{"id":"W2136000647","doi":"10.1093/hmg/ddn292","title":"Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease","year":2008,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Autophagy in Disease and Therapy","field":"Medicine","cited_by":348,"is_retracted":false,"has_abstract":true,"ca_institutions":"","funders":"National Institutes of Health; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Neurological Disorders and Stroke; Institut National de la Santé et de la Recherche Médicale; York University","keywords":"Autophagy; Lysosome; Biology; Skeletal muscle; Cell biology; Glycogen storage disease type II; Glycogen; Myocyte; Ubiquitin; ATG16L1; Biochemistry; Endocrinology; Enzyme replacement therapy; Internal medicine; Enzyme; Disease; Gene; Medicine; Apoptosis","routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":true},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.01993376988578649,"score_gpt":0.2868402945148623,"score_spread":0.2669065246290758,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}