Genetic and biochemical studies of SNPs of the mitochondrial Aβ-degrading protease, hPreP

Neuroscience Letters

Volumn 469, Issue 2, 2010, Pages 204-208

  Pinho, Catarina Moreira ^a   Björk, Behnosh F ^b   Alikhani, Nyosha ^a   Bäckman, Hans G ^a   Eneqvist, Therese ^a   Fratiglioni, Laura ^b,c   Glaser, Elzbieta ^a   Graff, Caroline ^b,c  

^a STOCKHOLM UNIVERSITY   (Sweden)

^b KAROLINSKA INSTITUTE   (Sweden)

^c KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Alzheimer disease; Amyloid peptide; Mitochondria; PreP; Proteolysis; SNP

Indexed keywords

AMYLOID BETA PROTEIN; MAGNESIUM ION; PRESEQUENCE PROTEASE; PROTEINASE; UNCLASSIFIED DRUG;

ALZHEIMER DISEASE; ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME ACTIVITY; ENZYME ANALYSIS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MITOCHONDRION; MOLECULAR GENETICS; MUTATIONAL ANALYSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN DEGRADATION; SINGLE NUCLEOTIDE POLYMORPHISM;

AGED; ALLELES; ALZHEIMER DISEASE; AMYLOID BETA-PROTEIN; CASE-CONTROL STUDIES; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LINKAGE DISEQUILIBRIUM; MAGNESIUM; MALE; METALLOENDOPEPTIDASES; MODELS, MOLECULAR; PEPTIDE FRAGMENTS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 73049110916     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2009.11.075     Document Type: Article

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