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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: HLA histocompatibility antigens. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (413 pages)
    Edition: 1st ed.
    ISBN: 9780080542508
    Series Statement: Factsbook Series
    Language: English
    Note: Front Cover -- The HLA FactsBook -- Copyright Page -- Contents -- Preface -- Abbreviations -- SECTION I: THE INTRODUCTORY CHAPTERS -- Chapter 1. Introduction -- Chapter 2. Human Leukocyte Antigens (HLA) Determine Histocompatibility in Transplantation -- Chapter 3. The Organization of HLA Genes Within the HLA Complex -- Chapter 4. HLA Class I Antigens and Alleles: Workshops and Nomenclature -- Chapter 5. HLA Class II Antigens and Alleles: Workshops and Nomenclature -- Chapter 6. HLA Typing at the DNA Level -- Chapter 7. HLA Class I and II Molecules Present Peptide Antigens to Different Types of T Cell -- Chapter 8. HLA Class I Molecules Control Natural Killer Cell Function -- Chapter 9. Three-Dimensional Structures of HLA Class I Molecules -- Chapter 10. Three-Dimensional Structures of HLA Class II Molecules -- Chapter 11. HLA Polymorphism, Peptide-binding Motifs and T-Cell Epitopes -- Chapter 12. Evolution and Anthropology of HLA -- Chapter 13. HLA and Disease -- Chapter 14. Alloreactions in Transplantation -- SECTION II: THE HLA CLASS I AND CLASS II LOCI -- Guide to FactsBook Tables -- PART 1: HLA-A -- PART 2: HLA-B -- PART 3: HLA-C -- PART 4: HLA-E -- PART 5: HLA-F -- PART 6: HLA-G -- PART 7: HLA-DM -- PART 8: HLA-DO -- PART 9: HLA-DP -- PART 10: HLA-DQ -- PART 11: HLA-DR -- Index.
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  • 2
    ISSN: 1432-1211
    Keywords: Key words MICA ; MICB ; HLA-B ; SSOP ; Haplotypes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1211
    Keywords: Key words MICA ; HLA ; Polymorphism ; Oligonucleotide typing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract  A large number of diseases occur in association with specific HLA-B or –C alleles. Recently a new gene, termed major histocompatibility complex class I chain-related gene A (MICA), has been identified in close proximity to HLA-B. The function of this gene is still unknown, but, it is structurally related to HLA class I genes, is polymorphic, and is potentially associated with several diseases. Some DNA-based techniques have previously been described to type for MICA including sequencing and single-strand conformational polymorphism. In this paper we describe the application of sequence-specific oligonucleotide probe based typing for the analysis of the MICA gene. We used a set of 30 oligonucleotide probes to screen for the polymorphisms in exons 2, 3, and 4, which account for the 16 known alleles. We report here the typing results of MICA for 103 B-cell lines that have been well characterized for HLA and describe the linkage disequilibrium between MICA and HLA-B. Unequivocal MICA typing was achieved for 85 of the 103 cells tested, 6 cells gave ambiguous MICA types, and a further 12 cells showed patterns consistent with them expressing at least one new MICA allele.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 30 (1989), S. 515-519 
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 37 (1993), S. 79-94 
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The HLA class II sequences included in this compilation are taken from publications listed in the papers: Nomenclature for factors of the HLA system, 1989, Nomenclature for factors of the HLA system, 1990, and Nomenclature for factors of the HLA system, 1991 (WHO Nomenclature Committee 1990, 1991, 1992). Where discrepancies have arisen between reported sequences, the original authors have been contacted where possible, and necessary amendments to published sequences have been incorporated into this alignment. Future sequencing may identify errors in this list, and we would welcome any evidence that helps to maintain the accuracy of this compilation. In the sequence alignments, identity between residues is indicated by a hyphen (-), an unavailable sequence is indicated by an asterisk (*), and gaps in the sequence are inserted to maintain the alignment between different alleles showing variation in amino acid number.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 31 (1990), S. 141-144 
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 33 (1991), S. 321-334 
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The HLA class II sequences included in this compilation are taken from publications listed in the accompanying paper, Nomenclature for factors of the HLA system, 1990 (Bodmer et al. 1991) and Nomenclature for factors of the HLA system, 1989 (Bodmer et al. 1990). Where discrepancies have arisen between reported sequences the original authors have been contacted where possible, and necessary amendments to published sequences have been incorporated into this alignment. Future sequencing may identify errors in this list and we would welcome any evidence that helps to maintain the accuracy of this compilation. In the sequence alignments identity between residues is indicated by a hyphen (-). Unavailable sequence is indicated by an asterisk (*). Gaps in the sequence are inserted to maintain the alignment between different alleles showing variation in amino acid number.
    Type of Medium: Electronic Resource
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