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Volumn 79, Issue 5, 2001, Pages 1109-1112
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N ε-(γ-L-glutamyl)-L-lysine (GGEL) is increased in cerebrospinal fluid of patients with Huntington's disease
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Author keywords
Cerebrospinal fluid; Huntington's disease; N ( L Glutamyl) L lysine; Neurodegenerative diseases; Transglutaminases
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Indexed keywords
HUNTINGTIN;
LYSINE DERIVATIVE;
N EPSILON (GAMMA GLUTAMYL)LYSINE;
POLYGLUTAMINE;
PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE;
UNCLASSIFIED DRUG;
DIPEPTIDE;
EPSILON (GAMMA GLUTAMYL) LYSINE;
EPSILON-(GAMMA-GLUTAMYL)-LYSINE;
PHTHALALDEHYDE;
ARTICLE;
CEREBROSPINAL FLUID ANALYSIS;
CONTROLLED STUDY;
DEGENERATIVE DISEASE;
DEMENTIA;
ENZYME ACTIVITY;
GENE MUTATION;
HUMAN;
HUMAN TISSUE;
HUNTINGTON CHOREA;
PRIORITY JOURNAL;
ADULT;
CEREBROSPINAL FLUID;
CHEMISTRY;
ELECTROCHEMISTRY;
FEMALE;
ISOTOPE DILUTION ASSAY;
LIQUID CHROMATOGRAPHY;
MALE;
METABOLISM;
ADULT;
CHROMATOGRAPHY, LIQUID;
DIPEPTIDES;
ELECTROCHEMISTRY;
FEMALE;
HUMAN;
HUNTINGTON DISEASE;
MALE;
O-PHTHALALDEHYDE;
RADIOISOTOPE DILUTION TECHNIQUE;
SUPPORT, U.S. GOV'T, P.H.S.;
TRANSGLUTAMINASES;
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EID: 0034747325
PISSN: 00223042
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1471-4159.2001.00673.x Document Type: Article |
Times cited : (84)
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References (30)
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