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  • Annual Reviews  (3)
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  • Annual Reviews  (3)
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  • 1
    Online Resource
    Online Resource
    Annual Reviews ; 2013
    In:  Annual Review of Immunology Vol. 31, No. 1 ( 2013-03-21), p. 1-29
    In: Annual Review of Immunology, Annual Reviews, Vol. 31, No. 1 ( 2013-03-21), p. 1-29
    Abstract: This review describes the building and scientific activity of the Immunology Department at the Institute for Genetics in Cologne, cofounded by Max Delbrück in post–World War II Germany. The protagonist, a child of Russian emigrants, became interested in antibodies as a postdoc at the Pasteur Institute in Paris and a proponent of the antigen-bridge model of T-B cell collaboration during his early time in Cologne. He was challenged by the gap between cellular immunology and molecular genetics and profited from the advances of the latter as well as postwar economic growth in Germany. The Immunology Department became a place, and little universe in itself, where young scientists from all over the world came together to study cellular and molecular mechanisms of antibody formation. This included work on normal and malignant B cells in the human, particularly the origin of Hodgkin lymphoma, but the main focus was on B cell development and homeostasis, the germinal center reaction, and immunological memory, developing recombinase-assisted and conditional gene targeting in mice as a main technical tool.
    Type of Medium: Online Resource
    ISSN: 0732-0582 , 1545-3278
    URL: Issue
    RVK:
    Language: English
    Publisher: Annual Reviews
    Publication Date: 2013
    detail.hit.zdb_id: 1470451-1
    SSG: 12
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    Annual Reviews ; 1998
    In:  Annual Review of Immunology Vol. 16, No. 1 ( 1998-04), p. 471-493
    In: Annual Review of Immunology, Annual Reviews, Vol. 16, No. 1 ( 1998-04), p. 471-493
    Abstract: ▪ Abstract  One of the characteristic features of Hodgkin's disease (HD) is the presence of a small population of often bizarre-looking large mono- or multinucleated Hodgkin and Reed-Sternberg (HRS) cells within the affected tissue. Recent cytogenetic investigations, studies of Epstein-Barr virus (EBV) genomes present in HRS cells, and analyses of Ig gene rearrangements amplified from single, micromanipulated HRS cells show that these cells largely represent clonal populations. The finding of Ig gene rearrangements in HRS cells in most cases of HD identifies B cells as the precursors of HRS cells in most if not all cases. Furthermore, the presence and pattern of somatic mutations within the rearranged Ig genes show that HRS cells in classical (i.e. nodular sclerosis, mixed cellularity, and lymphocyte depletion HD) as well as lymphocyte predominant (LP) HD originate from germinal center (GC) B cells. Ongoing somatic mutation and evidence for selection link HRS cells from LP HD to a mutating, antigen-selected GC B cell. In classical HD, the finding of “crippling” mutations and lack of stringent selection for antigen receptor expression suggests that in this case HRS cells are derived from a compartment of GC B cells that were destined to die but escaped apoptosis by some transforming event. One candidate for the latter is EBV infection.
    Type of Medium: Online Resource
    ISSN: 0732-0582 , 1545-3278
    URL: Issue
    RVK:
    Language: English
    Publisher: Annual Reviews
    Publication Date: 1998
    detail.hit.zdb_id: 1470451-1
    SSG: 12
    Location Call Number Limitation Availability
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  • 3
    Online Resource
    Online Resource
    Annual Reviews ; 1983
    In:  Annual Review of Immunology Vol. 1, No. 1 ( 1983-04), p. 569-607
    In: Annual Review of Immunology, Annual Reviews, Vol. 1, No. 1 ( 1983-04), p. 569-607
    Type of Medium: Online Resource
    ISSN: 0732-0582 , 1545-3278
    URL: Issue
    RVK:
    Language: English
    Publisher: Annual Reviews
    Publication Date: 1983
    detail.hit.zdb_id: 1470451-1
    SSG: 12
    Location Call Number Limitation Availability
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