P62/SQSTM1 analysis in frontotemporal lobar degeneration

Neurobiology of Aging

Volumn 36, Issue 3, 2015, Pages 1603.e5-1603.e9

  Miller, Louise ^a   Rollinson, Sara ^a   Callister, Janis Bennion ^a   Young, Kate ^a   Harris, Jenny ^b   Gerhard, Alex ^b   Neary, David ^b   Richardson, Anna ^b   Snowden, Julie ^b   Mann, David M A ^b   Pickering Brown, Stuart M ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b HOPE HOSPITAL   (United Kingdom)

Author keywords

C9orf72; Frontotemporal lobar degeneration; FTLD; P62; SQSTM1

Indexed keywords

MEMBRANE PROTEIN; PROTEIN P62; SEQUESTOSOME 1; UNCLASSIFIED DRUG; AMINO ACID; C9ORF72 PROTEIN, HUMAN; PROTEIN; REPETITIVE DNA; SIGNAL TRANSDUCING ADAPTOR PROTEIN; SQSTM1 PROTEIN, HUMAN; STOP CODON;

ADULT; AGED; ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; EXPANSION MUTATION; FEMALE; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; MOLECULAR PATHOLOGY; OPEN READING FRAME; P62 GENE; PREMATURE STOP CODON; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SOUTHERN BLOTTING; SQSTM1 GENE; UNITED KINGDOM; CHEMISTRY; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; GREAT BRITAIN; MIDDLE AGED; MUTATION; STOP CODON; VERY ELDERLY;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADULT; AGED; AGED, 80 AND OVER; AMINO ACIDS; CODON, NONSENSE; COHORT STUDIES; DNA REPEAT EXPANSION; FEMALE; FRONTOTEMPORAL LOBAR DEGENERATION; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GREAT BRITAIN; HUMANS; MALE; MIDDLE AGED; MUTATION; OPEN READING FRAMES; PROTEINS;

EID: 84923412754     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2014.08.035     Document Type: Article

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