 Nov 5.

Memory Unit, Neurology Department and Sant Pau Biomedical Research Institute, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain; CIBERNED, Center for Networked Biomedical Research into Neurodegenerative Diseases, Madrid, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2015.10.030DOI Listing
February 2016

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy.

Hum Mol Genet 2015 Dec 1;24(24):7111-20. Epub 2015 Oct 1.

Department of Neurology, Department of Psychiatry, Department of Genetics and Genomic Sciences, Friedman Brain Institute, Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, USA and

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http://dx.doi.org/10.1093/hmg/ddv410DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654061PMC
December 2015

GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment.

J Hum Genet 2015 Oct 2;60(10):637-40. Epub 2015 Jul 2.

Department of Neurology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY, USA.

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http://dx.doi.org/10.1038/jhg.2015.69DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624020PMC
October 2015

Beyond asexual development: modifications in the gene expression profile caused by the absence of the Aspergillus nidulans transcription factor FlbB.

Genetics 2015 Apr 20;199(4):1127-42. Epub 2015 Feb 20.

Department of Applied Chemistry, Faculty of Chemistry, University of The Basque Country, Manuel de Lardizabal, 3, 20018, San Sebastian, Spain

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http://dx.doi.org/10.1534/genetics.115.174342DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391568PMC
April 2015

Epitope Mapping of Antibodies to Alpha-Synuclein in LRRK2 Mutation Carriers, Idiopathic Parkinson Disease Patients, and Healthy Controls.

Front Aging Neurosci 2014 15;6:169. Epub 2014 Jul 15.

Departamento de Bioquímica, Instituto de Investigaciones Biomédicas "Alberto Sols", UAM-CSIC, Facultad de Medicina, Universidad Autónoma de Madrid , Madrid , Spain ; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED) , Madrid , Spain.

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http://dx.doi.org/10.3389/fnagi.2014.00169DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4097207PMC
July 2014

Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2.

Mov Disord 2014 May 19;29(6):750-5. Epub 2013 Dec 19.

Department of Neurology, University Hospital Donostia, San Sebastián, Spain; Center for Biomedical Research in Neurodegenerative Diseases Network (CIBERNED), San Sebastián, Spain; Neurosciences Area, Biodonostia Institute, San Sebastián, Spain.

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http://dx.doi.org/10.1002/mds.25778DOI Listing
May 2014

Leucine-rich repeat kinase 2 modulates cyclooxygenase 2 and the inflammatory response in idiopathic and genetic Parkinson's disease.

Neurobiol Aging 2014 May 22;35(5):1116-24. Epub 2013 Nov 22.

Laboratory of Stem Cells and Neural Repair, Fundación Inbiomed, San Sebastián, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.11.018DOI Listing
May 2014

Genetic variability related to serum uric acid concentration and risk of Parkinson's disease.

Mov Disord 2013 Oct 27;28(12):1737-40. Epub 2013 May 27.

Service of Neurology, Universitary Hospital Marqués de Valdecilla (IFIMAV), University of Cantabria (UC), Santander, Spain.

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http://dx.doi.org/10.1002/mds.25507DOI Listing
October 2013

The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathway.

Cell Mol Life Sci 2013 Jan 8;70(1):121-36. Epub 2012 Jul 8.

Departamento de Bioquímica y Biología Molecular y Genética, E. Enfermería y T.O., Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Universidad de Extremadura, Avda Universidad, s/n, 10003, Cáceres, Spain.

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http://dx.doi.org/10.1007/s00018-012-1061-yDOI Listing
January 2013

The MAPK1/3 pathway is essential for the deregulation of autophagy observed in G2019S LRRK2 mutant fibroblasts.

Autophagy 2012 Oct 23;8(10):1537-9. Epub 2012 Aug 23.

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Departamento de Bioquímica y Biología Molecular y Genética, E. Enfermería y T.O., Universidad de Extremadura, Cáceres, Spain.

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http://dx.doi.org/10.4161/auto.21270DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463455PMC
October 2012

Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2.

Mov Disord 2009 Oct;24(13):1998-2001

Department of Neurology, Hospital Donostia, Paseo Dr. Beguiristain s.n, 20014 Donostia, San Sebastián, Gipuzkoa, Spain.

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http://dx.doi.org/10.1002/mds.22677DOI Listing
October 2009