Reelin-Related Neurological Disorders and Animal Models

The Reeler mutation was so named because of the alterations in gait that characterize homozygous mice. Several decades after the description of the Reeler phenotype, the mutated protein was discovered and named Reelin (Reln). Reln controls a number of fundamental steps in embryonic and postnatal bra...

Descripció completa

Dades bibliogràfiques

Autors principals:	Laura Lossi, Adalberto Merighi, Gabriella D'Arcangelo
Format:	Online
Idioma:	anglès
Publicat:	Frontiers Media SA 2021
Matèries:	RC321-571 Q1-390 Neurons neuronal migration Schizophrenia Depression Neuronal Death Reeler Synapses autism intracellular pathways thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAN Neurosciences
Accés en línia:	22962
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!