Bazua-Valenti S, Brown MR, Zavras J, et al. Disrupted uromodulin trafficking is rescued by targeting TMED cargo receptors. The Journal of clinical investigation. 2024;134(24). doi:10.1172/JCI180347
Tahir UA, Barber JL, Cruz DE, et al. Proteogenomic analysis integrated with electronic health records data reveals disease-associated variants in Black Americans. The Journal of clinical investigation. 2024;134(21). doi:10.1172/JCI181802
Maio N, Orbach R, Zaharieva IT, et al. CIAO1 loss of function causes a neuromuscular disorder with compromise of nucleocytoplasmic Fe-S enzymes. The Journal of clinical investigation. 2024;134(12). doi:10.1172/JCI179559
Li Y, Ma K, Dong Z, et al. Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models. The Journal of clinical investigation. 2024;134(12). doi:10.1172/JCI177172
Szot JO, Cuny H, Martin EM, et al. A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder. The Journal of clinical investigation. 2024;134(4). doi:10.1172/JCI174824
Lofrano-Porto A, Pereira SA, Dauber A, et al. OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivity. The Journal of clinical investigation. 2023;133(23). doi:10.1172/JCI161701
Fletcher SC, Hall C, Kennedy TJ, et al. Impaired protein hydroxylase activity causes replication stress and developmental abnormalities in humans. The Journal of clinical investigation. 2023;133(7). doi:10.1172/JCI152784