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  • 1
    In: Cell Biochemistry and Function, Wiley, Vol. 32, No. 4 ( 2014-06), p. 344-350
    Abstract: Glycosaminoglycans (GAGs) from breast cyst fluid (BCF) of gross cysts, subdivided into apocrine and flattened, directly collected from 27 gross‐cystic‐breast‐disease (GCBD)‐affected women were analysed. Heparan sulfate, not further investigated, and chondroitin sulfate were identified. This last polysaccharide, in a content of 25–27 µg ml −1 BCF and having a high molecular mass (~20 000–22 000), was found rich in glucuronic acid (~96%–98%) and mainly sulfated in position 4 of the N ‐acetyl‐galactosamine (~60%–64%). Moreover, the presence of ~19%–24% of uncommon 4,6‐ O ‐disulfated disaccharides CS‐E inside the polysaccharide chains with a high charge density of ~1.15–1.20 was determined. No substantial differences between apocrine and flattened cysts were observed. The current study describes the first effort to examine the yield and distribution of complex macromolecules like GAGs in BCF, and the understanding of their structure may help explain some functions associated with physiological and pathological conditions. Copyright © 2013 John Wiley & Sons, Ltd.
    Type of Medium: Online Resource
    ISSN: 0263-6484 , 1099-0844
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 1496553-7
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Elsevier BV ; 2023
    In:  Research and Practice in Thrombosis and Haemostasis Vol. 7, No. 3 ( 2023-03), p. 100141-
    In: Research and Practice in Thrombosis and Haemostasis, Elsevier BV, Vol. 7, No. 3 ( 2023-03), p. 100141-
    Type of Medium: Online Resource
    ISSN: 2475-0379
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2023
    detail.hit.zdb_id: 2901840-7
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  • 3
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 2023
    In:  Clinical Chemistry and Laboratory Medicine (CCLM) Vol. 61, No. 6 ( 2023-05-25), p. 960-973
    In: Clinical Chemistry and Laboratory Medicine (CCLM), Walter de Gruyter GmbH, Vol. 61, No. 6 ( 2023-05-25), p. 960-973
    Abstract: The SARS-CoV-2 infection is characterized by both systemic and organ hyper-thromboinflammation, with a clinical course ranging from mild up-to critical systemic dysfunction and death. In patients with coronavirus disease 2019 (COVID-19) the monocyte/macrophage population is deeply involved as both trigger and target, assuming the value of useful diagnostic/prognostic marker of innate cellular immunity. Several studies correlated morphological and immunophenotypic alterations of circulating monocytes with clinical outcomes in COVID-19 patients, concluding that monocyte distribution width (MDW) may retain clinical value in stratifying the risk of disease worsening. Through an electronic search in Medline and Scopus we performed an updated literature review and meta-analysis aimed to explore the association between increased MDW levels and illness severity in COVID-19 patients, deciphering role(s) and function(s) of monocytes in the harmful network underlining SARS-CoV-2 infection. We found that significantly elevated MDW values were frequently present in COVID-19 patients who developed unfavorable clinical outcomes, compounded by a significant association between monocyte anisocytosis and SARS-CoV-2 outcomes. These findings suggest that blood MDW index and its scatter plot could represent useful routine laboratory tools for early identification of patients at higher risk of unfavorable COVID-19 and for monitoring the progression of viral infection, clinical outcomes, and therapeutic efficacy throughout hospitalization. According to this evidence, therapeutic decisions in patients with SARS-CoV-2 infection could benefit from monitoring MDW value, with administration of drugs limiting thrombo-inflammation due to monocyte hyper-activation in patients with severe/critical COVID-19 disease.
    Type of Medium: Online Resource
    ISSN: 1434-6621 , 1437-4331
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2023
    detail.hit.zdb_id: 1492732-9
    SSG: 15,3
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  • 4
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 2023
    In:  Clinical Chemistry and Laboratory Medicine (CCLM) Vol. 61, No. 8 ( 2023-07-26), p. 1525-1535
    In: Clinical Chemistry and Laboratory Medicine (CCLM), Walter de Gruyter GmbH, Vol. 61, No. 8 ( 2023-07-26), p. 1525-1535
    Abstract: Extracellular histone levels are associated with the severity of many human pathologies, including sepsis and COVID-19. This study aimed to investigate the role of extracellular histones on monocyte distribution width (MDW), and their effect on the release of cytokines by blood cells. Methods Peripheral venous blood was collected from healthy subjects and treated with different doses of a histone mixture (range 0–200 μg/mL) to analyze MDW modifications up-to 3 h and digital microscopy of blood smears. Plasma obtained after 3 h of histone treatment were assayed to evaluate a panel of 24 inflammatory cytokines. Results MDW values significantly increased in a time- and dose-dependent manner. These findings are associated with the histone-induced modifications of cell volume, cytoplasmic granularity, vacuolization, and nuclear structure of monocytes, promoting their heterogeneity without affecting their count. After 3 h of treatment almost all cytokines significantly increased in a dose-dependent manner. The most relevant response was shown by the significantly increased G-CSF levels, and by the increase of IL-1β, IL-6, MIP-1β, and IL-8 at the histone doses of 50, 100, and 200 µg/mL. VEGF, IP-10, GM-CSF, TNF-α, Eotaxin, and IL-2 were also up-regulated, and a lower but significant increase was observed for IL-15, IL-5, IL-17, bFGF, IL-10, IFN-γ, MCP-1, and IL-9. Conclusions Circulating histones critically induce functional alterations of monocytes mirrored by MDW, monocyte anisocytosis, and hyperinflammation/cytokine storm in sepsis and COVID-19. MDW and circulating histones may be useful tools to predict higher risks of worst outcomes.
    Type of Medium: Online Resource
    ISSN: 1434-6621 , 1437-4331
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2023
    detail.hit.zdb_id: 1492732-9
    SSG: 15,3
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  • 5
    In: Clinical Chemistry and Laboratory Medicine (CCLM), Walter de Gruyter GmbH, Vol. 0, No. 0 ( 2023-09-20)
    Abstract: SARS-CoV-2 infection may cause a wide spectrum of symptoms, from asymptomatic, to mild respiratory symptoms and life-threatening sepsis. Among the clinical laboratory biomarkers analyzed during COVID-19 pandemic, platelet indices have raised great interest, due to the critical involvement of platelets in COVID-19-related thromboinflammation. Through an electronic literature search on MEDLINE, CINAHL, PubMed, EMBASE, Web of Science, and preprint servers we performed and updated a systematic review aimed at providing a detailed analysis of studies addressing the potential clinical utility of platelet distribution width, platelet distribution width (PDW), in laboratory medicine, exploring the possible association between increased PDW levels, disease severity, and mortality in COVID-19. Our systematic review revealed a wide heterogeneity of COVID-19 cohorts examined and a lack of homogenous expression of platelet indices. We found that 75 % of studies reported significantly elevated PDW values in COVID-19 infected cohorts compared to healthy/non-COVID-19 controls, and 40 % of studies reported that patients with severe COVID-19 showed increased PDW values than those with less-than-severe illness. Interestingly, 71.4 % of studies demonstrated significant increased PDW values in non survivors vs. survivors. Overall, these results suggest that platelets are critically involved as major players in the process of immunothrombosis in COVID-19, and platelet reactivity and morphofunctional alterations are mirrored by PDW, as indicator of platelet heterogeneity. Our results confirm that the use of PDW as prognostic biomarkers of COVID-19 sepsis still remains debated due to the limited number of studies to draw a conclusion, but new opportunities to investigate the crucial role of platelets in thrombo-inflammation are warranted.
    Type of Medium: Online Resource
    ISSN: 1434-6621 , 1437-4331
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2023
    detail.hit.zdb_id: 1492732-9
    SSG: 15,3
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  • 6
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2013
    In:  BMC Cancer Vol. 13, No. 1 ( 2013-12)
    In: BMC Cancer, Springer Science and Business Media LLC, Vol. 13, No. 1 ( 2013-12)
    Type of Medium: Online Resource
    ISSN: 1471-2407
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2013
    detail.hit.zdb_id: 2041352-X
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  • 7
    In: Geology, Geological Society of America, Vol. 51, No. 2 ( 2023-02-01), p. 146-150
    Abstract: The Pacific, Antarctic, and Macquarie lithospheric plates diverge from the Macquarie Triple Junction (MTJ) in the southwestern Pacific Ocean, south of Macquarie Island. Morphobathymetric, magnetic, and gravity data have been used to understand the evolution of the three accretionary/transform boundaries that meet at the MTJ. Plate velocities, estimated near the MTJ and averaged over the past 3 m.y., indicate an unstable ridge–fault–fault triple junction. The long life ( & gt;6 m.y.) of this configuration can be attributed to a rapid increase in spreading asymmetry along the Southeast Indian Ridge segment as it approaches the MTJ, and to transtension along the southernmost strand of the Macquarie–Pacific transform boundary. A major change in plate motion triggered the development of the Macquarie plate at ca. 6 Ma and makes clear the recent evolution of the MTJ, including (1) shortening of the Southeast Indian Ridge segment; (2) formation of the westernmost Pacific-Antarctic Ridge, which increased its length over time; and (3) lengthening of the two transform boundaries converging in the MTJ. The clockwise change of the Pacific-Antarctic motion (ca. 12–10 Ma) led to complex geodynamic evolution of the plate boundary to the east of the triple junction, with fragmentation of the long-offset Emerald transform fault and its replacement over a short time interval (1–2 m.y.) with closely spaced, highly variable transform offsets that were joined by short ridge segments with time-varying asymmetries in the spreading rates.
    Type of Medium: Online Resource
    ISSN: 0091-7613 , 1943-2682
    Language: English
    Publisher: Geological Society of America
    Publication Date: 2023
    detail.hit.zdb_id: 184929-3
    detail.hit.zdb_id: 2041152-2
    SSG: 13
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  • 8
    Online Resource
    Online Resource
    Elsevier BV ; 2016
    In:  Journal of Vascular Surgery: Venous and Lymphatic Disorders Vol. 4, No. 3 ( 2016-07), p. 371-374
    In: Journal of Vascular Surgery: Venous and Lymphatic Disorders, Elsevier BV, Vol. 4, No. 3 ( 2016-07), p. 371-374
    Type of Medium: Online Resource
    ISSN: 2213-333X
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 2701667-5
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  • 9
    Online Resource
    Online Resource
    Elsevier BV ; 2018
    In:  Journal of Vascular Surgery: Venous and Lymphatic Disorders Vol. 6, No. 2 ( 2018-03), p. 296-297
    In: Journal of Vascular Surgery: Venous and Lymphatic Disorders, Elsevier BV, Vol. 6, No. 2 ( 2018-03), p. 296-297
    Type of Medium: Online Resource
    ISSN: 2213-333X
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2018
    detail.hit.zdb_id: 2701667-5
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  • 10
    In: Journal of Clinical Medicine, MDPI AG, Vol. 9, No. 11 ( 2020-11-11), p. 3634-
    Abstract: Diabetes mellitus is a heterogeneous and dysmetabolic chronic disease in which the laboratory plays a fundamental role, from diagnosis to monitoring therapy and studying complications. Early diagnosis and good glycemic control should start as early as possible to delay and prevent metabolic and cardio-vascular complications secondary to this disease. Glycated hemoglobin is currently used as the reference parameter. The accuracy of the glycated hemoglobin dosage may be compromised in subjects suffering from chronic renal failure and terminal nephropathy, affected by the reduction in the survival of erythrocytes, with consequent decrease in the time available for glucose to attach to the hemoglobin. In the presence of these renal comorbidities as well as hemoglobinopathies and pregnancy, glycated hemoglobin is not reliable. In such conditions, dosage of glycated albumin can help. Glycated albumin is not only useful for short-term diagnosis and monitoring but predicts the risk of diabetes, even in the presence of euglycemia. This protein is modified in subjects who do not yet have a glycemic alteration but, as a predictive factor, heralds the risk of diabetic disease. This review summarizes the importance of glycated albumin as a biomarker for predicting and stratifying the cardiovascular risk linked to multiorgan metabolic alterations.
    Type of Medium: Online Resource
    ISSN: 2077-0383
    Language: English
    Publisher: MDPI AG
    Publication Date: 2020
    detail.hit.zdb_id: 2662592-1
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