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Nature Communications|April 18, 2026
Wastewater intelligence predicts the emergence of clinically-relevant and drug-resistant Candidozyma auris at healthcare facilitiesChing-Lan Chang, Michael A Moshi, Quang-Huy Nguyen, et al.
Medrxiv : the Preprint Server for Health Sciences|August 6, 2025
Wastewater intelligence predicts the emergence of clinically-relevant and drug-resistant Candida auris at healthcare facilitiesChing-Lan Chang, Michael A Moshi, Quang-Huy Nguyen, et al.
Journal of Cancer Prevention|October 23, 2014
Correlations among endoscopic, histologic and serologic diagnoses for the assessment of atrophic gastritisJu Yup Lee, Nayoung Kim, Hye Seung Lee, et al.
Nutrients|April 28, 2025
Myths and Facts Regarding Low-Carbohydrate DietsNina Teicholz, Steven M Croft, Ignacio Cuaranta, et al.
Journal of Cancer Prevention|October 23, 2014
Risk factors of atrophic gastritis and intestinal metaplasia in first-degree relatives of gastric cancer patients compared with age-sex matched controlsSooyeon Oh, Nayoung Kim, Hyuk Yoon, et al.
American Journal of Human Genetics|November 20, 2012
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndromeJanneke H M Schuurs-Hoeijmakers, Edwin C Oh, Lisenka E L M Vissers, et al.
The Journal of Biological Chemistry|February 8, 2026
Cytomegalovirus (CMV)-encoded immediate early 1 (IE1) protein perturbs neural progenitor proliferation via interfering with host PML-DISC1 interactionAtsushi Saito, Stephanie Tankou, Kazuhiro Ishii, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
DISC1-PML protein interaction for congenital CMV infection-induced cortical neural progenitor deficit: perturbance of host signaling via viral IE1Atsushi Saito, Stephanie Tankou, Kazuhiro Ishii, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 2013
Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease geneKoji M Nishiguchi, Richard G Tearle, Yangfan P Liu, et al.
American Journal of Human Genetics|May 5, 2015
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 PathologyEugenia Migliavacca, Christelle Golzio, Katrin Männik, et al.
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