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Ana Gorostidi

Showing results (31-40 of 43) with videos related to

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Autophagy|August 24, 2012
The MAPK1/3 pathway is essential for the deregulation of autophagy observed in G2019S LRRK2 mutant fibroblastsJosé M Bravo-San Pedro, Rubén Gómez-Sánchez, Mireia Niso-Santano, et al.
Cellular and Molecular Life Sciences : CMLS|July 10, 2012
The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathwayJosé M Bravo-San Pedro, Mireia Niso-Santano, Rubén Gómez-Sánchez, et al.
Biological Psychiatry|October 24, 2007
Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findingsAdolfo López de Munain, Ainhoa Alzualde, Ana Gorostidi, et al.
Acta Neuropathologica|June 14, 2021
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophilsYing Fan, Raja S Nirujogi, Alicia Garrido, et al.
Neurobiology of Aging|December 18, 2015
Assessing the role of TUBA4A gene in frontotemporal degenerationOriol Dols-Icardo, Oriol Iborra, Jessica Valdivia, et al.
Human Molecular Genetics|April 30, 2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsyJosé M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.
Neurobiology of Aging|September 18, 2013
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementiaAgustín Ruiz, Oriol Dols-Icardo, María J Bullido, et al.
Brain : a Journal of Neurology|July 30, 2015
Alzheimer's disease cerebrospinal fluid biomarker in cognitively normal subjectsJon B Toledo, Henrik Zetterberg, Argonde C van Harten, et al.
Brain : a Journal of Neurology|July 9, 2015
Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from SpainOriol Dols-Icardo, Irene Nebot, Ana Gorostidi, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2015
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish ConsortiumPau Pastor, Fermín Moreno, Jordi Clarimón, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Autophagy|August 24, 2012
The MAPK1/3 pathway is essential for the deregulation of autophagy observed in G2019S LRRK2 mutant fibroblastsJosé M Bravo-San Pedro, Rubén Gómez-Sánchez, Mireia Niso-Santano, et al.
Cellular and Molecular Life Sciences : CMLS|July 10, 2012
The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathwayJosé M Bravo-San Pedro, Mireia Niso-Santano, Rubén Gómez-Sánchez, et al.
Biological Psychiatry|October 24, 2007
Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findingsAdolfo López de Munain, Ainhoa Alzualde, Ana Gorostidi, et al.
Acta Neuropathologica|June 14, 2021
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophilsYing Fan, Raja S Nirujogi, Alicia Garrido, et al.
Neurobiology of Aging|December 18, 2015
Assessing the role of TUBA4A gene in frontotemporal degenerationOriol Dols-Icardo, Oriol Iborra, Jessica Valdivia, et al.
Human Molecular Genetics|April 30, 2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsyJosé M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.
Neurobiology of Aging|September 18, 2013
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementiaAgustín Ruiz, Oriol Dols-Icardo, María J Bullido, et al.
Brain : a Journal of Neurology|July 30, 2015
Alzheimer's disease cerebrospinal fluid biomarker in cognitively normal subjectsJon B Toledo, Henrik Zetterberg, Argonde C van Harten, et al.
Brain : a Journal of Neurology|July 9, 2015
Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from SpainOriol Dols-Icardo, Irene Nebot, Ana Gorostidi, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2015
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish ConsortiumPau Pastor, Fermín Moreno, Jordi Clarimón, et al.
Pageof 5