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1 - 7 of 7 results found for NCF1. Did you mean: nf1

  1. Conditional haploinsufficiency of NCF1 (encoding p47 (phox), a signalling gene with a...

    http://iris.ucl.ac.uk/iris/publication/56482/1

  2. Prenatal diagnosis in two families with autosomal, P47 (phox)- deficient chronic...

    http://iris.ucl.ac.uk/iris/publication/23615/1

  3. CD68-expressing cells can prime T cells and initiate autoimmune arthritis in the absence...

    It is widely believed that DC, but not macrophages, prime naïve T cells in vivo. Here, we investigated the ability of CD68-expressing cells (commonly defined as macrophages) in priming autoreactive T cells and initiating collagen-induced arthritis

    http://iris.ucl.ac.uk/iris/publication/423674/2

  4. Targeted Repair of p47-CGD in iPSCs by CRISPR/Cas9: Functional Correction without...

    © 2019 The Author(s) Klatt, Schambach and colleagues generated patient-like p47-ΔGT iPSCs for disease modeling of chronic granulomatous disease and subsequent gene correction of NCF1 (encodes p47phox) using CRISPR/Cas9. Their strategy avoided

    http://iris.ucl.ac.uk/iris/publication/1700700/1

  5. Lentiviral gene therapy rescues p47phox chronic granulomatous disease and the ability to...

    Chronic granulomatous disease (CGD) is an inherited primary immunodeficiency disorder characterised by recurrent and often life-threatening infections and hyperinflammation. It is caused by defects of the phagocytic NADPH oxidase, a multicomponent

    http://iris.ucl.ac.uk/iris/publication/1790456/1

  6. Monogenic mimics of Behçet's disease in the young.

    Objectives: Monogenic autoinflammatory disorders (AID) and primary immunodeficiencies can present early in life with features that may be mistaken for Behçet's disease (BD). We aimed to retrospectively describe the clinical and laboratory features

    http://iris.ucl.ac.uk/iris/publication/1625976/1

  7. Pulmonary metastatic colonisation and granulomas in NOX2-deficient mice.

    Metastasis is the leading cause of death in cancer patients and successful colonisation of a secondary organ by circulating tumour cells (CTCs) is the rate-limiting step of this process. We used tail-vein injection of B16-F10 melanoma cells into

    http://iris.ucl.ac.uk/iris/publication/1574205/1

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