PRO136ALA CTLA4 Mutation

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PRO136ALA CTLA4 Mutation

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Title: PRO136ALA CTLA4 Mutation
Author: Palmer, Cody
Citation: Palmer, Cody. 2017. PRO136ALA CTLA4 Mutation. Master's thesis, Harvard Medical School.
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Abstract: Cytotoxic T lymphocyte antigen–4 (CTLA-4) is an inhibitory receptor involved in the regulation of immune responses. Deficiency of Ctla4 in mice causes fatal multiorgan lymphocytic infiltration. We identified a heterozygous, missense c.406C>G, p.P136A mutation in CTLA4 in a CVID patient. This mutation is within the binding motif of CTLA-4 and is predicted to interfere with ligand binding. To test whether this mutation is causal in the phenotype of the patient, we will use CRISPR/Cas9-mediated genome editing to clone the mutation into a regulatory T cell-like cell line and use the edited cell line for functional studies.
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33820495
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