A cre-inducible DUX4 transgenic mouse model for investigating facioscapulohumeral muscular dystrophy von Jones, Takako, Jones, Peter L

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CRISPR/dCas9-mediated Transcriptional Inhibition Ameliorates the Epigenetic Dysregulation at D4Z4 and Represses DUX4-fl in FSH Muscular Dystrophy von Himeda, Charis L, Jones, Takako I, Jones, Peter L

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The Genetics and Epigenetics of Facioscapulohumeral Muscular Dystrophy von Himeda, Charis L, Jones, Peter L

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Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia von El-Osta, Assam, Brasacchio, Daniella, Yao, Dachun, Pocai, Alessandro, Jones, Peter L, Roeder, Robert G, Cooper, Mark E, Brownlee, Michael

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Identification of candidate miRNA biomarkers for facioscapulohumeral muscular dystrophy using DUX4-based mouse models von Nunes, Andreia M, Ramirez, Monique, Jones, Takako I, Jones, Peter L

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Targeted epigenetic repression by CRISPR/dSaCas9 suppresses pathogenic DUX4-fl expression in FSHD von Himeda, Charis L., Jones, Takako I., Jones, Peter L.

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Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD) von Jones, Takako I, Parilla, Megan, Jones, Peter L

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Myogenic Enhancers Regulate Expression of the Facioscapulohumeral Muscular Dystrophy-Associated DUX4 Gene von Himeda, Charis L., Debarnot, Céline, Homma, Sachiko, Beermann, Mary Lou, Miller, Jeffrey B., Jones, Peter L., Jones, Takako I.

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Emerging preclinical animal models for FSHD von Lek, Angela, Rahimov, Fedik, Jones, Peter L, Kunkel, Louis M

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Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity von Jones, Takako I, Chew, Guo-Liang, Barraza-Flores, Pamela, Schreier, Spencer, Ramirez, Monique, Wuebbles, Ryan D, Burkin, Dean J, Bradley, Robert K, Jones, Peter L

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Precise Epigenetic Analysis Using Targeted Bisulfite Genomic Sequencing Distinguishes FSHD1, FSHD2, and Healthy Subjects von Gould, Taylor, Jones, Takako I., Jones, Peter L.

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Functional CpG Methylation System in a Social Insect von Wang, Ying, Jorda, Mireia, Jones, Peter L, Maleszka, Ryszard, Ling, Xu, Robertson, Hugh M, Mizzen, Craig A, Peinado, Miguel A, Robinson, Gene E

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mTOR is required for pulmonary arterial vascular smooth muscle cell proliferation under chronic hypoxia von Krymskaya, Vera P., Snow, Jennifer, Cesarone, Gregory, Khavin, Irene, Goncharov, Dmitry A., Lim, Poay N., Veasey, Sigrid C., Ihida‐Stansbury, Kaori, Jones, Peter L., Goncharova, Elena A.

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Temporal uncoupling of the DNA methylome and transcriptional repression during embryogenesis von Bogdanovic, Ozren, Long, Steven W, van Heeringen, Simon J, Brinkman, Arie B, Gómez-Skarmeta, Jose Luis, Stunnenberg, Hendrik G, Jones, Peter L, Veenstra, Gert Jan C

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Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing von Jones, Takako I, Yan, Chi, Sapp, Peter C, McKenna-Yasek, Diane, Kang, Peter B, Quinn, Colin, Salameh, Johnny S, King, Oliver D, Jones, Peter L

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription von Wolffe, Alan P, Jones, Peter L, Jan Veenstra, Gert C, Wade, Paul A, Vermaak, Danielle, Kass, Stefan U, Landsberger, Nicoletta, Strouboulis, John

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Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis von LIDA JONES, Takako, CHEN, Jennifer C. J, WAGNER, Kathryn R, JONES, Peter L, RAHIMOV, Fedik, HOMMA, Sachiko, ARASHIRO, Patricia, BEERMANN, Mary Lou, KING, Oliver D, MILLER, Jeffrey B, KUNKEL, Louis M, EMERSON, Charles P

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Human DUX4 and porcine DUXC activate similar early embryonic programs in pig muscle cells: implications for preclinical models of FSHD von Nip, Yee, Bennett, Sean R, Smith, Andrew A, Jones, Takako I, Jones, Peter L, Tapscott, Stephen J

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Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy von Nunes, Andreia M, Ramirez, Monique M, Garcia-Collazo, Enrique, Jones, Takako Iida, Jones, Peter L

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Muscular dystrophy candidate gene FRG1 is critical for muscle development von Hanel, Meredith L., Wuebbles, Ryan D., Jones, Peter L.

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