Zobrazeno 1 - 10 of 29 pro vyhledávání: '"R E, Callard"'
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An interaction between the IL-4Rα gene and infection is associated with atopic eczema in young children
Autor: C. Blanco, Richard Jones, John Henderson, C. Chatterton, R. E. Callard, Andrea Sherriff, R Hamvas, Marcus Pembrey
Publikováno v: Clinical & Experimental Allergy. 32:990-993
Summary Background A gain of function mutation (Q551- > R) in the IL-4 receptor α-chain (IL-4Rα) has been found to be associated with atopy in some studies but not others. The different results may be explained by interactions between the IL-4Rα p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8660a29ce718f9cb6dd9c4e9e33b304b
https://doi.org/10.1046/j.1365-2222.2002.01414.x
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3
CD40 ligand (CD40L) expression and B cell function in agammaglobulinemia with normal or elevated levels of IgM (HIM). Comparison of X-linked, autosomal recessive, and non-X-linked forms of the disease, and obligate carriers
Autor: R E Callard, S H Smith, J Herbert, G Morgan, M Padayachee, S Lederman, L Chess, R A Kroczek, W C Fanslow, R J Armitage
Publikováno v: The Journal of Immunology. 153:3295-3306
Hyper-IgM syndrome is a rare immunodeficiency characterized by low or absent IgG, IgA, and IgE with normal or elevated levels of IgM. It can occur as an acquired or familial disorder with either X-linked or autosomal modes of inheritance. The X-linke
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c32a32b881bd6cf121bc34a04906378c
https://doi.org/10.4049/jimmunol.153.7.3295
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4
CD19 regulation of human B cell responses. B cell proliferation and antibody secretion are inhibited or enhanced by ligation of the CD19 surface glycoprotein depending on the stimulating signal used
Autor: R E Callard, K P Rigley, S H Smith, S Thurstan, J G Shields
Publikováno v: The Journal of Immunology. 148:2983-2987
The regulation of human B cell proliferation and differentiation by the CD19 surface glycoprotein was investigated. As expected, proliferation induced by costimulation with anti-IgM plus IL-4 or IL-2, or with G28.8 antibody plus IL-4 was inhibited by
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ebf064746c18c389365e43bc8f91cd22
https://doi.org/10.4049/jimmunol.148.10.2983
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5
An interaction between the IL-4Ralpha gene and infection is associated with atopic eczema in young children
Autor: R E, Callard, R, Hamvas, C, Chatterton, C, Blanco, M, Pembrey, R, Jones, A, Sherriff, J, Henderson
Publikováno v: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 32(7)
A gain of function mutation (Q551-R) in the IL-4 receptor alpha-chain (IL-4Ralpha) has been found to be associated with atopy in some studies but not others. The different results may be explained by interactions between the IL-4Ralpha polymorphism a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::59ffa68a1373c8fd3c58ab00ba55dcfc
https://pubmed.ncbi.nlm.nih.gov/12100043
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6
Impaired Ca2+ mobilization by X-linked agammaglobulinaemia (XLA) B cells in response to ligation of the B cell receptor (BCR)
Autor: R. E. Callard, H. C. Genevier
SUMMARY XLA bone marrow samples were shown to contain B cells expressing IgM, and pre-B cells that express the μ-surrogate light chain (μψLC) complex, albeit at a reduced frequency to that found in normal bone marrow. Antibody ligation of μ heavy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb98b9a9a9283096be87968fd7b0da6f
https://europepmc.org/articles/PMC1904822/
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9
T-lymphocyte activation in steroid-sensitive nephrotic syndrome in childhood
Autor: T J, Neuhaus, V, Shah, R E, Callard, T M, Barratt
Publikováno v: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 10(8)
We undertook a sequential study in 29 children with steroid-sensitive nephrotic syndrome (SSNS) off treatment to seek evidence for T-cell activation in relapse. T-cell subsets and activation markers were analysed using two-colour flow cytometry. Solu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b323f56e296d036ff019362ac25d12ff
https://pubmed.ncbi.nlm.nih.gov/8538925
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10
CD40 ligand (CD40L) expression and B cell function in agammaglobulinemia with normal or elevated levels of IgM (HIM). Comparison of X-linked, autosomal recessive, and non-X-linked forms of the disease, and obligate carriers
Autor: R E, Callard, S H, Smith, J, Herbert, G, Morgan, M, Padayachee, S, Lederman, L, Chess, R A, Kroczek, W C, Fanslow, R J, Armitage
Publikováno v: Journal of immunology (Baltimore, Md. : 1950). 153(7)
Hyper-IgM syndrome is a rare immunodeficiency characterized by low or absent IgG, IgA, and IgE with normal or elevated levels of IgM. It can occur as an acquired or familial disorder with either X-linked or autosomal modes of inheritance. The X-linke
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4b2e221d1920c888e7df07e3511f4107
https://pubmed.ncbi.nlm.nih.gov/7916370
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