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Expression Profiling Analysis Reveals Key MicroRNA– mRNA Interactions in Early Retinal Degeneration in Retinitis Pigmentosa
(Association Research Vision Ophthalmology, 2018-05)
PURPOSE. The aim of this study was to identify differentially expressed microRNAs (miRNAs) that might play an important role in the etiology of retinal degeneration in a genetic mouse model of retinitis pigmentosa (rd10 ...
Dbx1-Derived Pyramidal Neurons Are Generated Locally in the Developing Murine Neocortex
(Frontiers Media, 2018-10-31)
The neocortex (NCx) generates at the dorsal region of the pallium in the forebrain. Several adjacent structures also contribute with neurons to NCx. Ventral pallium (VP) is considered to generate several populations of ...
Development and Maintenance of the Brain’s Immune Toolkit: Microglia and Non-Parenchymal Brain Macrophages
(Wiley, 2018-06)
Microglia and non-parenchymal macrophages located in the perivascular space, the meninges and the choroid plexus are independent immune populations that play vital roles in brain development, homeostasis, and tissue healing. ...
iPS Cell Cultures from a Gerstmann-Sträussler-Scheinker Patient with the Y218N PRNP Mutation Recapitulate tau Pathology
(Humana Press, 2018-04)
Gerstmann-Straussler-Scheinker (GSS) syndrome is a fatal autosomal dominant neurodegenerative prionopathy clinically characterized by ataxia, spastic paraparesis, extrapyramidal signs and dementia. In some GSS familiar ...
A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies
(Nature Publishing, 2018-09-18)
Inherited retinal diseases (IRD) are a heterogeneous group of diseases that mainly affect the retina; more than 250 genes have been linked to the disease and more than 20 different clinical phenotypes have been described. ...
FRZB gene expression regulation in vitro to restore muscle fibre homeostasis in limb-girdle muscular dystrophy type 2A (LGMD2A) and Frzb-/- murine model muscle analysis.
(2018-09-26)
Este trabajo se centra en el estudio de la distrofia muscular de cinturas tipo 2A (LGMD2A) causada por mutaciones en el gen de la calpaina 3. El trabajo ha sido enfocado en el estudio a nivel celular y molecular de esta ...
Acetylome in Human Fibroblasts From Parkinson's Disease Patients
(Frontiers Media SA, 2018-04-17)
Parkinson's disease (PD) is amultifactorial neurodegenerative disorder. The pathogenesis of this disease is associated with gene and environmental factors. Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most ...
Role of amyloid B oligomers in oligodendrocyte and myelin pathology in Alzheimers's disease
(2018-01-18)
La enfermedad de Alzheimer (EA) es un desorden neurodegenerativo caracterizado por la presencia de placas seniles compuestas por agregados del péptido beta amiloide (Aß), siendo las formas solubles las que mejor correlacionan ...
How aging, seizures and ATP change the intrinsic properties of adult hippocampal neural stem cells.
(2018-12-14)
El hipocampo del cerebro de la mayoría de los mamíferos, incluyendo humanos, es capaz de generar nuevas neuronas a partir de de células madre neurales (NSCs) lo largo de la vida adulta mediante un proceso llamado neurogénesis ...
Differences in the Use and Opinions About New eHealth Technologies Among Patients With Psychosis: Structured Questionnaire
(JMIR Publications, 2018-07-25)
Background: Despite a growing interest in the use of technology in order to support the treatment of psychotic disorders, limited knowledge exists about the viability and acceptability of these eHealth interventions in ...