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Journal Abstract Search

143 related items for PubMed ID: 6320877

  • 1. Self-adaptive modification of red-cell membrane lipids in lecithin: cholesterol acyltransferase deficiency. Lipid analysis and spin labeling.
    Yawata Y, Miyashima K, Sugihara T, Murayama N, Hosoda S, Nakashima S, Iida H, Nozawa Y.
    Biochim Biophys Acta; 1984 Jan 25; 769(2):440-8. PubMed ID: 6320877
    [Abstract] [Full Text] [Related]

  • 2. Spin label studies of erythrocytes with abnormal lipid composition: comparison of red cells in a hereditary hemolytic syndrome and lecithin: cholesterol acyltransferase deficiency.
    Godin DV, Herring FG.
    J Supramol Struct Cell Biochem; 1981 Jan 25; 15(3):213-8. PubMed ID: 6267314
    [Abstract] [Full Text] [Related]

  • 3. Erythrocyte membrane alterations in lecithin:cholesterol acyltransferase deficiency.
    Godin DV, Gray GR, Frohlich J.
    Scand J Clin Lab Invest Suppl; 1978 Jan 25; 150():162-7. PubMed ID: 218274
    [Abstract] [Full Text] [Related]

  • 4. Alterations in erythrocyte membrane lipid and its fragility in a patient with familial lecithin:cholesterol acyltrasferase (LCAT) deficiency.
    Suda T, Akamatsu A, Nakaya Y, Masuda Y, Desaki J.
    J Med Invest; 2002 Aug 25; 49(3-4):147-55. PubMed ID: 12323004
    [Abstract] [Full Text] [Related]

  • 5. Detection of erythrocyte membrane structural abnormalities in lecithin: cholesterol acyltransferase deficiency using a spin label approach.
    Maraviglia B, Herring FG, Weeks G, Godin DV.
    J Supramol Struct; 1979 Aug 25; 11(1):1-7. PubMed ID: 230389
    [Abstract] [Full Text] [Related]

  • 6. Lecithin:cholesterol acyltransferase deficiency and cell membrane lipids and function in human liver disease.
    Owen JS, Hutton RA, Hope MJ, Harry DS, Bruckdorfer KR, Day RC, McIntyre N, Lucy JA.
    Scand J Clin Lab Invest Suppl; 1978 Aug 25; 150():228-32. PubMed ID: 746354
    [No Abstract] [Full Text] [Related]

  • 7. [A case of familial lecithin: cholesterol acyltransferase deficiency].
    Baba Y, Hamada F, Aozaki S, Hagihara R, Ohashi T, Yasumoto Y, Ohsaki K, Yamashita W, Harada R, Arima T.
    Nihon Jinzo Gakkai Shi; 1992 Mar 25; 34(3):309-16. PubMed ID: 1630033
    [Abstract] [Full Text] [Related]

  • 8. Decreased sodium influx and abnormal red cell membrane lipids in a patient with familial plasma lecithin: cholesterol acyltransferase deficiency.
    Murayama N, Asano Y, Hosoda S, Maesawa M, Saito M, Takaku F, Sugihara T, Miyashima K, Yawata Y.
    Am J Hematol; 1984 Feb 25; 16(2):129-37. PubMed ID: 6695915
    [Abstract] [Full Text] [Related]

  • 9. Study of erythrocytes in a hereditary hemolytic syndrome (HHS): comparison with erythrocytes in lecithin:cholesterol acyltransferase (LCAT) deficiency.
    Godin DV, Gray GR, Frohlich J.
    Scand J Haematol; 1980 Feb 25; 24(2):122-30. PubMed ID: 6246569
    [Abstract] [Full Text] [Related]

  • 10. Lipid analyses and fluidity studies by electron spin resonance of red cell membranes in hereditary high red cell membrane phosphatidylcholine hemolytic anemia.
    Yawata Y, Sugihara T, Mori M, Nakashima S, Nozawa Y.
    Blood; 1984 Nov 25; 64(5):1129-34. PubMed ID: 6091816
    [Abstract] [Full Text] [Related]

  • 11. [Decreased sodium influx in leaky red cell membranes in familial lecithin-cholesterol acyltransferase deficiency].
    Murayama N, Asano Y, Hosoda S, Maesawa S, Saito M, Takaku F, Sugihara H, Miyashima K, Yawata Y.
    Rinsho Ketsueki; 1983 Oct 25; 24(10):1342-8. PubMed ID: 6672267
    [No Abstract] [Full Text] [Related]

  • 12. Decreased fluidity of red cell membrane lipids in abetalipoproteinemia.
    Cooper RA, Durocher JR, Leslie MH.
    J Clin Invest; 1977 Jul 25; 60(1):115-21. PubMed ID: 874076
    [Abstract] [Full Text] [Related]

  • 13. Hereditary plasma lecithin-cholesterol acyl transferase deficiency: a heterozygous variant with erythrocyte membrane abnormalities.
    Jain SK, Mohandas N, Sensabaugh GF, Shojania AM, Shohet SB.
    J Lab Clin Med; 1982 Jun 25; 99(6):816-26. PubMed ID: 7077125
    [Abstract] [Full Text] [Related]

  • 14. [Membrane cholesterol and insulin receptor in erythrocytes].
    Maehara K.
    Fukuoka Igaku Zasshi; 1991 Nov 25; 82(11):586-602. PubMed ID: 1774014
    [Abstract] [Full Text] [Related]

  • 15. Molecular species of phosphatidylcholine in familial lecithin-cholesterol acyltransferase deficiency: effect of enzyme supplementation.
    Subbaiah PV, Pritchard PH.
    Biochim Biophys Acta; 1989 Jun 08; 1003(2):145-50. PubMed ID: 2730888
    [Abstract] [Full Text] [Related]

  • 16. A study of the small spherical high density lipoproteins of patients afflicted with familial lecithin: cholesterol acyltransferase deficiency.
    Chen C, Applegate K, King WC, Glomset JA, Norum KR, Gjone E.
    J Lipid Res; 1984 Mar 08; 25(3):269-82. PubMed ID: 6726080
    [Abstract] [Full Text] [Related]

  • 17. Lipoprotein morphology in some LCAT-deficient states.
    Bode G, Klör HU, Ditschuneit H.
    Scand J Clin Lab Invest Suppl; 1978 Mar 08; 150():199-207. PubMed ID: 746349
    [No Abstract] [Full Text] [Related]

  • 18. Lower levels of erythrocyte membrane fluidity in diabetic patients. A spin label study.
    Kamada T, Otsuji S.
    Diabetes; 1983 Jul 08; 32(7):585-91. PubMed ID: 6305749
    [Abstract] [Full Text] [Related]

  • 19. Changes in membrane lipid composition of human erythrocytes after dietary supplementation of (n-3) polyunsaturated fatty acids. Maintenance of membrane fluidity.
    Popp-Snijders C, Schouten JA, van Blitterswijk WJ, van der Veen EA.
    Biochim Biophys Acta; 1986 Jan 16; 854(1):31-7. PubMed ID: 3002462
    [Abstract] [Full Text] [Related]

  • 20. Alpha-lecithin:cholesterol acyltransferase deficiency. Lack of both phospholipase A2 and acyltransferase activities characteristic of high density lipoprotein lecithin:cholesterol acyltransferase in fish eye disease.
    Holmquist L, Carlson LA.
    Acta Med Scand; 1987 Jan 16; 222(1):23-6. PubMed ID: 3630775
    [Abstract] [Full Text] [Related]

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