Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD)

Por Jones, Takako I., Parilla, Megan, Jones, Peter L.
Publicado no PLoS One (2016)

Facioscapulohumeral Muscular Dystrophy As a Model for Epigenetic Regulation and Disease

Por Himeda, Charis L., Jones, Takako I., Jones, Peter L.
Publicado no Antioxid Redox Signal (2015)

CRISPR/dCas9-mediated Transcriptional Inhibition Ameliorates the Epigenetic Dysregulation at D4Z4 and Represses DUX4-fl in FSH Muscular Dystrophy

Por Himeda, Charis L, Jones, Takako I, Jones, Peter L
Publicado no Mol Ther (2016)

Scalpel or Straitjacket: CRISPR/Cas9 Approaches for Muscular Dystrophies

Por Himeda, Charis L., Jones, Takako I., Jones, Peter L.
Publicado no Trends Pharmacol Sci (2016)

Myogenic Enhancers Regulate Expression of the Facioscapulohumeral Muscular Dystrophy-Associated DUX4 Gene

Por Himeda, Charis L., Debarnot, Céline, Homma, Sachiko, Beermann, Mary Lou, Miller, Jeffrey B., Jones, Peter L., Jones, Takako I.
Publicado em 2014

Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein

Por Hanel, Meredith L., Sun, Chia-Yun Jessica, Jones, Takako I., Long, Steven W., Zanotti, Simona, Milner, Derek, Jones, Peter L.
Publicado em 2011

Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing

Por 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
Publicado no Clin Epigenetics (2014)

Human skeletal muscle xenograft as a new preclinical model for muscle disorders

Por Zhang, Yuanfan, King, Oliver D., Rahimov, Fedik, Jones, Takako I., Ward, Christopher W., Kerr, Jaclyn P., Liu, Naili, Emerson, Charles P., Kunkel, Louis M., Partridge, Terence A., Wagner, Kathryn R.
Publicado em 2014

Facioscapulohumeral muscular dystrophy region gene 1 (FRG1) is a dynamic RNA-associated and actin bundling protein

Por Jessica Sun, Chia-Yun, van Koningsbruggen, Silvana, Long, Steven W., Straasheijm, Kirsten, Klooster, Rinse, Jones, Takako I., Bellini, Michel, Levesque, Lyne, Brieher, William M., van der Maarel, Silvère M., Jones, Peter L.
Publicado em 2011

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

Por Jones, Takako I, King, Oliver D, Himeda, Charis L, Homma, Sachiko, Chen, Jennifer C J, Beermann, Mary Lou, Yan, Chi, Emerson, Charles P, Miller, Jeffrey B, Wagner, Kathryn R, Jones, Peter L
Publicado no Clin Epigenetics (2015)

Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2

Por Mitsuhashi, Satomi, Boyden, Steven E, Estrella, Elicia A, Jones, Takako I, Rahimov, Fedik, Yu, Timothy W, Darras, Basil T, Amato, Anthony A, Folkerth, Rebecca D, Jones, Peter L, Kunkel, Louis M, Kang, Peter B
Publicado em 2013