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Autophagy
|
August 24, 2012
The MAPK1/3 pathway is essential for the deregulation of autophagy observed in G2019S LRRK2 mutant fibroblasts
José 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 pathway
José 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 findings
Adolfo 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 neutrophils
Ying Fan, Raja S Nirujogi, Alicia Garrido, et al.
Neurobiology of Aging
|
December 18, 2015
Assessing the role of TUBA4A gene in frontotemporal degeneration
Oriol 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 epilepsy
José 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 dementia
Agustín 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 subjects
Jon 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 Spain
Oriol 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 Consortium
Pau Pastor, Fermín Moreno, Jordi Clarimón, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
Autophagy
|
August 24, 2012
The MAPK1/3 pathway is essential for the deregulation of autophagy observed in G2019S LRRK2 mutant fibroblasts
José 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 pathway
José 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 findings
Adolfo 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 neutrophils
Ying Fan, Raja S Nirujogi, Alicia Garrido, et al.
Neurobiology of Aging
|
December 18, 2015
Assessing the role of TUBA4A gene in frontotemporal degeneration
Oriol 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 epilepsy
José 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 dementia
Agustín 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 subjects
Jon 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 Spain
Oriol 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 Consortium
Pau Pastor, Fermín Moreno, Jordi Clarimón, et al.
Page
of 5