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  • 1
    Publication Date: 2004-09-18
    Description: Eosinophils are often dominant inflammatory cells present in the lungs of asthma patients. Nonetheless, the role of these leukocytes remains poorly understood. We have created a transgenic line of mice (PHIL) that are specifically devoid of eosinophils, but otherwise have a full complement of hematopoietically derived cells. Allergen challenge of PHIL mice demonstrated that eosinophils were required for pulmonary mucus accumulation and the airway hyperresponsiveness associated with asthma. The development of an eosinophil-less mouse now permits an unambiguous assessment of a number of human diseases that have been linked to this granulocyte, including allergic diseases, parasite infections, and tumorigenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lee, James J -- Dimina, Dawn -- Macias, MiMi P -- Ochkur, Sergei I -- McGarry, Michael P -- O'Neill, Katie R -- Protheroe, Cheryl -- Pero, Ralph -- Nguyen, Thanh -- Cormier, Stephania A -- Lenkiewicz, Elizabeth -- Colbert, Dana -- Rinaldi, Lisa -- Ackerman, Steven J -- Irvin, Charles G -- Lee, Nancy A -- AI025230/AI/NIAID NIH HHS/ -- AI033043/AI/NIAID NIH HHS/ -- AR08545/AR/NIAMS NIH HHS/ -- F32 AR008545/AR/NIAMS NIH HHS/ -- F32 AR008545-01/AR/NIAMS NIH HHS/ -- F32 AR008545-02/AR/NIAMS NIH HHS/ -- F32 AR008545-03/AR/NIAMS NIH HHS/ -- HL058723/HL/NHLBI NIH HHS/ -- HL065228/HL/NHLBI NIH HHS/ -- HL10105/HL/NHLBI NIH HHS/ -- HLEB67273/HL/NHLBI NIH HHS/ -- NCRR-COBRE P20RR1555/RR/NCRR NIH HHS/ -- P01-HL67004/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 17;305(5691):1773-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Pulmonary Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA. jjlee@mayo.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15375267" target="_blank"〉PubMed〈/a〉
    Keywords: Allergens/immunology ; Animals ; Asthma/immunology/*pathology/*physiopathology ; Diphtheria Toxin/genetics ; Eosinophil Peroxidase ; Eosinophils/*physiology ; Gene Targeting ; Leukocyte Count ; Lung/immunology/*pathology/*physiopathology ; Mice ; Mice, Transgenic ; Models, Animal ; Mucus/secretion ; Ovalbumin/immunology ; Peptide Fragments/genetics ; Peroxidases/genetics ; Respiratory Hypersensitivity/immunology/pathology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 1980-02-15
    Description: The composite vagus nerve was stimulated during intravenous infusion of 5-hydroxytryptamine in cats subjected to pharmacologic autonomic blockade with atropine, propranolol, and phentolamine. Bronchial caliber, as assessed by changes in pulmonary resistance, demonstrated a marked dilatation, and dilatation could still be demonstrated after preliminary treatment with reserpine. By stimulating the component branches of the vagus nerve, it was determined that the parasympathetic branch is responsible for this phenomenon.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Irvin, C G -- Boileau, R -- Tremblay, J -- Martin, R R -- Macklem, P T -- New York, N.Y. -- Science. 1980 Feb 15;207(4432):791-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7352292" target="_blank"〉PubMed〈/a〉
    Keywords: Airway Resistance/drug effects ; Animals ; Bronchi/*innervation ; Cats ; Electric Stimulation ; Parasympatholytics/*pharmacology ; Sympatholytics/*pharmacology ; Vagus Nerve/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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