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International Journal of Molecular Sciences|February 11, 2023
Dietary-Induced Bacterial Metabolites Reduce Inflammation and Inflammation-Associated Cancer via Vitamin D PathwayCaitlin O'Mahony, Adam Clooney, Siobhan F Clarke, et al.Biological Reviews of the Cambridge Philosophical Society|February 9, 2021
How fire interacts with habitat loss and fragmentationDon A Driscoll, Dolors Armenteras, Andrew F Bennett, et al.Neuromuscular Disorders : NMD|March 16, 2010
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathyRachel D Susman, Susana Quijano-Roy, Nan Yang, et al.Nature Biotechnology|November 15, 2011
Single-cell dissection of transcriptional heterogeneity in human colon tumorsPiero Dalerba, Tomer Kalisky, Debashis Sahoo, et al.Redox Biology|September 14, 2021
Genetic screening reveals phospholipid metabolism as a key regulator of the biosynthesis of the redox-active lipid coenzyme QAnita Ayer, Daniel J Fazakerley, Cacang Suarna, et al.Journal of Neuromuscular Diseases|November 18, 2016
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 CasesJaya Punetha, Akanchha Kesari, Prech Uapinyoying, et al.Annals of Neurology|June 14, 2008
De novo LMNA mutations cause a new form of congenital muscular dystrophySusana Quijano-Roy, Blaise Mbieleu, Carsten G Bönnemann, et al.Intensive Care Medicine|September 12, 2013
Physicians declining patient enrollment in a critical care trial: a case study in thromboprophylaxisD Cook, Y Arabi, N Ferguson, et al.Annals of Neurology|September 30, 2015
TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotypeS Donkervoort, M Papadaki, J M de Winter, et al.Human Molecular Genetics|August 22, 2015
Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficienciesBiljana Ilkovski, Alistair T Pagnamenta, Gina L O'Grady, et al.Pageof 83