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Journal of Clinical Immunology|October 20, 2011

Phenotypic heterogeneity in a family with a CD40 ligand intracellular domain mutationS Kiani-Alikhan, P F K Yong, K C Gilmour, et al.

Journal of Clinical Pathology|October 29, 2008

Cerebral toxoplasmosis in a middle-aged man as first presentation of primary immunodeficiency due to a hypomorphic mutation in the CD40 ligand geneP F K Yong, F A Post, K C Gilmour, et al.

The Journal of Biological Chemistry|April 7, 1995

Transmembrane signaling by the alpha subunit of the type I interferon receptor is essential for activation of the JAK kinases and the transcriptional factor ISGF3O R Colamonici, L C Platanias, P Domanski, et al.

European Journal of Immunology|July 18, 2000

Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expressionK C Gilmour, T Cranston, A Jones, et al.

Clinical and Experimental Immunology|August 24, 2004

Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiencyD Eastwood, K C Gilmour, K Nistala, et al.

British Journal of Haematology|July 10, 2001

Protein assays for diagnosis of Wiskott-Aldrich syndrome and X-linked thrombocytopeniaW Qasim, K C Gilmour, S Heath, et al.

British Journal of Haematology|March 22, 2001

Rapid protein-based assays for the diagnosis of T-B+ severe combined immunodeficiencyK C Gilmour, T Cranston, S Loughlin, et al.

Cell|May 30, 1997

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone developmentF Otto, A P Thornell, T Crompton, et al.

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Showing results (11-20 of 18) with videos related to

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You have reached the last page of results.This site can display upto 18 results.

Journal of Clinical Immunology|October 20, 2011

Phenotypic heterogeneity in a family with a CD40 ligand intracellular domain mutationS Kiani-Alikhan, P F K Yong, K C Gilmour, et al.

Journal of Clinical Pathology|October 29, 2008

Cerebral toxoplasmosis in a middle-aged man as first presentation of primary immunodeficiency due to a hypomorphic mutation in the CD40 ligand geneP F K Yong, F A Post, K C Gilmour, et al.

The Journal of Biological Chemistry|April 7, 1995

Transmembrane signaling by the alpha subunit of the type I interferon receptor is essential for activation of the JAK kinases and the transcriptional factor ISGF3O R Colamonici, L C Platanias, P Domanski, et al.

European Journal of Immunology|July 18, 2000

Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expressionK C Gilmour, T Cranston, A Jones, et al.

Clinical and Experimental Immunology|August 24, 2004

Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiencyD Eastwood, K C Gilmour, K Nistala, et al.

British Journal of Haematology|July 10, 2001

Protein assays for diagnosis of Wiskott-Aldrich syndrome and X-linked thrombocytopeniaW Qasim, K C Gilmour, S Heath, et al.

British Journal of Haematology|March 22, 2001

Rapid protein-based assays for the diagnosis of T-B+ severe combined immunodeficiencyK C Gilmour, T Cranston, S Loughlin, et al.

Cell|May 30, 1997

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone developmentF Otto, A P Thornell, T Crompton, et al.

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