About: The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features

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About: The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features Goto Sponge NotDistinct Permalink

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Attributes	Values
rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1985 (uk) article scientifique publié en 1985 (fr) im Oktober 1985 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57997160-44790BDE-3173-4516-87FD-154ED0C71F62
publication date	1985-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57997160-F8BBA7B0-C866-4807-B886-3B6C5F6C49C7
language of work or name	English
author name string	wds:Q57997160-00BC7CB3-3FBE-4A66-9078-55B30B498A9A wds:Q57997160-04817222-67B8-4D37-AC5D-A2532ADD8856 wds:Q57997160-5B58F6F2-4753-4F61-9502-C1409151F1B0 wds:Q57997160-68CC429A-13E1-4ADB-B849-51803CB81F8B wds:Q57997160-9552B553-FF4F-4F9D-BAB3-04B58D3EB65E wds:Q57997160-99492143-31C8-4587-AF20-B962263AEEA2 wds:Q57997160-A96DC7BB-381B-4A72-95C0-19F4EAB0D6F7 wds:Q57997160-B8BE9FD0-0DF0-4BB3-992A-46CF2219B7D9 wds:Q57997160-C0A34025-1734-436F-88D7-35E5F75C54E6 wds:Q57997160-DC180FB9-38AF-49AC-A749-3F13648AC37F
author name string	D C Anderson L J Miller M J Finegold M F Tosi B J Hughes R Rothlein S Kohl T C Waldrop R L Jacobs F C Schmalsteig
rdfs:label	The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features (en) The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features (nl)
skos:prefLabel	The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features (en) The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features (nl)
name	The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features (en) The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features (nl)
title	wds:Q57997160-665252CF-7587-4782-8AF6-F81BFEECE231
title	The severe and moderate phenotypes of heritable Mac-1, LFA-1 deficiency: their quantitative definition and relation to leukocyte dysfunction and clinical features (en)
page(s)	wds:Q57997160-2876F495-1B57-43D4-8A5F-6C36F7C9B062
page(s)	668-689
instance of	wds:Q57997160-885D7144-4B08-4F2A-9FD2-BC4F8D3C40BC
instance of	scholarly article
main subject	wds:Q57997160-C3D4756B-8ACA-4DC0-B828-99C4F08A0C43
main subject	phenotype
PubMed ID	wds:Q57997160-6C07025B-594C-4C21-9625-B901547333C0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3900232
PubMed ID	3900232
published in	wds:Q57997160-CB773245-B0BB-41B9-A449-210ADB86F09B
published in	Journal of Infectious Diseases
issue	wds:Q57997160-1DDEC63F-2F7F-4336-A661-BE8931D90B3E
volume	wds:Q57997160-100A94DE-3103-458B-99FB-3ED5E670C2CF
issue	4
volume	152
number of pages	wds:Q57997160-315D3D38-1777-4E17-BF3C-4C4A59665C4D
number of pages	22 (xsd:decimal)
DOI	wds:Q57997160-E1BDBEAF-A226-4B68-AE48-480F4CD32732
DOI	http://dx.doi.org/10.1093/INFDIS/152.4.668
DOI	10.1093/INFDIS/152.4.668
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57997160
is cites work of	The molecular basis of leukocytosis Leukocyte adhesion-deficient neutrophils fail to amplify phagocytic function in response to stimulation. Evidence for CD11b/CD18-dependent and -independent mechanisms of phagocytosis Demystified...adhesion molecule deficiencies The leukocyte integrins The requirement for lymphocyte function-associated antigen 1 in homotypic leukocyte adhesion stimulated by phorbol ester Distinct mutations in two patients with leukocyte adhesion deficiency and their functional correlates Noma in children with severe combined immunodeficiency Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations Determination of the adhesive capability of canine polymorphonuclear neutrophil granulocytes using a fluorometric microtiter plate cellular adhesion assay Neutrophil emigration in the skin, lungs, and peritoneum: different requirements for CD11/CD18 revealed by CD18-deficient mice Role of CD18 in the accumulation of eosinophils and neutrophils and local oedema formation in inflammatory reactions in guinea-pig skin Leucocyte adhesion to cells. Molecular basis, physiological relevance, and abnormalities Chemotaxis of non‐compressed blood polymorphonuclear leukocytes from an adolescent with severe leukocyte adhesion deficiency Familial genetic defect in a case of leukocyte adhesion deficiency Molecular characterization of leukocyte adhesion deficiency in six patients Characterization of four CD18 mutants in leucocyte adhesion deficient (LAD) patients with differential capacities to support expression and function of the CD11/CD18 integrins LFA-1, Mac-1 and p150,95 Association of intercellular adhesion molecule-1 (ICAM-1) with actin-containing cytoskeleton and alpha-actinin Role of endothelial selectins in wound repair Genetic analysis of integrin function in man: LAD-1 and other syndromes. Leukocyte adhesion deficiency type 1 (LAD-1)/variant. A novel immunodeficiency syndrome characterized by dysfunctional beta2 integrins Monoclonal antibody to the murine type 3 complement receptor inhibits adhesion of myelomonocytic cells in vitro and inflammatory cell recruitment in vivo CD18-independent neutrophil and mononuclear leukocyte emigration into the peritoneum of rabbits Recognition of an endothelial determinant for CD 18-dependent human neutrophil adherence and transendothelial migration Vascular and nonvascular expression of INCAM-110. A target for mononuclear leukocyte adhesion in normal and inflamed human tissues Leukocyte adhesion deficiency: recurrent childhood skin infections VLA-4 integrin can mediate CD11/CD18-independent transendothelial migration of human monocytes Cooperative interactions of LFA-1 and Mac-1 with intercellular adhesion molecule-1 in facilitating adherence and transendothelial migration of human neutrophils in vitro Neutrophil migration across monolayers of cytokine-prestimulated endothelial cells: a role for platelet-activating factor and IL-8 CD43 interferes with T-lymphocyte adhesion Leukocyte response integrin and integrin-associated protein act as a signal transduction unit in generation of a phagocyte respiratory burst Local chemokine paralysis, a novel pathogenic mechanism for Porphyromonas gingivalis. Complement and antibody participation in opsonophagocytosis of type IV and V group B streptococci Neutrophil granule constituents and their release in health and disease. The cytoplasmic domain of the integrin lymphocyte function-associated antigen 1 beta subunit: sites required for binding to intercellular adhesion molecule 1 and the phorbol ester-stimulated phosphorylation site Human natural killer cell deficiencies and susceptibility to infection Inverse association between endogenous glucocorticoid secretion and L-selectin (CD62L) expression in trauma patients Canine leukocyte adhesion deficiency colony for investigation of novel hematopoietic therapies The road less traveled: regulation of leukocyte migration across vascular and lymphatic endothelium by galectins LFA-1 immunodeficiency disease. Definition of the genetic defect and chromosomal mapping of alpha and beta subunits of the lymphocyte function-associated antigen 1 (LFA-1) by complementation in hybrid cells Infectious diseases associated with complement deficiencies Infections of People with Complement Deficiencies and Patients Who Have Undergone Splenectomy

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