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Volumn 73, Issue 1, 1999, Pages 1-5

Glutathione reductase activity deficiency in homozygous Gr1(a1Neu) mice does not cause haemolytic anaemia

Author keywords

[No Author keywords available]

Indexed keywords

GLUTATHIONE REDUCTASE;

EID: 0033009796     PISSN: 00166723     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0016672398003590     Document Type: Article
Times cited : (20)

References (23)
  • 1
    • 0014592051 scopus 로고
    • Effect of flavin compounds on glutathione reductase activity: In vivo and in vitro studies
    • Beutler, E. (1969a). Effect of flavin compounds on glutathione reductase activity: in vivo and in vitro studies. Journal of Clinical Investigation 48, 1957-1966.
    • (1969) Journal of Clinical Investigation , vol.48 , pp. 1957-1966
    • Beutler, E.1
  • 2
    • 0014668145 scopus 로고
    • Glutathione reductase: Stimulation in normal subjects by riboflavin supplementation
    • Beutler, E. (1969b). Glutathione reductase: stimulation in normal subjects by riboflavin supplementation. Science 165, 613-615.
    • (1969) Science , vol.165 , pp. 613-615
    • Beutler, E.1
  • 5
    • 0028961615 scopus 로고
    • Induction of specific-locus and dominant lethal mutations in male mice by n-propyl and isopropyl methanesulfonate
    • Ehling, U. H. & Neuhäuser-Klaus, A. (1995). Induction of specific-locus and dominant lethal mutations in male mice by n-propyl and isopropyl methanesulfonate. Mutation Research 328, 73-82.
    • (1995) Mutation Research , vol.328 , pp. 73-82
    • Ehling, U.H.1    Neuhäuser-Klaus, A.2
  • 6
    • 0014027996 scopus 로고
    • Effects of sulfhydryl inhibition on red blood cells. III. Glutathione in the regulation of the hexose monophosphate pathway
    • Jacob, H. S. & Jandl, J. H. (1966). Effects of sulfhydryl inhibition on red blood cells. III. Glutathione in the regulation of the hexose monophosphate pathway. Journal of Biological Chemistry 241, 4243-4250.
    • (1966) Journal of Biological Chemistry , vol.241 , pp. 4243-4250
    • Jacob, H.S.1    Jandl, J.H.2
  • 8
    • 0022621945 scopus 로고
    • A model of hemopoietic stress in a lactate dehydrogenase mouse mutant with hemolytic anemia
    • Kremer, J.-P., Datta, T. & Dörmer, P. (1986). A model of hemopoietic stress in a lactate dehydrogenase mouse mutant with hemolytic anemia. Blut 52, 179-183.
    • (1986) Blut , vol.52 , pp. 179-183
    • Kremer, J.-P.1    Datta, T.2    Dörmer, P.3
  • 9
    • 0023626769 scopus 로고
    • Mechanisms of compensation of hemolytic anemia in a lactate dehydrogenase mouse mutant
    • Kremer, J.-P., Datta, T., Pretsch, W., Charles. D. J. & Dörmer, P. (1987). Mechanisms of compensation of hemolytic anemia in a lactate dehydrogenase mouse mutant. Experimental Hematology 15, 664-670.
    • (1987) Experimental Hematology , vol.15 , pp. 664-670
    • Kremer, J.-P.1    Datta, T.2    Pretsch, W.3    Charles, D.J.4    Dörmer, P.5
  • 10
    • 0014875052 scopus 로고
    • Familiärer glutathionreduktasemangel und störung der glutathionsynthese im erythrozyten
    • Kurz, R. & Hohenwallner, W. (1970). Familiärer Glutathionreduktasemangel und Störung der Glutathionsynthese im Erythrozyten. Helvetica Paedriatica Acta 25, 542-552.
    • (1970) Helvetica Paedriatica Acta , vol.25 , pp. 542-552
    • Kurz, R.1    Hohenwallner, W.2
  • 11
    • 24444469328 scopus 로고
    • Eine neue enzymopenische hämolytische anämie mit glutathionreduktase-mangel
    • Löhr, G.-W. & Waller, H. D. (1962). Eine neue enzymopenische hämolytische Anämie mit Glutathionreduktase-Mangel. Medizinische Klinik 36, 1521-1525.
    • (1962) Medizinische Klinik , vol.36 , pp. 1521-1525
    • Löhr, G.-W.1    Waller, H.D.2
  • 12
    • 0017062372 scopus 로고
    • Familial deficiency of glutathione reductase in human blood cells
    • Loos, H., Roos, D., Weening, R. & Houwerzijl, J. (1976). Familial deficiency of glutathione reductase in human blood cells. Blood 48, 53-62.
    • (1976) Blood , vol.48 , pp. 53-62
    • Loos, H.1    Roos, D.2    Weening, R.3    Houwerzijl, J.4
  • 13
    • 0026299006 scopus 로고
    • RI manager, a microcomputer program for analysis of data from recombinant inbred strains
    • Manly, K. F. & Elliot, R. W. (1991). RI Manager, a microcomputer program for analysis of data from recombinant inbred strains. Mammalian Genome 1, 123-126.
    • (1991) Mammalian Genome , vol.1 , pp. 123-126
    • Manly, K.F.1    Elliot, R.W.2
  • 14
    • 0024379013 scopus 로고
    • Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus
    • Merkle, S. & Pretsch, W. (1989). Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus. Genetics 123, 837-844.
    • (1989) Genetics , vol.123 , pp. 837-844
    • Merkle, S.1    Pretsch, W.2
  • 15
    • 0027389765 scopus 로고
    • Glucose-6-phosphate isomerase deficiency associated with nonspherocytic hemolytic anemia in the mouse: An animal model for the human disease
    • Merkle, S. & Pretsch, W. (1993). Glucose-6-phosphate isomerase deficiency associated with nonspherocytic hemolytic anemia in the mouse: an animal model for the human disease. Blood 81, 206-213.
    • (1993) Blood , vol.81 , pp. 206-213
    • Merkle, S.1    Pretsch, W.2
  • 16
    • 0016699430 scopus 로고
    • Polymorphism and linkage of glutathione reductase in Mus musculus
    • Nichols, E. A. & Ruddle, F. H. (1975). Polymorphism and linkage of glutathione reductase in Mus musculus. Biochemical Genetics 13, 323-329.
    • (1975) Biochemical Genetics , vol.13 , pp. 323-329
    • Nichols, E.A.1    Ruddle, F.H.2
  • 18
    • 0017162701 scopus 로고
    • Glutathionreduktasemangel mit membrandefekt bei hereditärer hämolylischer anämie
    • Pohl, A., Bugajer-Gleitmann, H. E., Lachmann, D. & Moser, K. (1976). Glutathionreduktasemangel mit Membrandefekt bei hereditärer Hämolylischer Anämie. Acta Haematologica (Basel) 56, 47-57.
    • (1976) Acta Haematologica (Basel) , vol.56 , pp. 47-57
    • Pohl, A.1    Bugajer-Gleitmann, H.E.2    Lachmann, D.3    Moser, K.4
  • 19
    • 0344540559 scopus 로고
    • Genetical and biochemical characterization of a dominant mutation of mouse lactate dehydrogenase
    • ed. B. J. Radola. Berlin: Walter de Gruyter
    • Pretsch, W. & Charles, D. (1980). Genetical and biochemical characterization of a dominant mutation of mouse lactate dehydrogenase. In Electrophoresis '79 (ed. B. J. Radola), pp. 817-824. Berlin: Walter de Gruyter.
    • (1980) Electrophoresis '79 , pp. 817-824
    • Pretsch, W.1    Charles, D.2
  • 20
    • 0023957185 scopus 로고
    • X-linked glucose-6-phosphate dehydrogenase deficiency in Mus musculus
    • Pretsch, W., Charles, D. J. & Merkle, S. (1988). X-linked glucose-6-phosphate dehydrogenase deficiency in Mus musculus. Biochemical Genetics 26, 89-103.
    • (1988) Biochemical Genetics , vol.26 , pp. 89-103
    • Pretsch, W.1    Charles, D.J.2    Merkle, S.3
  • 22
    • 0345402992 scopus 로고
    • Glutathione reductase deficiency
    • New York: Grune & Stratton
    • Waller, H. D. (1968). Glutathione reductase deficiency. In Hereditary Disorders of Erythrocyte Metabolism, pp. 185-204. New York: Grune & Stratton.
    • (1968) Hereditary Disorders of Erythrocyte Metabolism , pp. 185-204
    • Waller, H.D.1
  • 23
    • 0344109005 scopus 로고
    • Glutathionreduktasemangel mit hämatologischen und neurologischen störungen (autosomal dominant vererbliche bildung eines pathologischen enzyms)
    • Waller, H. D., Löhr, G. W., Zysno, E., Gerok, W., Voss, D. & Strauss, G. (1965). Glutathionreduktasemangel mit hämatologischen und neurologischen Störungen (Autosomal dominant vererbliche Bildung eines pathologischen Enzyms). Klinische Wochenschrift 43, 413-426.
    • (1965) Klinische Wochenschrift , vol.43 , pp. 413-426
    • Waller, H.D.1    Löhr, G.W.2    Zysno, E.3    Gerok, W.4    Voss, D.5    Strauss, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.