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Structure and mechanism of the human NHE1-CHP1 complex.
Dong Y, Gao Y, Ilie A, Kim D, Boucher A, Li B, Zhang XC, Orlowski J, Zhao Y. Dong Y, et al. Among authors: ilie a. Nat Commun. 2021 Jun 9;12(1):3474. doi: 10.1038/s41467-021-23496-z. Nat Commun. 2021. PMID: 34108458 Free PMC article.
Structural basis of autoinhibition of the human NHE3-CHP1 complex.
Dong Y, Li H, Ilie A, Gao Y, Boucher A, Zhang XC, Orlowski J, Zhao Y. Dong Y, et al. Among authors: ilie a. Sci Adv. 2022 May 27;8(21):eabn3925. doi: 10.1126/sciadv.abn3925. Epub 2022 May 25. Sci Adv. 2022. PMID: 35613257 Free PMC article.
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation.
Khayat W, Hackett A, Shaw M, Ilie A, Dudding-Byth T, Kalscheuer VM, Christie L, Corbett MA, Juusola J, Friend KL, Kirmse BM, Gecz J, Field M, Orlowski J. Khayat W, et al. Among authors: ilie a. Hum Mol Genet. 2019 Feb 15;28(4):598-614. doi: 10.1093/hmg/ddy371. Hum Mol Genet. 2019. PMID: 30335141 Free PMC article.
15 results