ER network formation and membrane fusion by atlastin1/SPG3A disease variants

Molecular Biology of the Cell

Volumn 26, Issue 9, 2015, Pages 1616-1628

  Ulengin, Idil ^a   Park, John J ^a   Lee, Tina H ^a  

^a CARNEGIE MELLON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATLASTIN 1; GUANOSINE TRIPHOSPHATASE; GUANOSINE TRIPHOSPHATE; PEPTIDES AND PROTEINS; UNCLASSIFIED DRUG; ATL1 PROTEIN, HUMAN; CARRIER PROTEIN; DROSOPHILA PROTEIN; GUANINE NUCLEOTIDE BINDING PROTEIN; MEMBRANE PROTEIN; REEP1 PROTEIN, HUMAN;

ARTICLE; CONTROLLED STUDY; COS 7 CELL LINE; DIMERIZATION; ENDOPLASMIC RETICULUM MEMBRANE; GENE LOCUS; GENE SILENCING; HELA CELL LINE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; LIMB WEAKNESS; MEMBRANE FUSION; MOTOR NEUROPATHY; PC12 CELL LINE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN CROSS LINKING; PROTEIN DEPLETION; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN HYDROLYSIS; PROTEIN STABILITY; PYRAMIDAL NERVE CELL; PYRAMIDAL TRACT; RNA INTERFERENCE; SPASTICITY; ANIMAL; CHLOROCEBUS AETHIOPS; COS CELL LINE; DROSOPHILA MELANOGASTER; ENDOPLASMIC RETICULUM; GENETICS; METABOLISM; MISSENSE MUTATION; PHYSIOLOGY; RAT;

ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; ENDOPLASMIC RETICULUM; GTP-BINDING PROTEINS; HELA CELLS; HUMANS; MEMBRANE FUSION; MEMBRANE PROTEINS; MEMBRANE TRANSPORT PROTEINS; MUTATION, MISSENSE; PC12 CELLS; PROTEIN STABILITY; RATS; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 84929492909     PISSN: 10591524     EISSN: 19394586     Source Type: Journal    
DOI: 10.1091/mbc.E14-10-1447     Document Type: Article

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