A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia
Articolo
Data di Pubblicazione:
2015
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Association study; Case-control; Frontotemporal dementia; Functional annotation; Genetic risk factors; Population; Aged; Aged, 80 and over; Alleles; Apoptosis Regulatory Proteins; Axons; Brain; Case-Control Studies; Cell Differentiation; Cohort Studies; Female; Frontotemporal Dementia; Genome-Wide Association Study; Glucosyltransferases; Haplotypes; Humans; Intercellular Signaling Peptides and Proteins; Male; Middle Aged; Neurogenesis; Neurons; Polymorphism, Single Nucleotide; Protein-Tyrosine Kinases; Risk Factors; Neuroscience (all); Aging; Developmental Biology; Geriatrics and Gerontology; Neurology (clinical)
Elenco autori:
Ferrari, Raffaele; Grassi, Mario; Salvi, Erika; Borroni, Barbara; Palluzzi, Fernando; Pepe, Daniele; D'Avila, Francesca; Padovani, Alessandro; Archetti, Silvana; Rainero, Innocenzo; Rubino, Elisa; Pinessi, Lorenzo; Benussi, Luisa; Binetti, Giuliano; Ghidoni, Roberta; Galimberti, Daniela; Scarpini, Elio; Serpente, Maria; Rossi, Giacomina; Giaccone, Giorgio; Tagliavini, Fabrizio; Nacmias, Benedetta; Piaceri, Irene; Bagnoli, Silvia; Bruni, Amalia C.; Maletta, Raffaele G.; Bernardi, Livia; Postiglione, Alfredo; Milan, Graziella; Franceschi, Massimo; Puca, Annibale A.; Novelli, Valeria; Barlassina, Cristina; Glorioso, Nicola; Manunta, Paolo; Singleton, Andrew; Cusi, Daniele; Hardy, John; Momeni, Parastoo
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