Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Isidro Ferrer

Showing results (191-200 of 300) with videos related to

Pageof 30
Sort By:
Frontiers in Aging Neuroscience|June 28, 2019
Early-Onset Molecular Derangements in the Olfactory Bulb of Tg2576 Mice: Novel Insights Into the Stress-Responsive Olfactory Kinase Dynamics in Alzheimer's DiseaseMercedes Lachen-Montes, Andrea González-Morales, Maialen Palomino, et al.
Human Molecular Genetics|November 3, 2012
Kidins220 accumulates with tau in human Alzheimer's disease and related models: modulation of its calpain-processing by GSK3β/PP1 imbalanceCelia López-Menéndez, Andrea Gamir-Morralla, Jerónimo Jurado-Arjona, et al.
Nature Medicine|July 21, 2014
Huntington's disease is a four-repeat tauopathy with tau nuclear rodsMarta Fernández-Nogales, Jorge R Cabrera, María Santos-Galindo, et al.
International Journal of Molecular Sciences|April 13, 2024
Neurodegeneration Biomarkers in Adult Spinal Muscular Atrophy (SMA) Patients Treated with NusinersenPol Andrés-Benito, Juan Francisco Vázquez-Costa, Nancy Carolina Ñungo Garzón, et al.
Neuropathology and Applied Neurobiology|May 6, 2021
Transcriptional signatures of synaptic vesicle genes define myotonic dystrophy type I neurodegenerationAntonio Jimenez-Marin, Ibai Diez, Garazi Labayru, et al.
Journal of the Neurological Sciences|March 31, 2004
Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studiesMontse Olivé, Lev Goldfarb, Dolores Moreno, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 22, 2005
Prognostic significance of O6-methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in anaplastic gliomasMarta Brell, Avelina Tortosa, Eugenia Verger, et al.
BMC Neurology|October 27, 2010
A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case reportAna B Rodríguez-Martínez, Joseba M Garrido, Juan J Zarranz, et al.
Journal of Neurochemistry|April 11, 2015
Anatomical location of LPA1 activation and LPA phospholipid precursors in rodent and human brainEstibaliz González de San Román, Iván Manuel, María Teresa Giralt, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|September 29, 2017
Lipid Profile in Human Frontal Cortex Is Sustained Throughout Healthy Adult Life Span to Decay at Advanced AgesRosanna Cabré, Alba Naudí, Mayelin Dominguez-Gonzalez, et al.
Pageof 30

Showing results (191-200 of 300) with videos related to

Sort By:
Pageof 30
Frontiers in Aging Neuroscience|June 28, 2019
Early-Onset Molecular Derangements in the Olfactory Bulb of Tg2576 Mice: Novel Insights Into the Stress-Responsive Olfactory Kinase Dynamics in Alzheimer's DiseaseMercedes Lachen-Montes, Andrea González-Morales, Maialen Palomino, et al.
Human Molecular Genetics|November 3, 2012
Kidins220 accumulates with tau in human Alzheimer's disease and related models: modulation of its calpain-processing by GSK3β/PP1 imbalanceCelia López-Menéndez, Andrea Gamir-Morralla, Jerónimo Jurado-Arjona, et al.
Nature Medicine|July 21, 2014
Huntington's disease is a four-repeat tauopathy with tau nuclear rodsMarta Fernández-Nogales, Jorge R Cabrera, María Santos-Galindo, et al.
International Journal of Molecular Sciences|April 13, 2024
Neurodegeneration Biomarkers in Adult Spinal Muscular Atrophy (SMA) Patients Treated with NusinersenPol Andrés-Benito, Juan Francisco Vázquez-Costa, Nancy Carolina Ñungo Garzón, et al.
Neuropathology and Applied Neurobiology|May 6, 2021
Transcriptional signatures of synaptic vesicle genes define myotonic dystrophy type I neurodegenerationAntonio Jimenez-Marin, Ibai Diez, Garazi Labayru, et al.
Journal of the Neurological Sciences|March 31, 2004
Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studiesMontse Olivé, Lev Goldfarb, Dolores Moreno, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 22, 2005
Prognostic significance of O6-methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in anaplastic gliomasMarta Brell, Avelina Tortosa, Eugenia Verger, et al.
BMC Neurology|October 27, 2010
A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case reportAna B Rodríguez-Martínez, Joseba M Garrido, Juan J Zarranz, et al.
Journal of Neurochemistry|April 11, 2015
Anatomical location of LPA1 activation and LPA phospholipid precursors in rodent and human brainEstibaliz González de San Román, Iván Manuel, María Teresa Giralt, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|September 29, 2017
Lipid Profile in Human Frontal Cortex Is Sustained Throughout Healthy Adult Life Span to Decay at Advanced AgesRosanna Cabré, Alba Naudí, Mayelin Dominguez-Gonzalez, et al.
Pageof 30