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C
Frietze KK, Pappy AL, Melson JW, O'Driscoll EE, Tyler CM, Perlman DH, et al. Cryptic protein-protein interaction motifs in the cytoplasmic domain of MHCI proteins. BMC Immunol. 2016 ;17(1):24.
Koch IJanowitz, Clark MM, Thompson MJ, Deere-Machemer KA, Wang J, Duarte L, et al. The concerted impact of domestication and transposon insertions on methylation patterns between dogs and grey wolves. Mol Ecol. 2016 ;25(8):1838-55.
Lee Y-S, Krishnan A, Oughtred R, Rust J, Chang CS, Ryu J, et al. A Computational Framework for Genome-wide Characterization of the Human Disease Landscape. Cell Syst. 2019 ;8(2):152-162.e6.
Jonikas MC, Collins SR, Denic V, Oh E, Quan EM, Schmid V, et al. Comprehensive characterization of genes required for protein folding in the endoplasmic reticulum. Science. 2009 ;323(5922):1693-7.
Armitage JP, Becker A, Christie PJ, de Boer PAJ, DiRita VJ, Gourse RL, et al. Classic Spotlights: Selected Highlights from the First 100 Years of the . J Bacteriol. 2017 ;199(13).
Deverett B, Koay SAnn, Oostland M, Wang SS-H. Cerebellar involvement in an evidence-accumulation decision-making task. Elife. 2018 ;7.
Giovannucci A, Badura A, Deverett B, Najafi F, Pereira TD, Gao Z, et al. Cerebellar granule cells acquire a widespread predictive feedback signal during motor learning. Nat Neurosci. 2017 ;20(5):727-734.
Oberstein A, Shenk T. Cellular responses to human cytomegalovirus infection: Induction of a mesenchymal-to-epithelial transition (MET) phenotype. Proc Natl Acad Sci U S A. 2017 ;114(39):E8244-E8253.
Hjeij R, Onoufriadis A, Watson CM, Slagle CE, Klena NT, Dougherty GW, et al. CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation. Am J Hum Genet. 2014 ;95(3):257-74.
Hjeij R, Onoufriadis A, Watson CM, Slagle CE, Klena NT, Dougherty GW, et al. CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation. Am J Hum Genet. 2014 ;95(3):257-74.
Hjeij R, Onoufriadis A, Watson CM, Slagle CE, Klena NT, Dougherty GW, et al. CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation. Am J Hum Genet. 2014 ;95(3):257-74.
B
Jang C, Oh SF, Wada S, Rowe GC, Liu L, Chan MChun, et al. A branched-chain amino acid metabolite drives vascular fatty acid transport and causes insulin resistance. Nat Med. 2016 ;22(4):421-6.
Oslund RC, Su X, Haugbro M, Kee J-M, Esposito M, David Y, et al. Bisphosphoglycerate mutase controls serine pathway flux via 3-phosphoglycerate. Nat Chem Biol. 2017 ;13(10):1081-1087.
Ochoa A, Storey JD, Llinás M, Singh M. Beyond the E-Value: Stratified Statistics for Protein Domain Prediction. PLoS Comput Biol. 2015 ;11(11):e1004509.
A
Shrine N, Guyatt AL, A Erzurumluoglu M, Jackson VE, Hobbs BD, Melbourne CA, et al. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat Genet. 2019 ;51(6):1067.
Okada BK, Seyedsayamdost MR. Antibiotic dialogues: induction of silent biosynthetic gene clusters by exogenous small molecules. FEMS Microbiol Rev. 2017 ;41(1):19-33.
Orman MA, Henry TC, DeCoste CJ, Brynildsen MP. Analyzing Persister Physiology with Fluorescence-Activated Cell Sorting. Methods Mol Biol. 2016 ;1333:83-100.
Orman MA, Mok WWK, Brynildsen MP. Aminoglycoside-enabled elucidation of bacterial persister metabolism. Curr Protoc Microbiol. 2015 ;36:17.9.1-17.9.14.