Evidence for the deregulation of protein turnover pathways in Atm-deficient mouse cerebellum: An organotypic study

Journal of Neuropathology and Experimental Neurology

Volumn 76, Issue 7, 2017, Pages 578-584

  Kim, Catherine D ^a   Reed, Ryan E ^a   Juncker, Meredith A ^a   Fang, Zhide ^b   Desai, Shyamal D ^a  

^a LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b LOUISIANA STATE UNIVERSITY HEALTH SCIENCES CENTER   (United States)

Author keywords

Ataxia telangiectasia; Autophagy; Genotoxic stress; ISG15; Organotypic cerebellar culture model; Proteinopathy; Ubiquitin

Indexed keywords

ATM PROTEIN; BETA ACTIN; ISG15 PROTEIN; UBIQUITIN; UNCLASSIFIED DRUG; ATM PROTEIN, MOUSE; CYTOKINE; G1P2 PROTEIN, MOUSE; MAP1LC3 PROTEIN, MOUSE; MICROTUBULE ASSOCIATED PROTEIN;

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; ATAXIA TELANGIECTASIA CELL LINE; AUTOPHAGY; BRAIN CELL CULTURE; CEREBELLAR SLICE; CEREBELLUM; CONTROLLED STUDY; EX VIVO STUDY; IMMUNOFLUORESCENCE; IMMUNOHISTOCHEMISTRY; KIDNEY TISSUE; LIVER TISSUE; LUNG PARENCHYMA; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN METABOLISM; SKIN FIBROBLAST; SPLEEN TISSUE; THYMUS TISSUE; ULTRAVIOLET RADIATION; WESTERN BLOTTING; ANIMAL; ATAXIA TELANGIECTASIA; DEFICIENCY; DISEASE MODEL; GENE EXPRESSION REGULATION; GENETICS; GENOTYPE; KNOCKOUT MOUSE; METABOLISM; MUTATION; ORGAN CULTURE TECHNIQUE; PATHOLOGY; RADIATION RESPONSE; UBIQUITINATION;

ANIMALS; ATAXIA TELANGIECTASIA; ATAXIA TELANGIECTASIA MUTATED PROTEINS; AUTOPHAGY; CEREBELLUM; CYTOKINES; DISEASE MODELS, ANIMAL; GENE EXPRESSION REGULATION; GENOTYPE; MICE; MICE, KNOCKOUT; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION; ORGAN CULTURE TECHNIQUES; UBIQUITINATION; UBIQUITINS; ULTRAVIOLET RAYS;

EID: 85019594259     PISSN: 00223069     EISSN: 15546578     Source Type: Journal    
DOI: 10.1093/jnen/nlx038     Document Type: Article

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