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T Warren

Showing results (231-240 of 471) with videos related to

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Nucleus (Austin, Tex.)|September 28, 2016
Disruption of PCNA-lamins A/C interactions by prelamin A induces DNA replication fork stallingAndrew M Cobb, Thomas V Murray, Derek T Warren, et al.
Mechanisms of Development|February 19, 2002
A quantitative analysis of the kinetics of Gal4 activator and effector gene expression in the zebrafishNico Scheer, Iris Riedl, J T Warren, et al.
Human Molecular Genetics|October 23, 2003
Phosphorylation influences the translation state of FMRP-associated polyribosomesStephanie Ceman, William T O'Donnell, Matt Reed, et al.
Cells|November 18, 2016
Prelamin A Accumulation Attenuates Rac1 Activity and Increases the Intrinsic Migrational Persistence of Aged Vascular Smooth Muscle CellsLauren J Porter, Mark R Holt, Daniel Soong, et al.
Human Molecular Genetics|May 31, 2014
Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequencesJoshua A Suhl, Pankaj Chopra, Bart R Anderson, et al.
Journal of Medical Genetics|August 1, 1997
The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typingC B Kunst, E P Leeflang, J C Iber, et al.
Neurobiology of Disease|September 25, 2002
Gene expression profiles in a transgenic animal model of fragile X syndromeVelia D'Agata, Stephen T Warren, Weiqin Zhao, et al.
The Journal of Biological Chemistry|October 29, 2009
Novel nuclear nesprin-2 variants tether active extracellular signal-regulated MAPK1 and MAPK2 at promyelocytic leukemia protein nuclear bodies and act to regulate smooth muscle cell proliferationDerek T Warren, Tamara Tajsic, Jason A Mellad, et al.
BMC Medical Genetics|January 30, 2013
Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locusReid S Alisch, Tao Wang, Pankaj Chopra, et al.
Developmental Biology|September 20, 2000
The mutation without children(rgl) causes ecdysteroid deficiency in third-instar larvae of Drosophila melanogasterJ Wismar, N Habtemichael, J T Warren, et al.
Pageof 48

Showing results (231-240 of 471) with videos related to

Sort By:
Pageof 48
Nucleus (Austin, Tex.)|September 28, 2016
Disruption of PCNA-lamins A/C interactions by prelamin A induces DNA replication fork stallingAndrew M Cobb, Thomas V Murray, Derek T Warren, et al.
Mechanisms of Development|February 19, 2002
A quantitative analysis of the kinetics of Gal4 activator and effector gene expression in the zebrafishNico Scheer, Iris Riedl, J T Warren, et al.
Human Molecular Genetics|October 23, 2003
Phosphorylation influences the translation state of FMRP-associated polyribosomesStephanie Ceman, William T O'Donnell, Matt Reed, et al.
Cells|November 18, 2016
Prelamin A Accumulation Attenuates Rac1 Activity and Increases the Intrinsic Migrational Persistence of Aged Vascular Smooth Muscle CellsLauren J Porter, Mark R Holt, Daniel Soong, et al.
Human Molecular Genetics|May 31, 2014
Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequencesJoshua A Suhl, Pankaj Chopra, Bart R Anderson, et al.
Journal of Medical Genetics|August 1, 1997
The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typingC B Kunst, E P Leeflang, J C Iber, et al.
Neurobiology of Disease|September 25, 2002
Gene expression profiles in a transgenic animal model of fragile X syndromeVelia D'Agata, Stephen T Warren, Weiqin Zhao, et al.
The Journal of Biological Chemistry|October 29, 2009
Novel nuclear nesprin-2 variants tether active extracellular signal-regulated MAPK1 and MAPK2 at promyelocytic leukemia protein nuclear bodies and act to regulate smooth muscle cell proliferationDerek T Warren, Tamara Tajsic, Jason A Mellad, et al.
BMC Medical Genetics|January 30, 2013
Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locusReid S Alisch, Tao Wang, Pankaj Chopra, et al.
Developmental Biology|September 20, 2000
The mutation without children(rgl) causes ecdysteroid deficiency in third-instar larvae of Drosophila melanogasterJ Wismar, N Habtemichael, J T Warren, et al.
Pageof 48