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Methods in Molecular Biology (Clifton, N.J.)|August 6, 2010
Loss-of-function studies in mouse embryonic stem cells using the pHYPER shRNA plasmid vectorSoizik Berlivet, Martin Houlard, Matthieu Gérard
Biotechniques|July 7, 2007
pHYPER, a shRNA vector for high-efficiency RNA interference in embryonic stem cellsSoizik Berlivet, Virginie Guiraud, Martin Houlard, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 5, 2017
Efficient Depletion of Essential Gene Products for Loss-of-Function Studies in Embryonic Stem CellsSoizik Berlivet, Isabelle Hmitou, Hélène Picaud, et al.
Genome Research|August 2, 2011
Histone H3 trimethylation at lysine 36 is associated with constitutive and facultative heterochromatinSophie Chantalat, Arnaud Depaux, Patrick Héry, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal miceJun Ren, Syann Lee, Silvia Pagliardini, et al.
Plos Genetics|November 7, 2006
CAF-1 is essential for heterochromatin organization in pluripotent embryonic cellsMartin Houlard, Soizik Berlivet, Aline V Probst, et al.
Journal of Molecular Biology|April 2, 2008
Regulation of RNA polymerase III transcription by Maf1 in mammalian cellsSarah J Goodfellow, Emma L Graham, Theodoros Kantidakis, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|September 12, 2019
Urinary ketone body loss leads to degeneration of brain white matter in elderly SLC5A8-deficient miceLaurent Suissa, Virginie Flachon, Jean-Marie Guigonis, et al.
Neurobiology of Aging|February 28, 2012
Capucin does not modify the toxicity of a mutant Huntingtin fragment in vivoLaurie Galvan, Nad'a Lepejová, Marie-Claude Gaillard, et al.
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