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Peter L Jones

Showing results (51-60 of 71) with videos related to

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Circulation Research|December 20, 2012
Myeloid cell 5-lipoxygenase activating protein modulates the response to vascular injuryZhou Yu, Emanuela Ricciotti, Takashi Miwa, et al.
Nature Genetics|February 8, 2005
Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencingK N Harikrishnan, Maggie Z Chow, Emma K Baker, et al.
Experimental Neurology|July 16, 2019
Muscle xenografts reproduce key molecular features of facioscapulohumeral muscular dystrophyAmber L Mueller, Andrea O'Neill, Takako I Jones, et al.
Pulmonary Circulation|July 10, 2014
Erythropoietin upregulation in pulmonary arterial hypertensionVanesa A Karamanian, Michael Harhay, Gregory R Grant, et al.
Circulation|February 2, 2011
Microsomal prostaglandin e2 synthase-1 modulates the response to vascular injuryMiao Wang, Kaori Ihida-Stansbury, Devashish Kothapalli, et al.
Pulmonary Circulation|June 12, 2015
Role played by Prx1-dependent extracellular matrix properties in vascular smooth muscle development in embryonic lungsKaori Ihida-Stansbury, Juliana Ames, Mithil Chokshi, et al.
Journal of Molecular Biology|June 25, 2011
Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling proteinChia-Yun Jessica Sun, Silvana van Koningsbruggen, Steven W Long, et al.
Clinical Epigenetics|April 24, 2015
Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophyTakako I Jones, Oliver D King, Charis L Himeda, et al.
Neuromuscular Disorders : NMD|October 17, 2013
Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2Satomi Mitsuhashi, Steven E Boyden, Elicia A Estrella, et al.
Human Molecular Genetics|July 17, 2012
Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesisTakako Iida Jones, Jennifer C J Chen, Fedik Rahimov, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Circulation Research|December 20, 2012
Myeloid cell 5-lipoxygenase activating protein modulates the response to vascular injuryZhou Yu, Emanuela Ricciotti, Takashi Miwa, et al.
Nature Genetics|February 8, 2005
Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencingK N Harikrishnan, Maggie Z Chow, Emma K Baker, et al.
Experimental Neurology|July 16, 2019
Muscle xenografts reproduce key molecular features of facioscapulohumeral muscular dystrophyAmber L Mueller, Andrea O'Neill, Takako I Jones, et al.
Pulmonary Circulation|July 10, 2014
Erythropoietin upregulation in pulmonary arterial hypertensionVanesa A Karamanian, Michael Harhay, Gregory R Grant, et al.
Circulation|February 2, 2011
Microsomal prostaglandin e2 synthase-1 modulates the response to vascular injuryMiao Wang, Kaori Ihida-Stansbury, Devashish Kothapalli, et al.
Pulmonary Circulation|June 12, 2015
Role played by Prx1-dependent extracellular matrix properties in vascular smooth muscle development in embryonic lungsKaori Ihida-Stansbury, Juliana Ames, Mithil Chokshi, et al.
Journal of Molecular Biology|June 25, 2011
Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling proteinChia-Yun Jessica Sun, Silvana van Koningsbruggen, Steven W Long, et al.
Clinical Epigenetics|April 24, 2015
Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophyTakako I Jones, Oliver D King, Charis L Himeda, et al.
Neuromuscular Disorders : NMD|October 17, 2013
Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2Satomi Mitsuhashi, Steven E Boyden, Elicia A Estrella, et al.
Human Molecular Genetics|July 17, 2012
Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesisTakako Iida Jones, Jennifer C J Chen, Fedik Rahimov, et al.
Pageof 8