Deconstructing pompe disease by analyzing single muscle fibers: To see a world in a grain of sand...

Autophagy

Volumn 3, Issue 6, 2007, Pages 546-552

  Raben, Nina ^a   Takikita, Shoichi ^a   Pittis, Maria G ^b   Bembi, Bruno ^b   Marie, Suely K N ^c   Roberts, Ashley ^a   Page, Laura ^a   Kishnani, Priya S ^d   Schoser, Benedikt G H ^e   Chien, Yin Hsiu ^f   Ralston, Evelyn ^a   Nagaraju, Kanneboyina ^g   Plotz, Paul H ^a  

^a NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES   (United States)

^b INSTITUTE FOR MATERNAL AND CHILD HEALTH IRCCS BURLO GAROFOLO   (Italy)

^c University of San Paolo Medical School   (Brazil)

^d DUKE UNIVERSITY MEDICAL CENTER   (United States)

^e LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^f NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^g CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

Author keywords

Autophagosome; Glycogen storage; Lysosomal storage disorder; Lysosome; Metabolic disorder; Myopathy; Skeletal muscle

Indexed keywords

ALPHA GLUCOSIDASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUTOPHAGY; CELL ORGANELLE; CONTROLLED STUDY; GLYCOGEN STORAGE DISEASE TYPE 2; GLYCOGEN STORAGE DISEASE TYPE 3; LYSOSOME; MOUSE; MUSCLE CELL; MUSCLE INJURY; MYOPATHY; NONHUMAN; PATHOGENESIS; PHAGOSOME; PROTEIN DEGRADATION; SKELETAL MUSCLE;

EID: 34548621869     PISSN: 15548627     EISSN: 15548635     Source Type: Journal    
DOI: 10.4161/auto.4591     Document Type: Article

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