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Human Mutation|August 23, 2020
Renal dysfunction, rod-cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2BLisa Roberts, Stephanie Julius, Shrinav Dawlat, et al.Human Molecular Genetics|May 29, 2015
Epigenetic changes as a common trigger of muscle weakness in congenital myopathiesOri Rokach, Marijana Sekulic-Jablanovic, Nicol Voermans, et al.Journal of the National Cancer Institute|January 31, 2008
Predictive value of tumor Ki-67 expression in two randomized trials of adjuvant chemoendocrine therapy for node-negative breast cancerGiuseppe Viale, Meredith M Regan, Mauro G Mastropasqua, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 20, 2008
Chemoendocrine compared with endocrine adjuvant therapies for node-negative breast cancer: predictive value of centrally reviewed expression of estrogen and progesterone receptors--International Breast Cancer Study GroupGiuseppe Viale, Meredith M Regan, Eugenio Maiorano, et al.American Journal of Human Genetics|November 26, 2013
Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosisSandra Mercier, Sébastien Küry, Gasnat Shaboodien, et al.American Journal of Respiratory and Critical Care Medicine|January 16, 2024
SARS-CoV-2 Viral Replication Persists in the Human Lung for Several Weeks after Symptom OnsetMichele Tomasicchio, Shameem Jaumdally, Lindsay Wilson, et al.Pageof 5