Below are the most recent publications written about "Genetic Techniques" by people in Profiles.
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Marion MC, Ramos PS, Bachali P, Labonte AC, Zimmerman KD, Ainsworth HC, Heuer SE, Robl RD, Catalina MD, Kelly JA, Howard TD, Lipsky PE, Grammer AC, Langefeld CD. Nucleic Acid-Sensing and Interferon-Inducible Pathways Show Differential Methylation in MZ Twins Discordant for Lupus and Overexpression in Independent Lupus Samples: Implications for Pathogenic Mechanism and Drug Targeting. Genes (Basel). 2021 11 26; 12(12).
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Anderson RI, Lopez MF, Griffin WC, Haun HL, Bloodgood DW, Pati D, Boyt KM, Kash TL, Becker HC. Dynorphin-kappa opioid receptor activity in the central amygdala modulates binge-like alcohol drinking in mice. Neuropsychopharmacology. 2019 05; 44(6):1084-1092.
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Peters J, Scofield MD, Reichel CM. Chemogenetic activation of the perirhinal cortex reverses methamphetamine-induced memory deficits and reduces relapse. Learn Mem. 2018 09; 25(9):410-415.
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Mueller LD, Phillips MA, Barter TT, Greenspan ZS, Rose MR. Genome-Wide Mapping of Gene-Phenotype Relationships in Experimentally Evolved Populations. Mol Biol Evol. 2018 08 01; 35(8):2085-2095.
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Jones ME, Paniccia JE, Lebonville CL, Reissner KJ, Lysle DT. Chemogenetic Manipulation of Dorsal Hippocampal Astrocytes Protects Against the Development of Stress-enhanced Fear Learning. Neuroscience. 2018 09 15; 388:45-56.
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Krishna I, Badell M, Loucks TL, Lindsay M, Samuel A. Adverse perinatal outcomes are more frequent in pregnancies with a low fetal fraction result on noninvasive prenatal testing. Prenat Diagn. 2016 Mar; 36(3):210-5.
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Cooper LA, Kong J, Gutman DA, Dunn WD, Nalisnik M, Brat DJ. Novel genotype-phenotype associations in human cancers enabled by advanced molecular platforms and computational analysis of whole slide images. Lab Invest. 2015 Apr; 95(4):366-76.
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Rose MR, Mueller LD, Burke MK. New experiments for an undivided genetics. Genetics. 2011 May; 188(1):1-10.
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Shtutman M, Maliyekkel A, Shao Y, Carmack CS, Baig M, Warholic N, Cole K, Broude EV, Harkins TT, Ding Y, Roninson IB. Function-based gene identification using enzymatically generated normalized shRNA library and massive parallel sequencing. Proc Natl Acad Sci U S A. 2010 Apr 20; 107(16):7377-82.
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Gonzalez JH, Shirali GS, Atz AM, Taylor SN, Forbus GA, Zyblewski SC, Hlavacek AM. Universal screening for extracardiac abnormalities in neonates with congenital heart disease. Pediatr Cardiol. 2009 Apr; 30(3):269-73.