Burns M, Amaya A, Bodi C, et al. Helicobacter pylori infection and low dietary iron alter behavior, induce iron deficiency anemia, and modulate hippocampal gene expression in female C57BL/6 mice. PLoS One. 2017;12(3):e0173108. doi:10.1371/journal.pone.0173108.

Kamer KJ, Grabarek Z, Mootha VK. High-affinity cooperative Ca binding by MICU1-MICU2 serves as an on-off switch for the uniporter. EMBO Rep. 2017;18(8):1397-1411. doi:10.15252/embr.201643748.

Kamer KJ, Sancak Y, Fomina Y, et al. MICU1 imparts the mitochondrial uniporter with the ability to discriminate between Ca and Mn. Proc Natl Acad Sci U S A. 2018;115(34):E7960-E7969. doi:10.1073/pnas.1807811115.

Nakata T, Creasey EA, Kadoki M, et al. A missense variant in confers risk for Crohn’s disease by disrupting manganese homeostasis and intestinal barrier integrity. Proc Natl Acad Sci U S A. 2020;117(46):28930-28938. doi:10.1073/pnas.2014742117.

Bick AG, Calvo SE, Mootha VK. Evolutionary diversity of the mitochondrial calcium uniporter. Science. 2012;336(6083):886. doi:10.1126/science.1214977.

Perocchi F, Gohil VM, Girgis HS, et al. MICU1 encodes a mitochondrial EF hand protein required for Ca(2+) uptake. Nature. 2010;467(7313):291-6. doi:10.1038/nature09358.

Plovanich M, Bogorad RL, Sancak Y, et al. MICU2, a paralog of MICU1, resides within the mitochondrial uniporter complex to regulate calcium handling. PLoS One. 2013;8(2):e55785. doi:10.1371/journal.pone.0055785.

Sancak Y, Markhard AL, Kitami T, et al. EMRE is an essential component of the mitochondrial calcium uniporter complex. Science. 2013;342(6164):1379-82. doi:10.1126/science.1242993.

Tukiainen T, Pirinen M, Sarin A-P, et al. Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation. PLoS Genet. 2014;10(2):e1004127. doi:10.1371/journal.pgen.1004127.

Flannick J, Thorleifsson G, Beer NL, et al. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat Genet. 2014;46(4):357-63. doi:10.1038/ng.2915.