Matches in Nanopublications for { ?s ?p "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523717.RAv8jnsXcWs4B2uE-zP1-wW0_-xNN5WhV9kcDcIo1D0dE130_provenance.
- NP821732.RA6oR4i_1PhU9u9SJeUtJhr2tR-Z_o2Sx4sFD-vJ3yAck130_assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821732.RA6oR4i_1PhU9u9SJeUtJhr2tR-Z_o2Sx4sFD-vJ3yAck130_provenance.
- NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410197.RA2rAL0_wVBNsG6aNhJZQX0eFyApW0wXpxz7HH0ISGTI0130_provenance.
- NP556107.RA-rKr7pzueuXpCk5LLJBwXkEuwOVqKPKnTkKWit577Bo130_assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556107.RA-rKr7pzueuXpCk5LLJBwXkEuwOVqKPKnTkKWit577Bo130_provenance.
- assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by mutations in the FOXP3 gene that result in the defective development of CD4+CD25+ regulatory T cells which constitute an important T cell subset involved in immune homeostasis and protection against autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.