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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 36 (1992), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Patients with gamma heavy chain disease (γ-HCD) generally produce incomplete immunoglobulin (Ig) γ-heavy chains (yγ-HCD protein) which cannot associate with light chains (IgL). In most patients Bence Jones proteins (BJP) are not observed. However, in the 61-year-old patienl WIN we found γl-HCD proteins and λ BJP in serum and urine. WIN -γl-HCD protein does not carry the Ig Fd region, has a molecular weight of 33.5 kDa, and the seven N-terminal amino acid residues are not translated from any of the known immunoglobulin heavy chain (IgH) gene sequences. These residues are followed by the Cγl-hinge region. In DNA from peripheral blood lymphocytes of patient WIN we found bands representing dominant rearrangements in one ofthe two alleles of the IgH, IgK and Igλ locus. Taken together, the data from protein and DNA analysis strongly suggest, albeit do not formally prove, that one dominant B-cell clone which carries it rearranged and a non-rearranged allele of each Ig locus produces γ-HCD protein and λ BJP. The productive λ-gene rearrangement in this clone thus has not been preceded by abortive rearrangements in both γ-locus alleles. Lymphocytes with an unusual sequence of IgL-chain gene activation seem to be involved in the case of γ-HCD described here.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 465 (1986), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 61 (1983), S. 349-356 
    ISSN: 1432-1440
    Keywords: Pulmonary sarcoidosis ; Immunology ; Lung T-lymphocytes ; Immunoenzyme technology ; Bronchoalveolar lavage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The aim of this study was to determine the value of the destination of T-lymphocyte subpopulations in bronchoalveolar lavage (BAL) fluid for the assessment of disease activity in pulmonary sarcoidosis in comparison with other tests of activity, i.e., lung function tests, angiotensin-converting enzyme (ACE), and gallium lung scan. According to clinical and roentgenographic data, 20 patients with biopsy-proven sarcoidosis were classified as having either active (nine patients) or inactive (11 patients) disease. Helper and suppressor T-lymphocyte subsets in BAL were identified by the peroxidase-antiperoxidase method performed on glass slides using murine monoclonal antibodies (OKT 3 for pan T-, OKT 4 for helper, and OKT 8 for suppressor T-lymphocytes). Patients with active sarcoidosis had significantly higher proportions of lung helper cells (90±5% of T-lymphocytes) than did patients with inactive sarcoidosis (65±11%) or control patients (63±7%),P〈0.001. The proportion of lung helper cells correlated significantly with vital capacity (r=−0.72,P〈0.001), with total lung capacity (r=−0.60,P〈0.01), with PaO2 at rest (r=−0.46,P〈0.05) and during exercise (r=−0.54,P〈0.05), and with CO-diffusing capacity/1 lung volume (r=−0.53,P〈0.05). There was, however, no correlation between lung lymphocyte subsets and serum ACE or gallium lung scan, nor between ACE and gallium scan. Although ACE and gallium uptake were higher in active sarcoidosis than in inactive disease, considerable overlap existed between groups, and the difference was not significant. Thus, the proportion of helper cells in BAL fluid appears to be a most useful parameter to assess activity of pulmonary sarcoidosis.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 56 (1988), S. 261-264 
    ISSN: 1432-0584
    Keywords: Acute leukemia ; Bone marrow transplantation ; Twins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The development of acute lymphoblastic leukemia (c-ALL) in identical twins is reported. The first born had ALL in 1982 and bone marrow transplantation was performed in first complete remission (CR) from his healthy twin-brother the same year. The bone marrow donor developed ALL in 1985; he received an autologous bone marrow transplantation in first CR in 1986. Unfortunately, both patients relapsed in 1986. Cytogenetic studies of the first born revealed multiple chromosomal abnormalities and a marker chromosome whereas the second patient had a Philadelphia chromosome. Genetic reasons or exposure to leukemogenic agents may be responsible for the onset of these leukemias.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 67 (1993), S. 133-134 
    ISSN: 1432-0584
    Keywords: Hydroxyurea ; Side effect ; Fever ; Acute alveolitis ; Chronic myeloid leukemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Hydroxyurea is increasingly being used to control myeloproliferative disorders, in part because of its relative lack of side effects. We present a case of life-threatening alveolitis in a patient treated with hydroxyurea for myeloproliferative syndrome. Absence of exposure to other drugs and the clinical course suggest that the alveolitis was induced by hydroxyurea.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-0584
    Keywords: Knochenmarktransplantation ; Genetischer Marker ; Lymphozyten-Phosphoglukomutase ; Bone marrow transplantation ; Genetic marker ; Lymphocyte phosphoglucomutase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Lymphocyte phosphoglucomutase can be used as a genetic marker to document successful engraftment in bone marrow transplant recipients. Two patients who underwent marrow transplantation as a treatment for acute leukemia showed a change into donor-type isozyme pattern.
    Notes: Zusammenfassung Phosphoglukomutase aus Lymphozyten kann als genetischer Marker in der Knochenmarktransplantation verwendet werden. Nach Knochenmarktransplantation von zwei Patienten mit akuter Leukose konnte der Übergang in das Iso-Enzymmuster des Spenders beobachtet werden.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0584
    Keywords: Ferritin ; Iron metabolism ; Erythrocytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Ferritin concentration has been determined with an immunoradiometric assay in plasma and washed sedimented erythrocytes after hypotonic lysis. There was a gradual decrease of plasma ferritin in the sequence normal males, normal females, blood donors and patients with iron deficiency anemia. Erythrocyte ferritin remained unchanged in normal males and females and in blood donors, but dropped significantly in the anemic patients. Correspondingly, the ratio of erythrocyte to plasma ferritin rose from less than 2 in healthy males up to 8 in persons with iron deficiency. Little, if any effect on plasma and erythrocyte ferritin was observed in 12 male and female volunteers when taking iron for 4 weeks. In 2 patients with iron deficiency anemia the blood counts were normalized within 2–3 months during oral iron substitution, accompanied by a drastic increase of the erythrocyte ferritin concentration to values far above normal. In contrast, the plasma ferritin concentration remained below normal. Thus, in iron deficiency erythrocyte ferritin is synthesized with priority in the presence of iron and, in addition to plasma ferritin, appears to be a useful parameter of the iron status.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-0584
    Keywords: Monocyte-Macrophages ; Differentiation ; Transferrin receptors ; Ferritin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Human blood monocytes when cultured on hydrophobic Teflon membranes differentiate into mature macrophages. The expression of transferrin receptors was monitored by monoclonal antibody (OKT9) binding as detected by immunperoxidase staining. Whereas monocytes were negative, an increasing percentage of macrophages, starting from day 2 in culture, labelled with the anti-transferrin receptor antibody as these cells undergo differentiation. After completion of maturation more than 90% of macrophages expressed transferrin receptors. While 90–95% of macrophages from broncho-alveolar lavage fluids labelled with the OKT9 antibody, only a minor portion of macrophages obtained from peritoneal and pleural cavities did so. In parallel, intracellular ferritin in cells of the monocyte-macrophage lineage increased from 10ng/106 cells to 350–1,500ng/106 cells during maturation in vitro. Alveolar macrophages proved to have the highest ferritin content which ranged from 355–8,400ng/106. The results may indicate that iron uptake and storage is a function of cells at late stages of macrophage maturation and that the occurrence of surface receptors for transferrin can be regarded as differentiation dependent marker.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0584
    Keywords: Lymphocytic leukemia ; Immunoglobulin light chains ; Western blotting
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The combination of two-dimensional mini gel electrophoresis with the ‘western blot’ technique proves to be a powerful tool in characterizing lymphoid cells. By testing for kappa and lambda immunoglobulin light chains we were able to differentiate between mono-, oligo-, and polyclonal B-cell diseases. The distribution of the lambda isotypes of 24 cases with chronic lymphocytic B-cell leukemia (B-CLL) tested was not random when compared to the distribution of the lambda light chains in B-lymphocytes of normal persons. This might implicate a genetic link between the lambda loci (chromosome 22) and the development of the lambda-CLL.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-0584
    Keywords: Human lymphoma clonogenic assay ; Human bone marrow stroma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We have analyzed cultures of malignant lymphoma cells and cells from patients with acute lymphoid leukemia in methylcellulose for their ability to from colonies. Clonogenic growth was examined in the presence or absence of fetal calf serum (FCS), platelet-poor plasma (PPP), medium conditioned by phytohemagglutininstimulated leukocytes (PHA-LCM), or irradiated allogeneic bone marrow stroma cells. Cells from 25 lymphoma patients — 17 with non-Hodgkin's lymphoma (NHL), eight with Hodgkin's disease (HD) — and from 19 patients with acute lymphocytic leukemia (ALL) were investigated. We show that colony growth can be obtained in a minority of cases (in 3 NHL, 5 HD, and 2 ALL) and that the use of FCS and allogeneic irradiated stroma cells may be required for optimal colony formation.
    Type of Medium: Electronic Resource
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