Cargando…
Modelling of human Wiskott–Aldrich syndrome protein mutants in zebrafish larvae using in vivo live imaging
Wiskott–Aldrich syndrome (WAS) and X-linked neutropenia (XLN) are immunodeficiencies in which the function of several haematopoietic cell lineages is perturbed as a result of mutations in the actin regulator WASp. From in vitro cell biology experiments, and biochemical and structural approaches, we...
Autores principales: | Jones, Rebecca A., Feng, Yi, Worth, Austen J., Thrasher, Adrian J., Burns, Siobhan O., Martin, Paul |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772384/ https://www.ncbi.nlm.nih.gov/pubmed/23868979 http://dx.doi.org/10.1242/jcs.128728 |
Ejemplares similares
-
The Wiskott-Aldrich Syndrome: The Actin Cytoskeleton and Immune Cell Function
por: Blundell, Michael P., et al.
Publicado: (2010) -
IL‐18: A potential inflammation biomarker in Wiskott–Aldrich syndrome
por: Rivers, Elizabeth, et al.
Publicado: (2021) -
Wiskott–Aldrich Syndrome: Immunodeficiency resulting from defective cell migration and impaired immunostimulatory activation
por: Bouma, Gerben, et al.
Publicado: (2009) -
Wiskott Aldrich syndrome protein regulates non-selective autophagy and mitochondrial homeostasis in human myeloid cells
por: Rivers, Elizabeth, et al.
Publicado: (2020) -
Exacerbated experimental arthritis in Wiskott–Aldrich syndrome protein deficiency: Modulatory role of regulatory B cells
por: Bouma, Gerben, et al.
Publicado: (2014)