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However, many preclinical models remain insufficiently characterised, hindering our understanding of the diseases and the development of effective therapeutic approaches. The present study provides a comprehensive phenotypic and molecular characterisation of the woozy (\n                    <jats:italic>Sil1<\/jats:italic>\n                    <jats:sup>\n                      <jats:italic>wz<\/jats:italic>\n                    <\/jats:sup>\n                    ) mouse model of Marinesco-Sj\u00f6gren Syndrome (MSS), a rare autosomal recessive cerebellar ataxia characterised by cerebellar dysfunction, congenital cataracts, and progressive myopathy. Disease progression was monitored from 5 to 26\u00a0weeks using a series of motor assessments, including the accelerating rotarod, beam walking, pole test, and inverted grid test. These evaluations revealed progressive cerebellar ataxia in\n                    <jats:italic>Sil1<\/jats:italic>\n                    <jats:sup>\n                      <jats:italic>wz<\/jats:italic>\n                    <\/jats:sup>\n                    mice, with symptoms emerging around the ninth week of age. A clear sex-related difference was observed in the motor tests, with female\n                    <jats:italic>Sil1<\/jats:italic>\n                    <jats:sup>\n                      <jats:italic>wz<\/jats:italic>\n                    <\/jats:sup>\n                    mice outperforming their male counterparts across all assessments. Histological analysis revealed significant muscular atrophy in glycolytic muscles (gastrocnemius and quadriceps) but not in oxidative muscles (soleus) of 26-week-old\n                    <jats:italic>Sil1<\/jats:italic>\n                    <jats:sup>\n                      <jats:italic>wz<\/jats:italic>\n                    <\/jats:sup>\n                    mice. Molecular analyses confirmed the upregulation of unfolded protein response markers (BiP and pEIF2\u03b1) and proteolysis-associated proteins (Rab11 and LC3-II) in glycolytic but not oxidative muscles. Cognitive assessment using nesting behaviour showed deficits in\n                    <jats:italic>Sil1<\/jats:italic>\n                    <jats:sup>\n                      <jats:italic>wz<\/jats:italic>\n                    <\/jats:sup>\n                    mice at 14\u00a0weeks, assuming similarities with mental retardation shown by MSS patients. Our findings established a comprehensive timeline of disease progression in this MSS model and highlighted the differential vulnerability of glycolytic versus oxidative muscles and cerebellar regions. These insights pave the way for the development of therapeutic strategies for MSS and related cerebellar ataxias.\n                  <\/jats:p>","DOI":"10.1007\/s12035-025-05577-y","type":"journal-article","created":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T03:59:06Z","timestamp":1764993546000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Systematic Phenotyping and Molecular Analysis of the Woozy Mouse: A Preclinical Model of Cerebellar Ataxia"],"prefix":"10.1007","volume":"63","author":[{"given":"Fabio","family":"Bellia","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Laura","family":"Amodei","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anna Giulia","family":"Ruggieri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francesca","family":"Potenza","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marianna","family":"Viele","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Manuela","family":"Bomba","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francesco","family":"Del Pizzo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Manuela","family":"Iezzi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alberto","family":"Granzotto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Luca","family":"Federici","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michele","family":"Sallese","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2025,12,6]]},"reference":[{"key":"5577_CR1","first-page":"1","volume":"61","author":"AE Harding","year":"1993","unstructured":"Harding AE (1993) Clinical features and classification of inherited ataxias. 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