Detection of a novel familial catalase mutation (Hungarian type D) and the possible risk of inherited catalase deficiency for diabetes mellitus

Electrophoresis

Volumn 26, Issue 9, 2005, Pages 1646-1649

  Góth, László ^a   Vitai, Márta ^b   Rass, Péter ^c   Sükei, Eszter ^a   Páy, Anikó ^d  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b DRC Drug Research Center Ltd   (Hungary)

^c Sigma Aldrich   (Hungary)

^d INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

Author keywords

Blood catalase activity; Catalase mutation; Diabetes mellitus

Indexed keywords

BLOOD; CELL SIGNALING; OXIDATION;

BLOOD CATALASE ACTIVITY; CATALASE ACTIVITY; CATALASE MUTATION; DIABETES MELLITUS; ENZYME CATALASE; HETEROGENEOUS CONDITIONS; HUNGARIANS; LARGE-SCALES; LOW CONCENTRATIONS; SIGNALLING PATHWAYS;

HYDROGEN PEROXIDE;

CATALASE; HYDROGEN PEROXIDE;

AGAR GEL ELECTROPHORESIS; AMINO ACID SUBSTITUTION; ARTICLE; CATALASE DEFICIENCY; CLINICAL ARTICLE; DIABETES MELLITUS; DNA EXTRACTION; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENETIC POLYMORPHISM; GENOME ANALYSIS; HUMAN; HUNGARY; INTRON; MALE; MASS SCREENING; MUTATIONAL ANALYSIS; NUCLEIC ACID BASE SUBSTITUTION; POLYMERASE CHAIN REACTION; RISK ASSESSMENT; SEQUENCE ANALYSIS; SPECTROPHOTOMETRY; STEADY STATE;

EID: 18844424909     PISSN: 01730835     EISSN: None     Source Type: Journal    
DOI: 10.1002/elps.200410384     Document Type: Article

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