Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases

Brain

Volumn 133, Issue 10, 2010, Pages 2920-2941

  Clemen, Christoph S ^a   Tangavelou, Karthikeyan ^a   Strucksberg, Karl Heinz ^a   Just, Steffen ^b   Gaertner, Linda ^b   Regus Leidig, Hanna ^c   Stumpf, Maria ^a   Reimann, Jens ^d   Coras, Roland ^e   Morgan, Reginald O ^f   Fernandez, Maria Pilar ^f   Hofmann, Andreas ^g   Müller, Stefan ^a   Schoser, Benedikt ^h   Hanisch, Franz Georg ^a   Rottbauer, Wolfgang ^b,i   Blümcke, Ingmar ^e   Von Hörsten, Stephan ^c   Eichinger, Ludwig ^a   Schröder, Rolf ^e  

^a UNIVERSITY OF COLOGNE   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^d UNIVERSITY HOSPITAL BONN   (Germany)

^e UNIVERSITY HOSPITAL ERLANGEN   (Germany)

^f UNIVERSITY OF OVIEDO   (Spain)

^g GRIFFITH UNIVERSITY   (Australia)

^h LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

ⁱ UNIVERSITY OF ULM   (Germany)

Author keywords

hereditary spastic paraplegia; IBMPFD; protein aggregate diseases; strumpellin; VCP

Indexed keywords

STRUMPELLIN; UNCLASSIFIED DRUG; VALOSIN CONTAINING PROTEIN; HUNTINGTON PROTEIN, MOUSE; KIAA0196 PROTEIN, HUMAN; NERVE PROTEIN; NUCLEAR PROTEIN; PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BRAIN NERVE CELL; CELL INCLUSION; CENTRAL NERVOUS SYSTEM; CONTROLLED STUDY; CYTOSOL; DISEASE MODEL; EMBRYO; ENDOPLASMIC RETICULUM; FEMALE; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENE OVEREXPRESSION; GENE SILENCING; HEART CONTRACTION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; HUNTINGTON CHOREA; LOSS OF FUNCTION MUTATION; MALE; MOTONEURON; MOUSE; MYOCARDIAL DISEASE; NERVE FIBER GROWTH; NEUROBLASTOMA CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PAGET BONE DISEASE; PHENOTYPE; PRESYNAPTIC NERVE; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; WILD TYPE; WOUND CLOSURE; WOUND HEALING IMPAIRMENT; ZEBRA FISH; ANIMAL; CELL CULTURE; CELL LINE; GENETIC PREDISPOSITION; GENETICS; IMMUNOHISTOCHEMISTRY; IMMUNOPRECIPITATION; INCLUSION BODY MYOSITIS; MASS SPECTROMETRY; METABOLISM; NERVE CELL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; WESTERN BLOTTING; WOUND HEALING;

ANIMALS; BLOTTING, WESTERN; CELL LINE; CELLS, CULTURED; ENDOPLASMIC RETICULUM; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IMMUNOHISTOCHEMISTRY; IMMUNOPRECIPITATION; MASS SPECTROMETRY; MICE; MYOSITIS, INCLUSION BODY; NERVE TISSUE PROTEINS; NEURONS; NUCLEAR PROTEINS; PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SPASTIC PARAPLEGIA, HEREDITARY; WOUND HEALING; ZEBRAFISH;

EID: 77957678410     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awq222     Document Type: Article

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