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Jacqueline Cordell

Researcher at University of Oxford

Publications -  25
Citations -  4821

Jacqueline Cordell is an academic researcher from University of Oxford. The author has contributed to research in topics: Monoclonal antibody & Antibody. The author has an hindex of 17, co-authored 24 publications receiving 4769 citations. Previous affiliations of Jacqueline Cordell include John Radcliffe Hospital & Royal College of Surgeons in Ireland.

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Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes).

TL;DR: The APAAP technique was found particularly suitable for labeling cell smears and for detecting low numbers of antigen-bearing cells in a specimen and could be used in conjunction with immunoperoxidase methods for double immunoenzymatic staining.
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The FOXP1 winged helix transcription factor is a novel candidate tumor suppressor gene on chromosome 3p

TL;DR: The JC12 monoclonal antibody recognizes a previously unknown nuclear protein that showed a restricted distribution in normal tonsil and was also overexpressed in a subset of diffuse large B-cell lymphomas and identified this protein as a novel putative transcription factor, FOXP1.
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Lymphomas expressing ALK fusion protein(s) other than NPM-ALK.

TL;DR: The results suggest that lymphomas carrying variants of the NPM-ALK fusion protein can be detected by immunostaining for ALK and NPM and also that they can be grouped with classical t(2;5)-positive tumors as a single entity that shows a better prognosis than ALK-negative anaplastic large-cell lymphomas.
Journal Article

Expression of the FOXP1 Transcription Factor Is Strongly Associated with Inferior Survival in Patients with Diffuse Large B-Cell Lymphoma

TL;DR: In this article, the authors investigated the prognostic importance of FOXP1 protein expression in an independent series of diffuse large B-cell lymphoma (DLBCL) cases.
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A human macrophage-associated antigen (CD68) detected by six different monoclonal antibodies.

TL;DR: It was concluded that these six antibodies react with a macrophage‐associated antigen for which the gene has been cloned, and this group of antibodies has recently been designated CD68 by the Fourth Workshop on Human Leucocyte Differentiation Antigens.