Resultados da pesquisa - Chester A. Alper

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  1. 1
    Studies of the In Vivo Behavior of Human C′3 in Normal Subjects and Patients*

    Studies of the In Vivo Behavior of Human C′3 in Normal Subjects and Patients* Por Chester A. Alper, Fred S. Rosen

    Publicado em 1967
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  2. 2
    Genetic polymorphism of the third component of human complement (C′3)

    Genetic polymorphism of the third component of human complement (C′3) Por Chester A. Alper, Richard P. Propp

    Publicado em 1968
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  3. 3
    Inheritance of human α1-acid glycoprotein (orosomucoid) variants

    Inheritance of human α1-acid glycoprotein (orosomucoid) variants Por Amber Johnson, Karl Schmid, Chester A. Alper

    Publicado em 1969
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  4. 4
    GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEIN

    GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEIN Por Chester A. Alper, Thomas Boenisch, Lillian Watson

    Publicado em 1972
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  5. 5
    THE RELATIONSHIP OF GLYCINE-RICH ß-GLYCOPROTEIN TO FACTOR B IN THE PROPERDIN SYSTEM AND TO THE COBRA FACTOR-BINDING PROTEIN OF HUMAN SERUM

    THE RELATIONSHIP OF GLYCINE-RICH ß-GLYCOPROTEIN TO FACTOR B IN THE PROPERDIN SYSTEM AND TO THE COBRA FACTOR-BINDING PROTEIN OF HUMAN SERUM Por Chester A. Alper, Ira Goodkofsky, Irwin H. Lepow

    Publicado em 1973
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  6. 6
    SERUM-DEPENDENT PHAGOCYTOSIS OF PARAFFIN OIL EMULSIFIED WITH BACTERIAL LIPOPOLYSACCHARIDE

    SERUM-DEPENDENT PHAGOCYTOSIS OF PARAFFIN OIL EMULSIFIED WITH BACTERIAL LIPOPOLYSACCHARIDE Por Thomas P. Stossel, Chester A. Alper, Fred S. Rosen

    Publicado em 1973
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  7. 7
    Study of Four New Kindreds with Inherited Thyroxine-Binding Globulin Abnormalities POSSIBLE MUTATIONS OF A SINGLE GENE LOCUS

    Study of Four New Kindreds with Inherited Thyroxine-Binding Globulin Abnormalities POSSIBLE MUTATIONS OF A SINGLE GENE LOCUS Por Samuel Refetoff, Noel I. Robin, Chester A. Alper

    Publicado em 1972
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  8. 8
    Inactivator of the Third Component of Complement as an Inhibitor in the Properdin Pathway

    Inactivator of the Third Component of Complement as an Inhibitor in the Properdin Pathway Por Chester A. Alper, Fred S. Rosen, Peter J. Lachmann

    Publicado em 1972
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  9. 9
    Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

    Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man. Por Z Awdeh, D Raum, Edmond J. Yunis, Chester A. Alper

    Publicado em 1983
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  10. 10
    THE ENHANCEMENT OF BACTERIAL PHAGOCYTOSIS BY SERUM

    THE ENHANCEMENT OF BACTERIAL PHAGOCYTOSIS BY SERUM Por Richard B. Johnston, Martin R. Klemperer, Chester A. Alper, Fred S. Rosen

    Publicado em 1969
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  11. 11
    Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy.

    Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy. Por Chester A. Alper, E. Fleischnick, Z Awdeh, A. Katz, Edmond J. Yunis

    Publicado em 1987
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  12. 12
    The opsonic fragment of the third component of human complement (C3).

    The opsonic fragment of the third component of human complement (C3). Por T P Stossel, R J Field, JD Gitlin, Chester A. Alper, F S Rosen

    Publicado em 1975
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  13. 13
    Deficiency of C3 Inactivator in Man

    Deficiency of C3 Inactivator in Man Por Neil Abramson, Chester A. Alper, Peter J. Lachmann, Fred S. Rosen, James H. Jandl

    Publicado em 1971
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  14. 14
    The immune response to hepatitis B vaccine in humans: inheritance patterns in families.

    The immune response to hepatitis B vaccine in humans: inheritance patterns in families. Por Margot S. Kruskall, Chester A. Alper, Z Awdeh, Edmond J. Yunis, Deborah Marcus-Bagley

    Publicado em 1992
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  15. 15
    Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.

    Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema. Por Michael R. Quastel, R. A. Harrison, Marco Cicardi, Chester A. Alper, Fred S. Rosen

    Publicado em 1983
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  16. 16
    Restoration by purified C3b inactivator of complement-mediated function in vivo in a patient with C3b inactivator deficiency.

    Restoration by purified C3b inactivator of complement-mediated function in vivo in a patient with C3b inactivator deficiency. Por John B. Ziegler, Chester A. Alper, R S Rosen, P. J. Lachmann, Lisa Sherington

    Publicado em 1975
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  17. 17
    Homozygous human C3 deficiency. The role of C3 in antibody production, C-1s-induced vasopermeability, and cobra venom-induced passive hemolysis.

    Homozygous human C3 deficiency. The role of C3 in antibody production, C-1s-induced vasopermeability, and cobra venom-induced passive hemolysis. Por Chester A. Alper, Harvey R. Colten, J. S. S. Gear, Arthur R. Rabson, Fred S. Rosen

    Publicado em 1976
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  18. 18
    Studies in vivo and in vitro on an abnormality in the metabolism of C3 in a patient with increased susceptibility to infection

    Studies in vivo and in vitro on an abnormality in the metabolism of C3 in a patient with increased susceptibility to infection Por Chester A. Alper, Neil Abramson, Richard B. Johnston, James H. Jandl, Fred S. Rosen

    Publicado em 1970
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  19. 19
    Inherited deficiency of the third component of human complement (C′3)

    Inherited deficiency of the third component of human complement (C′3) Por Chester A. Alper, Richard P. Propp, Martin R. Klemperer, Fred S. Rosen, Lillian Watson

    Publicado em 1969
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  20. 20
    Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema

    Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema Por Fred S. Rosen, Chester A. Alper, Jack Pensky, Martin R. Klemperer, Virginia H. Donaldson

    Publicado em 1971
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