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Daniel G Miller

Showing results (41-50 of 49) with videos related to

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Stem Cells and Development|February 5, 2010
Characterization of microRNAs involved in embryonic stem cell statesBradford Stadler, Irena Ivanovska, Kshama Mehta, et al.
Plos Genetics|November 7, 2017
Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cellsMinseung Choi, Diane P Genereux, Jamie Goodson, et al.
Human Molecular Genetics|April 11, 2009
RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophyLauren Snider, Amy Asawachaicharn, Ashlee E Tyler, et al.
Annals of Emergency Medicine|July 17, 2021
The Rapid Evaluation of COVID-19 Vaccination in Emergency Departments for Underserved Patients StudyRobert M Rodriguez, Jesus R Torres, Anna Marie Chang, et al.
Plos One|April 13, 2022
Facemasks: Perceptions and use in an ED population during COVID-19Vidya Eswaran, Anna Marie Chang, R Gentry Wilkerson, et al.
Science (New York, N.Y.)|August 21, 2010
A unifying genetic model for facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, et al.
American Journal of Human Genetics|December 18, 2018
GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott SyndromeAmy J LaCroix, Deborah Stabley, Rebecca Sahraoui, et al.
Human Molecular Genetics|September 27, 2014
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2Richard J L F Lemmers, Jelle J Goeman, Patrick J van der Vliet, et al.
Nature Genetics|November 13, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Rabi Tawil, Lisa M Petek, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Stem Cells and Development|February 5, 2010
Characterization of microRNAs involved in embryonic stem cell statesBradford Stadler, Irena Ivanovska, Kshama Mehta, et al.
Plos Genetics|November 7, 2017
Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cellsMinseung Choi, Diane P Genereux, Jamie Goodson, et al.
Human Molecular Genetics|April 11, 2009
RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophyLauren Snider, Amy Asawachaicharn, Ashlee E Tyler, et al.
Annals of Emergency Medicine|July 17, 2021
The Rapid Evaluation of COVID-19 Vaccination in Emergency Departments for Underserved Patients StudyRobert M Rodriguez, Jesus R Torres, Anna Marie Chang, et al.
Plos One|April 13, 2022
Facemasks: Perceptions and use in an ED population during COVID-19Vidya Eswaran, Anna Marie Chang, R Gentry Wilkerson, et al.
Science (New York, N.Y.)|August 21, 2010
A unifying genetic model for facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, et al.
American Journal of Human Genetics|December 18, 2018
GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott SyndromeAmy J LaCroix, Deborah Stabley, Rebecca Sahraoui, et al.
Human Molecular Genetics|September 27, 2014
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2Richard J L F Lemmers, Jelle J Goeman, Patrick J van der Vliet, et al.
Nature Genetics|November 13, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Rabi Tawil, Lisa M Petek, et al.
Pageof 5