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  • 1975-1979  (21)
  • 1965-1969  (3)
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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Biochemistry 8 (1969), S. 3937-3944 
    ISSN: 1520-4995
    Quelle: ACS Legacy Archives
    Thema: Biologie , Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Biochemistry 16 (1977), S. 3514-3518 
    ISSN: 1520-4995
    Quelle: ACS Legacy Archives
    Thema: Biologie , Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract Responses to GLPhe5 were generated in vitro, using the GLPhe helper factor. A plaque assay, using GLPhe-coated SRC, was used to measure antibody responses to GLPhe. Mice of differentH-2 haplotypes were tested for the ability to produce the GLPhe helper factor or to respond to a known GLPhe helper factor. We report here defects in nonresponder mice of different strains in both the production of helper factor and in the capacity to respond to it.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Immunogenetics 6 (1978), S. 283-291 
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract C57BL/6 (H-2 b) mice, when immunized with the sequential polymer (T-G-A-Gly)n and its low-molecular-weight oligomers, respond only to theα-helical oligomers with molecular weights of 9700 and above. Only the sameα-helical oligomers were able to inhibit the homologous antigen-antibody reaction. Random copolymers of GA, GT, and GAT10 did not inhibit. In vitro stimulation of peritoneal exudate lymphocyte (PETLES) cultures showed that the cellular response (T-cell) against (T-G-A-Gly)n is antigen-specific. In vitro antigen-induced stimulation of whole spleen or lymph node lymphocytes indicated that (T-G-A-Gly)n might also be a B-cell mitogen.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Immunogenetics 9 (1979), S. 183-192 
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract A series of known sequential polypeptides is being synthesized and used in our laboratory to study the contribution of antigen structure, i. e., amino acid sequence and conformation in antigen recognition and specificity of the immune response. The capacity to respond to one such α-helical polypeptide (T-G-A-Gly)n, is T-cell dependent and restricted to mice of theH- 2b haplotype. The response is controlled by anIr gene mapping to theK region and/or theIA subregion which allows the animal to make both a T-cell mediated response, as well as a humoral response to the polypeptide. The response of three mutant strains at theK end of the major histocompatibility locus (MHC) need not differ from that of the responder parental haplotype. PETLES obtained from mice possessing a responder haplotype proliferate when cultured in vitro with (T-G-A-Gly)n. The antibody level of individual inbred mice of a given strain at a given time differs significantly (from 80% binding to less than 10% antigen bound in 3 out of 57 mice). There is also great individual variability in time of appearance of the antibody response and where peak optimal levels are seen. Possible explanations for the variation in the antibody expression include: (a) the polymer is a weak immunogen, (b) the presence of modifier gene(s) outside of the major histocompatibility complex controlling the magnitude of the antibody level, (c) the possible effect of the polymer which is a B cell mitogen as a generator of suppressor T cells and, (d) a feedback mechanism effect on B cells controlling the antibody level.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Immunogenetics 6 (1978), S. 149-159 
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract The immune responses of inbred mice to the terpolymers poly(glu48-Iys32 ala20) GLA20, poly(glu36lys24ala40) GLA40, and poly(glu24lys16ala60) GLA60 were studied. Antibody levels were measured with the homologous, as well as with the crossreacting polymers (glu60ala40) GA and (glu60lys40) GL. It was determined that the terpolymers consist of many determinants of varying immunogenic strengths which account for the dose dependency requirements for responsiveness as follows: mice ofH-2 haplotypesa, b, d, k, ands respond to ten and 100μg GLA20 and GLA40 and to one, ten, and 100 μg GLA60; mice ofH-2 haplotypesp, q, andr do not respond well to any concentration of GLA20 but respond well to 100 μg GLA40 and tenμg GLA60. That the congenic mice C3H.NB (H-2 p) and B10.R111 (H-2 r), having responder backgrounds of C3H (H-2 k) and C57BL/10 (H-2 b) mice, respectively, do not respond would suggest strongly that there is linkage of responsiveness toH-2 in the above strains. In addition, the responsiveness of AQR mice to GLA60 would map theIr gene(s) to the right of theK region, and most likely in theI region. The antibody against GLA20 was directed against GL. Responses of miceof H-2 haplotypesp, q, andr against GLA40 and GLA60 were directed predominantly against unique GLA determinants that were neither GA nor GL. Mice of the other respondingH-2 haplotypes (a, b, d, k, ands) produced antibody against these unique GLA specificities, as well as against GL and/or GA determinants. The importance of measuring responses with the homologous polymer is therefore demonstrated. It was postulated that the recognition of GLA20 at the T-cell level is via GLA determinants having a limited amount of alanine, which are different from those helical GLA determinants recognized in the polymers GLA40 and GLA60.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract The immune response of inbred lines of chickens to the terpolymer poly(glu60ala30tyr10) and copolymer poly(glu60ala40) was determined. Of six lines immunized, one (line 7) contained birds that either did not respond or were low responders to two injections of 1 mg each of the polymers in Freund's complete adjuvant. As indicated by radioimmunoelectrophoresis, low responders produced a 7S response, although the switch from 17S (high molecular weight immunoglobulin) to 7S antibody production was slower than in high-responder lines. Analysis of the distribution of responders and nonresponders in F2 generations produced byinter se mating of F1 hybrids of line 7 with high-responder lines, showed that immune responses were clearly determined by certain alloalleles of theB blood group locus, the major histocompatibility system in the chicken.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract The immune response of allophenic mice of type C57BL/6↔(A × SJL) F1 to GLΦ administered in complete Freund's adjuvant was tested. Control mice of the three strains C57BL/6, A, and SJL are all nonresponders to this antigen. However, the F1 generations of C57BL/6 × A, C57BL/6 × SJL, and A × SJL were all responders to the antigen, so that the complementarity of at least two genes is confirmed. The allophenic mice showed no further complementation beyond the F1 generation, a result which may argue against the possibility that more than two genes control the response to GLΦ in these mouse strains. Characterization of the allophenic mice over several months showed that they exhibit “chimeric drift,” both in their coat color and in peripheral white blood cell population. There is no apparent correlation of coat color to the lymphocyte composition of the mice at any one time. The mice are true chimeras, since killing of the two populations of white blood cells with two different anti-H-2 sera produced a 100 percent killing. The immune response of individual allophenic mice to GLΦ showed a good correlation to the number of A × SJL lympho-cytes in the animal.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Springer
    Immunogenetics 4 (1977), S. 199-204 
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    ISSN: 1432-1211
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract Immune responses to the sequential helical polypeptide (Tyr-Ala-Glu-Gly)n [(T-A-G-Gly)n] in mice is under the control of at least two separate genes. One gene,Ir-(T-A-G-Gly)-1, which is linked, toH-2 haplotypesb, f, andr, controls the ability to respond and maps to theIA subregion. A non-H-2-linked locus,Ir-(T-A-G-Gly)-2. is responsible for the magnitude of the antibody response, which is expressed as a high, intermediate, or low level of antibody production. The antibody produced is of the IgG class, and does not crossreact even with the closely related sequential helical polymer (Tyr-Glu-Ala-Gly)n [(T-G-A-Gly)n]. Immune responsiveness is a dominant trait,i.e., the F1 generations of responder x nonresponder crosses are responders. However, the data obtained with both backcross populations are not easily interpretable. The contribution of the B-cell mitogenic activity of the sequential polymer to activation of suppressor T cells is considered as a possible explanation for the backcross results. The possible role of the Ia. W29 specificity present in the mouse strains responding to both (T-A-G-Gly)n and calf skin collagen type I in modulating responses to the polymers is discussed.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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