Results 301 to 310 of about 607,266 (334)
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Cell surface antigens

Cytogenetic and Genome Research, 1976
A stable human-Chinese hamster ovary cell hybrid has been produced which, in addition to the complement of Chinese hamster ovary (CHO-K1) chromosomes, contains only one human chromosome, No. 11. The human cell-surface antigens whose expression is controlled by human chromosome 11, and are expressed by this hybrid, have been defined as the A<sub>L&
E.E. Moore, C. Jones, T.T. Puck
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Murine Lymphocyte Surface Antigens

1979
Publisher Summary This chapter discusses the multiple lymphocyte surface antigens of the mouse. A wide range of different antigens is described, ranging from those that have a broad tissue distribution to those highly restricted to specific lymphocytes and including others, such as viral-associated antigens.
I F, McKenzie, T, Potter
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Embryonic surface antigens: A “quasi-endodermal” teratoma antigen

Developmental Biology, 1976
Abstract Hyperimmune antisera against a teratoma-derived endodermal carcinoma of the mouse were used in cytotoxicity tests and by absorption analysis to define a surface antigen. This antigen was found to be present on all tumor cells tested that were of endodermal origin as well as on embryonic liver, and was therefore designated “Endo.” Further ...
Artzt, K   +3 more
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Melanocytes Express 3G5 Surface Antigen

The American Journal of Dermatopathology, 2004
The 3G5-reactive ganglioside antigen (3G5 antigen) is expressed on the surface of various cell types including pericytes, pancreatic islet cells, thyroid follicular cells, and cells of the pituitary and the adrenal medulla. Expression on melanocytes has not yet been reported.
Eckhard, Fiedler   +3 more
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Surface antigens of human trophoblasts

Developmental & Comparative Immunology, 1977
Abstract Single cells and cell aggregates of human trophoblasts were studied by immunofluorescence and mixed haemadsorption for the presence of different surface antigens. Results indicate that fresh trophoblast cells do not express HL-A in detectable amounts but carry human chorionic gonadotropin (HCG) and Con-A receptors.
K G, Sundqvist   +2 more
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Trypanosoma cruzi: Surface antigenic determinants

Zeitschrift f�r Parasitenkunde Parasitology Research, 1983
A fraction (FAd) capable of inhibiting specific agglutination reactions of anti-epimastigote sera (anti-LE) was obtained by extracting the sediment of lyophilized epimastigote lysates (LE) with 0.05 M phosphate buffered saline, at 37 degrees C for 1 h.
W M, Tamashiro   +6 more
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Surface antigens of Schistosoma mansoni

Molecular and Biochemical Parasitology, 1981
Abstract The outer tegument membrane of 18 h artificially prepared schistosomula of Schistosoma mansoni was labelled using the non-permeant diazonium salt of [ 125 I]iodosulphanilic acid. Eight iodinated surface proteins were identified by SDS-polyacrylamide gel electrophoresis.
D W, Taylor, E G, Hayunga, W E, Vannier
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Surface Antigens of Haemophilus pertussis

Nature, 1958
IT has been shown by Frappier and Guerault1,2, and Frappier, Guerault and De Repentigny3, that the antigen of Haemophilus pertussis which protects mice against intracerebral infection could be washed off the bacteria by saline (0.85 per cent sodium chloride).
A, GUERAULT, H B, MAITLAND
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Surface Antigens of Bordetella Pertussis

1985
Bordetella pertussis and other Bordetella species cause respiratory infections in humans and in a variety of animals. Clinical isolates of B. pertussis have multiple virulence factors, several of which have been reported to induce protective immunity.
C D, Parker, S K, Armstrong, D W, Frank
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Surface Antigens of Smooth Brucellae

Journal of Bacteriology, 1968
Surface antigens of smooth brucellae were extracted by ether-water, phenol-water, trichloroacetic acid, and saline and examined by immunoelectrophoresis and gel diffusion with antisera from infected and immunized rabbits. Ether-water extracts ofBrucella melitensiscontained a lipopolysaccharide protein component, which was specific for the surface of ...
R, Diaz   +3 more
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