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Volumn 13, Issue 1, 2000, Pages 83-88

Hexokinase: Gene structure and mutations

Author keywords

Erythroid specific expression; Glycolysis; Haemolytic anaemia; Isozyme

Indexed keywords

ERYTHROID SPECIFIC HEXOKINASE R; HEXOKINASE; HEXOKINASE ISOENZYME; ISOENZYME; UNCLASSIFIED DRUG;

EID: 0034432367     PISSN: 15216926     EISSN: None     Source Type: Journal    
DOI: 10.1053/beha.1999.0058     Document Type: Article
Times cited : (25)

References (39)
  • 11
    • 0030998691 scopus 로고    scopus 로고
    • Identification of the cDNA for human red blood cell-specific hexokinase isozyme
    • (1997) Blood , vol.89 , pp. 762-766
    • Murakami, K.1    Piomelli, S.2
  • 15
    • 0026754672 scopus 로고
    • Primary pancreatic beta-cell secretory defect caused by mutations in glucokinase gene in kindreds of maturity onset diabetes of the young
    • (1992) Lancet , vol.340 , pp. 444-448
    • Velho, G.1    Froguel, P.2    Clement, K.3
  • 18
    • 0032518372 scopus 로고    scopus 로고
    • The mechanism of regulation of hexokinase: New insights from the crystal structure of recombinant human brain hexokinase complexed with glucose and glucose-6-phosphate
    • (1998) Structure , vol.6 , pp. 39-50
    • Aleshin, A.E.1    Zeng, C.2    Bourenkov, G.P.3
  • 35
    • 4244094961 scopus 로고    scopus 로고
    • Severe hexokinase deficiency as a cause of hemolytic anemia, periventricular leucomalacia and intrauterine death of the fetus
    • (1997) Blood , vol.90
    • Kanno, H.1    Ishikawa, K.2    Fujii, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.