{"product_id":"clevio-nobrega-nobrega-polyglutamine-disorders-9783319717807","title":"Polyglutamine Disorders","description":"Clinical features of Huntington's disease.- Genetic rodent models of Huntington's disease.- Mitochondrial dysfunction in Huntington's disease.- RNA related pathology in Huntington's disease.- Spinal and bulbar musar atrophy: from clinical genetic features and molear pathology to mechanisms underlying disease toxicity.- Spinocerebellar Ataxia Type 1: Molear Mechanisms Of Neurodegeneration And Preclinical Studies.- Spinocerebellar Ataxia, type 6.- Spinocerebellar ataxia type 2.- Molear mechanisms and therapeutic strategies in Spinocerebellar ataxia type 7.- Spinocerebellar ataxia type 17 (SCA17).- The neuropatholy of spinocerebellar ataxia type 3\/Machado-Joseph disease.- Origins and spread of Machado-Joseph disease ancestral mutational events.- Clinical features in Machado-Joseph disease.- Polyglutamine-independent features in ataxin-3 aggregation and pathogenesis of Machado-Joseph disease.- Animal models in Machado-Joseph disease.- Towards the identification of molear biomarkers of Spinocerebellar ataxia type 3\/Machado-Joseph disease.- Planning future clinical trials for Machado Joseph Disease.- Molear mechanisms and cellular pathways implicated in Machado-Joseph disease pathogenesis.- Pharmacological therapies for Machado-Joseph disease.- Gene therapy for Polyglutamine diseases.- Stem cell-based therapies for Polyglutamine diseases.","brand":"Springer Nature B.V.","offers":[{"title":"Default Title","offer_id":53883206959446,"sku":null,"price":0.0,"currency_code":"EUR","in_stock":false}],"url":"https:\/\/www.momoxbooks.com\/products\/clevio-nobrega-nobrega-polyglutamine-disorders-9783319717807","provider":"momoxbooks","version":"1.0","type":"link"}