Zobrazeno 1 - 10
of 36
pro vyhledávání: '"J. D. Isaacs"'
Autor:
M. Cole, C. Yap, C. Buckley, W. F. Ng, I. McInnes, A. Filer, S. Siebert, A. Pratt, J. D. Isaacs, D. D. Stocken
Publikováno v:
Trials, Vol 22, Iss 1, Pp 1-10 (2021)
Abstract Background Adaptive model-based dose-finding designs have demonstrated advantages over traditional rule-based designs but have increased statistical complexity but uptake has been slow especially outside of cancer trials. TRAFIC is a multi-c
Externí odkaz:
https://doaj.org/article/e288990549964c93a1c4b9c09a373ddf
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Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 81(10)
Autor:
J D, Isaacs, S, Greer, S, Sharma, D, Symmons, M, Smith, J, Johnston, H, Waldmann, G, Hale, B L, Hazleman
Publikováno v:
Arthritis and rheumatism. 44(9)
Therapies that deplete lymphocytes often improve symptoms in patients with otherwise refractory autoimmune disease but may result in long-term lymphopenia, the consequences of which are uncertain. To assess the impact of prolonged lymphopenia on morb
Autor:
R J, Wakefield, W W, Gibbon, P G, Conaghan, P, O'Connor, D, McGonagle, C, Pease, M J, Green, D J, Veale, J D, Isaacs, P, Emery
Publikováno v:
Arthritis and rheumatism. 43(12)
The ability to make an early, accurate diagnosis of rheumatoid arthritis (RA) has become increasingly important with the availability of new, expensive, and targeted therapies. However, plain radiography, the traditional method of detecting the chara
Autor:
A W, Morgan, B, Griffiths, F, Ponchel, B M, Montague, M, Ali, P P, Gardner, H C, Gooi, R D, Situnayake, A F, Markham, P, Emery, J D, Isaacs
Publikováno v:
Arthritis and rheumatism. 43(10)
To investigate a possible association between a functional polymorphism in the intermediate-affinity receptor for IgG called Fc-gamma receptor type IIIA (FcgammaRIIIA [CD16]) and rheumatoid arthritis (RA).This was an allelic association study in whic
Publikováno v:
Clinical and experimental rheumatology. 17(6 Suppl 18)
Biologic therapies refer to genetically engineered treatments such as monoclonal antibodies and receptor-immunoglobulin fusion proteins. Following many disappointments, the introduction of anti-tumor necrosis factor (anti-TNF alpha) therapies into th
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 161(8)
An in vivo model is used to define Fc motifs engaged by mAbs to deplete target cells. Human IgG1 and human IgG4 were very potent, and mutations within a motif critical for Fc gammaR binding (glutamate 233 to proline, leucine/phenylalanine 234 to vali