Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron disease

Proceedings of the National Academy of Sciences of the United States of America

Volumn 111, Issue 35, 2014, Pages

  Nguyen, Tammy T ^a   Oh, Sang S ^b   Weaver, David ^c   Lewandowska, Agnieszka ^a   Maxfield, Dane ^d   Schuler, Max Hinderk ^a   Smith, Nathan K ^a   Macfarlane, Jane ^a   Saunders, Gerald ^d   Palmer, Cheryl A ^a   Debattisti, Valentina ^c   Koshiba, Takumi ^e   Pulst, Stefan ^a   Feldman, Eva L ^b   Hajnóczky, György ^c   Shaw, Janet M ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^c THOMAS JEFFERSON UNIVERSITY   (United States)

^d UNIVERSITY OF UTAH   (United States)

^e KYUSHU UNIVERSITY   (Japan)

Author keywords

Miro GTPase; Mitochondrial respiration

Indexed keywords

CA2+-DEPENDENT MOTILITY; MIRO GTPASE; MITOCHONDRIAL RESPIRATION;

ADENOSINE TRIPHOSPHATE; AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; AXONAL TRANSPORT; CALCIUM; CELL RESPIRATION; DISEASE MODELS, ANIMAL; FEMALE; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MICROTUBULES; MITOCHONDRIA; MOTOR NEURONS; PARAPLEGIA; PHENOTYPE; RHO GTP-BINDING PROTEINS;

EID: 84907228136     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1402449111     Document Type: Article

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