Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulation

Human Molecular Genetics

Volumn 25, Issue 23, 2016, Pages 5111-5125

  Renvoisé, Benoît ^a   Malone, Brianna ^a   Falgairolle, Melanie ^b   Munasinghe, Jeeva ^c   Stadler, Julia ^a   Sibilla, Caroline ^a,d   Park, Seong H ^a   Blackstone, Craig ^a  

^a Cell Biology Section   (United States)

^b Laboratory of Neurochemistry   (United States)

^c NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^d MRC LABORATORY OF MOLECULAR BIOLOGY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FAT DROPLET; PERILIPIN; PROTEIN DERIVATIVE; PROTEIN REEP1; SPASTIN; UNCLASSIFIED DRUG; BSCL2 PROTEIN, MOUSE; CARRIER PROTEIN; HETEROTRIMERIC GUANINE NUCLEOTIDE BINDING PROTEIN; REEP1 PROTEIN, HUMAN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN CORTEX; CONGENITAL GENERALIZED LIPODYSTROPHY; CONTROLLED STUDY; EMBRYO; FIBROBLAST; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; KNOCKOUT MOUSE; MALE; MOTONEURON; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; ANIMAL; AXON; ENDOPLASMIC RETICULUM; GENETICS; HUMAN; METABOLISM; MORPHOGENESIS; MUTATION; PATHOLOGY; PATHOPHYSIOLOGY; PYRAMIDAL TRACT;

ANIMALS; AXONS; CEREBRAL CORTEX; ENDOPLASMIC RETICULUM; HETEROTRIMERIC GTP-BINDING PROTEINS; HUMANS; LIPID DROPLETS; LIPODYSTROPHY, CONGENITAL GENERALIZED; MEMBRANE TRANSPORT PROTEINS; MICE; MICE, KNOCKOUT; MORPHOGENESIS; MUTATION; PYRAMIDAL TRACTS; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 85014075342     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddw315     Document Type: Article

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