Matches in Nanopublications for { ?s ?p "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520153.RAipMKi5ch2aoUX8VIgNh2u2XLYpSTV4C9GBywGYkwoq0130_provenance.
- NP623871.RAW-hv7ELgiri73T5SOW64xvMIP116fE2XphsSdV7DDk4130_assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623871.RAW-hv7ELgiri73T5SOW64xvMIP116fE2XphsSdV7DDk4130_provenance.
- assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP801656.RABck1aXQN073yC3JiAsghrHZf9AwSrTM-I46g0fn7diw130_assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801656.RABck1aXQN073yC3JiAsghrHZf9AwSrTM-I46g0fn7diw130_provenance.
- NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899432.RAsAgmOLAlzT-PTGPPG_ZZj1kfKnwCi9Sk_t_OmZjfo7c130_provenance.
- NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801655.RAi_yWYvuxel3K7bSHbhUYJq8vbPp6gRo8eqjt5dkeBA4130_provenance.
- NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_assertion description "[Patients with IPEX (immune dysfunction, polyendocrinopathy, enteropathy, X-linked) syndrome harbor mutations in the forkhead box P3 (FOXP3) gene in regulatory T cells, which leads to severe autoimmunity and immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899442.RA6dc_IwT63yUeKOKC-ivYC2n_VyVv2wEx1x4f4L6HiRs130_provenance.