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  • 1
    Keywords: Medicine ; Immunology ; Molecular biology ; Cell biology ; Biomedicine ; Molecular Medicine ; Immunology ; Cell Biology
    Description / Table of Contents: Part I Basic Research for Innovative Medicine --- 1. Diverting Glycolysis to Combat Oxidative Stress --- 2. Metabolic Regulation by Nuclear Receptors --- 3. Fighting Fire with Fire in Cancer --- 4. Linear Polyubiquitination: a Crucial Regulator of NF-kB Activation --- 5. VCP, a major ATPase in the cells, as a novel drug target for currently incurable disorders --- 6. Roles of E-cadherin in hepatocarcinogenesis --- 7. The Hippo Signaling Pathway: A Candidate New Drug Target for Malignant Tumors --- 8. Inhibitory immunoreceptors on mast cells in allergy and inflammation --- 9. Doxycycline-inducible Autoimmune Blistering Skin Disease Model --- 10. T-cell Senescence and Autoimmunity --- Part II Translational Research for Innovative Medicine --- 11. IL-6: A new era for the treatment of autoimmune inflammatory diseases --- 12. Pathogenesis of Non-alcoholic Steatohepatitis and Its Potential Therapeutic Strategies --- 13. Multifaceted translational approach of major mental illness --- 14. Translational research of leptin in lipodystrophy and its related diseases --- 15. Translational research of the activation of the C-type natriuretic peptide (CNP)-guanylyl cyclase-B pathway for skeletal dysplasia --- 16. Clarity and Challenges in Tissue Fibrosis --- 17. TRP Channels: Their Function and Potentiality as Drug Targets --- 18. Autophagic Cell Death and Cancer Chemotherapeutics --- 19. Adrenomedullin as a Potential Therapeutic Agent for Refractory Ulcerative Colitis --- 20. RNA activation --- Part III New Technology for Innovative Medicine --- 21. Cardiac Reprogramming for Heart Repair --- 22. Development of a new in vivo optical probe for biological diagnosis and therapy --- 23. Introduction of mesenchymal stem cells for liver surgery (hepatectomy and transplantation) --- 24. Synaptic and axonal plasticity induction in the human cerebral cortex --- 25. TIM-3 is a novel therapeutic target for eradicating acute myelogenous leukemia stem cells --- 26. TGF-beta LAP degradation products, a novel biomarker and promising therapeutic target for liver fibrogenesis --- 27. Cell-based regenerative therapy for liver disease
    Pages: Online-Ressource (IX, 339 pages)
    ISBN: 9784431556510
    Language: English
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  • 2
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Achondroplasia is the most common genetic form of human dwarfism, for which there is presently no effective therapy. C-type natriuretic peptide (CNP) is a newly identified molecule that regulates endochondral bone growth through GC-B, a subtype of particulate guanylyl cyclase. Here we show that ...
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  • 3
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Leptin is a circulating hormone that is expressed abundantly and specifically in the adipose tissue1–5. It is involved in the regulation of energy homeostasis, as well as the neuroendocrine and reproductive systems6–11. Here, we demonstrate production of leptin by nonadipose tissue, ...
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  • 4
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Sir — The obese (ob) gene encodes a fat cell-derived blood-borne satiety factor (also known as leptin) that is involved in the regulation of energy homeostasis1–6. Mice homozygous for the ob mutation, ob/ob mice, develop severe hereditary obesity and non-insulin dependent diabetes ...
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  • 5
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Interaction between endothelial cells and mural cells (pericytes and vascular smooth muscle) is essential for vascular development and maintenance. Endothelial cells arise from Flk1-expressing (Flk1 +) mesoderm cells, whereas mural cells are believed to derive from mesoderm, ...
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  • 6
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Coronary spasm plays an important role in the pathogenesis of not only variant angina but also ischemic heart disease in general. However, the precise mechanism(s) by which coronary spasm occurs remains to be elucidated. Coronary spasm may arise from interactions between environmental and genetic factors. Endothelial derived nitric oxide (NO) has been implicated in the control of vascular tone. We have recently shown that both basal and acetylcholine (ACh)-induced NO activities are impaired in the coronary arteries of patients with coronary spasm. The purpose of this study has been to elucidate the possible variants that occur in the coding region of the endothelial nitric oxide synthase (eNOS) gene and that may be associated with coronary spasm. After initial screening in the entire 26 coding regions of the eNOS gene, we found a missense Glu298Asp variant in exon 7 in patients with coronary spasm. We subsequently performed a larger scale study involving 113 patients with coronary spasm and 100 control subjects, who were all diagnosed by intracoronary injection of ACh. The analysis revealed a significant difference in the distribution of the variant between the coronary spasm group (21.2%) and control group (9.0%; P=0.014 for dominant effect). Thus, we have found the missense Glu298Asp variant in the eNOS gene by the analysis of its entire 26 coding regions. The variant is significantly associated with coronary spasm.
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  • 7
    ISSN: 1573-6865
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Immunohistochemical examination of atrial natriuretic peptide (ANP) was performed on endomyocardial biopsy specimens from 8 patients with dilated cardiomyopathy (DCM), 10 human foetal hearts obtained from legal abortions, and 8 adult hearts from autopsy control subjects without cardiovascular diseases. The indirect immunoperoxidase method, using specific monoclonal antibody to α-human ANP was employed. Immunoreactivity was observed at the light microscope level in the working ventricular cardiocytes of all patients with DCM as dark-brown, granular deposits. Peripheral plasma levels of ANP in these patients were also increased. In control adult hearts without cardiovascular diseases, immunoreactivity was detected both in the atria and in the ventricular impulse-conducting system, although the working ventricular cardiocytes were not immunoreactive. In foetal hearts, immunoreactivity was detected not only in the atria and ventricular impulse-conducting system, but also in the working ventricular cardiocytes. We conclude that ANP is present in the ventricular impulse-conducting system of the human hearts, and that ANP is also present in the working ventricular cardiocytes in patients with DCM as well as in human foetuses.
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  • 8
    ISSN: 1573-904X
    Keywords: atrial natriuretic peptide ; brain natriuretic peptide ; clearance receptor ; neutral endopeptidase ; phosphoramidon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract To assess clearance mechanisms of atrial and brain natriuretic peptides in the circulation, we examined the effects of a neutral endopeptidase (NEP) inhibitor and a clearance receptor ligand on plasma concentrations of the peptides in normal rats. Plasma concentrations of endogenous α-rat atrial natriuretic peptide (α-rANP) were not significantly elevated by intravenous infusion of a NEP inhibitor, phosphoramidon, but were elevated threefold by intravenous infusion of a clearance receptor ligand, des(Gln18-Gly22)-rANP(4−23)-NH2 [C-ANF(4−23)]. On the other hand, the clearance of α-rANP given intravenously at the pharmacological dose, 600 pmol/ min/kg for 2 min, was decreased to one-third by the administration of phosphoramidon, although the administration of C-ANF(4−23) did not significantly decrease the clearance. The clearance of rat brain natriuretic peptide (rBNP) given at 600 pmol/min/kg for 2 min was approximately 38% lower than that of α-rANP. The effect of phosphoramidon on the clearance of rBNP was not significant and was similar to that of C-ANF(4−23). These results suggest that clearance receptor is involved in the clearance of the physiological levels of α-rANP and that NEP plays a major role in the clearance of a pharmacological dose of α-rANP, at which clearance receptors are thought to be saturated, and also indicate a pharmacokinetic difference between α-rANP and rBNP.
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  • 9
    ISSN: 1573-904X
    Keywords: arterio-venous fistula ; atrial natriuretic peptide ; heart failure ; myocardial infarction ; neutral endopeptidase ; phosphoramidon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract We developed a rat model of heart failure induced by myocardial infarction (MI) which preserves responsiveness to exogenously administered natriuretic peptide, and investigated the potentiating action of neutral endopeptidase (NEP) inhibition on the renal response to endogenous natriuretic peptide in MI rats, comparing with that in the established cardiac-failing model with arterio-venous fistula (AVF). The endogenous plasma concentration of α-rat atrial natriuretic peptide (α-rANP) in the MI rat was 6.4-fold higher than that in the normal rat, and intravenous infusion of phosphoramidon (165 nmol/min/kg), an NEP inhibitor, induced larger increases in circulating α-rANP levels and natriuresis in MI rats than in normal controls. The maximal natriuretic effect of phosphoramidon (165 nmol/ min/kg) was equal to that of exogenously administered α-rANP (100 pmol/min/kg) in MI rats, whereas plasma α-rANP concentration under NEP inhibition was much lower than that after administration of α-rANP. The endogenous α-rANP levels in AVF rats were as high as those in MI rats. However, the natriuretic effect of phosphoramidon was less in AVF rats than in MI rats, which was consistent with the decreased natriuretic activity observed with administration of exogenous to α-rANP in the AVF rat. These results indicate that the natriuretic effect of NEP inhibition is dependent on elevated endogenous α-rANP levels in cardiac-failing rats, but cannot be accounted for simply in terms of the increase in circulating α-rANP levels. Endogenous natriuretic peptide-mediated natriuresis under NEP inhibition also appears to correlate with the responsiveness to the exogenously administered peptide.
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  • 10
    ISSN: 1573-8744
    Keywords: atrial natriuretic peptide ; brain natriuretic peptide ; neutral endopeptidase ; NONMEM ; nonlinear mixed effect model ; pharmacodynamics ; phosphoramidon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Natriuretic peptides have not only natriuretic/diuretic but also hypotensive activities, and the decreased renal perfusion caused by the excessive hypotension is known to attenuate the diuretic actions. The present study was designed to examine the relationship between the dosing (intravenous constant infusion) rates and the diuretic actions of α-rat atrial natriuretic peptide (α-rANP) and rat brain natriuretic peptide (rBNP) in rats, and population (nonlinear mixed effect model) analysis was applied to these complicated diuretic actions. The intrinsic diuretic activities of α-rANP and rBNP could be analyzed, and the effects of blood pressure, heart rate, and also inhibition of degradation enzyme on the diuresis of natriuretic peptides were estimated simultaneously. The population analysis was useful for analyzing such pharmacodynamic data for which the individual analysis could not be applied easily.
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