Abnormal concentration and anomalous distribution of apolipoprotein A-I in Tangier disease.

[1]  R. Bradshaw,et al.  Structure of high density lipoprotein. The immunologic reactivities of the COOH- and NH2-terminal regions of apolipoprotein A-I. , 1976, The Journal of biological chemistry.

[2]  P. Wahl,et al.  Quantitation of apolipoprotein A-I of human plasma high density lipoprotein. , 1976, Metabolism: clinical and experimental.

[3]  G. Utermann,et al.  Plasma lipoprotein abnormalities in a case of primary high‐density‐lipoprotein (HDL) deficiency , 1975, Clinical genetics.

[4]  S. Eisenberg,et al.  Radioimmunoassay of human high density lipoprotein apo-protein A-1. , 1975, Biochimica et biophysica acta.

[5]  H. Greten,et al.  Lipoproteins and lipolytic plasma enzymes in a case of tangier disease. , 1974, The New England journal of medicine.

[6]  G. Schonfeld,et al.  The structure of human high density lipoprotein and the levels of apolipoprotein A-I in plasma as determined by radioimmunoassay. , 1974, The Journal of clinical investigation.

[7]  R. Krauss,et al.  Further Observations on the Activation and Inhibition of Lipoprotein Lipase by Apolipoproteins , 1973, Circulation research.

[8]  A. Gotto,et al.  Studies on the protein defect in Tangier disease. Isolation and characterization of an abnormal high density lipoprotein. , 1972, The Journal of clinical investigation.

[9]  K. Weber,et al.  The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis. , 1969, The Journal of biological chemistry.

[10]  A. Scanu,et al.  Fractionation of human serum high density lipoprotein in urea solutions. Evidence for polypeptide heterogeneity. , 1969, Biochemistry.

[11]  W. Engel,et al.  Neuropathy in Tangier disease. Alpha-Lipoprotein deficiency manifesting as familial recurrent neuropathy and intestinal lipid storage. , 1967, Archives of neurology.

[12]  Denis Williams,et al.  FAMILIAL α-LIPOPROTEIN DEFICIENCY (TANGIER DISEASE) WITH NEUROLOGICAL ABNORMALITIES , 1967 .

[13]  R. Lees,et al.  Fat transport in lipoproteins--an integrated approach to mechanisms and disorders. , 1967, The New England journal of medicine.

[14]  R. Reisfeld,et al.  Electrophoretic Heterogeneity of Polypeptide Chains of Specific Antibodies , 1966, Science.

[15]  D. Fredrickson,et al.  Tangier disease (familial high density lipoprotein deficiency). Clinical and genetic features in two adults. , 1965, The American journal of medicine.

[16]  R. Hubbard.  Studies in accelerated amino acid analysis. , 1965, Biochemical and biophysical research communications.

[17]  D. Fredrickson.  THE INHERITANCE OF HIGH DENSITY LIPOPROTEIN DEFICIENCY (TANGIER DISEASE). , 1964, The Journal of clinical investigation.

[18]  R. P. Howard,et al.  STUDIES OF THE METABOLISM OF RADIOIODINATED HUMAN SERUM ALPHA LIPOPROTEIN IN NORMAL AND HYPERLIPIDEMIC SUBJECTS. , 1964, The Journal of laboratory and clinical medicine.

[19]  L. Avioli,et al.  Tangier Disease: Combined Clinical Staff Conference at the National Institutes of Health , 1961 .

[20]  A. Scanu,et al.  Recombining capacity toward lipids of the protein moiety of human serum alpha 1-lipoprotein. , 1960, The Journal of biological chemistry.

[21]  R. Havel,et al.  The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum. , 1955, The Journal of clinical investigation.

[22]  S. Moore,et al.  Chromatography of amino acids on sulfonated polystyrene resins. , 1951, The Journal of biological chemistry.

[23]  G. Assmann.  Familial Lipoprotein Deficiency , 1978 .

[24]  A. Scanu,et al.  Measurement of human high density lipoprotein apolipoprotein A-1 in serum by radioimmunoassay. , 1976, Journal of lipid research.

[25]  V. Ferrans,et al.  The pathology of Tangier disease. A light and electron microscopic study. , 1975, The American journal of pathology.

[26]  C. Mitchell,et al.  Plasma lipoprotein metabolism in familial lecithin:cholesterol acyltransferase deficiency. , 1974, Scandinavian journal of clinical and laboratory investigation. Supplementum.