X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
By R. Wildin, F. Ramsdell, J. Peake, F. Faravelli, J. Casanova, N. Buist, E. Levy-Lahad, M. Mazzella, O. Goulet, L. Perroni and 6 more. Nature Genetics, 2001
2,018 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology, Surgery
View Paper: https://www.semanticscholar.org/paper/e3968a79a4a86db29843c3260ff23de0c765632e
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Citations in the corpus
- Treg cells expressing the co-inhibitory molecule TIGIT selectively inhibit pro-inflammatory Th1 and Th17 cell responses (2014, background): “Other regulatory populations also contribute to this balance, but Foxp3+ Treg cells are critical for maintaining immune homeostasis as demon- strated by the devastating multiorgan autoimmune disease caused by genetic deficiencies in Foxp3 (Brunkow et al., 2001; Wildin et al., 2001).”
- Control of regulatory T cell lineage commitment and maintenance (2009, background): “…identify the genetic basis for the autoimmune disorder in human patients suffering from IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome and in the spontaneous mouse mutant scurfy (Bennett et al., 2001; Brunkow et al., 2001; Chatila et al., 2000; Wildin et al., 2001).”